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dataset used in PMID:24144044 and elsewhere
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创建时间：
2013-11-21
相关数据集
In vitro potency and physicochemical properties for bicyclic 4-nitroimidazole analogs.
MIC99 = Minimum Inhibitory Concentration required to reduce the bacterial growth by 99%, MIC against both H37Rv (wild type) and F420 deficient (FbiC) mutants were tested. PAMPA = Parallel Artificial M
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Design and structural analysis of aromatic inhibitors of type II dehydroquinase dehydratase from Mycobacterium tuberculosis - compound 35c [3,4-dihydroxy-5-(3-nitrophenoxy)benzoic acid]
Design and structural analysis of aromatic inhibitors of type II dehydroquinase dehydratase from Mycobacterium tuberculosis - compound 35c [3,4-dihydroxy-5-(3-nitrophenoxy)benzoic acid]
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Mycobacterium tuberulosis H37Rv strains: Control vs. Osthole.
Transcriptional profiling of Mycobacterium tuberculosis H37Rv strains comparing control DMSO treated strains with Osthole treated strains. Goal was to determine the effects of Osthole against Mycobact
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Supplementary material. Discovery of novel and potent InhA inhibitors by an in silico screening and pharmacokinetic prediction
Figure S1. RMSD plots of template molecule (a), AG-690/13705356 (b), AG-690/14006355 (c), AP-845/40876827 (d), AE-848/34504008 (e), AP-845/40876825 (f), AP-845/40876828 (g), AP-845/4087683
NIAID Data Ecosystem80
Crystal structure of InhA(S94A) mutant in complex with pyridomycin
Crystal structure of InhA(S94A) mutant in complex with pyridomycin Descriptor: Enoyl-[acyl-carrier-protein] reductase [NADH], Pyridomycin Authors: Pojer, F, Hartkoorn, R.C, Cole, S.T. Deposit date: 20
Protein Data Bank Japan2023-12-20 更新70
