Bioactive amides from Polygonum cuspidatum

J Asian Nat Prod Res. 2021 Mar;23(3):228-234. doi: 10.1080/10286020.2021.1873298. Epub 2021 Jan 18.

Abstract

One pair of new amides enantiomers (1a and 1b) and two known amides were isolated from the rhizomes of Polygonum cuspidatum. Their structures were established using UV, IR, HRESIMS, and NMR data. Notably, compound 1 possesses unique C-C connection between feruloyltyramine and resveratrol. Their absolute configurations were determined by the ECD method. All compounds were evaluated for their α-glucosidase inhibitory activity and compounds 2 and 3 showed significant inhibitory activity with IC50 values of 2.82 and 13.06 μmol/L, respectively (positive control acarbose, IC50 385 μmol/L).

Keywords: Polygonaceae; Polygonum cuspidatum; amides; α-glucosidase inhibition.

MeSH terms

  • Amides / pharmacology
  • Fallopia japonica*
  • Molecular Structure
  • Plant Extracts
  • Polygonum*
  • Rhizome

Substances

  • Amides
  • Plant Extracts