Evaluation of lipoxygenase inhibitory activity of anacardic acids

Z Naturforsch C J Biosci. 2008 Jul-Aug;63(7-8):539-46. doi: 10.1515/znc-2008-7-812.

Abstract

6-Alkylsalicylic acids inhibit the linoleic acid peroxidation catalyzed by soybean lipoxygenase-1 (EC 1.13.11.12, type 1) competitively and without pro-oxidant effects. This activity is largely dependent on the nature of their alkyl side chains. Inhibitory activities of anacardic acids, viz. 6-pentadec(en)ylsalicylic acids, isolated from the cashew Anacardium occidentale, were initially used for comparison because their aromatic head portions are the same. Consequently, the data should be interpreted to mean that changes in the hydrophobic side chain tail portions of the molecules evaluated correlate with the specific activity determined.

MeSH terms

  • Anacardic Acids / chemistry
  • Anacardic Acids / pharmacokinetics
  • Anacardic Acids / pharmacology*
  • Drug Evaluation, Preclinical
  • Free Radical Scavengers / chemistry
  • Free Radical Scavengers / pharmacokinetics
  • Free Radical Scavengers / pharmacology
  • Lipoxygenase Inhibitors / chemistry
  • Lipoxygenase Inhibitors / pharmacokinetics
  • Lipoxygenase Inhibitors / pharmacology*
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Anacardic Acids
  • Free Radical Scavengers
  • Lipoxygenase Inhibitors