Structure-plant growth inhibitory activity relationship of lariciresinol

J Agric Food Chem. 2013 Dec 18;61(50):12297-306. doi: 10.1021/jf404292w. Epub 2013 Dec 4.

Abstract

The syntheses of 55 lariciresinol derivatives containing derivatives on the 9-position and an aryl group at both 7- and 7'-positions were successful to examine the effect of structure of (-)-lariciresinol (1) on plant growth regulatory activity. (-)-(7R,8R,8'S)-9-Dehydroxylariciresinol 9 showed activity 2-fold more potent than that of natural (-)-lariciresinol (1) and -95% growth inhibitory activity to negative control against rye grass root at 1 mM. The derivatives bearing hydrophobic and smaller groups at the 9-position showed higher activity. The importance of 4- and 4'-hydroxy groups and 3- and 3'-small hydrophobic groups on 7- and 7'-phenyl groups for higher activity was also suggested.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Furans / chemistry*
  • Furans / pharmacology*
  • Herbicides / chemistry*
  • Herbicides / pharmacology*
  • Lignans / chemistry*
  • Lignans / pharmacology*
  • Lolium / drug effects*
  • Lolium / growth & development*
  • Structure-Activity Relationship

Substances

  • Furans
  • Herbicides
  • Lignans
  • lariciresinol