CHEMBL4093140


SMILES CCCC[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(C)=O)C(=O)N[C@@H](CCC(=O)O)CN[C@@H](Cc1cnc[nH]1)C(=O)N[C@H](Cc1ccccc1)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N1CCC[C@H]1C(=O)N[C@H](C(N)=O)C(C)C
InChIKey RDCIPOBDQMOUKD-LXJGJVCSSA-N

Chemical properties

Hydrogen bond acceptors 21
Hydrogen bond donors 23
Rotatable bonds 51
Molecular weight (Da) 1631.9

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
MC1 MSHR Human Melanocortin A pIC50 11.0 11.0 11.0 ChEMBL
MC1 MSHR Human Melanocortin A pEC50 11.0 11.0 11.0 ChEMBL
MC5 MC5R Human Melanocortin A pIC50 8.66 8.66 8.66 ChEMBL
MC5 MC5R Human Melanocortin A pEC50 9.0 9.0 9.0 ChEMBL
MC3 MC3R Human Melanocortin A pEC50 9.1 9.1 9.1 ChEMBL
MC3 MC3R Human Melanocortin A pIC50 8.48 8.48 8.48 ChEMBL
MC4 MC4R Human Melanocortin A pEC50 9.7 9.7 9.7 ChEMBL
MC4 MC4R Human Melanocortin A pIC50 9.4 9.4 9.4 ChEMBL