Molecule Details
InChIKeyZAVYYYQORHVVFN-BDGVIKSFSA-N
Compound NameRediocide A
Canonical SMILESCC(C)CC(=O)O[C@H]1/C=C/C=C/C(=O)O[C@H]2[C@@H](C)C[C@@H]3[C@]2(O)[C@H](O)[C@@]2(CO)O[C@H]2[C@H]2[C@H]4OC5(c6ccccc6)O[C@@H]([C@@H](C)[C@@]23O5)[C@@]4(O)[C@](C)(O)C[C@H]2CC[C@H]1[C@H]2C
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)4
Pfam Stratification Cross-Family
Avg pChEMBL7.38
SourceChEMBL
2D Structure
2D structure
Activity Profile
Target Activities (4)
Target Gene Organism Category Pfam pChEMBL Type Source
P47871 GCGR Homo sapiens Human PF00002 PF02793 8.4 IC50 ChEMBL
P35348 ADRA1A Homo sapiens Human PF00001 7.9 IC50 ChEMBL
P35368 ADRA1B Homo sapiens Human PF00001 6.7 IC50 ChEMBL
P51684 CCR6 Homo sapiens Human PF00001 6.6 IC50 ChEMBL