Molecule Details
InChIKeyOSGCBUDLRBUEGW-JZCUZNMGSA-N
Compound NameGwtlnsagyllgpppalala-conh2
Canonical SMILESCC(C)C[C@H](NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CN)[C@@H](C)O)C(=O)N[C@@H](C)C(N)=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL7.99
SourceBindingDB;ChEMBL
2D Structure
2D structure
Activity Profile
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
O43603 GALR2 Homo sapiens Human PF00001 8.8 Ki ChEMBL;BindingDB
P47211 GALR1 Homo sapiens Human PF00001 8.6 Ki ChEMBL;BindingDB
O60755 GALR3 Homo sapiens Human PF00001 6.5 Ki BindingDB