In vitro cytotoxicity of some natural and semi-synthetic isocoumarins from Paepalanthus bromelioides

Z Naturforsch C J Biosci. 2002 Jan-Feb;57(1-2):85-8. doi: 10.1515/znc-2002-1-215.

Abstract

Numerous natural compounds have a potential for therapeutic applications, but may have to be chemically modified to alter toxic side effects. We investigated structural parameters that could affect the cytotoxicity of isocoumarins similar to 9,10-dihydroxy-5,7-dimethoxy-1H-naphtho(2,3c)pyran-1-one (paepalantine 1). Paepalantine 1 has antimicrobial activity, as well as significant in vitro cytotoxic effects in the McCoy cell line. Two other natural and two semi-synthetic isocoumarins with similar structures obtained from the capitula of Paepalanthus bromelioides were tested on the same cell line by the neutral red assay. Substitution of the 9 and/or 10-OH group made these compounds less cytotoxic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / metabolism
  • Cell Line
  • Cell Survival / drug effects
  • Cisplatin / toxicity
  • Coumarins / chemistry
  • Coumarins / metabolism*
  • Coumarins / toxicity*
  • Fibroblasts
  • Liliaceae / chemistry*
  • Liliaceae / metabolism
  • Mice
  • Structure-Activity Relationship

Substances

  • Anti-Infective Agents
  • Coumarins
  • Cisplatin