Alkyl side-chain derivatives of sordaricin as potent antifungal agents against yeast

Bioorg Med Chem Lett. 1998 Aug 18;8(16):2269-72. doi: 10.1016/s0960-894x(98)00401-6.

Abstract

Sordarin (1) was converted to 5 and 6, which showed potent antifungal activity against yeast. A series of C1-C9 alkyl side-chain derivatives was prepared, from which it was found that the optimal activity occurred with C5. A comparison of side chains with different unsaturation showed that the cis-alkene was the most active. This result suggested that the folding of the side chains might be crucial for the optimal activity.

MeSH terms

  • Antifungal Agents / chemical synthesis*
  • Antifungal Agents / chemistry*
  • Antifungal Agents / pharmacology
  • Diterpenes
  • Indenes
  • Indicators and Reagents
  • Microbial Sensitivity Tests
  • Molecular Conformation
  • Saccharomyces cerevisiae / drug effects*
  • Structure-Activity Relationship

Substances

  • Antifungal Agents
  • Diterpenes
  • Indenes
  • Indicators and Reagents
  • sordaricin
  • sordarin