ArticleCurrent issues in molecular biology2026
Antifungal Activity of Four Medium-Chain Fatty Acids and γ-Undecalactone Against
Article in Current issues in molecular biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
In this paper, the antifungal activity of medium-chain fatty acids with 8 to 11 carbon atoms in their chemical structures, medium-chain fatty acid lactones, and a partially fluorinated medium-chain fatty acid was determined. As the length of the alkyl chain increased in medium-chain fatty acids with 8 to 11 carbon atoms, the MIC and MFC became smaller, with increased antifungal activity (octanoic acid, 225 µg/mL(MIC), 450 µg/mL (MFC); nonanoic acid, 225 µg/mL (MIC), 450 µg/mL (MFC); decanoic acid, 112.5 µg/mL (MIC), 225 µg/mL (MFC); undecanoic acid, 112.5 µg/mL (MIC), 225 µg/mL (MFC)), whereas the antifungal activity of γ-undecalactone, in which the carboxyl group of the medium-chain fatty acid with 11 carbon atoms was converted to a five-membered lactone ring, also had antifungal activity (γ-undecalactone, 112.5 µg/mL (MIC), 225 µg/mL (MFC)). The antifungal activity of the partially fluorinated fatty acid with 11 carbon atoms and δ-undecalactone was not observed and their MICs were not evaluated in this study. The equation derived through multiple regression analysis revealed that the polarizability value was significantly related to the MICs or MFCs of fatty acids containing 8 to 11 carbon atoms and γ-undecalactone (R
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