Antiviral spirooliganones A and B with unprecedented skeletons from the roots of Illicium oligandrum

Org Lett. 2013 Sep 6;15(17):4450-3. doi: 10.1021/ol401992s. Epub 2013 Aug 12.

Abstract

Two novel spirooliganones A (1) and (2), a pair of spiro carbon epimers, with a rare dioxaspiro skeleton were isolated from the roots of Illicium oligandrum. The structures were fully determined by spectroscopic analysis and chemical methods, especially modified Mosher's method, and X-ray diffraction analysis. Spirooliganone B was found to exhibit more potent activities against coxsackie virus B3 and influenza virus A (H3N2) (IC50 3.70-5.05 μM) than spirooliganone A. The biosynthetic pathway involving a hetero-Diels-Alder reaction of the epimers was proposed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / chemistry
  • Antiviral Agents / isolation & purification*
  • Antiviral Agents / pharmacology*
  • Cycloaddition Reaction
  • Enterovirus B, Human / drug effects
  • Illicium / chemistry*
  • Influenza A Virus, H3N2 Subtype / drug effects
  • Molecular Structure
  • Plant Roots / chemistry
  • Spiro Compounds / chemistry
  • Spiro Compounds / isolation & purification*
  • Spiro Compounds / pharmacology*
  • Stereoisomerism

Substances

  • Antiviral Agents
  • Spiro Compounds
  • spirooliganone A