4.7 Article

Antifungal activity of Heterothalamus alienus metabolites

Journal

PHYTOTHERAPY RESEARCH
Volume 22, Issue 4, Pages 524-528

Publisher

WILEY
DOI: 10.1002/ptr.2380

Keywords

Heterothalamus alienus; 3-hydroxyflava nones; sakuranetin; sesquiterpenes; antifungal activity

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The chemical study of Heterothalamus alienus gave rutin, spathulenol (1), (IR,7S)-germacra-4(15),5,10(14)trien-1 ss-ol (2), sakuranetin (3), padmatin 3-acetate (4), (2R,.3R)-dihydroquercetin-7,3',4'-trimethyI ether (5), (2R,3R)-dihydroquereetin-7,4'-dimethyl ether (6), (2R,3R)-3-acetoxy-5,7,4'-trihydroxyflavanone (7), as the main components of an antifungal extract of the aerial parts of the plant. Compound 2 showed moderate activity, with Epidermophyton floccosum being the most susceptible species (MIC = 100 mu g/mL); compound 3 showed the best antifungal behavior having a broad spectrum of action and the lowest MICs. This flavanone along with flavanolol 5 showed very good activity against standardized (MIC = 31.2 mu g/mL) as well as clinical isolates of Trichophyton rubrum and T. mentagrophytes (MIC ranges 31.2-62.5 mu g/mL and 31.2-125 mu g/mL, respectively) and demonstrated not only fungistatic but also fungicide properties. Flavanolol 6 was active against all the dermatophytes tested with MICs of 62.5-250 mu g/mL. Rutin, spathulenol (1) and the 3-acetylated flavanones 4 and 7 were inactive or marginally active against the fungal panel. Copyright (c) 2008 John Wiley & Sons, Ltd.

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