CHEMBL267900


SMILES CC(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@H]1CSSC[C@@H](C(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)[C@H](CCC(=O)O)NC1=O
InChIKey UNXFCHHFXJFRRB-ABRXVHCYSA-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
MC4 MC4R Rat Melanocortin A pKi 9.41 9.41 9.41 ChEMBL
MC1 MSHR Human Melanocortin A pKi 7.78 7.78 7.78 ChEMBL
MC3 MC3R Human Melanocortin A pKi 7.25 7.25 7.25 ChEMBL
MC4 MC4R Human Melanocortin A pKi 9.26 9.26 9.26 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC3 MC3R Human Melanocortin A pEC50 8.79 8.79 8.79 ChEMBL
MC4 MC4R Human Melanocortin A pEC50 9.55 9.55 9.55 ChEMBL