CHEMBL1161323


SMILES CCCC[C@@H](NC(C)=O)C(=O)N[C@@H]1CC(=O)NCCCC[C@@H](C(N)=O)NC(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@@H](CCCNC(=N)N)NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)[C@H]2C[C@@]3(C)CCCC[C@@]3(C)N2C1=O
InChIKey KHGZKFBKKYRZCD-FFQWDCJVSA-N

Chemical properties

Hydrogen bond acceptors None
Hydrogen bond donors None
Rotatable bonds None
Molecular weight (Da)

Drug properties

Molecular type Protein
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC3 MC3R Human Melanocortin A pKd 8.2 8.2 8.2 ChEMBL
MC4 MC4R Human Melanocortin A pKd 8.9 8.9 8.9 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC5 MC5R Human Melanocortin A pIC50 9.96 9.96 9.96 ChEMBL
MC5 MC5R Human Melanocortin A pEC50 9.7 9.7 9.7 ChEMBL
MC3 MC3R Human Melanocortin A pIC50 8.6 8.6 8.6 ChEMBL
MC4 MC4R Human Melanocortin A pIC50 9.8 9.8 9.8 ChEMBL