Cytotoxic dimeric quinolone-terpene alkaloids from the root bark of Zanthoxylum rhetsa

Phytochemistry. 2014 Jul:103:8-12. doi: 10.1016/j.phytochem.2014.03.008. Epub 2014 Apr 22.

Abstract

Four quinolone-terpene alkaloids, chelerybulgarine (1), 2'-episimulanoquinoline (3), 2,11-didemethoxyvepridimerine B (4), and rhetsidimerine (5) were isolated from the root bark of Zanthoxylum rhetsa DC. Chelerybulgarine (1) is a C-C linked terpene alkaloid where the C-6 of dihydrochelerythrine is linked to C-11 of the sesquiterpenoid 10β-methoxybulgarene. 2'-Episimulanoquinoline is a dimeric alkaloid containing dihydrochelerythrine and 8-methoxy-N-methylflindersine moieties, whereas 2,11-didemethoxyvepridimerine B and rhetsidimerine are dimeric prenylated quinolone alkaloids. Seven of the isolated compounds exhibited weak cytotoxicity when tested against a panel of six human stomach-cancer cell lines.

Keywords: 2,11-Didemethoxyvepridimerine; 2′-Episimulanoquinoline; Chelerybulgarine; Dihydrochelerythrine; Rhetsidimerine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / chemistry*
  • Alkaloids / pharmacology*
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Humans
  • Molecular Structure
  • Plant Bark / chemistry*
  • Plant Extracts / chemistry*
  • Plant Extracts / pharmacology*
  • Plant Roots / chemistry*
  • Zanthoxylum / chemistry*

Substances

  • Alkaloids
  • Plant Extracts