Gamma-pyrone compounds as potential anti-cancer drugs

J Pharm Pharmacol. 1993 Sep;45(9):791-4. doi: 10.1111/j.2042-7158.1993.tb05686.x.

Abstract

The gamma-pyrones, artomunoxanthotrione epoxide, cyclocommunol, cyclomulberrin, and cyclocommunin exhibited potent inhibition of human PLC/PRF/5 and KB cells in-vitro. Dihydroisocycloartomunin showed significant and potent inhibition of human PLC/PRF/5 and KB cells in-vitro, respectively. Cyclomorusin, dihydrocycloartomunin and artomunoxanthone showed significant inhibition of KB cells in-vitro. Based on the above finding and the reported antileukaemic activity of xanthone psorospermin, a series of natural gamma-pyrones was prepared and the inhibition of human PLC/PRF/5 and KB cells in-vitro was measured. Structure-activity analysis indicated the epoxide group substituted at 3-hydroxyl and 2,6-; 3,6-; and 3,5-dihydroxyl xanthone enhanced the anti-tumour activity. The epoxide group substituted at the 6-hydroxyl group of 1,6-dihydroxyxanthone did not show anti-tumour activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / isolation & purification
  • Antineoplastic Agents / pharmacology*
  • Carcinoma, Hepatocellular / pathology
  • Cell Survival / drug effects*
  • Drug Screening Assays, Antitumor
  • Humans
  • KB Cells
  • Liver Neoplasms / pathology
  • Magnetic Resonance Spectroscopy
  • Plant Extracts
  • Pyrones / chemistry
  • Pyrones / isolation & purification
  • Pyrones / pharmacology*
  • Spectrophotometry, Infrared
  • Structure-Activity Relationship
  • Tumor Cells, Cultured
  • Xanthenes / isolation & purification
  • Xanthenes / pharmacology

Substances

  • Antineoplastic Agents
  • Plant Extracts
  • Pyrones
  • Xanthenes