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TargetEnoyl-[acyl-carrier-protein] reductase [NADH]
LigandBDBM15681
Substrate/CompetitorBDBM15648
Meas. Tech.Enoyl-CoA Reductase Inhibition Assay
IC50 1600±n/a nM
Citation He, XAlian, AStroud, ROrtiz de Montellano, PR Pyrrolidine carboxamides as a novel class of inhibitors of enoyl acyl carrier protein reductase from Mycobacterium tuberculosis. J Med Chem49:6308-23 (2006) [PubMed]  Article
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Enoyl-[acyl-carrier-protein] reductase [NADH]
Name:Enoyl-[acyl-carrier-protein] reductase [NADH]
Synonyms:Enoyl-ACP Reductase (InhA) | Enoyl-[acyl-carrier-protein] reductase | Enoyl-[acyl-carrier-protein] reductase [NADH] | INHA_MYCTU | NADH-dependent enoyl-ACP reductase | inhA
Type:Enzyme
Mol. Mass.:28526.00
Organism:Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv)
Description:P9WGR1
Residue:269
Sequence:
MTGLLDGKRILVSGIITDSSIAFHIARVAQEQGAQLVLTGFDRLRLIQRITDRLPAKAPL
LELDVQNEEHLASLAGRVTEAIGAGNKLDGVVHSIGFMPQTGMGINPFFDAPYADVSKGI
HISAYSYASMAKALLPIMNPGGSIVGMDFDPSRAMPAYNWMTVAKSALESVNRFVAREAG
KYGVRSNLVAAGPIRTLAMSAIVGGALGEEAGAQIQLLEEGWDQRAPIGWNMKDATPVAK
TVCALLSDWLPATTGDIIYADGGAHTQLL
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  Blast E-value cutoff:
BDBM15681
BDBM15648
NameBDBM15681
Synonyms:N-(5-chloro-2-methoxyphenyl)-1-cyclohexyl-5-oxopyrrolidine-3-carboxamide | Pyrrolidine Carboxamide Compound d15
TypeSmall organic molecule
Emp. Form.C18H23ClN2O3
Mol. Mass.350.84
SMILESCOc1ccc(Cl)cc1NC(=O)C1CN(C2CCCCC2)C(=O)C1
Structure
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