Abstract
We have identified two subseries of 2,6-disubstituted quinolines, consisting of 6-amide and 6-urea derivatives, which are characterized by fungicidal activity against Candida albicans with minimal fungicidal concentration (MFC) values < 15 μ M. The 6-amide derivatives displayed the highest fungicidal activity against C. albicans, in particular compounds 1, 5 and 6 characterized by MFC values of 6.25-12.5 μ M. Compounds 1 and 5 of this series displayed fungicidal activity against the emerging pathogen Candida glabrata (MFC < 50 μ M). The 6-amide derivatives 1, 2, 5, and 6 and the 6-urea derivatives 10, 12, 13 and 15 could also eradicate C. albicans biofilms. We found that the 6-urea derivatives 10, 13, and 15 induced accumulation of endogenous reactive oxygen species in Candida albicans biofilms. © 2012 by the authors; licensee MDPI, Basel, Switzerland.
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Delattin, N., Bardiot, D., Marchand, A., Chaltin, P., De Brucker, K., Cammue, B. P. A., & Thevissen, K. (2012). Identification of fungicidal 2,6-disubstituted quinolines with activity against candida biofilms. Molecules, 17(10), 12243–12251. https://doi.org/10.3390/molecules171012243
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