Hygrophorones A-G: fungicidal cyclopentenones from Hygrophorus species (Basidiomycetes)

Phytochemistry. 2004 Apr;65(8):1061-71. doi: 10.1016/j.phytochem.2004.01.023.

Abstract

Twenty new 5-(hydroxyalkyl)-2-cyclopentenone derivatives (hygrophorones) could be isolated from Hygrophorus latitabundus, H. olivaceoalbus, H. persoonii, and H. pustulatus. Their fungicidal activity was exemplarily tested. The hygrophorones have structural similarities to the antibiotic pentenomycin. Chemically, hygrophorones are 2-cyclopentenones with hydroxy or acetoxy substituents at C-4 and/or C-5. An odd-numbered 1' oxidized alkyl chain (C(11), C(13), C(15), or C(17)) is attached at C-5. In addition, from H. persoonii the new gamma-butyrolactone derivative [5-(E)-2-hydroxytetradexylidene-5H-furan-2-one] could be isolated. Some hygrophorones are responsible for the color reaction of the stipes of these fungi upon treatment with potassium hydroxide solution. Structural elucidations are based on 1D ((1)H, (13)C) and 2D (COSY, NOESY, HSQC, HMBC) NMR spectroscopic analyses as well as HR-FT-ICR-MS investigations.

MeSH terms

  • Antifungal Agents / chemistry*
  • Antifungal Agents / isolation & purification
  • Antifungal Agents / pharmacology*
  • Basidiomycota / chemistry*
  • Cladosporium / drug effects
  • Cyclopentanes / chemistry*
  • Cyclopentanes / isolation & purification
  • Cyclopentanes / pharmacology*
  • Molecular Structure
  • Nuclear Magnetic Resonance, Biomolecular

Substances

  • Antifungal Agents
  • Cyclopentanes
  • cyclopentenone