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• W2004707638 abstract "Benzothiazinones (BTZs) form a new class of potent antimycobacterial agents. Although the target of BTZs has been identified as decaprenylphosphoryl-β-d-ribose 2′-epimerase (DprE1), their detailed mechanism of action remains obscure. Here we demonstrate that BTZs are activated in the bacterium by reduction of an essential nitro group to a nitroso derivative, which then specifically reacts with a cysteine residue in the active site of DprE1." @default.
• W2004707638 created "2016-06-24" @default.
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• W2004707638 date "2010-09-09" @default.
• W2004707638 modified "2023-10-01" @default.
• W2004707638 title "Benzothiazinones: Prodrugs That Covalently Modify the Decaprenylphosphoryl-β-<scp>d</scp>-ribose 2′-epimerase DprE1 of <i>Mycobacterium tuberculosis</i>" @default.
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• W2004707638 doi "https://doi.org/10.1021/ja106357w" @default.
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