Ligand source activities (1 row/activity)





Ligands (move mouse cursor over ligand name to see structure) Receptor Assay information Chemical information
Sel. page Common
name
GPCRdb
ID
#Vendors

Reference
ligand
Fold
selectivity
# Tested
GPCRs
Species

p-value
(-log)
Activity
Type
Activity
Relation
Activity
Value
AssayType

Assay
Description
Source

Mol
weight
Rot
Bonds
H don

H acc

LogP

Smiles

DOI

CHEMBL1627325 208811 0 None 1 8 Human 10.5 pEC50 = 10.5 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None CSCC[C@H](NC(=O)CNC(=O)[C@@H](NC(=O)CNC(=O)[C@@H](NC(=O)[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](N)CO)C(C)(C)C)C(C)C)[C@@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)O)[C@@H](C)O 10.1021/jm900604g
3812 717 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
439201 717 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
649 717 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
CHEMBL406291 717 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
DB12126 717 42 None -1 3 Human 10.3 pEC50 = 10.3 Functional
Antagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilizationAntagonist activity at human recombinant bradykinin 2 receptor expressed in CHO cells assessed as inhibition of bradykinin-induced intracellular calcium mobilization
ChEMBL None None None None 10.1021/jm900604g
9851817 9681 0 None - 1 Guinea pig 7.0 pEC50 = 7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL112991 9681 0 None - 1 Guinea pig 7.0 pEC50 = 7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
44340964 9707 0 None - 1 Guinea pig 6.0 pEC50 = 6.0 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113176 9707 0 None - 1 Guinea pig 6.0 pEC50 = 6.0 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44341039 9511 0 None - 1 Guinea pig 6.9 pEC50 = 6.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112140 9511 0 None - 1 Guinea pig 6.9 pEC50 = 6.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44340818 110609 0 None - 1 Guinea pig 5.9 pEC50 = 5.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL325624 110609 0 None - 1 Guinea pig 5.9 pEC50 = 5.9 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
18941161 9729 0 None - 1 Guinea pig 4.7 pEC50 = 4.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL113320 9729 0 None - 1 Guinea pig 4.7 pEC50 = 4.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
44341214 110430 0 None - 1 Guinea pig 6.7 pEC50 = 6.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL324575 110430 0 None - 1 Guinea pig 6.7 pEC50 = 6.7 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
18941160 9915 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114401 9915 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
44214279 9716 0 None - 1 Guinea pig 6.6 pEC50 = 6.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL113222 9716 0 None - 1 Guinea pig 6.6 pEC50 = 6.6 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
10895913 9869 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL114180 9869 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
9831859 9706 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL113169 9706 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10257108 9831 1 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
CHEMBL113963 9831 1 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
44340760 110508 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL324950 110508 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
22008916 9762 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL113502 9762 0 None - 1 Guinea pig 6.4 pEC50 = 6.4 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
44214619 110605 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
CHEMBL325601 110605 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
18941145 9963 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
CHEMBL114732 9963 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
22008929 9750 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113465 9750 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
22008895 110558 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL325255 110558 0 None - 1 Guinea pig 7.3 pEC50 = 7.3 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
44340859 10043 0 None - 1 Guinea pig 7.2 pEC50 = 7.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL115163 10043 0 None - 1 Guinea pig 7.2 pEC50 = 7.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44340951 10002 0 None - 1 Guinea pig 6.2 pEC50 = 6.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114915 10002 0 None - 1 Guinea pig 6.2 pEC50 = 6.2 Functional
Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)Inhibition of BK-induced (4x10E-8M) contraction of isolated guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
3812 717 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
439201 717 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
649 717 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
CHEMBL406291 717 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
DB12126 717 42 None -1 3 Human 8.8 pED50 = 8.8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None None 10.1021/jm00144a008
CHEMBL2372138 210189 0 None - 1 Human 8.0 pED50 = 8 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None [N-]=[N+]=Nc1ccc(C[C@H](NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C(=O)N[C@@H](CO)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)cc1 10.1021/jm00144a008
CHEMBL2372165 210193 0 None - 1 Human 7.7 pED50 = 7.7 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccc(N)cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372173 210196 0 None - 1 Human 7.6 pED50 = 7.6 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc([N+](=O)[O-])cc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372157 210191 0 None - 1 Human 7.6 pED50 = 7.6 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None N#[N+]c1ccc(C[C@H](NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)cc1 10.1021/jm00144a008
CHEMBL2372164 210192 0 None - 1 Human 7.6 pED50 = 7.6 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None N#[N+]c1ccc(C[C@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)cc1 10.1021/jm00144a008
CHEMBL2372172 210195 0 None - 1 Human 7.2 pED50 = 7.2 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(N)cc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372156 210190 0 None - 1 Human 8.2 pED50 = 8.2 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccc([N+](=O)[O-])cc1)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00144a008
CHEMBL2372168 210194 0 None - 1 Human 8.2 pED50 = 8.2 Functional
In vitro 50 % Maximal response in jugular vein expressing B2 receptorIn vitro 50 % Maximal response in jugular vein expressing B2 receptor
ChEMBL None None None [N-]=[N+]=Nc1ccc(C[C@H](NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)cc1 10.1021/jm00144a008
44191040 195984 0 None - 1 Human 9.3 pIC50 = 9.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559825 195984 0 None - 1 Human 9.3 pIC50 = 9.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
667 1973 37 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
71364 1973 37 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
CHEMBL2028850 1973 37 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
DB06196 1973 37 None 2 2 Guinea pig 9.0 pIC50 = 9.0 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None None 10.1021/jm00015a001
25019714 196583 2 None - 1 Human 9.0 pIC50 = 9.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL563956 196583 2 None - 1 Human 9.0 pIC50 = 9.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
45272156 195059 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL549534 195059 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
44190944 195933 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559436 195933 0 None - 1 Human 8.9 pIC50 = 8.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
44190263 195954 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
CHEMBL559565 195954 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
10327403 78585 0 None 1 2 Rat 8.7 pIC50 = 8.7 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78585 0 None 1 2 Rat 8.7 pIC50 = 8.7 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
9987299 78601 0 None 2 2 Rat 7.0 pIC50 = 7.0 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78601 0 None 2 2 Rat 7.0 pIC50 = 7.0 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190941 195431 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
CHEMBL552296 195431 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
10327403 78585 0 None -1 2 Human 7.9 pIC50 = 7.9 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78585 0 None -1 2 Human 7.9 pIC50 = 7.9 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190852 195406 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552090 195406 0 None - 1 Human 7.9 pIC50 = 7.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
44191220 195030 0 None - 1 Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL549337 195030 0 None - 1 Human 5.9 pIC50 = 5.9 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL2370243 209812 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None N=C(N)NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)c1ccc(CN2CCCNCCNCCCNCC2)cc1)c1cccs1)C(=O)O 10.1021/jm00015a001
10327403 78585 0 None 1 2 Rat 6.9 pIC50 = 6.9 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78585 0 None 1 2 Rat 6.9 pIC50 = 6.9 Functional
Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2Inhibition of increase in [Ca2+] efflux from NG108-15 cells caused by activation of rat Bradykinin receptor B2
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190672 195344 0 None - 1 Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551757 195344 0 None - 1 Human 5.8 pIC50 = 5.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
9987299 78601 0 None -2 2 Human 7.8 pIC50 = 7.8 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78601 0 None -2 2 Human 7.8 pIC50 = 7.8 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44189787 196344 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562434 196344 0 None - 1 Human 6.8 pIC50 = 6.8 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190853 196289 4 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
CHEMBL562097 196289 4 None - 1 Human 6.7 pIC50 = 6.7 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
44190850 195223 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL550827 195223 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
9987299 78601 0 None 2 2 Rat 8.6 pIC50 = 8.6 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78601 0 None 2 2 Rat 8.6 pIC50 = 8.6 Functional
Inhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscleInhibition of Bradykinin receptor B2-mediated contractions of rat uterus smooth muscle
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190851 196570 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563878 196570 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
44190854 195445 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL552384 195445 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
44190753 196703 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL564841 196703 0 None - 1 Human 7.6 pIC50 = 7.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
44190077 196470 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563254 196470 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190266 195456 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL552442 195456 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191138 195916 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559273 195916 0 None - 1 Human 5.6 pIC50 = 5.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190943 195953 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
CHEMBL559564 195953 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
45267862 196320 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL562296 196320 0 None - 1 Human 6.6 pIC50 = 6.6 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
44190751 195345 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
CHEMBL551758 195345 0 None - 1 Human 7.5 pIC50 = 7.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
44190942 196227 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
CHEMBL561634 196227 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
44190581 195944 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL559506 195944 0 None - 1 Human 8.4 pIC50 = 8.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
44190267 195136 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550143 195136 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190168 195118 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550016 195118 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191224 196261 0 None - 1 Human 5.5 pIC50 = 5.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561839 196261 0 None - 1 Human 5.5 pIC50 = 5.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191226 195302 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551435 195302 0 None - 1 Human 6.5 pIC50 = 6.5 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190361 194803 0 None - 1 Human 5.4 pIC50 = 5.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL538865 194803 0 None - 1 Human 5.4 pIC50 = 5.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44189789 196153 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561223 196153 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190167 196489 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563391 196489 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44189792 195135 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550142 195135 0 None - 1 Human 6.4 pIC50 = 6.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190752 195346 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
CHEMBL551759 195346 0 None - 1 Human 7.4 pIC50 = 7.4 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
44190165 195963 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559645 195963 0 None - 1 Human 6.3 pIC50 = 6.3 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
667 1973 37 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
71364 1973 37 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
CHEMBL2028850 1973 37 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
DB06196 1973 37 None 2 2 Guinea pig 8.3 pIC50 = 8.3 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig pulmonary artery assay.
ChEMBL None None None None 10.1021/jm00015a001
10327403 78585 0 None -1 2 Human 7.3 pIC50 = 7.3 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78585 0 None -1 2 Human 7.3 pIC50 = 7.3 Functional
Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)Antagonism of the [Ca2+] efflux actions of the human Bradykinin receptor B2 (WI38 fibroblasts)
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44189790 196642 0 None - 1 Human 5.2 pIC50 = 5.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564341 196642 0 None - 1 Human 5.2 pIC50 = 5.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190166 196634 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564294 196634 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190269 196196 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561415 196196 0 None - 1 Human 7.2 pIC50 = 7.2 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190756 195437 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552359 195437 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
44190268 196511 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563516 196511 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190754 196448 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563068 196448 0 None - 1 Human 7.1 pIC50 = 7.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
44191223 196267 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561899 196267 0 None - 1 Human 6.1 pIC50 = 6.1 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL2370243 209812 0 None - 1 Guinea pig 8.1 pIC50 = 8.1 Functional
In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.In vitro antagonistic activity for Bradykinin receptor B2 by guinea pig ileal membrane receptor assay.
ChEMBL None None None N=C(N)NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)c1ccc(CN2CCCNCCNCCCNCC2)cc1)c1cccs1)C(=O)O 10.1021/jm00015a001
9987299 78601 0 None -2 2 Human 7.0 pIC50 = 7.0 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78601 0 None -2 2 Human 7.0 pIC50 = 7.0 Functional
Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)Antagonism of the [Ca2+] efflux actions of human Bradykinin receptor B2 (SK-N-SH neuroblastoma)
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44190755 195827 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL558279 195827 0 None - 1 Human 7.0 pIC50 = 7.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
44191225 196396 0 None - 1 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562747 196396 0 None - 1 Human 6.0 pIC50 = 6.0 Functional
Antagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilizationAntagonist activity at B2 receptor in human HF15 cells assessed as inhibition of bradykinin-induced calcium mobilization
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10463883 83833 0 None - 0 Guinea pig 10.4 pKd = 10.4 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220596 83833 0 None - 0 Guinea pig 10.4 pKd = 10.4 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
11498853 83188 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL218427 83188 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL541758 83188 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11498853 83188 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218427 83188 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL541758 83188 13 None - 1 Human 10.3 pKd = 10.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
57345657 71592 0 None - 0 Guinea pig 10.2 pKd = 10.2 Functional
Antagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responsesAntagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responses
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956722 71592 0 None - 0 Guinea pig 10.2 pKd = 10.2 Functional
Antagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responsesAntagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responses
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963183 71592 0 None - 0 Guinea pig 10.2 pKd = 10.2 Functional
Antagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responsesAntagonist activity at guinea pig bradykinin B2 receptor in longitudinal smooth muscle assessed as inhibition of bradykinin-induced contractile responses
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10439868 75926 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL205093 75926 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
10373970 137614 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375689 137614 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10032895 137631 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375820 137631 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
10101294 140154 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL380273 140154 0 None - 0 Guinea pig 10.0 pKd = 10 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
57403503 71665 0 None - 0 Human 9.9 pKd = 9.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956856 71665 0 None - 0 Human 9.9 pKd = 9.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963651 71665 0 None - 0 Human 9.9 pKd = 9.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105746 161930 0 None - 0 Human 9.8 pKd = 9.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415366 161930 0 None - 0 Human 9.8 pKd = 9.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
9988753 83832 0 None - 0 Guinea pig 9.8 pKd = 9.8 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220595 83832 0 None - 0 Guinea pig 9.8 pKd = 9.8 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10010104 141274 0 None - 0 Guinea pig 9.7 pKd = 9.7 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL383167 141274 0 None - 0 Guinea pig 9.7 pKd = 9.7 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
16105703 136480 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373607 136480 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
10373970 137614 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375689 137614 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44378635 168747 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL 1351 29 15 18 -2.0 C[C@@]12CCCC[C@]1(C)N(C(=O)[C@H]1Cc3ccccc3CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)c1ccc(NC(N)C=N)cc1)[C@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2 10.1016/S0960-894X(01)80847-7
CHEMBL437155 168747 0 None - 0 Human 9.6 pKd = 9.6 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL 1351 29 15 18 -2.0 C[C@@]12CCCC[C@]1(C)N(C(=O)[C@H]1Cc3ccccc3CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)c1ccc(NC(N)C=N)cc1)[C@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2 10.1016/S0960-894X(01)80847-7
667 1973 37 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
71364 1973 37 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
CHEMBL2028850 1973 37 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
DB06196 1973 37 None -2 2 Human 9.6 pKd = 9.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
57345657 71592 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956722 71592 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963183 71592 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11600324 141996 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL387452 141996 0 None - 0 Human 9.5 pKd = 9.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44412007 77211 1 None - 0 Guinea pig 9.5 pKd = 9.5 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL207939 77211 1 None - 0 Guinea pig 9.5 pKd = 9.5 Functional
Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleAntagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscle
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
667 1973 37 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
71364 1973 37 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
CHEMBL2028850 1973 37 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
DB06196 1973 37 None - 2 Rat 9.5 pKd = 9.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None None 10.1021/jm950716i
57399983 71575 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956859 71575 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963149 71575 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401772 71588 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956857 71588 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963175 71588 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
44412007 77211 1 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL207939 77211 1 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
57401770 71583 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956853 71583 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963162 71583 0 None - 0 Human 9.4 pKd = 9.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396534 71664 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956854 71664 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963650 71664 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL3038099 210932 0 None - 0 Rat 9.3 pKd = 9.3 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
10079793 94120 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL249235 94120 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105698 136346 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373459 136346 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10079797 137597 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375576 137597 0 None - 0 Human 9.3 pKd = 9.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105734 84272 0 None - 0 Human 9.2 pKd = 9.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221285 84272 0 None - 0 Human 9.2 pKd = 9.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
57394782 71643 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956855 71643 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963557 71643 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10101294 140154 0 None - 0 Human 9.1 pKd = 9.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380273 140154 0 None - 0 Human 9.1 pKd = 9.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
57399228 71572 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956720 71572 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963146 71572 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57402746 71573 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956721 71573 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963147 71573 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401778 71578 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956870 71578 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963152 71578 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57400986 71582 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956723 71582 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963161 71582 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
9988753 83832 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220595 83832 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10418701 97102 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL267493 97102 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10032895 137631 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375820 137631 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
10101294 140154 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL380273 140154 0 None - 0 Human 9.1 pKd = 9.1 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038100 210933 0 None - 0 Rat 9.1 pKd = 9.1 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None N=C(N)NCCCCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
667 1973 37 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
71364 1973 37 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
CHEMBL2028850 1973 37 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
DB06196 1973 37 None -2 2 Human 9.0 pKd = 9.0 Functional
Antagonist effect against bradykinin B2 receptor was determined in rabbit jugular veinAntagonist effect against bradykinin B2 receptor was determined in rabbit jugular vein
ChEMBL None None None None 10.1016/S0960-894X(01)80847-7
57396538 71589 0 None - 0 Human 9.0 pKd = 9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956861 71589 0 None - 0 Human 9.0 pKd = 9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963176 71589 0 None - 0 Human 9.0 pKd = 9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394780 71642 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956852 71642 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963556 71642 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105751 83229 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
CHEMBL218636 83229 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
16105690 83634 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220478 83634 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105729 136934 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374273 136934 0 None - 0 Human 8.9 pKd = 8.9 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038095 210929 0 None - 0 Rat 8.9 pKd = 8.9 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
CHEMBL2371961 210158 0 None - 0 Guinea pig 8.8 pKd = 8.8 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1CN(C(=O)[C@H]2c3ccccc3CCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C2CCCCC21)C(=O)O 10.1021/jm00069a016
57401776 71576 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956866 71576 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963150 71576 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401782 71586 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956873 71586 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963165 71586 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10463883 83833 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220596 83833 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105701 83969 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220693 83969 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
10441167 96988 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL266493 96988 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10102701 137438 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375354 137438 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105694 141894 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL386794 141894 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
9897921 161901 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415151 161901 0 None - 0 Human 8.8 pKd = 8.8 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL2372283 210209 0 None - 0 Rat 8.8 pKd = 8.8 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
57398324 71585 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956862 71585 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963164 71585 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105727 83811 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220591 83811 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10396101 84342 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221683 84342 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10441194 84622 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222156 84622 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105742 138154 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL376866 138154 0 None - 0 Human 8.7 pKd = 8.7 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10418495 77875 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209346 77875 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
44354187 116800 0 None - 0 Guinea pig 6.0 pKd = 6 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 29 11 10 0.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@@H](C(=O)O)C[C@H]2CCCC[C@H]21)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL337833 116800 0 None - 0 Guinea pig 6.0 pKd = 6 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 29 11 10 0.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@@H](C(=O)O)C[C@H]2CCCC[C@H]21)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL410363 212816 24 None - 0 Guinea pig 6.0 pKd = 6 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL None None None CC[C@H](C)[C@H](NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(C)=O)C(=O)O 10.1021/jm980495r
10010669 76811 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206938 76811 0 None - 0 Human 8.0 pKd = 8.0 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
70685700 74503 0 None - 0 Rabbit 6.9 pKd = 6.9 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 670 6 6 6 0.7 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CNC1=O 10.1021/jm950682e
CHEMBL2028840 74503 0 None - 0 Rabbit 6.9 pKd = 6.9 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 670 6 6 6 0.7 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2ccccc2)NC(=O)CNC1=O 10.1021/jm950682e
CHEMBL2370040 209773 0 None - 0 Guinea pig 7.9 pKd = 7.9 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None C[C@@](Cc1ccccc1)(NC(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44354059 117059 0 None - 0 Guinea pig 5.9 pKd = 5.9 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 34 11 10 1.8 CC[C@H](C)[C@H](NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(C)=O)C(=O)O 10.1021/jm980495r
CHEMBL339159 117059 0 None - 0 Guinea pig 5.9 pKd = 5.9 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 34 11 10 1.8 CC[C@H](C)[C@H](NC(=O)[C@@H](Cc1ccc2ccccc2c1)NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(C)=O)C(=O)O 10.1021/jm980495r
CHEMBL3038103 210936 0 None - 1 Rat 5.9 pKd = 5.9 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1)C1CCCC1 10.1021/jm950716i
70685699 74497 0 None - 0 Rabbit 6.8 pKd = 6.8 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 747 10 6 9 1.1 NCCCC[C@@H]1N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C(=O)NC1=O 10.1021/jm950682e
CHEMBL2028835 74497 0 None - 0 Rabbit 6.8 pKd = 6.8 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 747 10 6 9 1.1 NCCCC[C@@H]1N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C(=O)NC1=O 10.1021/jm950682e
CHEMBL3038104 210937 0 None - 1 Rat 6.8 pKd = 6.8 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL3038096 210930 0 None - 1 Rat 7.7 pKd = 7.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
10056816 77749 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209038 77749 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
11513471 138647 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
CHEMBL377612 138647 0 None - 0 Human 7.7 pKd = 7.7 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
56668285 63318 0 None - 0 Guinea pig 5.7 pKd = 5.7 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1145 26 13 15 -1.1 C=C([C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)CC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
CHEMBL1793829 63318 0 None - 0 Guinea pig 5.7 pKd = 5.7 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1145 26 13 15 -1.1 C=C([C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)CC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
10439868 75926 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL205093 75926 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
11600186 78297 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210788 78297 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10418252 138891 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378237 138891 0 None - 0 Human 8.6 pKd = 8.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
57401774 71593 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956863 71593 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963184 71593 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57391279 71594 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956876 71594 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963185 71594 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401784 71639 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956875 71639 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963532 71639 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57392147 71669 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1955876 71669 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963660 71669 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10439868 75926 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL205093 75926 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
16105696 83208 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218540 83208 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
57403505 71645 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956865 71645 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963559 71645 0 None - 0 Human 8.6 pKd = 8.6 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL3038101 210934 0 None - 0 Rat 7.7 pKd = 7.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
CHEMBL3038105 210938 0 None - 1 Rat 5.7 pKd = 5.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)O)Cc1ccccc1 10.1021/jm950716i
70696204 74498 0 None - 0 Rabbit 6.7 pKd = 6.7 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 690 6 4 7 0.9 CN1CC(=O)N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C1=O 10.1021/jm950682e
CHEMBL2028836 74498 0 None - 0 Rabbit 6.7 pKd = 6.7 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 690 6 4 7 0.9 CN1CC(=O)N[C@@H](Cc2cccs2)C(=O)N2Cc3ccccc3C[C@@H]2C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C1=O 10.1021/jm950682e
CHEMBL2372278 210207 0 None - 0 Rat 7.7 pKd = 7.7 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None N=C(N)NCCCCC(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL2370010 209767 0 None - 0 Guinea pig 6.6 pKd = 6.6 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N1)C(=O)O 10.1021/jm00069a016
70687850 74504 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 594 4 5 6 -0.7 C[C@@H]1NC(=O)CNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
CHEMBL2028841 74504 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 594 4 5 6 -0.7 C[C@@H]1NC(=O)CNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
11506007 78011 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209773 78011 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
10463758 138871 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378189 138871 0 None - 0 Human 7.6 pKd = 7.6 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
90662813 106567 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 722 15 6 8 1.3 NCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142191 106567 0 None - 0 Rabbit 6.6 pKd = 6.6 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 722 15 6 8 1.3 NCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL2370042 209775 0 None - 0 Guinea pig 5.6 pKd = 5.6 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None CN(C(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44410425 97139 0 None - 0 Human 5.6 pKd = 5.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
CHEMBL267822 97139 0 None - 0 Human 5.6 pKd = 5.6 Functional
Antagonist activity against bradykinin B2 receptorAntagonist activity against bradykinin B2 receptor
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
10010104 141274 0 None - 0 Human 8.5 pKd = 8.5 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383167 141274 0 None - 0 Human 8.5 pKd = 8.5 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
57396536 71584 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956860 71584 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963163 71584 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57393060 71587 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956851 71587 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963174 71587 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398326 71644 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956864 71644 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963558 71644 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11766718 136933 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374272 136933 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10010104 141274 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL383167 141274 0 None - 0 Human 8.5 pKd = 8.5 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038094 210928 0 None - 0 Rat 8.5 pKd = 8.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCC1 10.1021/jm950716i
CHEMBL3038106 210939 0 None - 0 Rat 8.5 pKd = 8.5 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1C[C@@H](O)C[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
57401780 71579 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956872 71579 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963153 71579 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398328 71668 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956874 71668 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963659 71668 0 None - 0 Human 8.4 pKd = 8.4 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
90662795 106564 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 778 17 9 8 1.4 N=C(N)NCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142173 106564 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 778 17 9 8 1.4 N=C(N)NCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
70681476 74506 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 709 5 7 8 -1.5 C[C@@H]1NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC1=O 10.1021/jm950682e
CHEMBL2028844 74506 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 709 5 7 8 -1.5 C[C@@H]1NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC1=O 10.1021/jm950682e
44354175 96908 0 None - 0 Guinea pig 5.5 pKd = 5.5 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1025 35 12 12 0.8 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@H]2CCCC[C@H]2C[C@@H]1C(=O)O)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL265814 96908 0 None - 0 Guinea pig 5.5 pKd = 5.5 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1025 35 12 12 0.8 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@H]2CCCC[C@H]2C[C@@H]1C(=O)O)C1Cc2ccccc2C1 10.1021/jm980495r
CHEMBL2370700 209916 0 None - 0 Guinea pig 5.5 pKd = 5.5 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL None None None NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21)C1Cc2ccccc2C1)C1Cc2ccccc2C1 10.1021/jm980495r
70696205 74501 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 704 6 6 7 1.5 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028839 74501 0 None - 0 Rabbit 6.5 pKd = 6.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 704 6 6 7 1.5 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
90662796 106565 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 792 18 9 8 1.8 N=C(N)NCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142174 106565 0 None - 0 Rabbit 5.5 pKd = 5.5 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 792 18 9 8 1.8 N=C(N)NCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/jm950682e
90662812 106566 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 716 15 6 7 1.2 NCCCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142190 106566 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 716 15 6 7 1.2 NCCCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
11527838 78358 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL211017 78358 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10008626 138678 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377800 138678 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10463818 139272 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379063 139272 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10102599 141404 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383989 141404 0 None - 0 Human 7.4 pKd = 7.4 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
44354176 96755 0 None - 0 Guinea pig 5.4 pKd = 5.4 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 28 10 10 0.6 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
CHEMBL264517 96755 0 None - 0 Guinea pig 5.4 pKd = 5.4 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 925 28 10 10 0.6 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1[C@H](C(=O)O)C[C@@H]2CCCC[C@@H]21 10.1021/jm980495r
10032469 74500 0 None - 0 Rabbit 7.4 pKd = 7.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 676 6 6 7 0.8 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CNC1=O 10.1021/jm950682e
CHEMBL2028838 74500 0 None - 0 Rabbit 7.4 pKd = 7.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 676 6 6 7 0.8 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC(=O)CNC1=O 10.1021/jm950682e
70696206 74509 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 797 5 7 8 0.2 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028847 74509 0 None - 0 Rabbit 6.4 pKd = 6.4 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 797 5 7 8 0.2 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@@H]2Cc3ccccc3CN2C(=O)CCCNC1=O 10.1021/jm950682e
70696207 74511 0 None - 0 Rabbit 7.3 pKd = 7.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 791 7 8 9 0.0 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028849 74511 0 None - 0 Rabbit 7.3 pKd = 7.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 791 7 8 9 0.0 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC1=O 10.1021/jm950682e
90662814 106568 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 806 21 6 8 3.6 NCCCCCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL3142192 106568 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 806 21 6 8 3.6 NCCCCCCCCCC(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
70694084 74505 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 808 6 7 7 1.3 C[C@@H]1NC(=O)[C@H](Cc2cc3ccccc3[nH]2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
CHEMBL2028843 74505 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 808 6 7 7 1.3 C[C@@H]1NC(=O)[C@H](Cc2cc3ccccc3[nH]2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
57396540 71590 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956867 71590 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963177 71590 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394784 71667 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956871 71667 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963658 71667 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometryAntagonist activity at human bradykinin B2 receptor expressed in dhfr-deficient CHO cells assessed as inhibition of bradykinin-induced inositol monophosphate accumulation preincubated for 15 mins prior bradykinin induction measured after 40 mins by liquid scintillation spectrometry
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10350966 84624 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222167 84624 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10102296 161902 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415152 161902 0 None - 0 Human 8.3 pKd = 8.3 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038102 210935 0 None - 0 Rat 7.3 pKd = 7.3 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)Cc1ccccc1 10.1021/jm950716i
CHEMBL2370011 209768 0 None - 0 Guinea pig 6.3 pKd = 6.3 Functional
Antagonism against bradykinin receptor B2 in guinea pig ileal tissueAntagonism against bradykinin receptor B2 in guinea pig ileal tissue
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N[C@@H](Cc2ccccc2)C(=O)N1)C(=O)O 10.1021/jm00069a016
CHEMBL2372276 210206 0 None - 1 Rat 7.3 pKd = 7.3 Functional
In vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assayIn vitro Bradykinin receptor B2 antagonist activity by using rat uterus functional assay
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm950716i
70694085 74508 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 771 6 8 8 0.1 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](c2ccccc2)NC(=O)CCCNC1=O 10.1021/jm950682e
CHEMBL2028846 74508 0 None - 0 Rabbit 6.3 pKd = 6.3 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 771 6 8 8 0.1 N=C(N)NCCC[C@@H]1NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](c2ccccc2)NC(=O)CCCNC1=O 10.1021/jm950682e
10441297 136888 0 None - 0 Human 8.2 pKd = 8.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374224 136888 0 None - 0 Human 8.2 pKd = 8.2 Functional
Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsAntagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL2370699 209915 7 None - 0 Guinea pig 8.2 pKd = 8.2 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2N1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1Cc2ccccc2C1)C1Cc2ccccc2C1)C(=O)O 10.1021/jm980495r
70681477 74507 0 None - 0 Rabbit 7.2 pKd = 7.2 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 6 6 8 0.8 C[C@@H]1NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
CHEMBL2028845 74507 0 None - 0 Rabbit 7.2 pKd = 7.2 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 6 6 8 0.8 C[C@@H]1NC(=O)[C@H](Cc2cccs2)NC(=O)CCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C1=O 10.1021/jm950682e
10349694 76583 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206312 76583 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10055774 76703 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206474 76703 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10260476 77997 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209719 77997 0 None - 0 Human 8.1 pKd = 8.1 Functional
Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationActivity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulation
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL2372276 210206 0 None - 1 Rabbit 5.1 pKd = 5.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
70692045 74499 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 10 9 8 0.4 N=C(N)NCCC[C@@H]1NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
CHEMBL2028837 74499 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 775 10 9 8 0.4 N=C(N)NCCC[C@@H]1NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
70689879 74510 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 777 7 7 9 -0.6 C[C@@H]1NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
CHEMBL2028848 74510 0 None - 0 Rabbit 7.1 pKd = 7.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 777 7 7 9 -0.6 C[C@@H]1NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC1=O 10.1021/jm950682e
44354174 141559 0 None - 0 Guinea pig 6.1 pKd = 6.1 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1081 35 14 12 -1.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2N1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1Cc2ccccc2C1)C(=O)O 10.1021/jm980495r
CHEMBL384846 141559 0 None - 0 Guinea pig 6.1 pKd = 6.1 Functional
Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.Antagonistic activity against Bradykinin receptor B2 of guinea pig ileum longitudinal smooth muscle.
ChEMBL 1081 35 14 12 -1.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1C[C@@H]2CCCC[C@@H]2N1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)CCCCCCCCCCNC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1Cc2ccccc2C1)C(=O)O 10.1021/jm980495r
73345363 89341 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 793 17 8 9 -0.1 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL2369364 89341 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 793 17 8 9 -0.1 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](Cc1cccs1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
73354461 89352 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 688 13 6 7 0.4 NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
CHEMBL2369400 89352 0 None - 0 Rabbit 6.1 pKd = 6.1 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 688 13 6 7 0.4 NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm950682e
73354460 89350 0 None - 0 Rabbit 6.0 pKd = 6.0 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 718 14 7 8 -0.2 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1ccccc1)C(=O)O 10.1021/jm950682e
CHEMBL2369392 89350 0 None - 0 Rabbit 6.0 pKd = 6.0 Functional
In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.In vitro antagonistic activity against kinin-induced rabbit jugular vein contraction.
ChEMBL 718 14 7 8 -0.2 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1ccccc1)C(=O)O 10.1021/jm950682e
119343 2874 22 None -30 2 Human 5.2 pA2 = 5.2 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
676 2874 22 None -30 2 Human 5.2 pA2 = 5.2 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
CHEMBL446325 2874 22 None -30 2 Human 5.2 pA2 = 5.2 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
653 565 0 None 5 3 Human 8.4 pA2 = 8.4 Functional
Apparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical veinApparent affinity for bradykinin B<sub>2</sub> receptor in human umbilical vein
Guide to Pharmacology None None None None 9650825
5311108 1686 18 None -9 2 Human 8.2 pA2 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9095082
674 1686 18 None -9 2 Human 8.2 pA2 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9095082
CHEMBL130517 1686 18 None -9 2 Human 8.2 pA2 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9095082
667 1973 37 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
71364 1973 37 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
CHEMBL2028850 1973 37 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
DB06196 1973 37 None -2 2 Human 8.4 pA2 = 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8735629
5128451 1380 0 None -1 2 Human 5.1 pIC50 = 5.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
646 1380 0 None -1 2 Human 5.1 pIC50 = 5.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
5128451 1380 0 None 1 2 Mouse 5.2 pIC50 = 5.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
646 1380 0 None 1 2 Mouse 5.2 pIC50 = 5.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
672 2267 21 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
6918284 2267 21 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
CHEMBL2105864 2267 21 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
DB06549 2267 21 None - 1 Human 7.5 pIC50 = 7.5 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 23362191
5311108 1686 18 None -9 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9203620
674 1686 18 None -9 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9203620
CHEMBL130517 1686 18 None -9 2 Human 8.1 pIC50 = 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 9203620
3812 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3812 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
439201 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
439201 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
649 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
649 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
CHEMBL406291 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL406291 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
DB12126 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB12126 717 42 None -1 3 Human 8.2 pIC50 = 8.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
667 1973 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
667 1973 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
71364 1973 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
71364 1973 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
CHEMBL2028850 1973 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL2028850 1973 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
DB06196 1973 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB06196 1973 37 None -2 2 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9203620
10255 2816 0 None - 1 Human 8.7 pIC50 = 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 19111586
5311111 2175 0 None -1 2 Mouse 9.3 pIC50 = 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
650 2175 0 None -1 2 Mouse 9.3 pIC50 = 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
122227 1378 31 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3825 1378 31 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
644 1378 31 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL264100 1378 31 None -28840 3 Mouse 4.6 pIC50 None 4.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
678 3808 0 None -5 2 Human 6.3 pIC50 None 6.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
119343 2874 22 None -30 2 Human 6.9 pIC50 None 6.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
676 2874 22 None -30 2 Human 6.9 pIC50 None 6.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL446325 2874 22 None -30 2 Human 6.9 pIC50 None 6.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
123973 2873 0 None -79 2 Human 7.0 pIC50 None 7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
675 2873 0 None -79 2 Human 7.0 pIC50 None 7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
678 3808 0 None 5 2 Mouse 7.0 pIC50 None 7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
673 1685 15 None -8 2 Human 7.2 pIC50 None 7.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 9203620
9810391 1685 15 None -8 2 Human 7.2 pIC50 None 7.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 9203620
CHEMBL1192627 1685 15 None -8 2 Human 7.2 pIC50 None 7.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 9203620
671 3897 0 None -1 2 Human 8.0 pIC50 None 8 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
671 3897 0 None 1 2 Mouse 8.1 pIC50 None 8.1 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3035449 2516 0 None -1 3 Mouse 8.4 pIC50 None 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
638 2516 0 None -1 3 Mouse 8.4 pIC50 None 8.4 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
3035449 2516 0 None 1 3 Human 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
638 2516 0 None 1 3 Human 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
119343 2874 22 None 30 2 Mouse 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
676 2874 22 None 30 2 Mouse 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL446325 2874 22 None 30 2 Mouse 8.7 pIC50 None 8.7 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
123973 2873 0 None 79 2 Mouse 8.9 pIC50 None 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
675 2873 0 None 79 2 Mouse 8.9 pIC50 None 8.9 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
10394861 1689 5 None 9 2 Human 9.2 pIC50 None 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 15139763
669 1689 5 None 9 2 Human 9.2 pIC50 None 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 15139763
CHEMBL329762 1689 5 None 9 2 Human 9.2 pIC50 None 9.2 Functional
UnclassifiedUnclassified
Guide to Pharmacology 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 15139763
3812 717 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
439201 717 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
649 717 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL406291 717 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB12126 717 42 None 1 3 Mouse 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
5311111 2175 0 None 1 2 Human 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
650 2175 0 None 1 2 Human 9.3 pIC50 None 9.3 Functional
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267




Ligands (move mouse cursor over ligand name to see structure) Receptor Assay information Chemical information
Sel. page Similar-
ity
Common
name
GPCRdb
ID
#Vendors

Reference
ligand
Fold
selectivity
# Tested
GPCRs
Species

p-value
(-log)
Activity
Type
Activity
Relation
Activity
Value
Assay
Type
Assay
Description
Source

Mol
weight
Rot
Bonds
H don

H acc

LogP

Smiles

DOI

11980903 14492 19 None - 0 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 382 4 0 2 5.3 Cc1cc(/C=C/c2ccc3cc(N(C)C)ccc3[n+]2C)c(C)n1-c1ccccc1 10.1038/s41467-023-40064-9
22526 14492 19 None - 0 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 382 4 0 2 5.3 Cc1cc(/C=C/c2ccc3cc(N(C)C)ccc3[n+]2C)c(C)n1-c1ccccc1 10.1038/s41467-023-40064-9
5281035 14492 19 None - 0 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 382 4 0 2 5.3 Cc1cc(/C=C/c2ccc3cc(N(C)C)ccc3[n+]2C)c(C)n1-c1ccccc1 10.1038/s41467-023-40064-9
CHEMBL1201303 14492 19 None - 0 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 382 4 0 2 5.3 Cc1cc(/C=C/c2ccc3cc(N(C)C)ccc3[n+]2C)c(C)n1-c1ccccc1 10.1038/s41467-023-40064-9
137 370 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
2119 370 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
563 370 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
66368 370 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
CHEMBL266195 370 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
DB00866 370 52 None - 12 Human 4.9 pAC50 = 4.9 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 249 8 2 3 2.2 C=CCc1ccccc1OCC(CNC(C)C)O 10.1038/s41467-023-40064-9
6436173 55116 45 None - 0 Human 4.8 pAC50 = 4.8 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 785 2 5 13 6.2 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c5c(nc6cc(C)ccn65)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
CHEMBL1617 55116 45 None - 0 Human 4.8 pAC50 = 4.8 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 785 2 5 13 6.2 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c5c(nc6cc(C)ccn65)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
135398735 136968 32 None - 0 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 822 4 6 15 4.3 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
136262914 136968 32 None - 0 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 822 4 6 15 4.3 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
CHEMBL374478 136968 32 None - 0 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 822 4 6 15 4.3 CO[C@H]1/C=C/O[C@@]2(C)Oc3c(C)c(O)c4c(O)c(c(/C=N/N5CCN(C)CC5)c(O)c4c3C2=O)NC(=O)/C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C 10.1038/s41467-023-40064-9
4495 196535 92 None - 29 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 308 5 1 5 2.8 CS(=O)(=O)Nc1ccc([N+](=O)[O-])cc1Oc1ccccc1 10.1038/s41467-023-40064-9
CHEMBL56367 196535 92 None - 29 Human 4.7 pAC50 = 4.7 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 308 5 1 5 2.8 CS(=O)(=O)Nc1ccc([N+](=O)[O-])cc1Oc1ccccc1 10.1038/s41467-023-40064-9
5329102 194726 86 None - 0 Human 5.6 pAC50 = 5.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 398 7 3 3 3.3 CCN(CC)CCNC(=O)c1c(C)[nH]c(/C=C2\C(=O)Nc3ccc(F)cc32)c1C 10.1038/s41467-023-40064-9
CHEMBL535 194726 86 None - 0 Human 5.6 pAC50 = 5.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 398 7 3 3 3.3 CCN(CC)CCNC(=O)c1c(C)[nH]c(/C=C2\C(=O)Nc3ccc(F)cc32)c1C 10.1038/s41467-023-40064-9
135564886 14493 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
135673376 14493 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
137157436 14493 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
145948239 14493 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
71587099 14493 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
CHEMBL1201304 14493 5 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 752 14 1 6 8.7 CC1(C)C(/C=C/C=C/C=C/C=C2\N(CCCCS(=O)(=O)O)c3ccc4ccccc4c3C2(C)C)=[N+](CCCCS(=O)(=O)[O-])c2ccc3ccccc3c21 10.1038/s41467-023-40064-9
26248 161539 102 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 368 3 1 7 2.0 CC(=O)Oc1cccc2c1C(=O)c1c(OC(C)=O)cc(C(=O)O)cc1C2=O 10.1038/s41467-023-40064-9
CHEMBL41286 161539 102 None - 0 Human 4.6 pAC50 = 4.6 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 368 3 1 7 2.0 CC(=O)Oc1cccc2c1C(=O)c1c(OC(C)=O)cc(C(=O)O)cc1C2=O 10.1038/s41467-023-40064-9
2335 11848 22 None - 12 Human 4.5 pAC50 = 4.5 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 412 11 0 2 6.1 CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1 10.1038/s41467-023-40064-9
8478 11848 22 None - 12 Human 4.5 pAC50 = 4.5 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 412 11 0 2 6.1 CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1 10.1038/s41467-023-40064-9
CHEMBL1182210 11848 22 None - 12 Human 4.5 pAC50 = 4.5 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 412 11 0 2 6.1 CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1 10.1038/s41467-023-40064-9
CHEMBL221753 11848 22 None - 12 Human 4.5 pAC50 = 4.5 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 412 11 0 2 6.1 CC(C)(C)CC(C)(C)c1ccc(OCCOCC[N+](C)(C)Cc2ccccc2)cc1 10.1038/s41467-023-40064-9
41684 31221 105 None - 0 Human 5.3 pAC50 = 5.3 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 307 4 1 7 2.2 CC(=O)Oc1ccccc1C(=O)Nc1ncc([N+](=O)[O-])s1 10.1038/s41467-023-40064-9
CHEMBL1401 31221 105 None - 0 Human 5.3 pAC50 = 5.3 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 307 4 1 7 2.2 CC(=O)Oc1ccccc1C(=O)Nc1ncc([N+](=O)[O-])s1 10.1038/s41467-023-40064-9
2179 167518 76 None - 0 Human 5.1 pAC50 = 5.1 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 393 5 2 5 4.5 COc1cc(NS(C)(=O)=O)ccc1Nc1c2ccccc2nc2ccccc12 10.1038/s41467-023-40064-9
CHEMBL1256655 167518 76 None - 0 Human 5.1 pAC50 = 5.1 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 393 5 2 5 4.5 COc1cc(NS(C)(=O)=O)ccc1Nc1c2ccccc2nc2ccccc12 10.1038/s41467-023-40064-9
CHEMBL43 167518 76 None - 0 Human 5.1 pAC50 = 5.1 Binding
Binding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assayBinding affinity towards human BDKRB2 in an in vitro assay with cellular components measured by scintillation proximity assay
ChEMBL 393 5 2 5 4.5 COc1cc(NS(C)(=O)=O)ccc1Nc1c2ccccc2nc2ccccc12 10.1038/s41467-023-40064-9
11498853 83188 13 None - 1 Human 10.3 pIC50 = 10.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm9002445
CHEMBL218427 83188 13 None - 1 Human 10.3 pIC50 = 10.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm9002445
CHEMBL541758 83188 13 None - 1 Human 10.3 pIC50 = 10.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm9002445
667 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
71364 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
CHEMBL2028850 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
DB06196 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980300f
667 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
71364 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
CHEMBL2028850 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
DB06196 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None None 10.1021/jm980214f
667 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
71364 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2028850 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
DB06196 1973 37 None 1 6 Guinea pig 10.1 pIC50 = 10.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2370160 209802 0 None - 0 Guinea pig 10.1 pIC50 = 10.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CS)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1c2ccccc2C[C@@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm030326t
11801968 13711 0 None - 0 Guinea pig 9.9 pIC50 = 9.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194974 13711 0 None - 0 Guinea pig 9.9 pIC50 = 9.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553614 13711 0 None - 0 Guinea pig 9.9 pIC50 = 9.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
11250851 13617 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1194270 13617 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3216880 13617 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
9874617 13306 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191908 13306 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543070 13306 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11250929 13835 0 None - 0 Guinea pig 9.7 pIC50 = 9.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1195824 13835 0 None - 0 Guinea pig 9.7 pIC50 = 9.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL555403 13835 0 None - 0 Guinea pig 9.7 pIC50 = 9.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
11158089 12917 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189084 12917 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538022 12917 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
18704946 13170 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1190879 13170 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3217081 13170 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
44214214 13261 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191492 13261 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL542598 13261 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
44360533 12892 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1188925 12892 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL537683 12892 0 None - 0 Guinea pig 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
10009762 12929 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counterDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counter
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1016/j.ejmech.2019.07.064
CHEMBL1189175 12929 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counterDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counter
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1016/j.ejmech.2019.07.064
CHEMBL3217072 12929 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counterDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells incubated for 2 hrs by liquid scintillation counter
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1016/j.ejmech.2019.07.064
10009762 12929 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1189175 12929 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217072 12929 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
10627384 13738 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL1195129 13738 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL553911 13738 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
11490839 13169 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190878 13169 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL541805 13169 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11273808 13798 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195573 13798 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3215979 13798 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
22008895 110558 0 None - 1 Guinea pig 9.5 pIC50 = 9.5 Binding
Displacement of [3H]bradykinin from guinea pig B2 receptorDisplacement of [3H]bradykinin from guinea pig B2 receptor
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1021/jm9002445
CHEMBL325255 110558 0 None - 1 Guinea pig 9.5 pIC50 = 9.5 Binding
Displacement of [3H]bradykinin from guinea pig B2 receptorDisplacement of [3H]bradykinin from guinea pig B2 receptor
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1021/jm9002445
11445288 13876 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1196072 13876 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217085 13876 0 None - 0 Human 9.5 pIC50 = 9.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11262728 138464 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1016/j.ejmech.2020.112948
CHEMBL3774617 138464 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1016/j.ejmech.2020.112948
11802489 13733 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1195106 13733 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL553844 13733 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
11262728 138464 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/acs.jmedchem.5b00982
CHEMBL3774617 138464 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 744 13 1 8 8.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/acs.jmedchem.5b00982
44329173 167812 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 787 14 2 9 7.4 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL430652 167812 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 787 14 2 9 7.4 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
44360597 13884 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL1196121 13884 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL555976 13884 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
10349737 13116 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1190430 13116 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL540840 13116 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
11411675 96495 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL262507 96495 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
5311114 1688 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1016/j.ejmech.2020.112948
668 1688 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1016/j.ejmech.2020.112948
CHEMBL99869 1688 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1016/j.ejmech.2020.112948
5311114 1688 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/acs.jmedchem.5b00982
668 1688 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/acs.jmedchem.5b00982
CHEMBL99869 1688 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/acs.jmedchem.5b00982
5311114 1688 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
668 1688 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
CHEMBL99869 1688 8 None - 1 Human 9.4 pIC50 = 9.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
44360533 12892 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1188925 12892 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL537683 12892 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 686 11 1 7 5.3 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
44360877 13687 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1194797 13687 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL553315 13687 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
11491041 13456 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1193122 13456 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL544480 13456 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
11227974 13305 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191906 13305 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543068 13305 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
10652092 13017 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189828 13017 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL539550 13017 0 None - 0 Guinea pig 9.4 pIC50 = 9.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
5311108 1686 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
674 1686 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
CHEMBL130517 1686 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
10531497 13213 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Displacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counterDisplacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counter
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1016/j.ejmech.2019.07.064
CHEMBL1191172 13213 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Displacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counterDisplacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counter
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1016/j.ejmech.2019.07.064
CHEMBL542232 13213 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Displacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counterDisplacement of [3H]BK from Bradykinin B2 Receptor in guinea pig ileum by liquid scintillation counter
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1016/j.ejmech.2019.07.064
5311108 1686 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
674 1686 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
CHEMBL130517 1686 18 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
10674687 13627 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1194363 13627 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL552543 13627 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
11251046 13205 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191121 13205 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542173 13205 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
667 1973 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
71364 1973 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2028850 1973 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
DB06196 1973 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL None None None None 10.1021/jm030159x
CHEMBL2370160 209802 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CS)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1c2ccccc2C[C@@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm030326t
667 1973 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
71364 1973 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
CHEMBL2028850 1973 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
DB06196 1973 37 None -1 6 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL None None None None 10.1021/jm980300f
11802476 12964 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1189415 12964 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL538732 12964 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
10698671 13468 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1193229 13468 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL544599 13468 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
11802476 12964 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189415 12964 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538732 12964 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
11802476 12964 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1189415 12964 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL538732 12964 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
10348414 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL439737 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL542096 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10348414 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membraneConcentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membrane
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL439737 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membraneConcentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membrane
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL542096 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membraneConcentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2 in guinea pig ileum membrane
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
10348414 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL439737 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL542096 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10348414 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL439737 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL542096 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10348414 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL439737 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL542096 169073 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
44360968 121084 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL357075 121084 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
10371910 20134 1 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130436 20134 1 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
11411594 12908 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189023 12908 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL537927 12908 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
44360818 13478 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL1193250 13478 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL544623 13478 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
10555818 13685 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194778 13685 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553293 13685 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
10675847 13417 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1192831 13417 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL544134 13417 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
44361029 13366 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1192448 13366 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL543685 13366 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
11479739 208203 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98460 208203 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
44360597 13884 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL1196121 13884 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
CHEMBL555976 13884 0 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 5.5 CC(=O)Nc1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(NC(C)=O)c(COc3cccc4ccc(C)nc34)c2NC(C)=O)cn1 10.1021/jm980330i
44360877 13687 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1194797 13687 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL553315 13687 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 722 11 1 7 6.6 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
10604613 13113 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1190420 13113 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL540828 13113 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10580156 13111 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1190412 13111 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL540819 13111 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
11239595 13723 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195041 13723 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553762 13723 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10627384 13738 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL1195129 13738 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL553911 13738 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 598 9 2 5 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10675243 96780 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL264751 96780 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
10675243 96780 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
CHEMBL264751 96780 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
673 1685 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
9810391 1685 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
CHEMBL1192627 1685 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
673 1685 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
9810391 1685 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
CHEMBL1192627 1685 15 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
45269613 194854 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 695 12 3 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@H]4C(=O)CCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm9002445
CHEMBL539924 194854 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 695 12 3 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@H]4C(=O)CCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm9002445
10531497 13213 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL1191172 13213 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL542232 13213 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
10394861 1689 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
669 1689 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
CHEMBL329762 1689 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
44360879 12971 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1189464 12971 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL538784 12971 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
10394861 1689 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1016/j.ejmech.2020.112948
669 1689 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1016/j.ejmech.2020.112948
CHEMBL329762 1689 5 None - 0 Human 9.2 pIC50 = 9.2 Binding
Agonist activity at bradykinin B2 receptor (unknown origin)Agonist activity at bradykinin B2 receptor (unknown origin)
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1016/j.ejmech.2020.112948
9958759 13471 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1193231 13471 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL544601 13471 0 None - 0 Guinea pig 9.2 pIC50 = 9.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
11445540 168173 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 727 13 2 8 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030468n
CHEMBL433214 168173 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 727 13 2 8 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030468n
10032884 13465 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193185 13465 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL544549 13465 0 None - 0 Human 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10257108 9831 1 None - 1 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
CHEMBL113963 9831 1 None - 1 Guinea pig 9.2 pIC50 = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
10371910 20134 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130436 20134 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 637 10 1 6 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
10651980 13418 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192832 13418 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544135 13418 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
11365972 13643 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1194477 13643 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216391 13643 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
44360968 121084 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL357075 121084 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 775 14 1 8 9.0 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
44353012 13389 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192626 13389 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL543898 13389 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10721082 13295 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1191809 13295 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL542958 13295 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
10818426 13361 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192425 13361 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543657 13361 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10746610 13416 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192829 13416 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL544132 13416 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10578612 13732 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1195105 13732 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL553843 13732 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
10722424 170959 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL44557 170959 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
10722424 170959 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL44557 170959 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
11491055 208201 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 723 12 1 7 7.3 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98459 208201 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 723 12 1 7 7.3 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030468n
44360553 13806 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1195619 13806 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL555006 13806 0 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
11377448 13055 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190058 13055 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216622 13055 0 None - 0 Human 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
10842202 13846 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1195903 13846 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL555555 13846 1 None - 0 Guinea pig 9.1 pIC50 = 9.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
9831859 9706 0 None - 1 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL113169 9706 0 None - 1 Guinea pig 9.1 pIC50 = 9.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
11422541 208167 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL98292 208167 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
10627732 22467 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL132510 22467 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
10769383 22865 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL132860 22865 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
10745254 35327 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL143697 35327 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL543781 35327 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
10745254 35327 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL143697 35327 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL543781 35327 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
10745254 35327 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL143697 35327 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL543781 35327 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10579332 13754 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195281 13754 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL554206 13754 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10579332 13754 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195281 13754 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL554206 13754 0 None - 0 Guinea pig 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11239019 13487 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL1193332 13487 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL544720 13487 0 None - 0 Human 9.0 pIC50 = 9 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
11468276 13513 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193590 13513 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL545021 13513 0 None - 0 Human 9.0 pIC50 = 9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10651897 13001 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1189702 13001 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL539294 13001 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
10841531 20558 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130782 20558 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
11801800 21160 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL131263 21160 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
10699672 12957 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189342 12957 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538531 12957 0 None - 0 Guinea pig 9.0 pIC50 = 9.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10348414 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/acs.jmedchem.5b00982
CHEMBL439737 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/acs.jmedchem.5b00982
CHEMBL542096 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/acs.jmedchem.5b00982
10348414 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL439737 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL542096 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10348414 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL439737 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL542096 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11456652 13207 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1191124 13207 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL542176 13207 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
11468051 13690 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1194820 13690 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215558 13690 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10348414 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL439737 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL542096 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10348414 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL439737 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL542096 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10348414 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL439737 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL542096 169073 0 None - 0 Human 9.0 pIC50 = 9.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
11216111 13290 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1191769 13290 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL542911 13290 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
11169915 13539 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1193789 13539 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL545255 13539 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11169975 208200 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
CHEMBL98458 208200 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
11169975 208200 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
CHEMBL98458 208200 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.5 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
11445066 13411 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1192789 13411 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL544087 13411 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
11456756 13809 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195624 13809 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216405 13809 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
22008895 110558 0 None - 1 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL325255 110558 0 None - 1 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10603710 13661 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194615 13661 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL552986 13661 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
10348414 169073 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL439737 169073 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL542096 169073 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 590 9 2 5 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10603710 13661 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1194615 13661 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL552986 13661 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
44360617 13477 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1193249 13477 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL544622 13477 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
10555195 13244 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1191388 13244 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL542479 13244 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
673 1685 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
9810391 1685 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
CHEMBL1192627 1685 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
11801941 13847 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1195904 13847 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL555556 13847 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10698666 14007 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1197062 14007 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL559195 14007 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10627456 20150 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130452 20150 0 None - 0 Guinea pig 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
673 1685 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
9810391 1685 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
CHEMBL1192627 1685 15 None - 0 Human 8.9 pIC50 = 8.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980214f
5311108 1686 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm9002445
674 1686 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm9002445
CHEMBL130517 1686 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm9002445
11204833 111633 1 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 711 12 1 7 6.9 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL328509 111633 1 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 711 12 1 7 6.9 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030468n
11433973 112395 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
CHEMBL329701 112395 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 698 12 2 8 6.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCc5ccccn5)cc(C)nc34)c2Cl)cn1 10.1021/jm030468n
5311108 1686 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
674 1686 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
CHEMBL130517 1686 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980330i
5311108 1686 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
674 1686 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
CHEMBL130517 1686 18 None - 0 Human 8.9 pIC50 = 8.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(cn1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2)Cl)C 10.1021/jm980300f
11802476 12964 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1189415 12964 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL538732 12964 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
11802476 12964 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189415 12964 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538732 12964 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
44360553 13806 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1195619 13806 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL555006 13806 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 645 11 4 8 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCc2cccn2-c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
10721752 169218 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL44087 169218 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
10675847 13417 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1192831 13417 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL544134 13417 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 657 9 2 6 6.0 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10721752 169218 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL44087 169218 0 None - 0 Guinea pig 8.8 pIC50 = 8.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
11308648 13035 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189935 13035 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539792 13035 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
11445066 13411 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1192789 13411 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL544087 13411 0 None - 0 Human 8.8 pIC50 = 8.8 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
122189857 123414 0 None - 2 Guinea pig 8.8 pIC50 = 8.8 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1742 42 23 22 -4.6 C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
CHEMBL3616881 123414 0 None - 2 Guinea pig 8.8 pIC50 = 8.8 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1742 42 23 22 -4.6 C[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
122189855 123412 0 None - 3 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
CHEMBL3616879 123412 0 None - 3 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
3812 717 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
439201 717 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
649 717 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
CHEMBL406291 717 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
DB12126 717 42 None 1 6 Human 8.7 pIC50 = 8.7 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
11399463 13457 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1193123 13457 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3143949 13457 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11399463 13457 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1193123 13457 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3143949 13457 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11445445 13718 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195018 13718 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3215999 13718 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
11204664 111573 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL328131 111573 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
10651897 13001 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1189702 13001 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL539294 13001 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm980300f
122189856 123413 0 None - 1 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1858 43 22 22 -2.5 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616880 123413 0 None - 1 Guinea pig 8.7 pIC50 = 8.7 Binding
Antagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced responseAntagonist activity against B2R in Hartley guinea pig ileum assessed as reduction in electrically-induced response
ChEMBL 1858 43 22 22 -2.5 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)O 10.1016/j.bmcl.2015.08.014
10531744 116343 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL335946 116343 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
10698671 13468 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1193229 13468 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL544599 13468 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 590 9 2 5 6.2 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980300f
119343 2874 22 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None None 10.1016/j.bmc.2013.03.016
676 2874 22 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None None 10.1016/j.bmc.2013.03.016
CHEMBL446325 2874 22 None - 0 Human 8.0 pIC50 = 8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None None 10.1016/j.bmc.2013.03.016
45272156 195059 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL549534 195059 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 556 6 0 7 6.8 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
44190263 195954 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
CHEMBL559565 195954 0 None - 0 Human 8.0 pIC50 = 8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 483 7 1 6 5.4 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C3CCCCC3)c2n1 10.1021/jm9002445
18941145 9963 0 None - 1 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
CHEMBL114732 9963 0 None - 1 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
10627129 101546 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL298320 101546 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
10627129 101546 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL298320 101546 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
10663541 119522 1 None - 0 Guinea pig 5.0 pIC50 = 5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 320 4 0 3 4.8 CCc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
CHEMBL345670 119522 1 None - 0 Guinea pig 5.0 pIC50 = 5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 320 4 0 3 4.8 CCc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
10818058 116584 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL336574 116584 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
10579547 13576 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194034 13576 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545534 13576 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10556247 23028 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL133005 23028 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
44341039 9511 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112140 9511 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
22008892 110162 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL323693 110162 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
10651074 101561 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL298463 101561 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
44189789 196153 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561223 196153 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2n[nH]cc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190166 196634 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564294 196634 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2scnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10651074 101561 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL298463 101561 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10626618 33475 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
CHEMBL142015 33475 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
10603982 80085 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL21311 80085 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
10603982 80085 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL21311 80085 0 None - 0 Guinea pig 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
10579143 168464 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL43510 168464 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10579143 168464 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL43510 168464 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
18941161 9729 0 None - 1 Guinea pig 5.0 pIC50 = 5.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL113320 9729 0 None - 1 Guinea pig 5.0 pIC50 = 5.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10675163 13242 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1191383 13242 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL542472 13242 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
44190854 195445 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL552384 195445 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 6 1 6 4.2 CC(=O)NCc1cncc(Cl)c1COc1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
19603349 13208 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191125 13208 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542177 13208 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
11296863 13410 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1192787 13410 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3216859 13410 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44353012 13389 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192626 13389 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL543898 13389 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 600 8 1 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C\c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10854681 120021 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 339 3 1 3 5.2 Cc1nc2c(NCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
CHEMBL350232 120021 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 339 3 1 3 5.2 Cc1nc2c(NCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
176 398 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2157 398 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2566 398 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
CHEMBL633 398 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
DB01118 398 66 None -5 31 Human 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
11169915 13539 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1193789 13539 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL545255 13539 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 11 2 6 6.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11445445 13718 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195018 13718 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3215999 13718 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 701 10 1 7 6.2 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
11801083 115248 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL334753 115248 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
10530740 165592 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL424268 165592 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
44189792 195135 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550142 195135 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cncs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44340818 110609 0 None - 1 Guinea pig 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL325624 110609 0 None - 1 Guinea pig 5.9 pIC50 = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
11801800 21160 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL131263 21160 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccc(C(=O)N(C)C)c4)c3Cl)c2n1 10.1021/jm980300f
119343 2874 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 bradykinin receptorDisplacement of [3H]bradykinin from human recombinant B2 bradykinin receptor
ChEMBL None None None None 10.1016/j.bmc.2016.03.006
676 2874 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 bradykinin receptorDisplacement of [3H]bradykinin from human recombinant B2 bradykinin receptor
ChEMBL None None None None 10.1016/j.bmc.2016.03.006
CHEMBL446325 2874 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 bradykinin receptorDisplacement of [3H]bradykinin from human recombinant B2 bradykinin receptor
ChEMBL None None None None 10.1016/j.bmc.2016.03.006
44190941 195431 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
CHEMBL552296 195431 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 1 7 3.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNS(C)(=O)=O)c2n1 10.1021/jm9002445
119343 2874 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
ChEMBL None None None None 10.1016/j.bmc.2016.11.014
676 2874 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
ChEMBL None None None None 10.1016/j.bmc.2016.11.014
CHEMBL446325 2874 22 None - 0 Human 7.9 pIC50 = 7.9 Binding
Displacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting methodDisplacement of [3H]bradykinin from human recombinant bradykinin B2 receptor expressed in CHO cells measured after 60 mins by scintillation counting method
ChEMBL None None None None 10.1016/j.bmc.2016.11.014
11800992 118782 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL342016 118782 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10627732 22467 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL132510 22467 0 None - 0 Human 7.9 pIC50 = 7.9 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 623 10 1 7 5.0 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
18941160 9915 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114401 9915 0 None - 1 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10651302 13317 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192012 13317 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543188 13317 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
44190943 195953 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
CHEMBL559564 195953 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 7 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COc3ccccn3)c2n1 10.1021/jm9002445
10743094 45304 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 471 4 0 5 5.5 COC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL152650 45304 0 None - 0 Guinea pig 5.9 pIC50 = 5.9 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 471 4 0 5 5.5 COC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL2392354 210415 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None N=C(N)NCCC[C@H](N)C(=O)N[C@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1016/j.ejmech.2013.01.044
10818067 13362 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1192427 13362 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL543659 13362 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
10722378 21340 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 7 3 6 5.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL131404 21340 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 7 3 6 5.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10698666 14007 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1197062 14007 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL559195 14007 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 589 7 2 5 6.1 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10651301 116528 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336209 116528 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10604425 165147 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL422794 165147 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10552342 47568 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCN(C(C)=O)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154625 47568 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCN(C(C)=O)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10744917 118836 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL342195 118836 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10503130 13004 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 399 3 1 4 4.9 Cc1nc2c(OCc3c(Cl)ccc(N)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL1189725 13004 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 399 3 1 4 4.9 Cc1nc2c(OCc3c(Cl)ccc(N)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL539324 13004 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 399 3 1 4 4.9 Cc1nc2c(OCc3c(Cl)ccc(N)c3Cl)cccn2c1Br 10.1021/jm970591c
10737855 45999 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 368 3 0 3 4.8 Cc1nc2c(OCc3c(F)cccc3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL153271 45999 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 368 3 0 3 4.8 Cc1nc2c(OCc3c(F)cccc3Cl)cccn2c1Br 10.1021/jm970591c
11239381 13144 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1190638 13144 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215541 13144 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10601892 47031 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL154188 47031 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL558018 47031 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10699672 12957 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1189342 12957 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL538531 12957 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 671 9 1 6 6.1 CC(=O)N(C)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10601892 47031 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154188 47031 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL558018 47031 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10531338 91707 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL240875 91707 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
10531338 91707 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL240875 91707 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
10506334 119639 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 0 5 4.7 CC(=O)N(C)CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL346718 119639 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 0 5 4.7 CC(=O)N(C)CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11491041 13456 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1193122 13456 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL544480 13456 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 719 11 2 8 7.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
11800992 118782 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL342016 118782 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C\c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10744917 118836 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL342195 118836 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 536 9 2 5 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2cccc(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10579159 119307 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
CHEMBL344021 119307 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
10674242 24157 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL133913 24157 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
11801594 100432 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL290431 100432 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
11801594 100432 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL290431 100432 0 None - 0 Guinea pig 6.8 pIC50 = 6.8 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
10693943 119610 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 428 3 0 3 5.4 Cc1nc2c(OCc3c(Br)cccc3Br)cccn2c1Cl 10.1021/jm970591c
CHEMBL346458 119610 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 428 3 0 3 5.4 Cc1nc2c(OCc3c(Br)cccc3Br)cccn2c1Cl 10.1021/jm970591c
10554743 115154 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL334421 115154 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
44190752 195346 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
CHEMBL551759 195346 0 None - 0 Human 7.8 pIC50 = 7.8 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 476 6 0 8 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccn3C)c2n1 10.1021/jm9002445
10508305 13609 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194233 13609 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545765 13609 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10836951 47490 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 4 1 4 5.2 CC(=O)Nc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154558 47490 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 4 1 4 5.2 CC(=O)Nc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10518915 119564 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 308 3 0 3 4.2 Cc1nc2c(OCc3c(F)cccc3F)cccn2c1Cl 10.1021/jm970591c
CHEMBL346034 119564 0 None - 0 Guinea pig 5.8 pIC50 = 5.8 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 308 3 0 3 4.2 Cc1nc2c(OCc3c(F)cccc3F)cccn2c1Cl 10.1021/jm970591c
10649831 13369 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1192462 13369 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL543700 13369 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11262636 13837 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1195841 13837 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215972 13837 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11801941 13847 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1195904 13847 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL555556 13847 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 614 7 2 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C#N)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10841637 13919 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1196403 13919 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL556816 13919 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
11181406 12938 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL1189212 12938 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL3217073 12938 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
11479285 13155 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190741 13155 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3143958 13155 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11479285 13155 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190741 13155 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3143958 13155 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
10650330 13160 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1190789 13160 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL541590 13160 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
10604425 165147 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL422794 165147 0 None - 0 Guinea pig 8.7 pIC50 = 8.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 661 9 2 7 6.3 CCOC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10722424 170959 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL44557 170959 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm030159x
19603349 13208 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191125 13208 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542177 13208 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 685 10 3 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)Nc5ccncc5)c4)c3Cl)c2n1 10.1021/jm030326t
673 1685 15 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
9810391 1685 15 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
CHEMBL1192627 1685 15 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 671 9 1 6 5.8 O=C(/C=C/c1ccc(cc1)C(=O)N(C)C)NCC(=O)N(c1ccc(c(c1Cl)COc1cccn2c1nc(c2Br)C)Cl)C 10.1021/jm980300f
10722424 170959 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL44557 170959 0 None - 0 Human 8.7 pIC50 = 8.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 609 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(OC)n4C)c2Cl)cc1 10.1021/jm980300f
5311114 1688 8 None - 1 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
668 1688 8 None - 1 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
CHEMBL99869 1688 8 None - 1 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 10.1021/jm030468n
10841582 13243 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1191384 13243 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL542473 13243 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
9894265 31538 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL140383 31538 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10793563 13840 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195858 13840 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL555465 13840 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10769517 23456 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL133339 23456 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
10840534 22573 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL132620 22573 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
10349737 13116 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1190430 13116 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL540840 13116 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
10840534 22573 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL132620 22573 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm970591c
11320262 208179 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 775 14 2 9 7.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)Cc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98349 208179 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 775 14 2 9 7.2 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)Cc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm030468n
11181524 208021 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
CHEMBL97393 208021 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
11193509 13737 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195125 13737 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553897 13737 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
10818067 13362 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1192427 13362 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL543659 13362 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
10793563 13840 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195858 13840 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL555465 13840 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10842202 13846 1 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1195903 13846 1 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL555555 13846 1 None - 0 Human 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 3 6 5.8 CNC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
11343115 13074 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1190165 13074 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL540300 13074 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
44360818 13478 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL1193250 13478 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
CHEMBL544623 13478 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 783 14 1 8 10.3 Cc1ccc2cccc(OCc3c(/C=C/c4ccncc4)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(/C=C/c5ccncc5)nc4)c3/C=C/c3ccncc3)c2n1 10.1021/jm980330i
9894265 31538 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL140383 31538 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 569 9 2 4 7.1 CNC(=O)c1ccc(/C=C/C(=O)NCc2ccccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10651302 13317 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192012 13317 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543188 13317 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10604560 20405 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL130660 20405 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
11250851 13617 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1194270 13617 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3216880 13617 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cccn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11296863 13410 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1192787 13410 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3216859 13410 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 675 10 2 7 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10769485 20550 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL130775 20550 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10746877 13818 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1195721 13818 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL555202 13818 0 None - 0 Human 8.6 pIC50 = 8.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
11479285 13155 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190741 13155 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3143958 13155 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
11479285 13155 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190741 13155 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3143958 13155 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 1 6 6.0 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
11343115 13074 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1190165 13074 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL540300 13074 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 692 13 2 8 5.5 CCOC(=O)COc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
10818426 13361 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192425 13361 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL543657 13361 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 690 11 3 7 5.5 COCCNC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
10651980 13418 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1192832 13418 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544135 13418 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 660 8 2 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)N(C)C)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190269 196196 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561415 196196 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2nscc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10555263 101096 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295005 101096 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
10841582 13243 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1191384 13243 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL542473 13243 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 8 2 6 6.1 COc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
44191220 195030 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL549337 195030 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.3 Cc1cc(-n2ccnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190168 195118 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550016 195118 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2csnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44191224 196261 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561839 196261 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 412 4 0 5 5.5 Cc1cc(-c2ncc(C)n2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10569271 49986 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 340 3 0 3 5.2 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
CHEMBL156902 49986 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 340 3 0 3 5.2 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Cl 10.1021/jm970591c
10555263 101096 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295005 101096 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
10699094 23261 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
CHEMBL133186 23261 0 None - 0 Human 5.7 pIC50 = 5.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
127034153 138564 0 None - 0 Human 4.7 pIC50 = 4.7 Binding
Inhibition of recombinant human bradykinin receptor 2 expressed in CHO cellsInhibition of recombinant human bradykinin receptor 2 expressed in CHO cells
ChEMBL 365 5 2 3 4.5 CC(C)CN1[C@H](C)Cc2cc(O)ccc2[C@H]1c1ccc(/C=C/C(=O)O)cc1 10.1021/acsmedchemlett.5b00413
CHEMBL3775378 138564 0 None - 0 Human 4.7 pIC50 = 4.7 Binding
Inhibition of recombinant human bradykinin receptor 2 expressed in CHO cellsInhibition of recombinant human bradykinin receptor 2 expressed in CHO cells
ChEMBL 365 5 2 3 4.5 CC(C)CN1[C@H](C)Cc2cc(O)ccc2[C@H]1c1ccc(/C=C/C(=O)O)cc1 10.1021/acsmedchemlett.5b00413
1016 3747 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2561 3747 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2733526 3747 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
5384 3747 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
CHEMBL83 3747 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
DB00675 3747 78 None -46 35 Human 4.7 pIC50 = 4.7 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
72548703 161567 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysisDisplacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysis
ChEMBL 583 8 3 6 5.8 CC(C)(C)NS(=O)(=O)c1ccc(-c2sc(C(=O)N[C@H]3C[C@H](C(=O)O)C3)nc2CC2CCCCC2)c2ccccc12 10.1016/j.bmcl.2018.03.093
CHEMBL4128926 161567 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysisDisplacement of [3H]bradykinin from human recombinant B2 receptor after 60 mins by scintillation counting analysis
ChEMBL 583 8 3 6 5.8 CC(C)(C)NS(=O)(=O)c1ccc(-c2sc(C(=O)N[C@H]3C[C@H](C(=O)O)C3)nc2CC2CCCCC2)c2ccccc12 10.1016/j.bmcl.2018.03.093
11296704 13825 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL1195759 13825 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL3216408 13825 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
22008929 9750 0 None - 1 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113465 9750 0 None - 1 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44190268 196511 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563516 196511 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2ncsc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10579159 119307 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
CHEMBL344021 119307 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 582 11 2 7 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(OC)c(COc3cccc4ccc(C)nc34)c2OC)cc1 10.1021/jm980330i
10791325 44762 0 None - 0 Guinea pig 5.7 pIC50 = 5.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 491 5 0 5 4.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)S(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL152158 44762 0 None - 0 Guinea pig 5.7 pIC50 = 5.7 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 491 5 0 5 4.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)S(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
10841393 13283 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL1191700 13283 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL542836 13283 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
10841393 13283 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL1191700 13283 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL542836 13283 0 None - 0 Human 7.7 pIC50 = 7.7 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
10792967 78527 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL2111974 78527 0 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
10507708 161823 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL41446 161823 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
10507708 161823 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL41446 161823 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
9851817 9681 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL112991 9681 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
10762703 47255 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 384 3 0 3 5.3 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL154386 47255 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 384 3 0 3 5.3 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1Br 10.1021/jm970591c
44323787 13016 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189812 13016 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215529 13016 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11468071 13037 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189943 13037 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL539800 13037 0 None - 0 Guinea pig 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10555061 116966 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL338682 116966 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
11411594 12908 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189023 12908 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL537927 12908 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
11239502 13703 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1194911 13703 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL553530 13703 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
44340760 110508 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL324950 110508 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
11468071 13037 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189943 13037 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL539800 13037 0 None - 0 Human 5.6 pIC50 = 5.6 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 676 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCN(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11181524 208021 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
CHEMBL97393 208021 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 686 12 2 8 6.1 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1Cc1ccccc1 10.1021/jm030468n
10816636 13767 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 2 5 5.0 CCCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1195365 13767 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 2 5 5.0 CCCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL554412 13767 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 555 8 2 5 5.0 CCCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10841531 20558 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL130782 20558 0 None - 0 Human 7.6 pIC50 = 7.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
44214279 9716 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL113222 9716 0 None - 1 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
10675163 13242 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL1191383 13242 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
CHEMBL542472 13242 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980214f
10507708 161823 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL41446 161823 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm030159x
10507708 161823 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL41446 161823 0 None - 0 Human 6.6 pIC50 = 6.6 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 5 6.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(C)c(C)oc34)c2Cl)cc1 10.1021/jm980300f
11422667 12985 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189575 12985 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539023 12985 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
11456756 13809 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195624 13809 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216405 13809 0 None - 0 Guinea pig 7.6 pIC50 = 7.6 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 699 10 1 6 7.3 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm030326t
10555202 116752 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
CHEMBL337555 116752 0 None - 0 Guinea pig 6.6 pIC50 = 6.6 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
11468276 13513 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193590 13513 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL545021 13513 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
15388873 114731 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL333832 114731 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
11801594 100432 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL290431 100432 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm030159x
11801594 100432 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL290431 100432 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
10009762 12929 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1189175 12929 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217072 12929 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 678 10 1 7 7.4 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
10579332 13754 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195281 13754 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL554206 13754 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
11239019 13487 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL1193332 13487 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL544720 13487 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 626 10 2 5 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c(-c5ccccc5)cc(C)nc34)c2C)cc1 10.1021/jm030159x
11399463 13457 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1193123 13457 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3143949 13457 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11399463 13457 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1193123 13457 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3143949 13457 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 633 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44361029 13366 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL1192448 13366 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
CHEMBL543685 13366 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 714 11 1 7 5.3 Cc1ccc2cccc(OCc3c(N4CCCC4=O)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3N3CCCC3=O)c2n1 10.1021/jm980330i
10555818 13685 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194778 13685 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553293 13685 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 616 9 1 5 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)c2n1 10.1021/jm980300f
10746877 13818 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1195721 13818 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL555202 13818 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 654 10 2 7 6.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)nc4)c3Cl)c2n1 10.1021/jm980300f
667 1973 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
71364 1973 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
CHEMBL2028850 1973 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
DB06196 1973 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980300f
667 1973 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
71364 1973 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
CHEMBL2028850 1973 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
DB06196 1973 37 None -1 6 Human 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL None None None None 10.1021/jm980214f
9874617 13306 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191908 13306 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543070 13306 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
10674242 24157 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL133913 24157 0 None - 0 Guinea pig 8.5 pIC50 = 8.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cc1 10.1021/jm980300f
11169752 112409 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL329758 112409 0 None - 0 Human 8.5 pIC50 = 8.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
10652092 13017 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189828 13017 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL539550 13017 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 672 9 1 7 5.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)cccn2c1Br 10.1021/jm980214f
11273808 13798 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195573 13798 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3215979 13798 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 656 10 2 7 5.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5ccnc5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11491069 12916 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189082 12916 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538020 12916 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
10841637 13919 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1196403 13919 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL556816 13919 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 623 7 2 5 6.7 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(Cl)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
10580536 12940 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189218 12940 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL538281 12940 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10603710 13661 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1194615 13661 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL552986 13661 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
44360617 13477 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL1193249 13477 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
CHEMBL544622 13477 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 678 11 1 7 4.0 Cc1ccc2cccc(OCc3c(C(=O)N(C)C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C(=O)N(C)C)c2n1 10.1021/jm980330i
10603710 13661 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194615 13661 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL552986 13661 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 604 9 1 5 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
11491069 12916 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189082 12916 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538020 12916 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 691 12 2 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)N(C)C)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11365972 13643 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1194477 13643 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216391 13643 0 None - 0 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 1 6 6.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
10818058 116584 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL336574 116584 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm980300f
10840241 116469 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336116 116469 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
44191226 195302 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551435 195302 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 1 4 5.2 Cc1cc(-c2ccn[nH]2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10756101 46081 4 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 292 3 0 3 4.2 Clc1cccc(Cl)c1COc1cccn2ccnc12 10.1021/jm970591c
CHEMBL153344 46081 4 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 292 3 0 3 4.2 Clc1cccc(Cl)c1COc1cccn2ccnc12 10.1021/jm970591c
44369201 121457 0 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 381 5 0 4 5.8 CCn1c(C)cc(C#N)c1-c1ccc(COc2cc(C)nc3ccccc23)cc1 10.1021/jm970591c
CHEMBL358232 121457 0 None - 0 Guinea pig 4.5 pIC50 = 4.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 381 5 0 4 5.8 CCn1c(C)cc(C#N)c1-c1ccc(COc2cc(C)nc3ccccc23)cc1 10.1021/jm970591c
44191225 196396 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562747 196396 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2cccn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL2372276 210206 0 None 3 3 Human 7.5 pIC50 = 7.5 Binding
Displacement of radiolabeled NPC 567 from human bradykinin B2 receptorDisplacement of radiolabeled NPC 567 from human bradykinin B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm8007618
44341214 110430 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL324575 110430 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44190853 196289 4 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
CHEMBL562097 196289 4 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 7 1 6 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(N)=O)c2n1 10.1021/jm9002445
11250929 13835 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/acs.jmedchem.5b00982
CHEMBL1195824 13835 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/acs.jmedchem.5b00982
CHEMBL555403 13835 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Displacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counterDisplacement of [3H]BK from cloned human B2 bradykinin receptor expressed in CHO cells after 2 hrs by liquid scintillation counter
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/acs.jmedchem.5b00982
11250929 13835 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1195824 13835 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL555403 13835 0 None - 0 Human 7.5 pIC50 = 7.5 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 634 11 2 6 6.0 CCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
10579723 21317 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL131380 21317 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
9958759 13471 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1193231 13471 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL544601 13471 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 533 8 1 4 6.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccccc4)c3Cl)c2n1 10.1021/jm980300f
10699094 23261 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
CHEMBL133186 23261 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
10627456 20150 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130452 20150 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 602 9 1 5 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10504612 121130 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 4 1 4 5.1 CNC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL357530 121130 0 None - 0 Guinea pig 6.5 pIC50 = 6.5 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 4 1 4 5.1 CNC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10699094 23261 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
CHEMBL133186 23261 0 None - 0 Human 5.5 pIC50 = 5.5 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 619 10 2 6 5.5 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccnc3-n3c(C)ccc3C)c2Cl)cc1 10.1021/jm980300f
44190756 195437 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552359 195437 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 0 6 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CCC(=O)N(C)C)c2n1 10.1021/jm9002445
44189790 196642 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL564341 196642 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 1 4 5.5 Cc1cc(-c2cn[nH]c2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44190754 196448 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563068 196448 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 497 7 0 7 3.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3[S+]([O-])CC(=O)N(C)C)c2n1 10.1021/jm9002445
11239595 13723 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195041 13723 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553762 13723 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 738 11 2 8 6.7 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
11433935 13206 1 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191123 13206 1 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215986 13206 1 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10531338 91707 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL240875 91707 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm980300f
10531338 91707 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL240875 91707 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 582 10 2 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(N(C)C)n4C)c2C)cc1 10.1021/jm030159x
10579143 168464 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL43510 168464 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10790603 45164 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 5 1 5 4.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CN)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL152542 45164 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 470 5 1 5 4.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CN)c3Cl)cccn2c1Br 10.1021/jm970591c
10579143 168464 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL43510 168464 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10555195 13244 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1191388 13244 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
CHEMBL542479 13244 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3C)c2n1 10.1021/jm980300f
44346506 11439 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
Compound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenatesCompound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenates
ChEMBL 545 29 0 0 12.9 CCCC[P+](CCCC)(CCCC)CCCCCCCCCC[P+](CCCC)(CCCC)CCCC 10.1016/0960-894X(95)00035-R
CHEMBL1180320 11439 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
Compound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenatesCompound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenates
ChEMBL 545 29 0 0 12.9 CCCC[P+](CCCC)(CCCC)CCCCCCCCCC[P+](CCCC)(CCCC)CCCC 10.1016/0960-894X(95)00035-R
CHEMBL121851 11439 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
Compound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenatesCompound was evaluated for competitive [3H]bradykinin binding to guinea pig ileum homogenates
ChEMBL 545 29 0 0 12.9 CCCC[P+](CCCC)(CCCC)CCCCCCCCCC[P+](CCCC)(CCCC)CCCC 10.1016/0960-894X(95)00035-R
44340964 9707 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113176 9707 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
44190944 195933 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559436 195933 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 539 6 0 7 5.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
11479294 13824 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195758 13824 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216404 13824 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
11801083 115248 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL334753 115248 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 565 9 1 6 4.6 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3C)c2n1 10.1021/jm980300f
10604613 13113 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1190420 13113 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL540828 13113 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 683 9 1 6 6.2 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
11422541 208167 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL98292 208167 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 682 13 2 10 4.6 CCOC(=O)Cn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
10508305 13609 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194233 13609 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545765 13609 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 8 2 7 6.0 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc([N+](=O)[O-])c4)c3Cl)cccn2c1Br 10.1021/jm980214f
18923274 19825 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130196 19825 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10675243 96780 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
CHEMBL264751 96780 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm030468n
11490605 13751 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1195242 13751 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL554127 13751 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
10675243 96780 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL264751 96780 0 None - 0 Human 8.4 pIC50 = 8.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 610 10 2 8 4.6 COc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc2n1C 10.1021/jm980300f
11445288 13876 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1196072 13876 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL3217085 13876 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 670 10 1 7 6.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
18704946 13170 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1190879 13170 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL3217081 13170 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 657 10 2 8 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(-n5cncn5)cc(C)nc34)c2Cl)cc1 10.1021/jm030159x
11169752 112409 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
CHEMBL329758 112409 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 654 13 2 9 4.7 COCCn1c(OC)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3Cl)cccc21 10.1021/jm030468n
44360879 12971 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL1189464 12971 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
CHEMBL538784 12971 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 637 11 4 8 2.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C(=O)NC)c(COc3cccc4ccc(C)nc34)c2C(=O)NC)cn1 10.1021/jm980330i
10531497 13213 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL1191172 13213 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
CHEMBL542232 13213 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980300f
10580536 12940 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1189218 12940 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL538281 12940 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 693 10 2 7 5.5 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NS(C)(=O)=O)cc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10745254 35327 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL143697 35327 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
CHEMBL543781 35327 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm030159x
11296704 13825 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL1195759 13825 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
CHEMBL3216408 13825 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 647 10 2 6 6.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1C 10.1021/jm030326t
10745254 35327 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL143697 35327 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL543781 35327 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
10745254 35327 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL143697 35327 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
CHEMBL543781 35327 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 550 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980300f
11193509 13737 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195125 13737 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL553897 13737 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 750 12 2 7 7.5 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
11331301 13287 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191763 13287 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215537 13287 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44375675 56506 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
In vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assayIn vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assay
ChEMBL 605 12 4 7 4.9 O=C(O)CN(Cc1ccccc1)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1016/s0960-894x(01)00044-0
CHEMBL163506 56506 0 None - 0 Rat 6.4 pIC50 = 6.4 Binding
In vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assayIn vitro binding affinity against Bradykinin receptor B2 in rat NG 108-15 neuroblastoma-glioma hybrid cell membranes using [3H]BK binding assay
ChEMBL 605 12 4 7 4.9 O=C(O)CN(Cc1ccccc1)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1016/s0960-894x(01)00044-0
10789357 47573 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 5 0 4 5.7 CCN(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154633 47573 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 441 5 0 4 5.7 CCN(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10601892 47031 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL154188 47031 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL558018 47031 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 512 6 1 5 4.4 CC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
11796916 49980 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 429 4 0 5 5.2 Cc1nc2c(OCc3c(Cl)ccc([N+](=O)[O-])c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL156899 49980 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 429 4 0 5 5.2 Cc1nc2c(OCc3c(Cl)ccc([N+](=O)[O-])c3Cl)cccn2c1Br 10.1021/jm970591c
44190165 195963 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559645 195963 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2nccs2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11799290 49925 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 489 4 0 4 5.9 CC(=O)N(C)c1c(Cl)cc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL156847 49925 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 489 4 0 4 5.9 CC(=O)N(C)c1c(Cl)cc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10555202 116752 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
CHEMBL337555 116752 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 577 9 3 6 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)Nc2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cn1 10.1021/jm980330i
9916589 100238 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL288603 100238 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
11377448 13055 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1190058 13055 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216622 13055 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 689 10 1 7 5.8 Cc1cc(N2CCOCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030326t
44190361 194803 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL538865 194803 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2conc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11801594 100432 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL290431 100432 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4nc(C)cnc34)c2Cl)cc1 10.1021/jm980300f
10531744 116343 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL335946 116343 0 None - 0 Human 7.4 pIC50 = 7.4 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 605 9 1 6 5.3 Cc1cnc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm980300f
44191221 196237 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2cncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561701 196237 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2cncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10852230 49617 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 306 3 0 3 4.5 Cc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
CHEMBL156606 49617 0 None - 0 Guinea pig 5.4 pIC50 = 5.4 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 306 3 0 3 4.5 Cc1cn2cccc(OCc3c(Cl)cccc3Cl)c2n1 10.1021/jm970591c
10792291 13895 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 527 6 2 5 4.2 CNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1196218 13895 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 527 6 2 5 4.2 CNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL556176 13895 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 527 6 2 5 4.2 CNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10769517 23456 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL133339 23456 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 577 9 1 6 5.1 Cc1cnc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
44214619 110605 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
CHEMBL325601 110605 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
44190751 195345 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from wild-type B2 receptorDisplacement of [3H]bradykinin from wild-type B2 receptor
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
CHEMBL551758 195345 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from wild-type B2 receptorDisplacement of [3H]bradykinin from wild-type B2 receptor
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
10721082 13295 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1191809 13295 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL542958 13295 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 534 8 1 5 5.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4cccnc4)c3Cl)c2n1 10.1021/jm980300f
10530740 165592 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL424268 165592 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 552 9 2 7 4.3 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
10675204 168780 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
CHEMBL43746 168780 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
10675204 168780 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
CHEMBL43746 168780 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
10603884 20137 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130438 20137 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
11331301 13287 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191763 13287 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215537 13287 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 13 3 7 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(NCCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
11796407 47775 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 418 3 0 3 5.9 Cc1nc2c(OCc3c(Cl)ccc(Cl)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL154823 47775 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 418 3 0 3 5.9 Cc1nc2c(OCc3c(Cl)ccc(Cl)c3Cl)cccn2c1Br 10.1021/jm970591c
44190942 196227 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
CHEMBL561634 196227 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 471 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cn3ccccc3=O)c2n1 10.1021/jm9002445
10032884 13465 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1193185 13465 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL544549 13465 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10626618 33475 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
CHEMBL142015 33475 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 556 9 2 5 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2)cc1 10.1021/jm980330i
10579332 13754 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1195281 13754 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL554206 13754 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm030159x
44340859 10043 0 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL115163 10043 0 None - 1 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
11801968 13711 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1194974 13711 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL553614 13711 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 617 9 1 6 5.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)nc4)c3Cl)c2n1 10.1021/jm980300f
10579332 13754 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1195281 13754 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL554206 13754 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ncc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10793528 13470 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1193230 13470 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544600 13470 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190581 195944 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL559506 195944 0 None - 0 Human 8.3 pIC50 = 8.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 443 7 1 6 4.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
10555061 116966 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL338682 116966 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 1 5 6.0 CCCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
11181406 12938 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL1189212 12938 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
CHEMBL3217073 12938 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 663 11 2 7 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cc1OC 10.1021/jm030326t
10769485 20550 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
CHEMBL130775 20550 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 575 9 2 5 7.2 CNC(=O)c1ccc(/C=C/C(=O)NCc2sccc2-c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cc1 10.1021/jm980330i
11422667 12985 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189575 12985 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539023 12985 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 710 12 2 7 6.6 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030326t
11158136 208444 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 664 12 3 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)O)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL99978 208444 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 664 12 3 7 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OCC(=O)O)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
44190751 195345 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
CHEMBL551758 195345 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 479 6 0 8 6.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Sc3nccs3)c2n1 10.1021/jm9002445
44189787 196344 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL562434 196344 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10553878 47630 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 513 6 0 6 4.8 CC(=O)OCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154682 47630 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 513 6 0 6 4.8 CC(=O)OCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10842026 96722 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 655 10 2 6 6.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(-c3ccccc3)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL264259 96722 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 655 10 2 6 6.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(-c3ccccc3)n4C)c2Cl)cc1 10.1021/jm980300f
18923274 19825 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130196 19825 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 604 9 1 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)COc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10579723 21317 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL131380 21317 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 617 7 2 6 5.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NC(=O)c4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190672 195344 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551757 195344 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 364 4 0 5 4.6 Cc1cc(-c2ccnn2C)c2cccc(OCc3ccncc3Cl)c2n1 10.1021/jm9002445
10722735 20064 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130379 20064 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
22008916 9762 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL113502 9762 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
44190363 195303 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 318 3 0 3 4.8 Cc1ccc2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551436 195303 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 318 3 0 3 4.8 Cc1ccc2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10575810 121478 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 455 4 0 4 5.3 CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL358234 121478 0 None - 0 Guinea pig 7.3 pIC50 = 7.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 455 4 0 4 5.3 CC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10693220 47367 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 414 4 0 4 5.3 COc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154465 47367 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 414 4 0 4 5.3 COc1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10651074 101561 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL298463 101561 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm030159x
10651074 101561 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL298463 101561 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
44340951 10002 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114915 10002 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
11262636 13837 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1195841 13837 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215972 13837 0 None - 0 Guinea pig 6.3 pIC50 = 6.3 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 721 16 2 8 5.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(CCOC)CCOC)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10579547 13576 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1194034 13576 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL545534 13576 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 603 8 2 5 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10650330 13160 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1190789 13160 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL541590 13160 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
44191138 195916 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL559273 195916 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 384 4 0 5 5.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10578574 13583 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 548 7 1 6 3.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNS(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL1194067 13583 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 548 7 1 6 3.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNS(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
CHEMBL545573 13583 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 548 7 1 6 3.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNS(C)(=O)=O)c3Cl)cccn2c1Br 10.1021/jm970591c
10743570 46944 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 485 6 0 5 4.9 COCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154122 46944 0 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 485 6 0 5 4.9 COCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10651074 101561 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL298463 101561 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 591 9 2 6 5.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4cnc(C)nc34)c2Cl)cc1 10.1021/jm980300f
10554743 115154 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL334421 115154 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 552 9 2 7 3.7 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ncc(C)nc34)c2C)cn1 10.1021/jm980300f
45267862 196320 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
CHEMBL562296 196320 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 434 5 0 7 4.3 CC(=O)OCc1cncc(Cl)c1C(=O)c1cccc2c(-c3ccnn3C)cc(C)nc12 10.1021/jm9002445
11227974 13305 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191906 13305 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL543068 13305 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 741 12 2 8 8.1 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(-n4cccc4CNC(=O)/C=C/c4ccc(C(=O)NCc5ccccn5)cc4)c3Cl)c2n1 10.1021/jm030159x
11479739 208203 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
CHEMBL98460 208203 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the B2 receptor in guinea pig ileum membrane;
ChEMBL 760 13 2 8 7.8 Cc1cc(OCc2ccccn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030468n
10556247 23028 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL133005 23028 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 652 10 2 5 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5ccccc5)cc4)c3Cl)c2n1 10.1021/jm980300f
10394861 1689 5 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
669 1689 5 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
CHEMBL329762 1689 5 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2Concentration required to inhibit specific binding of [3H]-BK(0.06 nM) to the bradykinin receptor B2
ChEMBL 687 12 2 9 5.5 COc1nc2c(n1Cc1ccccn1)cccc2OCc1c(Cl)ccc(c1Cl)N(C(=O)CNC(=O)/C=C/c1ccc(nc1)NC(=O)C)C 10.1021/jm030468n
11490605 13751 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1195242 13751 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL554127 13751 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 634 10 2 7 5.6 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N(C)C)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
44190755 195827 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL558279 195827 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 7 0 7 4.0 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3OCC(=O)N(C)C)c2n1 10.1021/jm9002445
44190851 196570 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL563878 196570 0 None - 0 Human 8.2 pIC50 = 8.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 464 6 1 6 4.3 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)N(C)C)c2n1 10.1021/jm9002445
44214214 13261 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1191492 13261 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL542598 13261 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 708 10 3 8 7.0 Cc1cc(-n2ccnc2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4ccc(C(=O)Nc5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030159x
11251046 13205 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1191121 13205 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL542173 13205 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 696 11 2 7 6.9 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
44190169 195288 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2ocnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL551354 195288 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 5 5.8 Cc1cc(-c2ocnc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10746610 13416 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL1192829 13416 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL544132 13416 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 631 8 2 6 6.3 CC(=O)c1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
11239502 13703 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1194911 13703 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL553530 13703 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 674 11 2 6 6.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
10506663 21432 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL131517 21432 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10722735 20064 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130379 20064 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 633 8 3 6 5.8 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Nc4cccc(C(=O)O)c4)c3Cl)cccn2c1Br 10.1021/jm980214f
44190167 196489 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563391 196489 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 415 4 0 5 6.3 Cc1cc(-c2ncsc2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10895913 9869 0 None - 1 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL114180 9869 0 None - 1 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
11204664 111573 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL328131 111573 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 5.4 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
9916589 100238 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL288603 100238 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
9916589 100238 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL288603 100238 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
10793528 13470 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL1193230 13470 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL544600 13470 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 588 8 1 5 5.6 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)Cc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10793125 100177 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL288079 100177 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
10793125 100177 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL288079 100177 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
44190077 196470 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563254 196470 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2ncnn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11468051 13690 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1194820 13690 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215558 13690 0 None - 0 Guinea pig 7.2 pIC50 = 7.2 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 673 10 2 6 6.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
119343 2874 22 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of human bradykinin B2 receptorInhibition of human bradykinin B2 receptor
ChEMBL None None None None 10.1021/jm701575k
676 2874 22 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of human bradykinin B2 receptorInhibition of human bradykinin B2 receptor
ChEMBL None None None None 10.1021/jm701575k
CHEMBL446325 2874 22 None - 0 Human 8.2 pIC50 = 8.2 Binding
Inhibition of human bradykinin B2 receptorInhibition of human bradykinin B2 receptor
ChEMBL None None None None 10.1021/jm701575k
10721752 169218 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL44087 169218 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm030159x
10721752 169218 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL44087 169218 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 569 10 2 7 3.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(OC)n4C)c2C)cc1 10.1021/jm980300f
44190753 196703 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL564841 196703 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 481 7 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3SCC(=O)N(C)C)c2n1 10.1021/jm9002445
10580156 13111 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL1190412 13111 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
CHEMBL540819 13111 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 653 10 2 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)Nc5cccnc5)cc4)c3Cl)c2n1 10.1021/jm980300f
44190850 195223 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
CHEMBL550827 195223 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 463 7 1 6 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3CNC(=O)C(C)C)c2n1 10.1021/jm9002445
10816618 13774 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 554 9 1 5 5.6 CCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL1195382 13774 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 554 9 1 5 5.6 CCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL554431 13774 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 554 9 1 5 5.6 CCCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10792967 78527 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
CHEMBL2111974 78527 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.Inhibition of the specific binding of [3H]BK to human recombinant Bradykinin receptor B2 expressed in CHO cells.
ChEMBL 559 9 2 4 6.6 CNC(=O)c1ccc(/C=C/C(=O)NC/C=C/c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm980330i
44189791 196566 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2nncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL563861 196566 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 399 4 0 6 4.6 Cc1cc(-c2nncn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
10672078 48284 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL155339 48284 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 469 5 0 4 5.7 CCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11801411 101344 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL296865 101344 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
11801411 101344 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL296865 101344 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
10604560 20405 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
CHEMBL130660 20405 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 676 10 3 7 5.7 COCC(=O)Nc1cccc(NC(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)c1 10.1021/jm980214f
11308648 13035 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1189935 13035 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL539792 13035 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 736 11 2 7 7.9 Cc1cc(N2CCCCC2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(=O)c5ccncc5)cc4)c3Cl)c2n1 10.1021/jm030326t
10568916 46668 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 336 4 1 4 4.0 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1CO 10.1021/jm970591c
CHEMBL153890 46668 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 336 4 1 4 4.0 Cc1nc2c(OCc3c(Cl)cccc3Cl)cccn2c1CO 10.1021/jm970591c
13825921 45060 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 374 6 0 4 4.7 C#CCOCc1c(C)nc2c(OCc3c(Cl)cccc3Cl)cccn12 10.1021/jm970591c
CHEMBL152439 45060 0 None - 0 Guinea pig 5.1 pIC50 = 5.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 374 6 0 4 4.7 C#CCOCc1c(C)nc2c(OCc3c(Cl)cccc3Cl)cccn12 10.1021/jm970591c
11216111 13290 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL1191769 13290 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
CHEMBL542911 13290 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 648 12 2 6 6.4 CCCOc1cc(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc12 10.1021/jm030468n
15388870 110633 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL325742 110633 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
10768499 46953 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 1 5 4.8 CC(=O)NC(C)C(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL154130 46953 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 6 1 5 4.8 CC(=O)NC(C)C(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10745895 101155 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295428 101155 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
10745895 101155 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295428 101155 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
11158089 12917 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL1189084 12917 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
CHEMBL538022 12917 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cellsInhibition of [3H]BK (1.0 nM) binding to the human bradykinin receptor B2, expressed in CHO cells
ChEMBL 620 10 2 6 5.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(OC)cc(C)nc34)c2Cl)cc1 10.1021/jm030468n
11479294 13824 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL1195758 13824 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
CHEMBL3216404 13824 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 648 10 1 7 5.4 Cc1cc(N(C)C)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)nc4)c3Cl)c2n1 10.1021/jm030326t
44190852 195406 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
CHEMBL552090 195406 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 465 6 0 7 4.8 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(Cl)cncc3COC(=O)N(C)C)c2n1 10.1021/jm9002445
10578612 13732 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL1195105 13732 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
CHEMBL553843 13732 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 551 9 2 6 4.9 CC(=O)Nc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1021/jm980300f
10769383 22865 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL132860 22865 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 570 10 2 8 3.9 COc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(NC(C)=O)nc4)c3C)cccc2n1C 10.1021/jm980300f
10841393 13283 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL1191700 13283 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
CHEMBL542836 13283 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm980300f
25019714 196583 2 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL563956 196583 2 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 1 6 5.8 Cc1cc(-c2[nH]ncc2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
10841393 13283 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL1191700 13283 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
CHEMBL542836 13283 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.2 CCc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc2n1C 10.1021/jm030159x
44191040 195984 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
CHEMBL559825 195984 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 519 6 0 7 5.5 Cc1cc(-c2ccnn2C)c2cccc(OCc3c(C)ccnc3Cn3cccc(C(F)(F)F)c3=O)c2n1 10.1021/jm9002445
10675204 168780 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
CHEMBL43746 168780 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm980300f
10603884 20137 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL130438 20137 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 616 10 1 5 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CCCc4ccccc4)c3Cl)cccn2c1Br 10.1021/jm980214f
10506663 21432 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL131517 21432 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10506663 21432 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL131517 21432 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 540 8 1 5 5.2 CCCC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10675204 168780 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
CHEMBL43746 168780 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 607 10 2 6 5.4 CCn1c(C)nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3Cl)cccc21 10.1021/jm030159x
44190267 195136 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL550143 195136 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 401 4 0 5 5.9 Cc1cc(-c2cscn2)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
44341060 9560 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112360 9560 0 None - 1 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
10625996 121008 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CC(=O)NCCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL356480 121008 0 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 526 7 1 5 4.8 CC(=O)NCCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
10651301 116528 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336209 116528 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 603 7 2 5 6.4 Cc1ccccc1NC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10840534 22573 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
CHEMBL132620 22573 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 555 8 1 6 3.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)CN(C)C)c3Cl)cccn2c1Br 10.1021/jm980214f
11433935 13206 1 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1191123 13206 1 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215986 13206 1 None - 0 Guinea pig 6.1 pIC50 = 6.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 687 10 2 6 7.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10603982 80085 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL21311 80085 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
10603982 80085 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL21311 80085 0 None - 0 Human 5.1 pIC50 = 5.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 625 12 2 8 4.0 CCOC(=O)Cc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
11456652 13207 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL1191124 13207 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
CHEMBL542176 13207 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Inhibition of specific binding of [3H]BK at 0.06 nM to bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 676 10 2 8 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCOCC5)cc(C)nc34)c2Cl)cn1 10.1021/jm030326t
10579143 168464 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL43510 168464 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK (1.2 nM) to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 580 9 2 6 5.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4oc(C)nc34)c2Cl)cc1 10.1021/jm980300f
44323787 13016 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1189812 13016 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215529 13016 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 659 10 2 6 6.2 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCCC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
10840241 116469 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
CHEMBL336116 116469 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [3H]BK at 0.06 nM to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm980214f
10840241 116469 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
CHEMBL336116 116469 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.In vitro for inhibition of specific binding of [3H]BK (0.06 nM) to bradykinin receptor B2 in guinea pig ileum membrane preparations.
ChEMBL 541 7 2 5 4.6 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccn3c(Br)c(C)nc23)c1Cl 10.1021/jm970591c
11802476 12964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL1189415 12964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
CHEMBL538732 12964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm030159x
11802476 12964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL1189415 12964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
CHEMBL538732 12964 0 None - 0 Human 8.1 pIC50 = 8.1 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 657 9 2 6 5.4 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cc1 10.1021/jm980300f
9916589 100238 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
CHEMBL288603 100238 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm980300f
11802489 13733 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL1195106 13733 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
CHEMBL553844 13733 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.Concentration required to inhibit specific binding of [3H]BK at 1.2 nM to A-431 cells (human epidermoid carcinoma) which express Bradykinin receptor B2 by 50%.
ChEMBL 658 9 2 7 4.8 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccn4c(Br)c(C)nc34)c2Cl)cn1 10.1021/jm980214f
11490839 13169 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL1190878 13169 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
CHEMBL541805 13169 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 671 10 1 8 5.5 Cc1cc(-n2ccnn2)c2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)N(C)C)cc4)c3Cl)c2n1 10.1021/jm030159x
9916589 100238 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
CHEMBL288603 100238 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 593 9 2 6 4.9 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c3nc(C)n4C)c2Cl)cc1 10.1021/jm030159x
10674687 13627 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL1194363 13627 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
CHEMBL552543 13627 0 None - 0 Human 8.0 pIC50 = 8.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 576 9 1 5 5.7 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(N5CCCC5=O)cc4)c3C)c2n1 10.1021/jm980300f
10745895 101155 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295428 101155 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm980300f
10745895 101155 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295428 101155 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 585 10 2 7 4.6 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(SC)n4C)c2C)cc1 10.1021/jm030159x
11801411 101344 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
CHEMBL296865 101344 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm980300f
44191223 196267 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL561899 196267 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 398 4 0 5 5.2 Cc1cc(-c2nccn2C)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
11801411 101344 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
CHEMBL296865 101344 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 583 11 2 7 4.3 CCOc1nc2c(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(=O)NC)cc4)c3C)cccc2n1C 10.1021/jm030159x
10627129 101546 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL298320 101546 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm030159x
10627129 101546 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL298320 101546 0 None - 0 Human 5.0 pIC50 = 5.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 583 11 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(COC)n4C)c2C)cc1 10.1021/jm980300f
10793125 100177 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL288079 100177 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.Concentration required to inhibit specific binding of [ 3H]BK (0.06 nM) to Bradykinin receptor B2 in guinea pig ileum membrane preparations by 50%.
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm980300f
10793125 100177 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL288079 100177 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparationIn vitro inhibitory activity towards bradykinin receptor B2 using [3H]BK (0.06 nM) as a radioligand in guinea pig ileum membrane preparation
ChEMBL 568 10 3 7 4.0 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(NC)n4C)c2C)cc1 10.1021/jm030159x
10555263 101096 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
CHEMBL295005 101096 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
In vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligandIn vitro inhibitory activity towards human bradykinin receptor B2 expressed in CHO cells using [3H]BK (1.0 nM) as a radioligand
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm030159x
10626599 30987 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 555 8 2 4 7.4 CNC(=O)c1ccc(/C=C/C(=O)Nc2cccc(-c3ccc(C)c(COc4cccc5ccc(C)nc45)c3C)c2)cc1 10.1021/jm980330i
CHEMBL139870 30987 0 None - 0 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparationsInhibition of the specific binding of [3H]BK to Bradykinin receptor B2 in guinea pig ileum membrane preparations
ChEMBL 555 8 2 4 7.4 CNC(=O)c1ccc(/C=C/C(=O)Nc2cccc(-c3ccc(C)c(COc4cccc5ccc(C)nc45)c3C)c2)cc1 10.1021/jm980330i
10555263 101096 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
CHEMBL295005 101096 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.Inhibition specific binding of [3H]BK (1.0 nM) to human Bradykinin receptor B2 which was expressed in CHO (Chinese hamster ovary) cells by 50%.
ChEMBL 581 10 2 7 4.1 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(C)c(COc3cccc4c3nc(C(C)=O)n4C)c2C)cc1 10.1021/jm980300f
11239381 13144 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL1190638 13144 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
CHEMBL3215541 13144 0 None - 0 Human 7.0 pIC50 = 7.0 Binding
Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.Inhibition of specific binding of [3H]BK at 1 nM to human bradykinin receptor B2 expressed in CHO cells by 50%.
ChEMBL 688 10 2 7 5.3 CNC(=O)c1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4c(N5CCN(C)CC5)cc(C)nc34)c2Cl)cc1 10.1021/jm030326t
44190266 195456 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL552442 195456 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cellsDisplacement of [3H]bradykinin from human recombinant B2 receptor expressed in HEK293 cells
ChEMBL 435 4 0 5 6.6 Cc1cc(-c2scnc2Cl)c2cccc(OCc3c(Cl)cncc3Cl)c2n1 10.1021/jm9002445
CHEMBL5274928 193831 0 None - 1 Human 9.4 pKd = 9.4 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1290 30 18 17 -4.8 N=C(N)NCCCC(NC(=O)[C@@H]1C[C@@H]2CCC[C@@H]2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
CHEMBL5280457 194068 0 None - 1 Human 9.1 pKd = 9.1 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1312 30 18 17 -4.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1Cc2ccccc2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
44317520 104889 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 601 12 5 5 3.6 N=C(N)NCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
CHEMBL311191 104889 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 601 12 5 5 3.6 N=C(N)NCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
44317577 205645 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 382 9 2 4 5.2 CCCCC1(CCCC)Oc2cccc(NC(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
CHEMBL81864 205645 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 382 9 2 4 5.2 CCCCC1(CCCC)Oc2cccc(NC(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
44317502 205733 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 439 12 2 5 5.0 CCCCC1(CCCC)Oc2cccc(N(CCCN)C(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
CHEMBL82600 205733 0 None - 1 Human 4.9 pKd = 4.9 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 439 12 2 5 5.0 CCCCC1(CCCC)Oc2cccc(N(CCCN)C(=O)c3ccc(CN)cc3)c2O1 10.1016/s0960-894x(00)00482-0
44317490 104696 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 402 6 3 3 3.1 N=C(N)NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
CHEMBL310531 104696 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 402 6 3 3 3.1 N=C(N)NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
44317519 105739 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 531 11 2 5 5.1 NCCCN1C(=O)C(CCN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
CHEMBL312658 105739 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 531 11 2 5 5.1 NCCCN1C(=O)C(CCN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
44317631 105125 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 501 11 4 5 3.7 NCc1ccc(CNC(=O)[C@@H](CN)n2cccc2CNC(=O)C(c2ccccc2)C2CCCCC2)cc1 10.1016/s0960-894x(00)00482-0
CHEMBL311420 105125 0 None - 1 Human 4.8 pKd = 4.8 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 501 11 4 5 3.7 NCc1ccc(CNC(=O)[C@@H](CN)n2cccc2CNC(=O)C(c2ccccc2)C2CCCCC2)cc1 10.1016/s0960-894x(00)00482-0
CHEMBL5268547 193570 0 None - 1 Human 5.7 pKd = 5.7 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1250 30 18 17 -5.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1CCC[C@@]12Cc1ccccc1CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C2=O 10.1021/acs.jmedchem.6b01029
73351522 89389 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 861 10 7 9 0.9 NCCCC[C@@H]1NC(=O)[C@H](c2ccccc2)NC(=O)[C@H](CNC(=O)Cc2ccccc2)NC(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H](CN)NC1=O 10.1016/s0960-894x(00)00482-0
CHEMBL2369879 89389 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 861 10 7 9 0.9 NCCCC[C@@H]1NC(=O)[C@H](c2ccccc2)NC(=O)[C@H](CNC(=O)Cc2ccccc2)NC(=O)[C@H]2Cc3ccccc3CN2C(=O)[C@@H]2CC3CCCCC3N2C(=O)[C@H](CN)NC1=O 10.1016/s0960-894x(00)00482-0
90662959 106587 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 769 8 7 7 1.6 N=C(N)NCCC[C@@H]1NC(=O)N2C3CCCCC3C[C@H]2C(=O)N2Cc3ccccc3C[C@@H]2C(=O)NCC[C@@H](NC(=O)CCc2ccccc2)C(=O)CCNC1=O 10.1016/s0960-894x(00)00482-0
CHEMBL3142416 106587 0 None - 1 Human 6.7 pKd = 6.7 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells; 0.2-16
ChEMBL 769 8 7 7 1.6 N=C(N)NCCC[C@@H]1NC(=O)N2C3CCCCC3C[C@H]2C(=O)N2Cc3ccccc3C[C@@H]2C(=O)NCC[C@@H](NC(=O)CCc2ccccc2)C(=O)CCNC1=O 10.1016/s0960-894x(00)00482-0
44317544 205688 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 471 18 1 3 7.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN(CCCC)CCCC)c1 10.1016/s0960-894x(00)00482-0
CHEMBL82249 205688 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 471 18 1 3 7.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN(CCCC)CCCC)c1 10.1016/s0960-894x(00)00482-0
CHEMBL5266183 193472 0 None - 1 Human 5.6 pKd = 5.6 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1210 31 19 17 -6.4 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1Cc2ccccc2CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
CHEMBL5271423 193683 0 None - 1 Human 5.6 pKd = 5.6 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1312 30 18 17 -4.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
44317810 105630 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 537 14 4 5 4.6 NCCCC[C@H](C(=O)NCc1ccc(CN)cc1)n1cccc1C(=O)NC(Cc1ccccc1)c1ccccc1 10.1016/s0960-894x(00)00482-0
CHEMBL312374 105630 0 None - 1 Human 4.6 pKd = 4.6 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 537 14 4 5 4.6 NCCCC[C@H](C(=O)NCc1ccc(CN)cc1)n1cccc1C(=O)NC(Cc1ccccc1)c1ccccc1 10.1016/s0960-894x(00)00482-0
CHEMBL5267275 193515 0 None - 1 Human 5.5 pKd = 5.5 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1250 30 18 17 -5.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1CCC[C@]12Cc1ccccc1CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C2=O 10.1021/acs.jmedchem.6b01029
90663066 106588 0 None - 1 Guinea pig 5.5 pKd = 5.5 Binding
Functional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assayFunctional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL3142595 106588 0 None - 1 Guinea pig 5.5 pKd = 5.5 Binding
Functional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assayFunctional antagonism against BK-induced contractions in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL5274916 193829 0 None - 1 Human 5.4 pKd = 5.4 Binding
Antagonist potency at B2 bradykinin receptor (unknown origin)Antagonist potency at B2 bradykinin receptor (unknown origin)
ChEMBL 1405 31 20 19 -4.2 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@H]1CSSC[C@@H](C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](Cc2ccccc2)NC1=O 10.1021/acs.jmedchem.6b01029
10481702 104405 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 517 10 2 5 4.8 NCCCN1C(=O)C(CN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
CHEMBL310300 104405 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 517 10 2 5 4.8 NCCCN1C(=O)C(CN)N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc21 10.1016/s0960-894x(00)00482-0
10371624 105424 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 615 13 5 5 4.0 N=C(N)NCCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
CHEMBL311969 105424 0 None - 1 Human 5.4 pKd = 5.4 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 615 13 5 5 4.0 N=C(N)NCCC1N=C(c2ccccc2)c2cc(N(Cc3ccccc3)Cc3ccccc3)ccc2N(CCCN=C(N)N)C1=O 10.1016/s0960-894x(00)00482-0
44317826 205275 0 None - 1 Human 5.3 pKd = 5.3 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 435 10 3 3 4.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN=C(N)N)cc2)c1 10.1016/s0960-894x(00)00482-0
CHEMBL79057 205275 0 None - 1 Human 5.3 pKd = 5.3 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 435 10 3 3 4.6 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN=C(N)N)cc2)c1 10.1016/s0960-894x(00)00482-0
44317458 205197 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 359 11 2 3 4.7 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN)c1 10.1016/s0960-894x(00)00482-0
CHEMBL78487 205197 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 359 11 2 3 4.7 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)CCCCN)c1 10.1016/s0960-894x(00)00482-0
44317602 205677 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 360 5 1 3 3.6 NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
CHEMBL82194 205677 0 None - 1 Human 4.2 pKd = 4.2 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 360 5 1 3 3.6 NC[C@H]1C[C@@H](OCc2ccccc2)CN1C(=O)c1ccc2ccccc2c1 10.1016/s0960-894x(00)00482-0
44317543 105325 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 393 9 2 3 5.3 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN)cc2)c1 10.1016/s0960-894x(00)00482-0
CHEMBL311593 105325 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 393 9 2 3 5.3 CCCCc1ccnc([C@H](CC2CCCCC2)NC(=O)c2ccc(CN)cc2)c1 10.1016/s0960-894x(00)00482-0
44317849 103902 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 434 7 1 3 5.6 NCc1cccc(Cn2ccc3c2C(=O)C(Cc2ccccc2)(Cc2ccccc2)CC3)c1 10.1016/s0960-894x(00)00482-0
CHEMBL309221 103902 0 None - 1 Human 5.1 pKd = 5.1 Binding
Compound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cellsCompound was assayed for binding against the human Bradykinin receptor B2 expressed in CHO cells
ChEMBL 434 7 1 3 5.6 NCc1cccc(Cn2ccc3c2C(=O)C(Cc2ccccc2)(Cc2ccccc2)CC3)c1 10.1016/s0960-894x(00)00482-0
11050762 67675 0 None 5248 2 Rat 10.6 pKi = 10.6 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907651 67675 0 None 5248 2 Rat 10.6 pKi = 10.6 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
667 1973 37 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
71364 1973 37 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
CHEMBL2028850 1973 37 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
DB06196 1973 37 None -1 6 Human 10.6 pKi = 10.6 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL None None None None 10.1016/j.bmcl.2006.01.125
57398326 71644 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956864 71644 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963558 71644 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 14 1 6 6.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401774 71593 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956863 71593 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963184 71593 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 749 13 1 6 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57391279 71594 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956876 71594 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963185 71594 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 2 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394782 71643 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956855 71643 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963557 71643 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 11 3 9 3.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57403503 71665 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956856 71665 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963651 71665 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 2 9 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11498853 83188 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL218427 83188 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL541758 83188 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11498853 83188 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218427 83188 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL541758 83188 13 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 763 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1021/jm061143k
11600324 141996 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL387452 141996 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105746 161930 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415366 161930 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 779 12 2 8 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCSCC4)c3Cl)c2n1 10.1021/jm061143k
667 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
71364 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
CHEMBL2028850 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
DB06196 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
57399981 71574 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 2 9 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956858 71574 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 2 9 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963148 71574 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 2 9 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401778 71578 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956870 71578 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963152 71578 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 14 1 7 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57390466 71640 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 13 5 9 3.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956719 71640 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 13 5 9 3.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963540 71640 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 13 5 9 3.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
667 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
71364 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL2028850 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB06196 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
3812 717 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
439201 717 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
649 717 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
CHEMBL406291 717 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
DB12126 717 42 None 1 6 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None None 10.1021/jm9901531
44355428 169134 0 None - 1 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1200 31 15 18 -5.4 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL440257 169134 0 None - 1 Human 10.2 pKi = 10.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1200 31 15 18 -5.4 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
667 1973 37 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
71364 1973 37 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL2028850 1973 37 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB06196 1973 37 None -1 6 Rat 10.1 pKi = 10.1 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
57399228 71572 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956720 71572 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963146 71572 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 9 1 7 3.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398324 71585 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956862 71585 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963164 71585 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 735 12 1 6 5.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57345657 71592 0 None -2 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956722 71592 0 None -2 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963183 71592 0 None -2 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 748 12 1 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396534 71664 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956854 71664 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963650 71664 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105703 136480 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373607 136480 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 776 12 2 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCN(C)CC4)c3Cl)c2n1 10.1021/jm061143k
90662945 106586 0 None - 1 Human 10.1 pKi = 10.1 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1298 30 15 17 -5.2 NC(N)=NCCC[C@H](N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1c2ccccc2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm990961s
CHEMBL3142396 106586 0 None - 1 Human 10.1 pKi = 10.1 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1298 30 15 17 -5.2 NC(N)=NCCC[C@H](N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@H]1C(=O)N1c2ccccc2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm990961s
CHEMBL2371961 210158 0 None - 1 Guinea pig 10.1 pKi = 10.1 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1CN(C(=O)[C@H]2c3ccccc3CCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C2CCCCC21)C(=O)O 10.1021/jm00069a016
57401770 71583 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956853 71583 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963162 71583 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 733 12 1 8 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCN(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57401772 71588 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956857 71588 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963175 71588 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 12 3 9 3.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396538 71589 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956861 71589 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963176 71589 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 721 11 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105734 84272 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221285 84272 0 None - 1 Human 10.0 pKi = 10 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 803 14 4 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCNC(=N)N)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
9831859 9706 0 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL113169 9706 0 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 508 10 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCCN)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10257108 9831 1 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
CHEMBL113963 9831 1 None - 1 Guinea pig 10.0 pKi = 10 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 554 9 1 6 5.4 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2C#N)c1 10.1016/s0960-894x(98)00736-7
3812 717 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
439201 717 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
649 717 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
CHEMBL406291 717 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
DB12126 717 42 None 1 6 Human 10.0 pKi = 10.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
CHEMBL2371961 210158 0 None - 1 Guinea pig 10.0 pKi = 10.0 Binding
Binding affinity towards bradykinin receptor B2 using [3H]bradykininBinding affinity towards bradykinin receptor B2 using [3H]bradykinin
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1CN(C(=O)[C@H]2c3ccccc3CCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C2CCCCC21)C(=O)O 10.1021/jm00035a015
667 1973 37 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
71364 1973 37 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
CHEMBL2028850 1973 37 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
DB06196 1973 37 None 1 6 Guinea pig 10.0 pKi = 10.0 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None None 10.1021/jm00062a018
57402746 71573 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956721 71573 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963147 71573 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 11 1 7 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57402744 71581 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 12 5 9 2.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956718 71581 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 12 5 9 2.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963160 71581 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 12 5 9 2.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCNC(=N)N)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57400986 71582 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956723 71582 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963161 71582 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 762 13 1 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105690 83634 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220478 83634 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10102701 137438 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375354 137438 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44337475 8082 0 None - 1 Human 9.8 pKi = 9.8 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 329 5 0 4 1.4 CC(=O)CN1CN(CCc2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL109123 8082 0 None - 1 Human 9.8 pKi = 9.8 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 329 5 0 4 1.4 CC(=O)CN1CN(CCc2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
57401784 71639 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956875 71639 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963532 71639 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 734 13 2 7 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105751 83229 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
CHEMBL218636 83229 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 12 2 8 3.9 CC(=O)N1CCC(NS(=O)(=O)c2ccc(Cl)c(COc3cccc4c(C)cc(C)nc34)c2Cl)(C(=O)N2CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC2)CC1 10.1021/jm061143k
CHEMBL2369941 209737 0 None - 1 Guinea pig 9.8 pKi = 9.8 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL None None None CCCC1C[C@H](C(=O)N2C3CCCCC3C[C@H]2C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)N(C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccsc2)NC(=O)CNC(=O)[C@@H]2CC[C@H](O)N2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1 10.1021/jm00062a018
CHEMBL3038098 210931 0 None - 1 Human 9.8 pKi = 9.8 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)CC1CCCCC1 10.1021/jm950716i
CHEMBL5274928 193831 0 None - 1 Human 9.7 pKi = 9.7 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1290 30 18 17 -4.8 N=C(N)NCCCC(NC(=O)[C@@H]1C[C@@H]2CCC[C@@H]2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1C[C@@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
667 1973 37 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
71364 1973 37 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
CHEMBL2028850 1973 37 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
DB06196 1973 37 None -1 6 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
57394780 71642 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956852 71642 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963556 71642 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 776 14 1 7 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57392147 71669 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1955876 71669 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963660 71669 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 720 12 2 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CNCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105696 83208 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL218540 83208 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 790 13 1 6 5.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10441297 136888 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374224 136888 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 804 14 1 6 6.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCC[N+](C)(C)C)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
11766718 136933 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374272 136933 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 774 14 1 8 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCCN(C)C)N(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
9897921 161901 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415151 161901 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL3038106 210939 0 None 16 2 Human 9.7 pKi = 9.7 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1C[C@@H](O)C[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL3038099 210932 0 None 2 2 Human 9.6 pKi = 9.6 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
57399983 71575 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956859 71575 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963149 71575 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 777 13 2 8 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396536 71584 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956860 71584 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963163 71584 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 707 10 1 6 4.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+](C)(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57396540 71590 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956867 71590 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963177 71590 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 7 1 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CC5)CC[N+](C)(C)CC6)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105698 136346 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL373459 136346 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 747 12 2 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@H](CCCN)[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105694 141894 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL386794 141894 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 12 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
22008895 110558 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL325255 110558 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 592 8 1 5 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
10996140 67676 0 None 309 2 Rat 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907652 67676 0 None 309 2 Rat 9.5 pKi = 9.5 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
57393062 71577 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 11 1 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956869 71577 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 11 1 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963151 71577 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 706 11 1 7 4.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
16105727 83811 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220591 83811 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105742 138154 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL376866 138154 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 733 11 2 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL5280457 194068 0 None - 1 Human 9.4 pKi = 9.4 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1312 30 18 17 -4.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1Cc2ccccc2C[C@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
CHEMBL3038094 210928 0 None 8 2 Human 9.4 pKi = 9.4 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCC1 10.1021/jm950716i
CHEMBL3038095 210929 0 None 3 2 Human 9.4 pKi = 9.4 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
57403505 71645 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956865 71645 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963559 71645 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 675 7 1 6 5.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57394784 71667 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956871 71667 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963658 71667 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 677 9 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(C[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10463758 138871 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378189 138871 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 692 12 2 8 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10101294 140154 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380273 140154 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
44412007 77211 1 None -1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL207939 77211 1 None -1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm061143k
10396101 84342 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL221683 84342 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 11 1 6 5.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10441167 96988 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL266493 96988 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 732 11 3 6 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10101294 140154 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL380273 140154 0 None -5 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 706 12 2 8 4.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
10102296 161902 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL415152 161902 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 690 9 1 6 4.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44316161 161516 0 None -1 2 Human 9.4 pKi = 9.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1043 25 12 16 -4.0 NCCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O 10.1021/jm990961s
CHEMBL412824 161516 0 None -1 2 Human 9.4 pKi = 9.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1043 25 12 16 -4.0 NCCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O 10.1021/jm990961s
122189902 123423 0 None 13489 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616944 123423 0 None 13489 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in guinea pig ileum membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
3812 717 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
439201 717 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
649 717 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL406291 717 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB12126 717 42 None -1 6 Rat 9.3 pKi = 9.3 Binding
Binding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against rat Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
5312119 718 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
680 718 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
CHEMBL308468 718 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
5312119 718 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
680 718 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
CHEMBL308468 718 4 None 1148 2 Rat 9.3 pKi = 9.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
57401782 71586 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956873 71586 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963165 71586 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 705 11 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
11600186 78297 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210788 78297 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 2 8 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
16105701 83969 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220693 83969 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 762 12 3 8 3.6 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCC[N+](C)(C)C)CC5)CCNCC4)c3Cl)c2n1 10.1021/jm061143k
10350966 84624 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222167 84624 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 1 6 6.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL2370040 209773 0 None - 1 Guinea pig 9.3 pKi = 9.3 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None C[C@@](Cc1ccccc1)(NC(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44337490 9168 0 None - 1 Human 9.2 pKi = 9.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 307 3 0 4 1.5 CC(=O)CN1CN(C2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL110188 9168 0 None - 1 Human 9.2 pKi = 9.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 307 3 0 4 1.5 CC(=O)CN1CN(C2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
10556495 167939 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL2112044 167939 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL431562 167939 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
10556495 167939 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112044 167939 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL431562 167939 0 None 2398 2 Rat 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
44340859 10043 0 None - 1 Guinea pig 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL115163 10043 0 None - 1 Guinea pig 9.2 pKi = 9.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 599 11 2 8 5.0 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(NC(C)=O)nc2)c(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
57393060 71587 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956851 71587 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963174 71587 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 661 7 1 6 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCCC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57398328 71668 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956874 71668 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963659 71668 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 719 12 1 6 6.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CCCC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10439868 75926 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL205093 75926 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10463818 139272 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379063 139272 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 14 2 8 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10010104 141274 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383167 141274 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10439868 75926 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL205093 75926 0 None -12 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
10463883 83833 0 None -25 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220596 83833 0 None -25 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10079793 94120 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL249235 94120 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 717 11 3 7 4.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=N)NCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
16105729 136934 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL374273 136934 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 761 13 2 7 5.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCC[N+](C)(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10079797 137597 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375576 137597 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 718 12 3 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCN)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10032895 137631 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375820 137631 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 734 13 5 8 3.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC4)c3Cl)c2n1 10.1021/jm061143k
10010104 141274 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL383167 141274 0 None -7 2 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 720 13 2 8 4.5 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm061143k
3812 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
439201 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
649 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL406291 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB12126 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
3812 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
439201 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
649 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
CHEMBL406291 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
DB12126 717 42 None 1 6 Human 9.2 pKi = 9.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None None 10.1021/jm950716i
71450888 78793 0 None 8 2 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2112698 78793 0 None 8 2 Human 9.2 pKi = 9.2 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL5284501 194256 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1228 31 19 18 -5.9 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
44355233 166656 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL428148 166656 0 None - 1 Human 9.2 pKi = 9.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
70683601 74518 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL 1270 33 15 15 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00062a018
CHEMBL2028979 74518 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
ChEMBL 1270 33 15 15 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2CCCCC2N1C(=O)[C@@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)O 10.1021/jm00062a018
667 1973 37 None -1 6 Human 9.1 pKi = 9.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL None None None None 10.1021/acs.jmedchem.6b01029
71364 1973 37 None -1 6 Human 9.1 pKi = 9.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL None None None None 10.1021/acs.jmedchem.6b01029
CHEMBL2028850 1973 37 None -1 6 Human 9.1 pKi = 9.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL None None None None 10.1021/acs.jmedchem.6b01029
DB06196 1973 37 None -1 6 Human 9.1 pKi = 9.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL None None None None 10.1021/acs.jmedchem.6b01029
9987299 78601 0 None 13 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78601 0 None 13 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
57401780 71579 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956872 71579 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963153 71579 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 691 10 1 6 5.9 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCC(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
57391277 71666 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 692 10 1 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956868 71666 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 692 10 1 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963652 71666 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 692 10 1 7 4.4 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(CC[N+](C)(C)C)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
44412007 77211 1 None -1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL207939 77211 1 None -1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 710 12 4 7 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)N4CCC[C@@H]4C(=O)NCCCNC(=O)c4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
10102599 141404 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL383989 141404 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
10418701 97102 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL267493 97102 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)C[C@@H](N)CCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
122189902 123423 0 None 13489 2 Guinea pig 9.0 pKi = 9 Binding
Binding affinity to B2R in guinea pig ileum membranesBinding affinity to B2R in guinea pig ileum membranes
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616944 123423 0 None 13489 2 Guinea pig 9.0 pKi = 9 Binding
Binding affinity to B2R in guinea pig ileum membranesBinding affinity to B2R in guinea pig ileum membranes
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
57401776 71576 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1956866 71576 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
CHEMBL1963150 71576 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation countingDisplacement of [3H]-Bradykinin from human bradykinin B2 receptor expressed in CHO cells membrane after 60 mins by scintillation counting
ChEMBL 690 7 1 7 4.2 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CC[N+]6(CCN(C)CC6)CC5)CCOCC4)c3Cl)c2n1 10.1016/j.bmc.2012.01.036
10349694 76583 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206312 76583 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 13 4 7 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10418252 138891 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378237 138891 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 663 10 4 7 3.8 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10373970 137614 0 None -5 2 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL375689 137614 0 None -5 2 Human 9.0 pKi = 9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 760 13 5 8 4.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
3812 717 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
439201 717 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
649 717 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
CHEMBL406291 717 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
DB12126 717 42 None 1 6 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 minsDisplacement of [3H]Bradykinin from human recombinant bradykinin B2 receptor expressed in CHEM1 cells after 60 mins
ChEMBL None None None None 10.1016/j.bmcl.2013.01.025
10055774 76703 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206474 76703 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 734 14 4 8 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)C[C@@H](N)CCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
10441194 84622 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL222156 84622 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 745 13 4 7 5.0 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)CCCCCNC(=N)N)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
44341039 9511 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112140 9511 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)c(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
18941145 9963 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
CHEMBL114732 9963 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 569 9 1 6 6.3 COc1cccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)c1 10.1016/s0960-894x(98)00736-7
22008892 110162 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL323693 110162 0 None - 1 Guinea pig 8.9 pKi = 8.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 561 8 1 4 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3C)c2n1 10.1016/s0960-894x(98)00736-7
11136263 78586 0 None 43 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112221 78586 0 None 43 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2370010 209767 0 None - 1 Guinea pig 8.8 pKi = 8.8 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N1)C(=O)O 10.1021/jm00069a016
10418495 77875 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209346 77875 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 10 4 7 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)NCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
10260476 77997 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209719 77997 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 691 14 3 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
9988753 83832 0 None -7 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
CHEMBL220595 83832 0 None -7 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human bradykinin B2 receptor transfected in CHO cells
ChEMBL 746 13 2 8 5.1 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC4(C(=O)N5CCN(C(=O)[C@@H](N)CCCCN(C)C)CC5)CCCC4)c3Cl)c2n1 10.1021/jm061143k
10788314 119967 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 421 7 4 5 3.7 NC(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL349817 119967 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 421 7 4 5 3.7 NC(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
18941160 9915 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114401 9915 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 8 1 5 6.6 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(C)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10010669 76811 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL206938 76811 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 13 2 8 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)[C@@H](N)CCCCN(C)C)CC4)c3Cl)c2n1 10.1021/jm060137l
44276460 99239 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.6 CCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL281706 99239 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.6 CCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
11527838 78358 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL211017 78358 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 635 10 3 7 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCN=C(N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
11513471 138647 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
CHEMBL377612 138647 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 748 14 2 8 4.4 CC(=O)N[C@@H](CCCCN(C)C)C(=O)N1CCN(C(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)CC1 10.1021/jm060137l
9987299 78601 0 None -13 2 Rat 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112283 78601 0 None -13 2 Rat 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 706 14 4 9 3.3 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44410425 97139 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
CHEMBL267822 97139 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
11699718 77087 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 524 9 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL207465 77087 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 524 9 3 6 3.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN)c3Cl)c2n1 10.1021/jm060137l
11513163 77776 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 7 2 6 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209130 77776 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 7 2 6 4.7 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCCC4)c3Cl)c2n1 10.1021/jm060137l
44320402 14348 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1162589 14348 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1200092 14348 0 None - 1 Human 6.0 pKi = 6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
44347466 14336 0 None - 1 Human 6.0 pKi = 6 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1162799 14336 0 None - 1 Human 6.0 pKi = 6 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1200034 14336 0 None - 1 Human 6.0 pKi = 6 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
44347552 12178 0 None - 1 Human 5.0 pKi = 5 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 613 17 1 2 9.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)CCCc2ccccc2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1184218 12178 0 None - 1 Human 5.0 pKi = 5 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 613 17 1 2 9.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)CCCc2ccccc2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL339723 12178 0 None - 1 Human 5.0 pKi = 5 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 613 17 1 2 9.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)CCCc2ccccc2)cc1 10.1016/0960-894X(95)00037-T
2324360 57193 12 None - 1 Rat 4.0 pKi = 4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 257 4 3 2 2.7 S=C(NCc1ccccc1)NNc1ccccc1 10.1021/jm991155o
CHEMBL164968 57193 12 None - 1 Rat 4.0 pKi = 4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 257 4 3 2 2.7 S=C(NCc1ccccc1)NNc1ccccc1 10.1021/jm991155o
44215785 95534 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 557 8 0 7 5.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL25751 95534 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 557 8 0 7 5.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
101653258 13782 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44320402 13782 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195447 13782 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554592 13782 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 18 3 2 11.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccc3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44355241 168724 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL436963 168724 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
118719116 115444 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL3350763 115444 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
44346315 13841 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 771 12 3 2 10.1 O=C(Nc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1195864 13841 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 771 12 3 2 10.1 O=C(Nc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL555493 13841 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 771 12 3 2 10.1 O=C(Nc1ccc(C[P+](c2ccccc2)(c2ccccc2)c2ccccc2)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44346282 12348 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 30 1 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1185367 12348 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 30 1 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL409910 12348 0 None - 1 Human 6.0 pKi = 6.0 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 712 30 1 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
9919335 106585 1 None -489 2 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligandBinding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligand
ChEMBL 922 22 9 13 -2.1 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC2(CC1)C(=O)N(CC(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc3ccccc3N(CC(=O)O)C1=O)CN2CCc1ccccc1 10.1021/jm990962k
CHEMBL3142392 106585 1 None -489 2 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligandBinding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligand
ChEMBL 922 22 9 13 -2.1 NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC2(CC1)C(=O)N(CC(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc3ccccc3N(CC(=O)O)C1=O)CN2CCc1ccccc1 10.1021/jm990962k
11050762 67675 0 None -5248 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907651 67675 0 None -5248 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 696 16 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
71456185 78529 0 None - 1 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL2111994 78529 0 None - 1 Human 4.9 pKi = 4.9 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL3038100 210933 0 None -14 2 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None N=C(N)NCCCCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@@H]1C(=O)N1C[C@@H](O)C[C@@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
CHEMBL2372276 210206 0 None 3 3 Human 7.9 pKi = 7.9 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm950716i
1016 3747 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2561 3747 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
2733526 3747 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
5384 3747 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
CHEMBL83 3747 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
DB00675 3747 78 None -46 35 Human 4.9 pKi = 4.9 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 nan
22288574 99578 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 606 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL283824 99578 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 606 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
11549560 78271 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 4 7 4.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(C(N)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210708 78271 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 4 7 4.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(C(N)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5268614 193575 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1024 24 13 13 -3.9 N=C(N)NCCCC(NC(=O)CN1CCCCC2(CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O)C(=O)O 10.1021/acs.jmedchem.6b01029
44276438 99445 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 580 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL282981 99445 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 580 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
44355038 161694 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1065 25 13 15 -5.1 NC(N)=NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901529
CHEMBL413386 161694 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1065 25 13 15 -5.1 NC(N)=NCCC[C@H](N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)NC1CSc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901529
CHEMBL5279008 194010 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1049 25 14 14 -3.7 N=C(N)NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)CSc2ccccc21)C(=O)O 10.1021/acs.jmedchem.6b01029
70695304 77450 0 None 17 2 Human 6.9 pKi = 6.9 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 556 8 2 6 4.0 Cc1ccc2cccc(OCc3cc(S(=O)(=O)N4CCC[C@H]4C(=O)NCC4CCNCC4)ccc3Cl)c2n1 10.1021/jm2016057
CHEMBL2087027 77450 0 None 17 2 Human 6.9 pKi = 6.9 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 556 8 2 6 4.0 Cc1ccc2cccc(OCc3cc(S(=O)(=O)N4CCC[C@H]4C(=O)NCC4CCNCC4)ccc3Cl)c2n1 10.1021/jm2016057
44346367 10251 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cnc2ccccc2c1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160972 10251 0 None - 1 Human 5.9 pKi = 5.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cnc2ccccc2c1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
18941161 9729 0 None - 1 Guinea pig 5.9 pKi = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL113320 9729 0 None - 1 Guinea pig 5.9 pKi = 5.9 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 615 9 1 5 8.0 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4sc(-c5ccccc5)nc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
11342079 161786 0 None - 1 Human 4.9 pKi = 4.9 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL414091 161786 0 None - 1 Human 4.9 pKi = 4.9 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
44355196 141524 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1328 35 16 18 -6.0 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@](Cc2ccccc2)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)C1Cc1ccccc1)C(=O)O 10.1021/jm9901531
CHEMBL384617 141524 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1328 35 16 18 -6.0 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@](Cc2ccccc2)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)C1Cc1ccccc1)C(=O)O 10.1021/jm9901531
CHEMBL3038101 210934 0 None 1 2 Human 7.8 pKi = 7.8 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)c1ccccc1 10.1021/jm950716i
57393602 67680 0 None -3 2 Rat 7.8 pKi = 7.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907656 67680 0 None -3 2 Rat 7.8 pKi = 7.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2370011 209768 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None NC(N)=NCCC[C@H](NC(=O)[C@@H]1C2CCCCC2CN1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CCC[C@H]2C(=O)NCC(=O)N[C@@H](Cc2ccccc2)C(=O)N1)C(=O)O 10.1021/jm00069a016
44346372 13104 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 727 18 3 2 12.3 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@@H](Cc2ccc3ccccc3c2)N/C(=N/c2ccc(C)cc2)Nc2ccc(C)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190356 13104 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 727 18 3 2 12.3 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@@H](Cc2ccc3ccccc3c2)N/C(=N/c2ccc(C)cc2)Nc2ccc(C)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540643 13104 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 727 18 3 2 12.3 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@@H](Cc2ccc3ccccc3c2)N/C(=N/c2ccc(C)cc2)Nc2ccc(C)cc2)cc1 10.1016/0960-894X(95)00035-R
71456177 78506 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
CHEMBL2111891 78506 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
11284303 66342 0 None 2 2 Human 5.9 pKi = 5.9 Binding
Binding affinity for Bradykinin receptor B2 expressed in COS7 cellsBinding affinity for Bradykinin receptor B2 expressed in COS7 cells
ChEMBL 553 15 1 7 4.7 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm049747g
CHEMBL185068 66342 0 None 2 2 Human 5.9 pKi = 5.9 Binding
Binding affinity for Bradykinin receptor B2 expressed in COS7 cellsBinding affinity for Bradykinin receptor B2 expressed in COS7 cells
ChEMBL 553 15 1 7 4.7 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm049747g
44276461 98273 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL27461 98273 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 9 0 6 7.0 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
10556495 167939 0 None -2398 2 Human 5.8 pKi = 5.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112044 167939 0 None -2398 2 Human 5.8 pKi = 5.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL431562 167939 0 None -2398 2 Human 5.8 pKi = 5.8 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(C)CCN(C)CCNC(=O)[C@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
10770256 57165 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 627 16 3 8 4.5 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL164754 57165 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 627 16 3 8 4.5 CN(C)CCCN(CCCN(C)C)S(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
44276793 99522 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 9 0 6 7.0 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL283394 99522 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 9 0 6 7.0 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
11467345 161951 0 None -489 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL415629 161951 0 None -489 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
11549562 77512 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 3 7 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(N(C)C)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208738 77512 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 671 14 3 7 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(N(C)C)cc4)c3Cl)c2n1 10.1021/jm060137l
11549335 140149 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 9 3 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380260 140149 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 578 9 3 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
11621618 140157 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 538 10 3 6 4.0 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380282 140157 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 538 10 3 6 4.0 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
11621850 166318 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 4 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4c[nH]cn4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL427217 166318 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 4 7 4.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4c[nH]cn4)c3Cl)c2n1 10.1021/jm060137l
51351563 58508 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL1683738 58508 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)[C@H](Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
71450890 78795 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
CHEMBL2112709 78795 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1222 30 16 17 -6.7 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H]1CCc2cccc3c2N(C1=O)[C@@H](C(=O)N[C@H](CCCN=C(N)N)C(=O)O)C3 10.1021/jm9901531
44340818 110609 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL325624 110609 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 8 1 5 6.3 Cc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(Cl)c(COc3cccc4scnc34)c2Cl)cc1 10.1016/s0960-894x(98)00736-7
10662116 56549 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 302 5 3 4 3.0 O=[N+]([O-])c1ccccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
CHEMBL163956 56549 0 None - 1 Rat 5.8 pKi = 5.8 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 302 5 3 4 3.0 O=[N+]([O-])c1ccccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
16108965 161330 0 None -1000 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
CHEMBL412552 161330 0 None -1000 2 Human 4.8 pKi = 4.8 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
71459890 78505 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2111889 78505 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2370038 209772 0 None - 1 Guinea pig 5.8 pKi = 5.8 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CN(CC(=O)N(C)[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N 10.1021/jm00069a016
44276753 165327 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 7 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C(C)(C)C)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL423482 165327 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 551 7 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C(C)(C)C)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10327403 78585 0 None -63 2 Rat 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78585 0 None -63 2 Rat 6.8 pKi = 6.8 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44276287 164819 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 5 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C5CCCCC5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL421863 164819 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 5 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)C5CCCCC5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44346451 10254 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 695 10 3 3 8.4 O=C(NC1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160979 10254 0 None - 1 Human 4.8 pKi = 4.8 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 695 10 3 3 8.4 O=C(NC1C2CCN(CC2)C1C(c1ccccc1)c1ccccc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44355256 157223 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1148 31 16 17 -8.0 NC(N)=NCCC[C@H](NC(=O)CN1CCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL407626 157223 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1148 31 16 17 -8.0 NC(N)=NCCC[C@H](NC(=O)CN1CCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
672 2267 21 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
6918284 2267 21 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
CHEMBL2105864 2267 21 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
DB06549 2267 21 None -1 2 Human 7.7 pKi = 7.7 Binding
Binding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligandBinding affinity against human cloned Bradykinin receptor B2 expressed in CHO cells using [3H]-bradykinin as radioligand
ChEMBL None None None None 10.1021/jm9901529
44276550 97298 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 570 9 0 6 6.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26908 97298 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 570 9 0 6 6.8 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL2370748 209918 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL None None None Cc1ccc(C[C@@H](CN[C@@H](CCCN=C(N)N)C(=O)O)NC(=O)[C@@H]2CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2C[C@@H](O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCN=C(N)N)cc1 10.1021/jm9901531
11577748 78097 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 10 4 6 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210217 78097 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 10 4 6 2.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
11505970 78181 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 656 13 5 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210472 78181 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 656 13 5 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5272490 193726 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1210 31 19 17 -6.4 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H]1Cc2ccccc2CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
11585604 77127 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 11 2 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN(C)C)c3Cl)c2n1 10.1021/jm060137l
CHEMBL207692 77127 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 566 11 2 6 4.6 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN(C)C)c3Cl)c2n1 10.1021/jm060137l
11672243 78198 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 658 14 3 7 5.8 COc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
CHEMBL210524 78198 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 658 14 3 7 5.8 COc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
11600235 138411 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 642 13 3 6 6.1 Cc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
CHEMBL377370 138411 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 642 13 3 6 6.1 Cc1ccc(CNCCCNC(=O)C(C)(C)NS(=O)(=O)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)cc1 10.1021/jm060137l
11707335 139319 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 11 3 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379259 139319 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 11 3 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCCN)c3Cl)c2n1 10.1021/jm060137l
11672186 139695 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 628 13 3 6 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379806 139695 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 628 13 3 6 5.8 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5266765 193491 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1212 31 19 18 -6.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1COc2ccccc2N(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
44355427 141877 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1212 31 16 18 -7.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1COc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL386697 141877 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1212 31 16 18 -7.2 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1COc2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
22008929 9750 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113465 9750 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 597 9 1 5 6.6 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(Cl)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
10056816 77749 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209038 77749 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 649 13 2 7 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(CCCCCCN)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL3038096 210930 0 None 6 2 Human 8.6 pKi = 8.6 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1 10.1021/jm950716i
10327403 78585 0 None 63 2 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112220 78585 0 None 63 2 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 702 14 4 10 3.8 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
9851817 9681 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL112991 9681 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 607 8 1 5 7.3 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccc(C(F)(F)F)cc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
44340760 110508 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL324950 110508 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 523 10 3 6 3.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)NCCCC(=O)O)c3C#N)c2n1 10.1016/s0960-894x(98)00736-7
CHEMBL2372276 210206 0 None 3 3 Human 7.7 pKi = 7.7 Binding
Displacement of radiolabeled NPC 567 from human bradykinin B2 receptorDisplacement of radiolabeled NPC 567 from human bradykinin B2 receptor
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)[C@@H]1CCCN1C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm8007618
22288598 97167 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 642 9 0 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(=O)N(C)C)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26810 97167 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 642 9 0 6 6.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(=O)N(C)C)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44355288 96774 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1224 33 16 17 -6.8 NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)N1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL264712 96774 0 None - 1 Human 5.7 pKi = 5.7 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1224 33 16 17 -6.8 NC(N)=NCCC[C@H](NC(=O)[C@H](Cc1ccccc1)N1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
44346465 11433 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 584 23 0 0 13.2 CCCC[P+](CCCC)(CCCC)Cc1ccc(-c2ccc(C[P+](CCCC)(CCCC)CCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1180311 11433 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 584 23 0 0 13.2 CCCC[P+](CCCC)(CCCC)Cc1ccc(-c2ccc(C[P+](CCCC)(CCCC)CCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL121350 11433 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 584 23 0 0 13.2 CCCC[P+](CCCC)(CCCC)Cc1ccc(-c2ccc(C[P+](CCCC)(CCCC)CCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
44346306 10247 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160968 10247 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44320168 10248 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL1160969 10248 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL444322 10248 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
9826248 34082 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 439 8 3 3 3.7 N=C(N)NCCCCN1C(=O)C(Cc2ccccc2)N=C(c2ccccc2)c2ccccc21 10.1016/s0960-894x(99)00015-3
CHEMBL142515 34082 0 None - 1 Human 4.7 pKi = 4.7 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 439 8 3 3 3.7 N=C(N)NCCCCN1C(=O)C(Cc2ccccc2)N=C(c2ccccc2)c2ccccc21 10.1016/s0960-894x(99)00015-3
CHEMBL3038103 210936 0 None 61 2 Human 7.6 pKi = 7.6 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H](C(=O)N(CC(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C1CCCCC1)C1CCCC1 10.1021/jm950716i
44276711 96931 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 571 8 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26604 96931 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 571 8 0 5 7.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
15952860 99248 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 596 8 0 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL281756 99248 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 596 8 0 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
11050689 102267 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 678 15 4 10 3.8 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL303258 102267 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 678 15 4 10 3.8 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
44276375 96720 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 585 9 0 5 7.4 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)Cc5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26422 96720 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 585 9 0 5 7.4 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)Cc5ccccc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44276380 99419 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL28282 99419 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 577 8 0 6 7.3 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44320404 13123 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 581 18 3 2 8.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190474 13123 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 581 18 3 2 8.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540896 13123 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 581 18 3 2 8.5 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL5267275 193515 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1250 30 18 17 -5.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1CCC[C@]12Cc1ccccc1CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C2=O 10.1021/acs.jmedchem.6b01029
11679144 77296 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 10 3 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208223 77296 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 552 10 3 6 4.3 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN)c3Cl)c2n1 10.1021/jm060137l
11636121 139011 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 7 2 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL378567 139011 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 7 2 6 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCCNCC4)c3Cl)c2n1 10.1021/jm060137l
44412412 168785 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 550 7 2 6 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL437491 168785 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 550 7 2 6 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
44346682 14243 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C/[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1162798 14243 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C/[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1199421 14243 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C/[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44320404 14349 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 582 18 3 2 8.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1021/jm00069a021
CHEMBL1162590 14349 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 582 18 3 2 8.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1021/jm00069a021
CHEMBL1200093 14349 0 None - 1 Human 4.6 pKi = 4.6 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 582 18 3 2 8.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C(C)C)NC(C)C)cc1 10.1021/jm00069a021
CHEMBL5268614 193575 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1024 24 13 13 -3.9 N=C(N)NCCCC(NC(=O)CN1CCCCC2(CCCN2C(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O)C(=O)O 10.1021/acs.jmedchem.6b01029
11707528 77771 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 621 11 2 7 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCN(C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209117 77771 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 621 11 2 7 4.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCN(C)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5284537 194257 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1032 25 14 13 -4.2 N=C(N)NCCC[C@H](NC(=O)CN1Cc2ccccc2C[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O)C(=O)O 10.1021/acs.jmedchem.6b01029
11657717 140067 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 594 10 2 7 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380045 140067 0 None - 1 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 594 10 2 7 3.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
10876210 78584 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 691 13 4 8 4.5 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c(Cl)c1 10.1021/jm0111088
CHEMBL2112219 78584 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 691 13 4 8 4.5 CN(C)CCCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(NNC(=O)NC2c3ccccc3CCc3ccccc32)c(Cl)c1 10.1021/jm0111088
44346347 10249 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cccc2ccncc12)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160970 10249 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 547 7 3 3 7.1 O=C(Nc1cccc2ccncc12)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44346416 13102 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 667 18 3 3 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccs2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190354 13102 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 667 18 3 3 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccs2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540641 13102 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 667 18 3 3 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cccs2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL2370042 209775 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CN(C(=O)CNC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44337466 5415 0 None - 1 Human 7.6 pKi = 7.6 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 267 4 0 4 0.6 CCCN1CN(CC(C)=O)C(=O)C12CCN(C)CC2 10.1021/jm950676i
CHEMBL107234 5415 0 None - 1 Human 7.6 pKi = 7.6 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 267 4 0 4 0.6 CCCN1CN(CC(C)=O)C(=O)C12CCN(C)CC2 10.1021/jm950676i
44276482 99503 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL283295 99503 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
44346410 13783 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 701 18 4 2 10.8 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2c[nH]c3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195448 13783 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 701 18 4 2 10.8 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2c[nH]c3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554593 13783 0 None - 1 Human 5.6 pKi = 5.6 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 701 18 4 2 10.8 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2c[nH]c3ccccc23)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44215784 99998 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 566 8 0 6 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL286710 99998 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 566 8 0 6 6.6 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
44276513 99970 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 638 11 0 6 8.3 CCCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL286520 99970 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 638 11 0 6 8.3 CCCCn1c(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)ccc1C(=O)c1ccc(C#N)cc1 10.1016/s0960-894x(03)00104-5
57395311 67679 0 None 2 2 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907655 67679 0 None 2 2 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44214279 9716 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL113222 9716 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 489 8 1 5 5.3 C=C/C=C/C(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3sc(C)nc23)c1Cl 10.1016/s0960-894x(98)00736-7
CHEMBL5268547 193570 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1250 30 18 17 -5.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1CCC[C@@]12Cc1ccccc1CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C2=O 10.1021/acs.jmedchem.6b01029
15388873 114731 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL333832 114731 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 529 8 1 6 5.9 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)/C=C/c4ccco4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
44341214 110430 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL324575 110430 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 621 12 1 6 6.7 CCCOc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
11506007 78011 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209773 78011 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 676 9 2 8 3.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=O)CN5CCNCC5)CC4)c3Cl)c2n1 10.1021/jm060137l
10008626 138678 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377800 138678 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 7 3 6 3.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N4CCN(C(=N)N)CC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL2370028 209770 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CN(CC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N 10.1021/jm00069a016
22288562 162954 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 8 1 6 6.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL417474 162954 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 586 8 1 6 6.8 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL2370035 209771 0 None - 1 Guinea pig 5.5 pKi = 5.5 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CC(NC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@](C)(Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44276439 96964 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 546 9 0 6 6.3 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26629 96964 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 546 9 0 6 6.3 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccnc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
44276474 97391 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 591 9 0 6 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26976 97391 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 591 9 0 6 7.7 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5cccs5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10504589 57177 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 471 9 4 6 3.5 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccccc2)ccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
CHEMBL164848 57177 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 471 9 4 6 3.5 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccccc2)ccc1N/N=C(/S)NCc1ccccc1 10.1021/jm991155o
44346389 10252 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 497 7 3 3 6.0 O=C(Nc1cccnc1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160975 10252 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 497 7 3 3 6.0 O=C(Nc1cccnc1)[C@@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL5266183 193472 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1210 31 19 17 -6.4 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N[C@@H]1Cc2ccccc2CN(CC(=O)N[C@@H](CCCNC(=N)N)C(=O)O)C1=O 10.1021/acs.jmedchem.6b01029
11614670 77654 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 3 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccoc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208859 77654 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 618 13 3 7 5.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccoc4)c3Cl)c2n1 10.1021/jm060137l
11571204 138710 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 10 2 6 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCCCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377966 138710 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 592 10 2 6 5.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCN4CCCCC4)c3Cl)c2n1 10.1021/jm060137l
44410526 83256 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
CHEMBL218749 83256 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity to human bradykinin B2 receptor transfected in CHO cellsBinding affinity to human bradykinin B2 receptor transfected in CHO cells
ChEMBL 1332 32 16 17 -4.3 NC(N)=NCCC[C@H](NC(=O)[C@@H]1CC2(CCCC2)C2CCC[C@@](Cc3ccccc3)(NC(=O)[C@H](CO)NC(=O)[C@H](Cc3cccs3)NC(=O)CNC(=O)[C@@H]3CC(O)CN3C(=O)[C@@H]3CCCN3C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N21)C(=O)O 10.1016/j.bmcl.2006.01.125
44316621 82116 0 None -57 2 Human 6.5 pKi = 6.5 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1091 24 13 15 -4.9 NC(N)=NCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
CHEMBL216618 82116 0 None -57 2 Human 6.5 pKi = 6.5 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1091 24 13 15 -4.9 NC(N)=NCCCC(N)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)NC(C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
101653256 13103 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44320170 13103 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190355 13103 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540642 13103 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 661 18 3 2 10.4 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44298960 195638 0 None - 1 Human 7.5 pKi = 7.5 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
CHEMBL55632 195638 0 None - 1 Human 7.5 pKi = 7.5 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
44346104 11424 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 643 28 0 0 15.0 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc2cc(C[P+](CCCCC)(CCCCC)CCCCC)ccc2c1 10.1016/0960-894X(95)00035-R
CHEMBL1180289 11424 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 643 28 0 0 15.0 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc2cc(C[P+](CCCCC)(CCCCC)CCCCC)ccc2c1 10.1016/0960-894X(95)00035-R
CHEMBL120282 11424 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 643 28 0 0 15.0 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc2cc(C[P+](CCCCC)(CCCCC)CCCCC)ccc2c1 10.1016/0960-894X(95)00035-R
44320170 14292 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 663 18 3 2 10.1 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1162585 14292 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 663 18 3 2 10.1 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1199851 14292 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 663 18 3 2 10.1 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
22288578 99112 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 649 9 0 7 6.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(C)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL280869 99112 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 649 9 0 7 6.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(C)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10930680 67678 0 None -6 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907654 67678 0 None -6 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
10100960 16489 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL123548 16489 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL333705 16489 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL539629 16489 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
10100960 16489 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL123548 16489 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL333705 16489 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL539629 16489 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 669 29 0 0 15.5 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(-c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
44346418 13758 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 17 3 2 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C(N/C(=N/C2CCCCC2)NC2CCCCC2)c2ccc3ccccc3c2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195322 13758 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 17 3 2 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C(N/C(=N/C2CCCCC2)NC2CCCCC2)c2ccc3ccccc3c2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554254 13758 0 None - 1 Human 5.5 pKi = 5.5 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 17 3 2 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C(N/C(=N/C2CCCCC2)NC2CCCCC2)c2ccc3ccccc3c2)cc1 10.1016/0960-894X(95)00035-R
11215913 136539 0 None -26915 2 Human 4.5 pKi = 4.5 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
CHEMBL373654 136539 0 None -26915 2 Human 4.5 pKi = 4.5 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 646 9 2 6 4.9 CN1c2cc(CN3CCCCC3)ccc2[C@@H](NC(=O)C[C@@H](NS(=O)(=O)c2ccc3ccccc3c2)c2ccccc2)CS1(=O)=O 10.1021/jm061224g
44276975 96515 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity towards bradykinin receptor B2 using [3H]bradykininBinding affinity towards bradykinin receptor B2 using [3H]bradykinin
ChEMBL 1081 34 13 12 -0.8 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2C1C(=O)N1CC(C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2CCCCC21 10.1021/jm00035a015
CHEMBL262639 96515 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity towards bradykinin receptor B2 using [3H]bradykininBinding affinity towards bradykinin receptor B2 using [3H]bradykinin
ChEMBL 1081 34 13 12 -0.8 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2C1C(=O)N1CC(C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)C2CCCCC21 10.1021/jm00035a015
90663066 106588 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assayCompound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL3142595 106588 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assayCompound was evaluated for inhibitory activity against [3H]BK in the classical guinea pig ileum B2 binding assay
ChEMBL 1081 34 14 12 -0.5 N=C(N)NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)NCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
22288581 99283 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 5 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)[nH]4)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL281951 99283 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 5 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)[nH]4)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
9830551 100048 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 620 9 0 6 7.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL287018 100048 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 620 9 0 6 7.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(Cl)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10571699 57152 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 378 6 3 4 4.6 O=[N+]([O-])c1ccccc1N/N=C(/S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
CHEMBL164636 57152 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 378 6 3 4 4.6 O=[N+]([O-])c1ccccc1N/N=C(/S)NC(c1ccccc1)c1ccccc1 10.1021/jm991155o
22288602 99729 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
CHEMBL284865 99729 0 None - 1 Human 5.4 pKi = 5.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 624 10 0 6 7.9 CCCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
11707423 78031 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 580 11 4 6 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
CHEMBL209873 78031 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 580 11 4 6 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN=C(N)N)c3Cl)c2n1 10.1021/jm060137l
11592927 139277 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 629 13 3 7 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccn4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379083 139277 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 629 13 3 7 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccccn4)c3Cl)c2n1 10.1021/jm060137l
11636064 78020 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 553 11 2 6 4.6 COCCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
CHEMBL209819 78020 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 553 11 2 6 4.6 COCCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
11498691 78253 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 646 13 3 6 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(F)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210662 78253 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 646 13 3 6 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(F)cc4)c3Cl)c2n1 10.1021/jm060137l
9916936 99711 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL284727 99711 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)CCc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
10790025 57458 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 457 7 4 6 3.2 NS(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
CHEMBL165627 57458 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 457 7 4 6 3.2 NS(=O)(=O)c1ccc(N/N=C(/S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm991155o
44316620 2121 0 None 19 2 Human 8.4 pKi = 8.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
656 2121 0 None 19 2 Human 8.4 pKi = 8.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
CHEMBL408846 2121 0 None 19 2 Human 8.4 pKi = 8.4 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None None 10.1021/jm990961s
57393602 67680 0 None 3 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907656 67680 0 None 3 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 708 13 4 9 3.0 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
44320168 10248 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160969 10248 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL444322 10248 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44320168 10248 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL1160969 10248 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL444322 10248 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
44346412 13100 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 717 18 3 3 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cc3ccccc3s2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190352 13100 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 717 18 3 3 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cc3ccccc3s2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540639 13100 0 None - 1 Human 6.4 pKi = 6.4 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 717 18 3 3 11.6 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2cc3ccccc3s2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
70688994 77451 0 None -18 2 Human 4.4 pKi = 4.4 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 433 5 2 4 2.6 Cc1c(Cl)ccc(S(=O)(=O)N2CCC[C@H]2C(=O)NCC2CCNCC2)c1Cl 10.1021/jm2016057
CHEMBL2087028 77451 0 None -18 2 Human 4.4 pKi = 4.4 Binding
Binding affinity to B2 receptorBinding affinity to B2 receptor
ChEMBL 433 5 2 4 2.6 Cc1c(Cl)ccc(S(=O)(=O)N2CCC[C@H]2C(=O)NCC2CCNCC2)c1Cl 10.1021/jm2016057
44276459 96357 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 652 11 0 6 8.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4CCC(C)C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26160 96357 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 652 11 0 6 8.6 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4CCC(C)C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
90663068 106589 0 None - 1 Human 7.4 pKi = 7.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptorCompound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptor
ChEMBL 1095 35 13 12 -0.3 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
CHEMBL3142597 106589 0 None - 1 Human 7.4 pKi = 7.4 Binding
Compound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptorCompound was evaluated for inhibitory activity against [3H]BK in membrane preparations from a stable cell line that expresses the human B2 receptor
ChEMBL 1095 35 13 12 -0.3 NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)NCCCCCCCCCCCCC(=O)N[C@@H](CO)C(=O)N1CCc2ccccc2[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1016/S0960-894X(97)10042-7
44340964 9707 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL113176 9707 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 609 10 1 6 6.7 COc1c(N(C)C(=O)CNC(=O)/C=C/c2ccc(C(F)(F)F)cc2)ccc(SC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
10482991 100650 0 None - 1 Human 7.3 pKi = 7.3 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
CHEMBL292181 100650 0 None - 1 Human 7.3 pKi = 7.3 Binding
In vitro binding affinity against Bradykinin receptor B2In vitro binding affinity against Bradykinin receptor B2
ChEMBL 563 9 2 6 5.9 CC(=O)Nc1ccc(/C=C/C(=O)NC[C@H]2CCCN2c2ccc(C)c(COc3cccc4ccc(C)nc34)c2C)cn1 10.1016/s0960-894x(03)00309-3
44346414 13759 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 676 19 3 2 10.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1195323 13759 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 676 19 3 2 10.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL554255 13759 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 676 19 3 2 10.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44276666 98617 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 639 8 0 5 8.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(F)(F)F)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL27701 98617 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 639 8 0 5 8.2 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C(F)(F)F)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44355289 161904 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL415209 161904 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1134 31 16 17 -8.4 NC(N)=NCCC[C@H](NC(=O)CN1CC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
16108960 169259 0 None -30902 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL441188 169259 0 None -30902 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 567 9 2 4 6.0 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
44300140 101609 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 526 8 4 3 6.1 O=C(Nc1ccc(CO)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL298832 101609 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 526 8 4 3 6.1 O=C(Nc1ccc(CO)cc1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44214619 110605 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
CHEMBL325601 110605 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 553 13 1 8 4.7 COC(=O)CCCCC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1SC 10.1016/s0960-894x(98)00736-7
10930680 67678 0 None 6 2 Rat 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907654 67678 0 None 6 2 Rat 8.3 pKi = 8.3 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 750 15 4 9 4.7 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2Cl)c2ccccc2Cl)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL5278855 194001 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1046 25 14 13 -3.8 C[C@H](C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)N1Cc2ccccc2C[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O 10.1021/acs.jmedchem.6b01029
44276716 99710 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 622 10 0 6 7.6 C=CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
CHEMBL284726 99710 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 622 10 0 6 7.6 C=CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
44355287 161879 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL415032 161879 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
122189855 123412 0 None -75 3 Rat 5.3 pKi = 5.3 Binding
Displacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
CHEMBL3616879 123412 0 None -75 3 Rat 5.3 pKi = 5.3 Binding
Displacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from B2R in rat brain membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1816 45 23 23 -3.5 CSCC[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@H](CCCNC(=N)N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)CC1C(=O)NCC(=O)NC(Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C(C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)CC2CCCCC21 10.1016/j.bmcl.2015.08.014
44346361 10250 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 536 7 4 3 6.5 O=C(Nc1nc2ccccc2[nH]1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160971 10250 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 536 7 4 3 6.5 O=C(Nc1nc2ccccc2[nH]1)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
10742229 120269 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 451 9 4 8 2.7 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccco2)ccc1N/N=C(/S)NCc1ccco1 10.1021/jm991155o
CHEMBL352459 120269 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 451 9 4 8 2.7 O=[N+]([O-])c1cc(S(=O)(=O)NCc2ccco2)ccc1N/N=C(/S)NCc1ccco1 10.1021/jm991155o
44276455 98377 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
CHEMBL27530 98377 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 610 9 0 6 7.5 CCN(C(=O)Cc1ccc(C(=O)c2ccc(C#N)cc2)n1C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1016/s0960-894x(03)00104-5
44346306 10247 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
CHEMBL1160968 10247 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)C(Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1016/0960-894X(95)00035-R
44320168 10248 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL1160969 10248 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
CHEMBL444322 10248 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 529 7 3 3 5.2 O=C(NC1CN2CCC1CC2)[C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1 10.1021/jm00069a021
44276487 99999 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(NC(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL286711 99999 0 None - 1 Human 5.3 pKi = 5.3 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 582 8 1 6 7.1 Cc1ccc2cccc(OCc3c(Cl)ccc(NC(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
16108967 84344 0 None -147 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 541 10 2 4 5.6 O=C(CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)NCc1ccc(CN2CCCCC2)cc1 10.1021/jm061224g
CHEMBL221691 84344 0 None -147 2 Human 4.3 pKi = 4.3 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 541 10 2 4 5.6 O=C(CC(NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)NCc1ccc(CN2CCCCC2)cc1 10.1021/jm061224g
10461651 99373 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL282562 99373 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
16108969 83031 0 None -239883 2 Human 4.2 pKi = 4.2 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL218152 83031 0 None -239883 2 Human 4.2 pKi = 4.2 Binding
Displacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cellsDisplacement of [3H]bradykinin from human bradykinin B2 receptor expressed in CHO-K1 cells
ChEMBL 581 9 2 4 6.4 O=C(C[C@@H](NS(=O)(=O)c1ccc2ccccc2c1)c1ccccc1)N[C@@H]1CCCc2cc(CN3CCCCC3)ccc21 10.1021/jm061224g
CHEMBL5271423 193683 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1312 30 18 17 -4.6 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1021/acs.jmedchem.6b01029
CHEMBL3038105 210938 0 None 3 2 Human 6.2 pKi = 6.2 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)O)Cc1ccccc1 10.1021/jm950716i
71450888 78793 0 None -8 2 Rat 8.2 pKi = 8.2 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
CHEMBL2112698 78793 0 None -8 2 Rat 8.2 pKi = 8.2 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
ChEMBL 1228 31 16 18 -6.5 NC(N)=NCCC[C@H](NC(=O)CN1C(=O)[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)CSc2ccccc21)C(=O)O 10.1021/jm9901529
44355234 96458 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1242 31 16 18 -6.2 Cc1ccc2c(c1)SCC(NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CC(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm9901531
CHEMBL262313 96458 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1242 31 16 18 -6.2 Cc1ccc2c(c1)SCC(NC(=O)[C@H](CO)NC(=O)[C@H](Cc1cccs1)NC(=O)CNC(=O)[C@@H]1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N2CC(=O)N[C@H](CCCN=C(N)N)C(=O)O 10.1021/jm9901531
22008916 9762 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL113502 9762 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 461 8 2 6 3.3 CCNC(=O)NCC(=O)N(C)c1ccc(OC)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
44337425 109877 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 315 3 0 4 1.7 CC(=O)CN1CN(c2ccc(C)cc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL323421 109877 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 315 3 0 4 1.7 CC(=O)CN1CN(c2ccc(C)cc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
44340951 10002 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
CHEMBL114915 10002 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 587 11 1 7 6.4 COc1ccc(/C=C/C(=O)NCC(=O)N(C)c2ccc(SC)c(COc3cccc4ccc(C)nc34)c2SC)cc1 10.1016/s0960-894x(98)00736-7
44337476 8128 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 321 4 0 4 1.7 CC(=O)CN1CN(CC2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL109172 8128 0 None - 1 Human 8.2 pKi = 8.2 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 321 4 0 4 1.7 CC(=O)CN1CN(CC2CCCCC2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
132927 4084 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
138398059 4084 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
677 4084 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
CHEMBL294453 4084 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
CHEMBL551291 4084 4 None 6 2 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 10.1016/0960-894X(95)00035-R
101005081 13101 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44346317 13101 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190353 13101 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540640 13101 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 754 21 3 2 12.7 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
132928 14297 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL1162586 14297 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL1199865 14297 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00036-S
132928 14297 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1162586 14297 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
CHEMBL1199865 14297 4 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligandBinding affinity against human bradykinin receptor B2 using [3H]bradykinin as radioligand
ChEMBL 713 18 3 2 11.2 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1021/jm00069a021
90662943 106584 0 None -1778 2 Human 7.2 pKi = 7.2 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1192 30 14 17 -4.3 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
CHEMBL3142391 106584 0 None -1778 2 Human 7.2 pKi = 7.2 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL 1192 30 14 17 -4.3 NCCCC[C@H](N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1CC(O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
11650337 138687 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 523 7 3 5 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N=C(N)N)c3Cl)c2n1 10.1021/jm060137l
CHEMBL377835 138687 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 523 7 3 5 3.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)N=C(N)N)c3Cl)c2n1 10.1021/jm060137l
11542210 77609 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 608 11 2 7 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL208807 77609 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 608 11 2 7 4.3 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCN4CCOCC4)c3Cl)c2n1 10.1021/jm060137l
11136263 78586 0 None -43 2 Rat 7.2 pKi = 7.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL2112221 78586 0 None -43 2 Rat 7.2 pKi = 7.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 704 13 4 10 3.9 CN(C)CCN(C)CCNC(=O)c1cccn1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3CCc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
10952583 67681 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 694 14 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3-c3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907657 67681 0 None - 1 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 694 14 4 9 3.7 CN(C)CCCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC2c3ccccc3-c3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
57395311 67679 0 None -2 2 Rat 6.2 pKi = 6.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907655 67679 0 None -2 2 Rat 6.2 pKi = 6.2 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 580 7 4 7 2.9 NC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=S)NC2Cc3ccccc3Cc3ccccc32)c([N+](=O)[O-])c1 10.1021/jm0111088
9915727 95525 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 556 8 0 6 6.4 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL25745 95525 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 556 8 0 6 6.4 Cc1ccc2cccc(OCc3c(C)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)cc5)n4C)c3C)c2n1 10.1016/s0960-894x(03)00104-5
10886849 67677 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 655 14 4 7 3.5 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC(c2ccccc2)c2ccccc2)c(Cl)c1 10.1021/jm0111088
CHEMBL1907653 67677 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranesInhibition of specific binding of [3H]-BK (1 nM) to rat Bradykinin receptor B2 by 50% in NG108-15 cell membranes
ChEMBL 655 14 4 7 3.5 CN(C)CCN(C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(NNC(=O)NC(c2ccccc2)c2ccccc2)c(Cl)c1 10.1021/jm0111088
44337489 9230 0 None - 1 Human 8.1 pKi = 8.1 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 301 3 0 4 1.3 CC(=O)CN1CN(c2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL110652 9230 0 None - 1 Human 8.1 pKi = 8.1 Binding
Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731Affinity to human Bradykinin receptor B2 in CHO cell membranes determined by displacement of [3H]-NPC 17731
ChEMBL 301 3 0 4 1.3 CC(=O)CN1CN(c2ccccc2)C2(CCN(C)CC2)C1=O 10.1021/jm950676i
CHEMBL2392354 210415 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity to human bradykinin B2 receptor by radioligand displacement assayBinding affinity to human bradykinin B2 receptor by radioligand displacement assay
ChEMBL None None None N=C(N)NCCC[C@H](N)C(=O)N[C@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)O 10.1016/j.ejmech.2013.01.044
11527906 140118 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 670 13 5 7 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380086 140118 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 670 13 5 7 5.7 Cc1cc(C)c2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNc4ccc(C(=N)N)cc4)c3Cl)c2n1 10.1021/jm060137l
45266122 13105 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 726 18 2 2 11.9 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N(C)/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190357 13105 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 726 18 2 2 11.9 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N(C)/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540644 13105 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 726 18 2 2 11.9 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N(C)/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
44346679 13122 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 631 18 3 2 9.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1190473 13122 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 631 18 3 2 9.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
CHEMBL540895 13122 0 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 631 18 3 2 9.7 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)[C@H](Cc2ccc3ccccc3c2)N/C(=N/C(C)C)NC(C)C)cc1 10.1016/0960-894X(95)00035-R
10542327 57413 0 None - 1 Rat 5.2 pKi = 5.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 301 5 2 3 3.2 O=[N+]([O-])c1ccccc1C/N=C(\S)NCc1ccccc1 10.1021/jm991155o
CHEMBL165240 57413 0 None - 1 Rat 5.2 pKi = 5.2 Binding
Inhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranesInhibition of binding of [3H]BK to rat bradykinin B2 receptor expressed in NG108-15 neuroblastoma-glioma hybrid cell membranes
ChEMBL 301 5 2 3 3.2 O=[N+]([O-])c1ccccc1C/N=C(\S)NCc1ccccc1 10.1021/jm991155o
44276840 99975 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1cccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)c1 10.1016/s0960-894x(03)00104-5
CHEMBL286556 99975 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1cccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)c1 10.1016/s0960-894x(03)00104-5
44276488 97209 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 597 8 0 7 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26847 97209 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 597 8 0 7 6.5 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(C#N)nc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44276624 96852 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 605 8 0 5 7.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26532 96852 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 605 8 0 5 7.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(Cl)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44276599 96408 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 650 9 1 7 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(N)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
CHEMBL26192 96408 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 650 9 1 7 5.9 Cc1ccc2cccc(OCc3c(Cl)ccc(N(C)C(=O)Cc4ccc(C(=O)c5ccc(S(N)(=O)=O)cc5)n4C)c3Cl)c2n1 10.1016/s0960-894x(03)00104-5
44346387 14335 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C\[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1162797 14335 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C\[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL1200033 14335 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 696 18 2 1 12.3 CCCC[PH](CCCC)(CCCC)Cc1ccc(/C=C\[C@H](Cc2ccc3ccccc3c2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00035-R
176 398 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2157 398 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
2566 398 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
CHEMBL633 398 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
DB01118 398 66 None -5 31 Human 5.1 pKi = 5.1 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
ChEMBL 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 nan
10373002 138311 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL121565 138311 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
CHEMBL377100 138311 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00035-R
10373002 138311 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL121565 138311 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
CHEMBL377100 138311 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluatedBinding affinity against human IMR90 fetal lung fibroblast bradykinin B2 receptor was evaluated
ChEMBL 697 30 0 1 15.1 CCCCC[P+](CCCCC)(CCCCC)Cc1ccc(C(=O)c2ccc(C[P+](CCCCC)(CCCCC)CCCCC)cc2)cc1 10.1016/0960-894X(95)00036-S
44355257 166462 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
CHEMBL427805 166462 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1162 31 16 17 -7.6 NC(N)=NCCC[C@H](NC(=O)CN1CCCC[C@@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc2cccs2)NC(=O)CNC(=O)[C@@H]2CC(O)CN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C1=O)C(=O)O 10.1021/jm9901531
5312119 718 4 None -1148 2 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
680 718 4 None -1148 2 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
CHEMBL308468 718 4 None -1148 2 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10.1021/jm0111088
11650783 52429 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 14 3 8 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(S(C)(=O)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL159066 52429 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 706 14 3 8 5.2 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(S(C)(=O)=O)cc4)c3Cl)c2n1 10.1021/jm060137l
11636119 78078 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 8 3 6 4.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210100 78078 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 564 8 3 6 4.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NC4CCNCC4)c3Cl)c2n1 10.1021/jm060137l
11686399 140137 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 644 13 4 7 5.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL380206 140137 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 644 13 4 7 5.5 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(O)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL5285641 194306 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1032 25 14 13 -4.2 N=C(N)NCCC[C@H](NC(=O)CN1Cc2ccccc2CC(NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@@H](N)CCCNC(=N)N)C1=O)C(=O)O 10.1021/acs.jmedchem.6b01029
11527892 139528 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 662 13 3 6 6.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(Cl)cc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL379541 139528 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 662 13 3 6 6.4 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)NCCCNCc4ccc(Cl)cc4)c3Cl)c2n1 10.1021/jm060137l
11671905 77759 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 539 10 2 6 4.2 COCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
CHEMBL209068 77759 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 539 10 2 6 4.2 COCCNC(=O)C(C)(C)NS(=O)(=O)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1Cl 10.1021/jm060137l
11513104 78168 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 557 8 2 5 6.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)Nc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
CHEMBL210427 78168 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2 receptor transfected in CHO cellsDisplacement of [3H]BK from human B2 receptor transfected in CHO cells
ChEMBL 557 8 2 5 6.1 Cc1ccc2cccc(OCc3c(Cl)ccc(S(=O)(=O)NC(C)(C)C(=O)Nc4ccccc4)c3Cl)c2n1 10.1021/jm060137l
10895913 9869 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL114180 9869 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 465 7 2 5 3.9 CCNC(=O)NCC(=O)N(C)c1ccc(Cl)c(COc2cccc3ccc(C)nc23)c1C#N 10.1016/s0960-894x(98)00736-7
CHEMBL3038102 210935 0 None 5 2 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Bradykinin receptor B2 in human S34 clone cellsBinding affinity towards Bradykinin receptor B2 in human S34 clone cells
ChEMBL None None None NC(N)=NCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)N(CC(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O)Cc1ccccc1 10.1021/jm950716i
44347466 14336 0 None - 1 Human 6.1 pKi = 6.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1162799 14336 0 None - 1 Human 6.1 pKi = 6.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1200034 14336 0 None - 1 Human 6.1 pKi = 6.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 836 20 3 3 11.4 CCCC[PH](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)[C@H](CCc2ccccc2)N/C(=N/C2CCCCC2)NC2CCCCC2)cc1 10.1016/0960-894X(95)00037-T
44347757 11447 0 None - 1 Human 5.1 pKi = 5.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 728 18 2 4 10.0 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)C(CCc2ccccc2)NC(=O)OC(C)(C)C)cc1 10.1016/0960-894X(95)00037-T
CHEMBL1180347 11447 0 None - 1 Human 5.1 pKi = 5.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 728 18 2 4 10.0 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)C(CCc2ccccc2)NC(=O)OC(C)(C)C)cc1 10.1016/0960-894X(95)00037-T
CHEMBL123124 11447 0 None - 1 Human 5.1 pKi = 5.1 Binding
Tested for binding affinity against human IMR-90 Bradykinin receptor B2Tested for binding affinity against human IMR-90 Bradykinin receptor B2
ChEMBL 728 18 2 4 10.0 CCCC[P+](CCCC)(CCCC)Cc1ccc(NC(=O)C2Cc3ccccc3CN2C(=O)C(CCc2ccccc2)NC(=O)OC(C)(C)C)cc1 10.1016/0960-894X(95)00037-T
CHEMBL2370041 209774 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membraneBinding affinity against [3H]bradykinin binding to bradykinin receptor B2 in guinea pig ileal membrane
ChEMBL None None None CC(NC(=O)[C@@H]1C[C@H](O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1C2CCCCC2C[C@H]1C(=O)N[C@@H](CCCN=C(N)N)C(=O)O 10.1021/jm00069a016
44346449 10253 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 619 9 2 3 7.1 O=C([C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1)N(Cc1ccccc1)C1CN2CCC1CC2 10.1016/0960-894X(95)00035-R
CHEMBL1160978 10253 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2Binding affinity against human IMR 90 fetal lung fibroblast bradykinin receptor B2
ChEMBL 619 9 2 3 7.1 O=C([C@H](Cc1ccc2ccccc2c1)N/C(=N/C1CCCCC1)NC1CCCCC1)N(Cc1ccccc1)C1CN2CCC1CC2 10.1016/0960-894X(95)00035-R
118719116 115444 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
CHEMBL3350763 115444 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
ChEMBL 1285 32 16 18 -5.8 NC(N)=NCCC[C@H](NC(=O)[C@H](N)CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@@H](CO)C(=O)NC1N=C(c2ccccc2)c2ccccc2N(CC(=O)N[C@H](CCCN=C(N)N)C(=O)O)C1=O 10.1021/jm9901531
44276841 95529 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccccc1C(=O)c1ccc(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)n1C 10.1016/s0960-894x(03)00104-5
CHEMBL25748 95529 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 628 9 1 6 7.2 CC(=O)Nc1ccccc1C(=O)c1ccc(CC(=O)N(C)c2ccc(Cl)c(COc3cccc4ccc(C)nc34)c2Cl)n1C 10.1016/s0960-894x(03)00104-5
CHEMBL5274916 193829 0 None - 1 Human 6.1 pKi = 6.1 Binding
Binding affinity to B2 bradykinin receptor (unknown origin)Binding affinity to B2 bradykinin receptor (unknown origin)
ChEMBL 1405 31 20 19 -4.2 N=C(N)NCCC[C@@H](N)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](Cc1cccs1)C(=O)N[C@H]1CSSC[C@@H](C(=O)N[C@@H](CCCNC(=N)N)C(=O)O)NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@H](Cc2ccccc2)NC1=O 10.1021/acs.jmedchem.6b01029
10005078 33767 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
CHEMBL142260 33767 0 None - 1 Human 5.1 pKi = 5.1 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 473 6 3 3 5.0 N=C(N)Nc1cccc(CN2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)c1 10.1016/s0960-894x(99)00015-3
15388870 110633 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL325742 110633 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 543 8 1 6 6.4 Cc1nc2c(OCc3c(Cl)ccc(N(C)C(=O)CNC(=O)OCc4ccccc4)c3Cl)cccc2s1 10.1016/s0960-894x(98)00736-7
CHEMBL3085458 210988 6 None -398 2 Human 8.0 pKi = 8.0 Binding
Binding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligandBinding affinity towards human cloned B2 receptor was determined using [3H]BK as radioligand
ChEMBL None None None NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990962k
CHEMBL3085458 210988 6 None -398 2 Human 8.0 pKi = 8.0 Binding
Ability to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykininAbility to bind to human cloned B2 receptor in competition binding experiments with [3H]- bradykinin
ChEMBL None None None NCCCC[C@H](N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@H](C(=O)N[C@@H](CO)C(=O)N[C@@H]1CSc2ccccc2N(CC(=O)O)C1=O)C1Cc2ccccc2C1 10.1021/jm990961s
44341060 9560 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
CHEMBL112360 9560 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)Inhibition of specific binding of [3H]BK to bradykinin B2 receptors of guinea pig ileum (GPI)
ChEMBL 539 10 1 6 5.2 COc1ccc(N(C)C(=O)CNC(=O)/C=C/c2cccc(C)c2)c(OC)c1COc1cccc2ccc(C)nc12 10.1016/s0960-894x(98)00736-7
122189902 123423 0 None -13489 2 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
CHEMBL3616944 123423 0 None -13489 2 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assayDisplacement of [3H]BK from human B2R expressed in HEK293 cell membranes by liquid scintillation counting in based radioligand competition assay
ChEMBL 1304 30 18 17 -4.4 N=C(N)NCCC[C@H](NC(=O)C1CC2CCCCC2N1C(=O)[C@H]1Cc2ccccc2CN1C(=O)[C@H](CO)NC(=O)C(Cc1cccs1)NC(=O)CNC(=O)C1CC(O)CN1C(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(=N)N)NC(=O)[C@H](N)CCCNC(=N)N)C(=O)O 10.1016/j.bmcl.2015.08.014
44276667 98618 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 601 9 0 6 7.2 COc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
CHEMBL27702 98618 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards human bradykinin receptor B2Binding affinity towards human bradykinin receptor B2
ChEMBL 601 9 0 6 7.2 COc1ccc(C(=O)c2ccc(CC(=O)N(C)c3ccc(Cl)c(COc4cccc5ccc(C)nc45)c3Cl)n2C)cc1 10.1016/s0960-894x(03)00104-5
44361937 169404 0 None - 1 Human 5.0 pKi = 5.0 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 459 5 3 3 5.1 N=C(N)Nc1ccc(N2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)cc1 10.1016/s0960-894x(99)00015-3
CHEMBL442294 169404 0 None - 1 Human 5.0 pKi = 5.0 Binding
Binding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligandBinding affinity towards human bradykinin B2 receptor (membranes from Cos-7 cells expressing human B2 receptor) using [3H]-BK as radioligand
ChEMBL 459 5 3 3 5.1 N=C(N)Nc1ccc(N2C(=O)C(Cc3ccccc3)N=C(c3ccccc3)c3ccccc32)cc1 10.1016/s0960-894x(99)00015-3
10996140 67676 0 None -309 2 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
CHEMBL1907652 67676 0 None -309 2 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cellsDisplacement of [3H]BK (1 nM) from human Bradykinin receptor B2 expressed in Cos-7 cells
ChEMBL 710 17 4 9 4.1 CN(C)CCCN(C)CCCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(N/N=C(\S)NC(c2ccccc2)c2ccccc2)c([N+](=O)[O-])c1 10.1021/jm0111088
3812 717 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
439201 717 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
649 717 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
CHEMBL406291 717 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
DB12126 717 42 None -1 6 Mouse 9.4 pKd = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9333122
122173054 217734 0 None -1 6 Rat 8.0 pKi = 8 Binding
Binding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligandBinding affinity against rat bradykinin B2 receptors expressed in CHO cells using [3H]bradykinin as radioligand
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
122173054 217734 0 None -1 6 Human 8.0 pKi = 8.0 Binding
Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.Binding affinity towards human cloned Bradykinin receptor B2 expressed in CHO cells by [3H]bradykinin displacement.
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
3075702 217332 0 3H-NPC 17731 -2 37 Human 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 198 3 1 3 1.5 C1CNC1COC2=CN=C(C=C2)Cl None
243 3202 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3052762 3202 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3502 3202 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
CHEMBL117287 3202 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
DB06480 3202 91 3H-BRADYKININ -1096 34 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
44208932 140707 7 UNDEFINED -89125 36 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 475 5 1 3 6.8 Cc1ccc(Cn2nc(C(=O)NC3C4(C)CCC(C4)C3(C)C)cc2-c2ccc(Cl)c(C)c2)cc1 None
CHEMBL381689 140707 7 UNDEFINED -89125 36 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 475 5 1 3 6.8 Cc1ccc(Cn2nc(C(=O)NC3C4(C)CCC(C4)C3(C)C)cc2-c2ccc(Cl)c(C)c2)cc1 None
1973 203483 15 3H-NPC 17731 -3 36 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 462 3 1 7 3.9 Nc1ncnc2nc(-c3ccc(N4CCOCC4)nc3)cc(-c3cccc(Br)c3)c12 None
CHEMBL1394464 203483 15 3H-NPC 17731 -3 36 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 462 3 1 7 3.9 Nc1ncnc2nc(-c3ccc(N4CCOCC4)nc3)cc(-c3cccc(Br)c3)c12 None
CHEMBL66089 203483 15 3H-NPC 17731 -3 36 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 462 3 1 7 3.9 Nc1ncnc2nc(-c3ccc(N4CCOCC4)nc3)cc(-c3cccc(Br)c3)c12 None
None 216493 0 3H-BRADYKININ -10471285 17 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 372 2 1 3 4.4 CC(C)(C)C1=CC=C(C=C1)NC(=O)N2CCN(CC2)C3=C(C=CC=N3)Cl None
1016 3747 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
2561 3747 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
2733526 3747 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
5384 3747 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
CHEMBL83 3747 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
DB00675 3747 78 None -46 35 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 371 8 0 2 6.0 CC/C(=C(\c1ccccc1)/c1ccc(cc1)OCCN(C)C)/c1ccccc1 None
176 398 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
2157 398 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
2566 398 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
CHEMBL633 398 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
DB01118 398 66 None -5 31 Human 8.3 pKi = 8.3 Binding
DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)DRUGMATRIX: Bradykinin B2 radioligand binding (ligand: [3H] Bradykinin)
Drug Central 645 11 0 4 6.9 CCCCc1oc2c(c1C(=O)c1cc(I)c(c(c1)I)OCCN(CC)CC)cccc2 None
122173054 217734 0 None -1 6 Mouse 8.0 pKi = 8.0 Binding
NoneNone
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
122173054 217734 0 None -1 6 Guinea pig 8.0 pKi = 8 Binding
In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.In vitro binding affinity against bradykinin receptor B2 from guinea pig ileum.
Drug Central 1304 30 18 17 -4.4 N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N1C[C@H](O)C[C@H]1C(=O)NCC(=O)N[C@@H](CC1=CC=CS1)C(=O)N[C@@H](CO)C(=O)N1CC2=C(C[C@@H]1C(=O)N1[C@H]3CCCC[C@H]3C[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(O)=O)C=CC=C2 None
12421 1399 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 32636746
12421 1399 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 35086057
154623230 1399 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 32636746
154623230 1399 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.Binding affinity to human bradykinin B<sub>2</sub> receptor derived from a [<sup>3</sup>H]BK binding competition assay.
Guide to Pharmacology 534 9 1 7 5.1 [2H][C@](C)(C1=C(C(=CC(=C1)F)Cl)COC=2C=CC=C3C(=CC(=NC23)C)C4=NC=NN4C)NC(COC(F)F)=O 35086057
11159 1092 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.
Guide to Pharmacology 533 9 1 7 5.1 FC(OCC(=O)N[C@H](c1cc(F)cc(c1COc1cccc2c1nc(C)cc2c1ncnn1C)Cl)C)F 32636746
138634054 1092 0 None - 1 Human 9.3 pKi = 9.3 Binding
Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.Ki values at the human B2 receptor derived from a [3H]BK binding competition assay.
Guide to Pharmacology 533 9 1 7 5.1 FC(OCC(=O)N[C@H](c1cc(F)cc(c1COc1cccc2c1nc(C)cc2c1ncnn1C)Cl)C)F 32636746
667 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
71364 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
CHEMBL2028850 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
DB06196 1973 37 None -1 6 Human 10.2 pKi = 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
679 414 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
9831652 414 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
CHEMBL2107725 414 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
DB05038 414 0 None 2 2 Human 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
670 2120 0 None 8 2 Rat 10.1 pKi None 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
667 1973 37 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
71364 1973 37 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
CHEMBL2028850 1973 37 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
DB06196 1973 37 None -1 6 Rat 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10694205
5312119 718 4 None -1148 2 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
680 718 4 None -1148 2 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
CHEMBL308468 718 4 None -1148 2 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
658 2872 0 None -3981 2 Human 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8995263
132927 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
132927 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
138398059 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
138398059 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
677 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
677 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
CHEMBL294453 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
CHEMBL294453 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
CHEMBL551291 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8197121
CHEMBL551291 4084 4 None 6 2 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 746 18 3 2 8.5 CCCC[P+](Cc1ccc(cc1)NC(=O)[C@H](Cc1ccc2c(c1)cccc2)NC(=NC1CCCCC1)NC1CCCCC1)(CCCC)CCCC.[Cl-] 8394936
5311114 1688 8 None - 1 Human 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 9224807
668 1688 8 None - 1 Human 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 9224807
CHEMBL99869 1688 8 None - 1 Human 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 697 12 2 7 6.6 CNC(=O)c1ccc(cc1)/C=C/C(=O)NCC(=O)N(c1ccc(c(c1Cl)COc1cccc2c1nc(C)cc2OCc1ccccn1)Cl)C 9224807
679 414 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
9831652 414 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
CHEMBL2107725 414 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
DB05038 414 0 None -2 2 Rat 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 710 12 4 7 5.1 Cc1cc(C)c2c(n1)c(ccc2)OCc1c(Cl)ccc(c1Cl)S(=O)(=O)N1CCC[C@H]1C(=O)NCCCNC(=O)c1ccc(cc1)C(=N)N 10596852
672 2267 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
672 2267 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
6918284 2267 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
6918284 2267 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
CHEMBL2105864 2267 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
CHEMBL2105864 2267 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
DB06549 2267 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
DB06549 2267 21 None 1 2 Rat 7.9 pKi None 7.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 7965719
3081308 2871 0 None 15 2 Human 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8995263
657 2871 0 None 15 2 Human 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8995263
44316620 2121 0 None 19 2 Human 8.4 pKi None 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10882364
656 2121 0 None 19 2 Human 8.4 pKi None 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10882364
CHEMBL408846 2121 0 None 19 2 Human 8.4 pKi None 8.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10882364
653 565 0 None -1 4 Mouse 9.0 pKi None 9 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9276157
653 565 0 None 1 4 Human 9.1 pKi None 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8856115
653 565 0 None 1 4 Human 9.1 pKi None 9.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 9276157
670 2120 0 None -8 2 Human 9.2 pKi None 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 10514288
5312119 718 4 None 1148 2 Rat 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
680 718 4 None 1148 2 Rat 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
CHEMBL308468 718 4 None 1148 2 Rat 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 682 15 4 9 2.9 CN(CCN(C)C)CCNC(=O)[C@@H]1CCCN1S(=O)(=O)c1ccc(c(c1)[N+](=O)[O-])NNC(=S)NC(c1ccccc1)c1ccccc1 10694205
667 1973 37 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
71364 1973 37 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
CHEMBL2028850 1973 37 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267
DB06196 1973 37 None -2 6 Mouse 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology None None None None 8302267