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A Pantetheinase-Resistant Pantothenamide with Potent, On Target, and Selective Antiplasmodial Activity

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Authors

Macuamule, Cristiano
Tjhin, Erick
Jana, Collins E.
Barnard, Leanne
Koekemoer, Lizbe
de Villiers, Marianne
Saliba, Kevin
Strauss, Erick

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American Society for Microbiology

Abstract

Pantothenamides inhibit blood-stage Plasmodium falciparum with potencies (50% inhibitory concentration [IC50], 20 nM) similar to that of chloroquine. They target processes dependent on pantothenate, a precursor of the essential metabolic cofactor coenzyme A. However, their antiplasmodial activity is reduced due to degradation by serum pantetheinase. Minor modification of the pantothenamide structure led to the identification of -methyl-N-phenethyl-pantothenamide, a pantothenamide resistant to degradation, with excellent antiplasmodial activity (IC50, 52 6 nM), target specificity, and low toxicity. O

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Source

Antimicrobial Agents and Chemotherapy

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Open Access

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