Molecule Details
InChIKeyDEQANNDTNATYII-JDBXKHNRSA-N
Compound NameH-D-Phe-Cys(1)-Phe-D-Trp-Lys-Thr-Cys(1)-D-aThr-ol
Canonical SMILESC[C@@H](O)[C@H](CO)NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](N)Cc2ccccc2)C(=O)N[C@@H](Cc2ccccc2)C(=O)N[C@H](Cc2c[nH]c3ccccc23)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N1
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)5
Pfam Stratification Homologous
Avg pChEMBL8.07
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (5)
Target Gene Organism Category Pfam pChEMBL Type Source
P30874 SSTR2 Homo sapiens Human PF00001 9.2 Ki ChEMBL;BindingDB
P31391 SSTR4 Homo sapiens Human PF00001 8.5 IC50 ChEMBL
P35346 SSTR5 Homo sapiens Human PF00001 8.2 Ki ChEMBL;BindingDB
P32745 SSTR3 Homo sapiens Human PF00001 7.9 Ki ChEMBL;BindingDB
P30872 SSTR1 Homo sapiens Human PF00001 6.6 Ki ChEMBL;BindingDB