Ligand source activities (1 row/activity)





Ligands (move mouse cursor over ligand name to see structure) Receptor Activity Chemical information
Sel. page Common
name
GPCRdb
ID
Reference
ligand
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Species

Assay
Type

Activity
Type
Activity
Relation
Activity
Value
p-value
(-log)
Fold
selectivity
Tested
GPCRs
Assay
Description
Source

Mol
weight
Rot
Bonds
H don

H acc

LogP

Smiles

DOI

118037818 134778 None 0 Human Functional pAC50 = 5.5 5.5 1 2
Agonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assayAgonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assay
ChEMBL 428 4 2 4 4.9 O=C(Nc1ccccc1C(=O)Nc1cccc(C(F)(F)F)c1)c1ccc2c(c1)OCO2 nan
CHEMBL3718470 134778 None 0 Human Functional pAC50 = 5.5 5.5 1 2
Agonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assayAgonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assay
ChEMBL 428 4 2 4 4.9 O=C(Nc1ccccc1C(=O)Nc1cccc(C(F)(F)F)c1)c1ccc2c(c1)OCO2 nan
90010773 133980 None 0 Human Functional pAC50 = 5.1 5.1 1 2
Agonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assayAgonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assay
ChEMBL 375 4 2 4 4.2 O=C(Nc1ccccc1C(=O)Nc1cccc(C(F)(F)F)c1)c1ccno1 nan
CHEMBL3715750 133980 None 0 Human Functional pAC50 = 5.1 5.1 1 2
Agonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assayAgonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assay
ChEMBL 375 4 2 4 4.2 O=C(Nc1ccccc1C(=O)Nc1cccc(C(F)(F)F)c1)c1ccno1 nan
127024071 134094 None 0 Human Functional pAC50 = 5.0 5.0 - 1
Agonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assayAgonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assay
ChEMBL 361 4 3 2 4.9 O=C(Nc1ccc2cc[nH]c2c1)c1ccccc1NC(=O)C1CCCCC1 nan
CHEMBL3716158 134094 None 0 Human Functional pAC50 = 5.0 5.0 - 1
Agonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assayAgonist activity at RXFP2 receptor (unknown origin) expressed in HEK293 cells assessed as stimulation of cAMP production incubated for 30 mins by HTRF assay
ChEMBL 361 4 3 2 4.9 O=C(Nc1ccc2cc[nH]c2c1)c1ccccc1NC(=O)C1CCCCC1 nan
12503 1127 None 0 Human Functional pEC50 = 6.4 6.4 - 1
Determined in a HTRF cAMP assay using HEK-RXFP2 cells.Determined in a HTRF cAMP assay using HEK-RXFP2 cells.
Guide to Pharmacology 787 5 1 5 6.6 FC(F)(F)OC1=CC(I)=C(OCC(=O)N2CCN3[C@@H](C2)C(=O)NC4=C(C=C(C=C4)C5=CC(=CC(=C5)C(F)(F)F)C(F)(F)F)C3=O)C=C1 36333465
167993647 1127 None 0 Human Functional pEC50 = 6.4 6.4 - 1
Determined in a HTRF cAMP assay using HEK-RXFP2 cells.Determined in a HTRF cAMP assay using HEK-RXFP2 cells.
Guide to Pharmacology 787 5 1 5 6.6 FC(F)(F)OC1=CC(I)=C(OCC(=O)N2CCN3[C@@H](C2)C(=O)NC4=C(C=C(C=C4)C5=CC(=CC(=C5)C(F)(F)F)C(F)(F)F)C3=O)C=C1 36333465
11914 2045 None 0 Human Functional pEC50 = 10 10.0 - 1
Receptor activationReceptor activation
Guide to Pharmacology None None None None 22654853
8346 202 None 0 Human Functional pEC50 = 6 6.0 -165 2
UnclassifiedUnclassified
Guide to Pharmacology None None None None 21878627
1989 3305 None 0 Human Functional pEC50 = 9.1 9.1 -17 3
UnclassifiedUnclassified
Guide to Pharmacology None None None None 18434306




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

Species

Assay
Type
Activity
Type
Activity
Relation
Activity
Value
p-value
(-log)
Fold
selectivity
Tested
GPCRs
Assay
Description
Source

Mol
weight
Rot
Bonds
H don

H acc

LogP

Smiles

DOI

11913 2731 None 0 Human Binding pKd = 8.7 8.7 - 1
Receptor binding affinityReceptor binding affinity
Guide to Pharmacology None None None None 24056075
1995 2044 None 0 Human Binding pKd = 10.4 10.4 16982 2
UnclassifiedUnclassified
Guide to Pharmacology None None None None 18434306
3875 1599 None 0 Human Binding pKd = 9 9.0 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 18529069
11914 2045 None 0 Human Binding pKi = 7.8 7.8 - 1
Receptor bindingReceptor binding
Guide to Pharmacology None None None None 22654853
3885 2046 None 0 Human Binding pKi = 5.1 5.1 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 16547350
8346 202 None 0 Human Binding pKi = 6 6.0 -9 2
UnclassifiedUnclassified
Guide to Pharmacology None None None None 21878627
8333 1279 None 0 Human Binding pKi = 6.7 6.7 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 17120268
8332 282 None 0 Human Binding pKi = 8.3 8.3 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 20570702
1989 3305 None 0 Human Binding pKi = 8.4 8.4 -40 3
UnclassifiedUnclassified
Guide to Pharmacology None None None None 15649866
1989 3305 None 0 Human Binding pKi = 8.4 8.4 -40 3
UnclassifiedUnclassified
Guide to Pharmacology None None None None 18434306
155817469 2047 None 0 Human Binding pKi = 8.5 8.5 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 20560146
4372 2047 None 0 Human Binding pKi = 8.5 8.5 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 20560146
8331 233 None 0 Human Binding pKi = 8.6 8.6 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 20570702
155817501 190 None 0 Human Binding pKi = 8.7 8.7 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 18434306
8330 190 None 0 Human Binding pKi = 8.7 8.7 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 18434306
134813893 214 None 0 Human Binding pKi = 9.1 9.1 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 18434306
8329 214 None 0 Human Binding pKi = 9.1 9.1 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 18434306
1995 2044 None 0 Human Binding pKi = 9.5 9.5 16982 2
UnclassifiedUnclassified
Guide to Pharmacology None None None None 15649866
1995 2044 None 0 Human Binding pKi = 9.5 9.5 16982 2
UnclassifiedUnclassified
Guide to Pharmacology None None None None 18434306
1990 3307 None 0 Human Binding pKi None 7 7.0 -81 4
UnclassifiedUnclassified
Guide to Pharmacology None None None None 16411781
1994 3302 None 0 Human Binding pKi None 7.8 7.8 -39 2
UnclassifiedUnclassified
Guide to Pharmacology None None None None 15649866
1992 3303 None 0 Human Binding pKi None 7.9 7.9 -15 2
UnclassifiedUnclassified
Guide to Pharmacology None None None None 15649866
1988 3306 None 0 Human Binding pKi None 8.8 8.8 - 1
UnclassifiedUnclassified
Guide to Pharmacology None None None None 16411781