CHEMBL2070250


SMILES CCCC[C@H](NC(=O)[C@@H](N)CNC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CO)NC(=O)CNC(=O)COCCOCCNC(=O)CCCCCCCCCCCCCCCc1nnn[nH]1)C(=O)N[C@H]1CCC(=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](Cc2ccccc2)NC(=O)[C@@H]2C[C@@H](O)CN2C1=O
InChIKey LKIXKBAXFLOUEW-NVTOBUBFSA-N

Chemical properties

Hydrogen bond acceptors 26
Hydrogen bond donors 24
Rotatable bonds 56
Molecular weight (Da) 1918.1

Drug properties

Molecular type Small molecule
Physiological/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 6.16 6.16 6.16 ChEMBL
MC5 MC5R Human Melanocortin A pKi 7.4 7.4 7.4 ChEMBL
MC3 MC3R Human Melanocortin A pKi 6.92 6.92 6.92 ChEMBL
MC4 MC4R Human Melanocortin A pKi 9.77 9.77 9.77 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC4 MC4R Human Melanocortin A pEC50 7.07 7.07 7.07 ChEMBL