Lignans from the Roots of Taxus wallichiana and Their α-Glucosidase Inhibitory Activities

J Nat Prod. 2017 Jun 23;80(6):1876-1882. doi: 10.1021/acs.jnatprod.7b00171. Epub 2017 Jun 5.

Abstract

From an EtOAc-soluble extract of the roots of Taxus wallichiana, six new (1-6) and 11 known lignans were isolated. The structures of the new compounds were elucidated based on interpretation of spectroscopic data. (+)-7'-epi-Tsugacetal (1) is a rare aryltetralin-type lignan having a cis-orientation of H-7' and H-8'. Compounds 3-6 were identified as the first naturally occurring tetrahydrofuranoid lignans having a cis-orientation of H-7 and H-8. All tested compounds were found to possess α-glucosidase inhibitory activity, with formosanol (9) showing the most potent effect with an IC50 value of 35.3 μM.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Dose-Response Relationship, Drug
  • Glycoside Hydrolase Inhibitors / chemistry
  • Glycoside Hydrolase Inhibitors / isolation & purification*
  • Glycoside Hydrolase Inhibitors / pharmacology*
  • Inhibitory Concentration 50
  • Lignans / chemistry
  • Lignans / isolation & purification*
  • Lignans / pharmacology*
  • Molecular Structure
  • Plant Roots / chemistry*
  • Taxus / chemistry*
  • Vietnam
  • alpha-Glucosidases / drug effects

Substances

  • Glycoside Hydrolase Inhibitors
  • Lignans
  • alpha-Glucosidases