Nordihydroguaiaretic acid autoxidation produces a schisandrin-like dibenzocyclooctadiene lignan

J Nat Prod. 2008 Sep;71(9):1612-5. doi: 10.1021/np8001354. Epub 2008 Aug 2.

Abstract

The lignan meso-nordihydroguaiaretic acid is known to undergo spontaneous oxidation in alkaline solution. In the presence of the trapping agent glutathione, the major oxidation products are consistent with the formation of a meso-nordihydroguaiaretic acid ortho-quinone. In the absence of a trapping agent however, the major oxidation product of meso-nordihydroguaiaretic acid in aqueous solution is a unique, stable schisandrin-like dibenzocyclooctadiene lignan that may be responsible for some of the biological effects of nordihydroguaiaretic acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclooctanes / chemistry*
  • Lignans / chemistry*
  • Masoprocol / chemistry*
  • Masoprocol / pharmacology
  • Molecular Structure
  • Oxidation-Reduction
  • Polycyclic Compounds / chemistry*
  • Stereoisomerism

Substances

  • Cyclooctanes
  • Lignans
  • Polycyclic Compounds
  • dibenzocyclooctadiene lignan
  • Masoprocol
  • schizandrin