CHEMBL263878
SMILES | CCCC[C@H](NC(=O)[C@@H](NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(C)C)C(=O)N[C@@H]1CSSC[C@H](C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](Cc2ccccc2)C(=O)NCC(N)=O)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)CNC1=O |
InChIKey | UKCAJRRGLXHDRO-JAKOWJIMSA-N |
Chemical properties
Hydrogen bond acceptors | None |
Hydrogen bond donors | None |
Rotatable bonds | None |
Molecular weight (Da) |
Drug properties
Molecular type | Protein |
Endogenous/Surrogate | Surrogate |
Approved drug | No |
Database connections
Bioactivities
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
MC5 | MC5R | Human | Melanocortin | A | pKi | 6.66 | 6.66 | 6.66 | ChEMBL |
MC3 | MC3R | Human | Melanocortin | A | pKi | 6.62 | 6.62 | 6.62 | ChEMBL |
MC4 | MC4R | Human | Melanocortin | A | pKi | 5.0 | 5.0 | 5.0 | ChEMBL |
Receptor | Activity | Source | |||||||
---|---|---|---|---|---|---|---|---|---|
GTP | Uniprot | Species | Family | Class | Type | Min | Avg | Max | Database |
MC5 | MC5R | Human | Melanocortin | A | pEC50 | 6.57 | 6.57 | 6.57 | ChEMBL |
MC3 | MC3R | Human | Melanocortin | A | pEC50 | 7.41 | 7.41 | 7.41 | ChEMBL |
MC4 | MC4R | Human | Melanocortin | A | pEC50 | 7.08 | 7.08 | 7.08 | ChEMBL |