CHEMBL3600912


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)N(C)C(=O)[C@@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](Cc2cnc[nH]2)N(C)C1=O
InChIKey KRKYTJXTDCSSJS-PGMQRQGHSA-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
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC1 MSHR Human Melanocortin A pIC50 7.83 8.12 8.4 ChEMBL
MC1 MSHR Human Melanocortin A pEC50 7.66 8.04 8.43 ChEMBL
MC3 MC3R Human Melanocortin A pIC50 7.82 7.82 7.82 ChEMBL
MC4 MC4R Human Melanocortin A pIC50 7.01 7.01 7.01 ChEMBL
MC5 MC5R Human Melanocortin A pIC50 8.2 8.2 8.2 ChEMBL