Synthesis and anti-Candida activity of novel 2-hydrazino-1,3-thiazole derivatives

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Abstract

Eighteen new hydrazino-1,3-thiazole derivatives were evaluated against 8 strains of multi-resistant Candida spp. Introduction of an indolyl moiety linked to the hydrazone function enhanced the in vitro anti-Candida activity, with an activity spectrum towards Candida albicans strains. Introduction of a (S)-2-aminoethyl chain on the thiazole nucleus largely enhanced the in vitro antifungal activity, with a selectivity oriented towards non-C. albicans species. © 2013 Elsevier Ltd. All rights reserved.

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Maillard, L. T., Bertout, S., Quinonéro, O., Akalin, G., Turan-Zitouni, G., Fulcrand, P., … Masurier, N. (2013). Synthesis and anti-Candida activity of novel 2-hydrazino-1,3-thiazole derivatives. Bioorganic and Medicinal Chemistry Letters, 23(6), 1803–1807. https://doi.org/10.1016/j.bmcl.2013.01.039

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