CHEMBL504349
SMILES | CCC[C@H]1C(=O)N([C@@H](Cc2ccc3ccccc3c2)C(=O)NC)CCN1C(=O)[C@@H](Cc1ccc(F)cc1)NC(=O)[C@H](C)NC |
InChIKey | AHYGIWNTGDKMRR-SUAIOLNFSA-N |
Chemical properties
Hydrogen bond acceptors | 5 |
Hydrogen bond donors | 3 |
Rotatable bonds | 12 |
Molecular weight (Da) | 603.3 |
Drug properties
Molecular type | Small molecule |
Physiological/Surrogate | Surrogate |
Approved drug | No |
Database connections
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
MC1 | MSHR | Human | Melanocortin | A | pKi | 7.0 | 7.0 | 7.0 | ChEMBL |
MC3 | MC3R | Human | Melanocortin | A | pKi | 6.68 | 6.68 | 6.68 | ChEMBL |
MC4 | MC4R | Human | Melanocortin | A | pKi | 8.22 | 8.22 | 8.22 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
MC1 | MSHR | Human | Melanocortin | A | pEC50 | 7.3 | 7.3 | 7.3 | ChEMBL |
MC3 | MC3R | Human | Melanocortin | A | pEC50 | 7.29 | 7.29 | 7.29 | ChEMBL |
MC4 | MC4R | Human | Melanocortin | A | pEC50 | 8.77 | 8.77 | 8.77 | ChEMBL |