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Generation of ATP via oxidative phosphorylation is an essential metabolic function for Mycobaterium tuberculosis (Mtb) regardless of the growth environment. The type II NADH dehydrogenase (Ndh-2) is the conduit for electrons into the pathway, and is absent in the mammalian genome, making it a potential drug target. Herein, we report the identification of two types of small molecules as selective inhibitors for Ndh-2 via a multi-component high-throughput screen.
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