Molecule Details
InChIKeyRSKAMAUHJHZMQX-ZFVVFXQTSA-N
Compound Namecyclo[Arg-Cys(1)-Thr-Tyr-Ser-Glu-Pro-Pro-Ile-Cys(1)-Phe-Pro-Asp-Gly]
Canonical SMILESCC[C@H](C)[C@@H]1NC(=O)[C@@H]2CCCN2C(=O)[C@@H]2CCCN2C(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H]([C@@H](C)O)NC(=O)[C@@H]2CSSC[C@H](NC1=O)C(=O)N[C@@H](Cc1ccccc1)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(=O)O)C(=O)NCC(=O)N[C@@H](CCCNC(=N)N)C(=O)N2
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)6
Pfam Stratification Homologous
Avg pChEMBL8.76
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (6)
Target Gene Organism Category Pfam pChEMBL Type Source
P17538 CTRB1 Homo sapiens Human PF00089 9.1 Ki ChEMBL
P40313 CTRL Homo sapiens Human PF00089 9.1 Ki ChEMBL
Q6GPI1 CTRB2 Homo sapiens Human PF00089 9.1 Ki ChEMBL;BindingDB
Q99895 CTRC Homo sapiens Human PF00089 9.1 Ki ChEMBL
P23946 CMA1 Homo sapiens Human PF00089 8.2 Ki ChEMBL;BindingDB
P08311 CTSG Homo sapiens Human PF00089 8.1 Ki ChEMBL;BindingDB