Antinociceptive properties of caffeic acid derivatives in mice

Eur J Med Chem. 2009 Nov;44(11):4596-602. doi: 10.1016/j.ejmech.2009.06.029. Epub 2009 Jul 3.

Abstract

Ten ester derivatives from caffeic acid were synthesized, and their antinociceptive properties are evaluated in mice. The most active compound, dodecyl ester derivative, exhibited potent and dose-related activity against the writhing test, with a calculated ID(50) value of 15.1 (11.9-19.1)micromol/kg and MI of 78.8% being several times more active than reference drugs. It was also effective in other experimental models, such as formalin, capsaicin and glutamate-induced pain tests, but was inactive in the hot-plate test. Although the mechanism of action has still not been elucidated, these results appear to support its therapeutic potential against painful diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics / chemistry*
  • Analgesics / therapeutic use*
  • Animals
  • Caffeic Acids / chemistry*
  • Caffeic Acids / therapeutic use*
  • Mice
  • Molecular Structure
  • Pain / chemically induced
  • Pain / drug therapy*
  • Structure-Activity Relationship

Substances

  • Analgesics
  • Caffeic Acids
  • caffeic acid