Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10593997 | Bioorganic & Medicinal Chemistry Letters | 2011 | 5 Pages |
Abstract
Antimalarial 4-pyridones are a novel class of inhibitors of the plasmodial mitochondrial electron transport chain targeting Cytochrome bc1 (complex III). In general, the most potent 4-pyridones are lipophilic molecules with poor solubility in aqueous media and low oral bioavailability in pre-clinical species from the solid dosage form. The strategy of introducing polar hydroxymethyl groups has enabled us to maintain the high levels of antimalarial potency observed for other more lipophilic analogues whilst improving the solubility and the oral bioavailability in pre-clinical species.
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Authors
José M. Bueno, Pilar Manzano, MarÃa C. GarcÃa, Jesús Chicharro, Margarita Puente, Milagros Lorenzo, Adolfo GarcÃa, Santiago Ferrer, Rubén M. Gómez, MarÃa T. Fraile, José L. Lavandera, José M. Fiandor, Jaume Vidal, Esperanza Herreros,