SR142948A
SMILES | COc1cccc(c1c1cc(nn1c1ccc(cc1C(C)C)C(=O)N(CCCN(C)C)C)C(=O)NC1(C(=O)O)C2CC3CC1CC(C2)C3)OC |
InChIKey | LWULHXVBLMWCHO-UHFFFAOYSA-N |
Chemical properties
Hydrogen bond acceptors | 8 |
Hydrogen bond donors | 2 |
Rotatable bonds | 13 |
Molecular weight (Da) | 685.4 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | No |
Database connections
Structure pdb | 6Z4Q |
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
NTS2 | NTR2 | Rat | Neurotensin | A | pKi | 8.15 | 8.2 | 8.24 | ChEMBL |
NTS1 | NTR1 | Rat | Neurotensin | A | pKi | 8.7 | 8.77 | 8.85 | ChEMBL |
NTS2 | NTR2 | Human | Neurotensin | A | pKi | 7.13 | 7.13 | 7.13 | ChEMBL |
NTS1 | NTR1 | Human | Neurotensin | A | pKi | 8.96 | 8.98 | 9.0 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
NTS1 | NTR1 | Human | Neurotensin | A | pIC50 | 8.9 | 8.9 | 8.9 | Guide to Pharmacology |
NTS2 | NTR2 | Rat | Neurotensin | A | pEC50 | 7.66 | 7.7 | 7.75 | ChEMBL |
NTS1 | NTR1 | Human | Neurotensin | A | pIC50 | 7.3 | 8.64 | 9.62 | ChEMBL |
NTS1 | NTR1 | Human | Neurotensin | A | pEC50 | 5.0 | 5.0 | 5.0 | ChEMBL |