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- W2487518043 abstract "Mycobacterium tuberculosis l-alanine dehydrogenase (MTB l-AlaDH) is one of the important drug targets for treating latent/persistent tuberculosis. In this study we used crystal structure of the MTB l-AlaDH bound with cofactor NAD+ as a structural framework for virtual screening of our in-house database to identified new classes of l-AlaDH inhibitor. We identified azetidine-2,4-dicarboxamide derivative as one of the potent inhibitor with IC50 of 9.22 ± 0.72 μM. Further lead optimization by synthesis leads to compound 1-(isonicotinamido)-N2,N4-bis(benzo[d]thiazol-2-yl)azetidine-2,4-dicarboxamide (18) with l-AlaDH IC50 of 3.83 ± 0.12 μM, 2.0 log reduction in nutrient starved dormant MTB model and MIC of 11.81 μM in actively replicative MTB." @default.
- W2487518043 created "2016-08-23" @default.
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- W2487518043 date "2016-09-01" @default.
- W2487518043 modified "2023-10-02" @default.
- W2487518043 title "Design and development of new class of Mycobacterium tuberculosis l-alanine dehydrogenase inhibitors" @default.
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- W2487518043 doi "https://doi.org/10.1016/j.bmc.2016.07.051" @default.
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