Molecule Details
InChIKeyMUUFKPHKUZXIMS-FTJBHMTQSA-N
Compound NamePHD Inhibitor, 12{2,5,2}
Canonical SMILESCC(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@H](Cc1ccccc1)C(=O)NCc1ccc2c(c1)c(O)c(C(=O)NCC(=O)O)c(=O)n2C
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL7.84
SourceBindingDB
2D Structure
2D structure
Activity Profile
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
Q96KS0 EGLN2 Homo sapiens Human PF13640 8.1 IC50 BindingDB
Q9H6Z9 EGLN3 Homo sapiens Human PF13640 8.1 IC50 BindingDB
Q9GZT9 EGLN1 Homo sapiens Human PF13640 PF01753 7.3 IC50 BindingDB