Molecule Details
InChIKeyAJJBWPRLFOMJCY-GUJGKPLJSA-N
Compound Name[(1R)-1-[(2S,5S,8S,14S,16S)-16-[[(2S)-2-[[(2S)-1-acetylpyrrolidine-2-carbonyl]amino]-4-methylpentanoyl]amino]-8-carbamoyl-2-(hydroxymethyl)-3,6,13,17-tetraoxo-14-(8-phenyloctyl)-1,4,7,12-tetrazacycloheptadec-5-yl]ethyl] dihydrogen phosphate
Canonical SMILESCC(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@H]1C[C@H](CCCCCCCCc2ccccc2)C(=O)NCCC[C@@H](C(N)=O)NC(=O)[C@H]([C@@H](C)OP(=O)(O)O)NC(=O)[C@H](CO)NC1=O
Clinical Status Data-mined Candidate
Targets (Human+Pathogen)3
Pfam Stratification Homologous
Avg pChEMBL6.82
SourceChEMBL;BindingDB
2D Structure
2D structure
Activity Profile
Target Activities (3)
Target Gene Organism Category Pfam pChEMBL Type Source
P53350 PLK1 Homo sapiens Human PF00069 PF00659 8.3 IC50 ChEMBL;BindingDB
Q9NYY3 PLK2 Homo sapiens Human PF00069 PF00659 6.2 IC50 ChEMBL;BindingDB
Q9H4B4 PLK3 Homo sapiens Human PF00069 PF00659 6.0 IC50 ChEMBL;BindingDB