Tomoeones A-H, cytotoxic phloroglucinol derivatives from Hypericum ascyron

Phytochemistry. 2008 Aug;69(11):2225-30. doi: 10.1016/j.phytochem.2008.04.026. Epub 2008 Jun 13.

Abstract

Phloroglucinol derivatives tomoeones A-H (1-8) and three known compounds were isolated from leaves of Hypericum ascyron. Their structures were established based on spectroscopic analyses. They are all acylphloroglucinol derivatives possessing a spiro skeleton with geminal isoprenyl groups and a monoterpene moiety, and they are stereoisomers to each other at C-4 and C-13. They appear to be a class of phloroglucinol derivatives. Cytotoxicities of the isolated phloroglucinol derivatives against human tumor cell lines, including multidrug-resistant (MDR) cancer cell lines, were evaluated. Tomoeone F (6) demonstrated significant cytotoxicity against KB cells with an IC50 value of 6.2 microM. Compound 6 was also cytotoxic against MDR cancer cell lines (KB-C2 and K562/Adr), which was more potent than doxorubicin.

MeSH terms

  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Humans
  • Hypericum / chemistry*
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Phloroglucinol / analogs & derivatives*
  • Phloroglucinol / chemistry
  • Phloroglucinol / metabolism
  • Phloroglucinol / toxicity*
  • Structure-Activity Relationship

Substances

  • Phloroglucinol