4.7 Article

Composition and antifungal activity of the essential oil from the rhizome and roots of Ferula hermonis

Journal

PHYTOCHEMISTRY
Volume 72, Issue 11-12, Pages 1406-1413

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2011.04.013

Keywords

Ferula hermonis; Essential oil; alpha-Pinene; 3,5-Nonadiyne; Jaeschkeanadiol benzoate; Antifungal activity; Dermatophytes

Funding

  1. Fundacion Maria Francisca de Roviralta (Barcelona, Spain)

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The analysis of the essential oil from rhizome and roots of Ferula hermonis Boiss. (Apiaceae) by GC-FID, GC-MS and C-13 NMR allowed the identification of 79 constituents, more than 90% of the oil, the major one being alpha-pinene (43.3%), followed by alpha-bisabolol (11.1%) and the unusual acetylenic compound 3,5-nonadiyne (4.4%). The antifungal activity of the essential oil before and after fractionation was assayed against several yeasts and filamentous fungi. Purification of the active fractions afforded 3,5-nonadiyne, alpha-bisabolol, jaeschkeanadiol angelate, alpha-bisabolol oxide B and trans-verbenol, as well as two purified fractions, one of them (JB73) with 73% of jaeschkeanadiol benzoate and the other with 50% of spathulenol. Determination of MIC and MFC values of all these products evidenced strong antifungal activities for JB73 and 3,5-nonadiyne. Particularly, against the dermatophyte Tricophyton mentagrophytes, MIC and MFC values were 0.25 mu g/ml for JB73, and 8 mu g/ml for 3,5-nonadiyne, the former being more active than amphotericin B and nystatin. (C) 2011 Elsevier Ltd. All rights reserved.

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