Antifungal Compounds from the Rhizome and Roots of Ferula hermonis

被引:16
作者
Al-Ja'fari, Abdel-Hadi [1 ,2 ]
Vila, Roser [1 ]
Freixa, Blanca [1 ]
Costa, Joan [2 ]
Canigueral, Salvador [1 ]
机构
[1] Univ Barcelona, Fac Farm, Unitat Farmacol & Farmacognosia, ES-08028 Barcelona, Spain
[2] Univ Autonoma Barcelona, Fac Med, Dept Farmacol Terapeut & Toxicol, Unitat Docent Hosp Univ Germans Trias & Pujol, ES-08916 Badalona, Spain
关键词
Ferula hermonis; jaeschkeanadiol p-hydroxybenzoate; jaeschkeanadiol benzoate; antifungal activity; dermatophytes; DAUCANE SESQUITERPENES; ESTERS; PLANTS; ERA;
D O I
10.1002/ptr.4806
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The antifungal activity of hexane, dichloromethane, methanol and aqueous extracts from the rhizome and root of Ferula hermonis was assayed in vitro by the agar disk diffusion method against a panel of human opportunistic and pathogenic fungi. Among them, the hexane and dichloromethane extracts showed the highest activity particularly against the dermatophytes Microsporum gypseum and Tricophyton mentagrophytes as well as the yeast Candida lactis-condensi. Activity-guided fractionation of both extracts using an agar overlay bioautographic method led to the isolation of two antifungal compounds which were identified as the daucane aryl esters jaeschkeanadiol p-hydroxybenzoate (ferutinin) and jaeschkeanadiol benzoate (teferidin). Determination of minimal inhibitory concentration (MIC) and minimal fungicidal concentration (MFC) values of both compounds evidenced a stronger antifungal activity for ferutinin than for teferidin. Particularly, T. mentagrophytes was the most sensitive strain with MIC and MFC values ranging from 8 to 256 mu g/mL. Copyright (c) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:911 / 915
页数:5
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