Molecule Details
InChIKeyVNKGTZHAAMHYKK-HBLZZUKZSA-N
Compound Namecyclo[Arg-Cys(1)-Gly-His-D-Phe-N(Me)Arg-Trp-D-Asp-Arg-Cys(1)-His-D-Phe-N(Me)Arg-N(Me)Trp]
Canonical SMILESCN1C(=O)[C@@H](Cc2ccccc2)NC(=O)[C@H](Cc2c[nH]cn2)NC(=O)CNC(=O)[C@@H]2CSSC[C@H](NC(=O)[C@H](CCCNC(=N)N)NC(=O)[C@@H](CC(=O)O)NC(=O)[C@H](Cc3c[nH]c4ccccc34)NC(=O)[C@@H]1CCCNC(=N)N)C(=O)N[C@@H](Cc1c[nH]cn1)C(=O)N[C@H](Cc1ccccc1)C(=O)N(C)[C@@H](CCCNC(=N)N)C(=O)N(C)[C@@H](Cc1c[nH]c3ccccc13)C(=O)N[C@@H](CCCNC(=N)N)C(=O)N2
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL7.31
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
Q01726 MC1R Homo sapiens Human PF00001 8.3 Ki ChEMBL;BindingDB
P41968 MC3R Homo sapiens Human PF00001 6.8 Ki ChEMBL;BindingDB
P32245 MC4R Homo sapiens Human PF00001 6.8 Ki ChEMBL;BindingDB