CHEMBL497746
SMILES | CC(C)[C@H](NC(=O)CCN(C)C)c1cccc(F)c1N1CCN(C(=O)[C@H](C)Cc2ccc(Cl)cc2)CC1 |
InChIKey | ROSDSGGMKIYLIM-ZBLYBZFDSA-N |
Chemical properties
Hydrogen bond acceptors | 4 |
Hydrogen bond donors | 1 |
Rotatable bonds | 10 |
Molecular weight (Da) | 530.3 |
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 |
MC3 | MC3R | Rat | Melanocortin | A | pKi | 6.47 | 6.47 | 6.47 | ChEMBL |
MC4 | MC4R | Rat | Melanocortin | A | pKi | 8.26 | 8.26 | 8.26 | ChEMBL |
MC3 | MC3R | Mouse | Melanocortin | A | pKi | 6.72 | 6.72 | 6.72 | ChEMBL |
MC4 | MC4R | Mouse | Melanocortin | A | pKi | 8.46 | 8.46 | 8.46 | ChEMBL |
ghrelin | GHSR | Human | Ghrelin | A | pKi | 6.62 | 6.62 | 6.62 | ChEMBL |
MC5 | MC5R | Human | Melanocortin | A | pKi | 5.96 | 5.96 | 5.96 | ChEMBL |
MC3 | MC3R | Human | Melanocortin | A | pKi | 6.31 | 6.31 | 6.31 | ChEMBL |
MC4 | MC4R | Human | Melanocortin | A | pKi | 8.12 | 8.12 | 8.12 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
MC4 | MC4R | Human | Melanocortin | A | pIC50 | 6.57 | 6.57 | 6.57 | ChEMBL |