Structural and conformational analysis of two native procyanidin trimers

Magn Reson Chem. 2007 Feb;45(2):157-66. doi: 10.1002/mrc.1938.

Abstract

The structure and conformation of two native procyanidin trimers in water have been determined using 2D NMR and molecular mechanics. The results show the existence of four rotameric forms, one of which is predominant (60 to 80%). These four rotamers are shown to be in slow to intermediate exchange on the NMR timescale. Both trimers, whose structures vary owing to a different substitution of one carbon atom, adopt conformations in which stacking between different phenolic rings is favored.

MeSH terms

  • Biflavonoids / chemistry*
  • Carbohydrate Conformation
  • Catechin / chemistry*
  • Magnetic Resonance Spectroscopy*
  • Models, Molecular
  • Polymers / chemistry
  • Proanthocyanidins / chemistry*

Substances

  • Biflavonoids
  • Polymers
  • Proanthocyanidins
  • procyanidin
  • Catechin