Molecule Details
InChIKeyAZSNMRSAGSSBNP-XPNPUAGNSA-N
Canonical SMILESCC[C@H](C)[C@H]1O[C@]2(CC[C@@H]1C)C[C@@H]1C[C@@H](C/C=C(\C)[C@@H](O[C@H]3C[C@H](OC)[C@@H](O[C@H]4C[C@H](OC)[C@@H](O)[C@H](C)O4)[C@H](C)O3)[C@@H](C)/C=C/C=C3\CO[C@@H]4[C@H](O)C(C)=C[C@@H](C(=O)O1)[C@]34O)O2
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)2
Pfam Stratification Homologous
Avg pChEMBL6.65
SourceBindingDB
2D Structure
2D structure
Activity Profile
Target Activities (2)
Target Gene Organism Category Pfam pChEMBL Type Source
P08183 ABCB1 Homo sapiens Human PF00664 PF00005 7.0 IC50 BindingDB
P33527 ABCC1 Homo sapiens Human PF00664 PF00005 PF24357 6.3 Ki BindingDB