A new benzyl ester and ergosterol derivatives from the fungus Gymnoascus reessii

Nat Prod Res. 2014;28(14):1045-51. doi: 10.1080/14786419.2014.903478. Epub 2014 Apr 7.

Abstract

A new benzyl ester, reessiate (1), anthraquinone, islandicin (2), ergosterol and seven ergosterol derivatives (3-9) were isolated from the fungus Gymnoascus reessii. All structures were identified by spectroscopic methods. This is the first report of their isolation from this fungus. Compounds 4-7 and 9 exhibited antimalarial activity against Plasmodium falciparum with IC50 values in the range of 3.3-4.5 μg/mL. In addition, 4 showed cytotoxicity against KB, MCF7 and NCI-H187 cancer cell lines. It was found that 4 has cytotoxic effect to MCF7 (IC50 = 7.9 μg/mL) lower than Doxorubicin (IC50 = 8.5 μg/mL).

Keywords: Gymnoascus reessii; antimalaria; benzyl ester; cytotoxicity; ergosterol derivative.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anthraquinones / chemistry
  • Anthraquinones / isolation & purification
  • Anthraquinones / pharmacology
  • Antimalarials / chemistry
  • Antimalarials / isolation & purification*
  • Antimalarials / pharmacology
  • Ascomycota / chemistry*
  • Benzyl Compounds / chemistry
  • Benzyl Compounds / isolation & purification*
  • Ergosterol / analogs & derivatives*
  • Ergosterol / chemistry
  • Ergosterol / isolation & purification*
  • Ergosterol / pharmacology
  • Esters
  • Female
  • Humans
  • Inhibitory Concentration 50
  • KB Cells
  • Molecular Structure
  • Plasmodium falciparum / drug effects*

Substances

  • Anthraquinones
  • Antimalarials
  • Benzyl Compounds
  • Esters
  • reessiate
  • funiculosin (anthraquinone)
  • Ergosterol