Acetylenic acids inhibiting azole-resistant Candida albicans from Pentagonia gigantifolia

J Nat Prod. 2003 Aug;66(8):1132-5. doi: 10.1021/np030196r.

Abstract

Antifungal bioassay-guided isolation of the ethanol extract of the roots of Pentagonia gigantifolia yielded 6-octadecynoic acid (1) and the new 6-nonadecynoic acid (2). Compounds 1 and 2 inhibited the growth of fluconazole-susceptible and -resistant Candida albicans strains. Their antifungal potencies were comparable to those of amphotericin B and fluconazole. Of particular significance is the low cytotoxicity and specific activity of 1 and 2 against C. albicans.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amphotericin B / pharmacology
  • Antifungal Agents / chemistry
  • Antifungal Agents / isolation & purification*
  • Antifungal Agents / pharmacology
  • Candida albicans / drug effects*
  • Drug Resistance, Microbial
  • Fatty Acids, Monounsaturated / chemistry
  • Fatty Acids, Monounsaturated / isolation & purification*
  • Fatty Acids, Monounsaturated / pharmacology
  • Fluconazole / pharmacology
  • Gas Chromatography-Mass Spectrometry
  • Methylation
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Peru
  • Plant Roots / chemistry
  • Sphingolipids

Substances

  • 6-nonadecynoic acid
  • 6-octadecynoic acid
  • Antifungal Agents
  • Fatty Acids, Monounsaturated
  • Sphingolipids
  • Amphotericin B
  • Fluconazole