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• W2415691649 abstract "ABSTRACT Endochin-like quinolones (ELQs) are potent and specific inhibitors of cytochrome bc 1 from Plasmodium falciparum and Toxoplasma gondii and show promise for novel antiparasitic drug development. To determine whether the mitochondrial electron transport chain of Leishmania parasites could be targeted similarly for drug development, we investigated the activity of 134 structurally diverse ELQs. A cohort of ELQs was selectively toxic to amastigotes of Leishmania mexicana and L. donovani , with 50% inhibitory concentrations (IC 50 s) in the low micromolar range, but the structurally similar hydroxynaphthoquinone buparvaquone was by far the most potent inhibitor of electron transport, ATP production, and intracellular amastigote growth. Cytochrome bc 1 is thus a promising target for novel antileishmanial drugs, and further improvements on the buparvaquone scaffold are warranted for development of enhanced therapeutics." @default.
• W2415691649 created "2016-06-24" @default.
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• W2415691649 date "2016-08-01" @default.
• W2415691649 modified "2023-10-04" @default.
• W2415691649 title "Targeting the Cytochrome <i>bc</i> ₁ Complex of Leishmania Parasites for Discovery of Novel Drugs" @default.
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• W2415691649 doi "https://doi.org/10.1128/aac.00850-16" @default.
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