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TargetEnoyl-acyl-carrier protein reductase
LigandBDBM50182378
Substrate/Competitorn/a
Meas. Tech.ChEMBL_347035 (CHEMBL866856)
IC50 26000±n/a nM
Citation Freundlich, JSYu, MLucumi, EKuo, MTsai, HCValderramos, JCKaragyozov, LJacobs, WRSchiehser, GAFidock, DAJacobus, DPSacchettini, JC Synthesis and biological activity of diaryl ether inhibitors of malarial enoyl acyl carrier protein reductase. Part 2: 2'-substituted triclosan derivatives. Bioorg Med Chem Lett16:2163-9 (2006) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Enoyl-acyl-carrier protein reductase
Name:Enoyl-acyl-carrier protein reductase
Synonyms:n/a
Type:PROTEIN
Mol. Mass.:49770.86
Organism:Plasmodium falciparum
Description:ChEMBL_795989
Residue:432
Sequence:
MNKISQRLLFLFLHFYTTVCFIQNNTQKTFHNVLQNEQIRGKEKAFYRKEKRENIFIGNK
MKHVHNMNNTHNNNHYMEKEEQDASNINKIKEENKNEDICFIAGIGDTNGYGWGIAKELS
KRNVKIIFGIWPPVYNIFMKNYKNGKFDNDMIIDKDKKMNILDMLPFDASFDTANDIDEE
TKNNKRYNMLQNYPIEDVANLIHQKYGKINMLVHSLANAKEVQKDLLNTSRKGYLDALSK
SSYSLISLCKYFVNIMKPQSSIISLTYHASQKVVPGYGGGMSSAKAALESDTRVLAYHLG
RNYNIRINTISAGPLKSRAATAINKLNNTYENNTNQNKNRNSHDVHNIMNNSGEKEEKKN
SASQNYTFIDYAIEYSEKYAPLRQKLLSTDIGSVASFLLSRESRAITGQTIYVDNGLNIM
FLPDDIYRNENE
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  Blast E-value cutoff:
BDBM50182378
n/a
NameBDBM50182378
Synonyms:5-chloro-2-(4-chloro-2-((naphthalen-2-ylamino)methyl)phenoxy)phenol | CHEMBL206263
TypeSmall organic molecule
Emp. Form.C23H17Cl2NO2
Mol. Mass.410.293
SMILESOc1cc(Cl)ccc1Oc1ccc(Cl)cc1CNc1ccc2ccccc2c1
Structure
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