Molecule Details
InChIKeyJHZKLNWCMALUKX-QWFCPSLTSA-N
Compound NameH-Phe-(1).cyclo[N(Bn)Gly-Phe-D-Trp-Lys(1)-Thr-Phe]
Canonical SMILESC[C@@H](O)[C@@H]1NC(=O)[C@H](CCCCNC(=O)[C@@H](N)Cc2ccccc2)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccccc2)NC(=O)CN(Cc2ccccc2)C(=O)[C@H](Cc2ccccc2)NC1=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL7.33
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P30874 SSTR2 Homo sapiens Human PF00001 8.3 Kd ChEMBL;BindingDB
P35346 SSTR5 Homo sapiens Human PF00001 7.1 Kd ChEMBL;BindingDB
P32745 SSTR3 Homo sapiens Human PF00001 6.6 Kd ChEMBL;BindingDB