Molecule Details
InChIKeyLWOMHJBSXPGKKS-REAJPLCASA-N
Compound NameH-Tyr-D-Ala-Gly-Phe-Pro-Leu-Trp-NH-3,5-Bzl(CF3)2
Canonical SMILESCC(C)C[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](Cc1ccccc1)NC(=O)CNC(=O)[C@@H](C)NC(=O)[C@@H](N)Cc1ccc(O)cc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)NCc1cc(C(F)(F)F)cc(C(F)(F)F)c1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL8.07
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P25103 TACR1 Homo sapiens Human PF00001 9.2 Ki ChEMBL;BindingDB
P35372 OPRM1 Homo sapiens Human PF00001 7.9 IC50 ChEMBL;BindingDB
P41143 OPRD1 Homo sapiens Human PF00001 7.1 Ki ChEMBL;BindingDB