CHEMBL5090285


SMILES CC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](CCCNC(=N)N)N(C)C(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@@H]2CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N2
InChIKey DPPBMHXXQRAKPB-RVMKJBODSA-N

Chemical properties

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

Drug properties

Molecular type Na
Endogenous/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC1 MSHR Human Melanocortin A pKi 8.55 8.55 8.55 ChEMBL
MC3 MC3R Human Melanocortin A pKi 6.41 6.41 6.41 ChEMBL
MC4 MC4R Human Melanocortin A pKi 7.97 7.97 7.97 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC1 MSHR Human Melanocortin A pEC50 9.1 9.1 9.1 ChEMBL
MC5 MC5R Human Melanocortin A pIC50 6.17 6.17 6.17 ChEMBL
MC3 MC3R Human Melanocortin A pEC50 8.18 8.18 8.18 ChEMBL
MC4 MC4R Human Melanocortin A pEC50 8.46 8.99 9.52 ChEMBL