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- W3006342248 abstract "In ϒ-proteobacteria and Actinomycetales, cysteine biosynthetic enzymes are indispensable during persistence and become dispensable during growth or acute infection. The biosynthetic machinery required to convert inorganic sulfur into cysteine is absent in mammals; therefore, it is a suitable drug target. We searched for inhibitors of Salmonella serine acetyltransferase (SAT), the enzyme that catalyzes the rate-limiting step of l-cysteine biosynthesis. The virtual screening of three ChemDiv focused libraries containing 91 243 compounds was performed to identify potential SAT inhibitors. Scaffold similarity and the analysis of the overall physicochemical properties allowed the selection of 73 compounds that were purchased and evaluated on the recombinant enzyme. Six compounds displaying an IC50 <100 μM were identified via an indirect assay using Ellman’s reagent and then tested on a Gram-negative model organism, with one of them being able to interfere with bacterial growth via SAT inhibition." @default.
- W3006342248 created "2020-02-24" @default.
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- W3006342248 date "2020-02-13" @default.
- W3006342248 modified "2023-09-27" @default.
- W3006342248 title "Inhibition of Nonessential Bacterial Targets: Discovery of a Novel Serine <i>O</i>-Acetyltransferase Inhibitor" @default.
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- W3006342248 doi "https://doi.org/10.1021/acsmedchemlett.9b00627" @default.
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