Reaction Details Report a problem with these data
Target
Enoyl-ACP reductase
Ligand
BDBM50240896
Substrate
n/a
Meas. Tech.
ChEMBL_761713 (CHEMBL1816807)
IC50
35200±n/a nM
Citation
 Bankeu, JJ; Khayala, R; Lenta, BN; Noungoué, DT; Ngouela, SA; Mustafa, SA; Asaad, K; Choudhary, MI; Prigge, ST; Hasanov, R; Nkengfack, AE; Tsamo, E; Ali, MS Isoflavone dimers and other bioactive constituents from the figs of Ficus mucuso. J Nat Prod 74:1370-8 (2011) [PubMed]  Article 
Target
Name:
Enoyl-ACP reductase
Synonyms:
Enoyl-ACP Reductase (PfENR) | Enoyl-ACP reductase
Type:
Enzyme
Mol. Mass.:
49844.02
Organism:
Plasmodium falciparum
Description:
Q9BJJ9
Residue:
432
Sequence:
MNKISQRLLFLFLHFYTTVCFIQNNTQKTFHNVLQNEQIRGKEKAFYRKEKRENIFIGNKMKHVHNMNNTHNNNHYMEKEEQDASNINKIKEENKNEDICFIAGIGDTNGYGWGIAKELSKRNVKIIFGIWPPVYNIFMKNYKNGKFDNDMIIDKDKKMNILDMLPFDASFDTANDIDEETKNNKRYNMLQNYTIEDVANLIHQKYGKINMLVHSLANAKEVQKDLLNTSRKGYLDALSKSSYSLISLCKYFVNIMKPQSSIISLTYHASQKVVPGYGGGMSSAKAALESDTRVLAYHLGRNYNIRINTISAGPLKSRAATAINKLNNTYENNTNQNKNRNRHDVHNIMNNSGEKEEKKISASQNYTFIDYAIEYSEKYAPLRQKLLSTDIGSVASFLLSRESRAITGQTIYVDNGLNIMFLPDDIYRNENE
  
Inhibitor
Name:
BDBM50240896
Synonyms:
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-methoxy-4H-chromen-4-one | 3',4',5,7-tetrahydroxy-3-methoxyflavone | CHEMBL163316 | cid_5280681
Type:
Small organic molecule
Emp. Form.:
C16H12O7
Mol. Mass.:
316.2623
SMILES:
COc1c(oc2cc(O)cc(O)c2c1=O)-c1ccc(O)c(O)c1
Structure:
Search PDB for entries with ligand similarity: