Structural elucidation and α‑glucosidase inhibitory activity of a new xanthone glycoside from Lomatogonium rotatum (L.) Fries es Nym

Nat Prod Res. 2022 Sep;36(17):4317-4321. doi: 10.1080/14786419.2021.1995864. Epub 2021 Nov 3.

Abstract

A new xanthone glycoside, 1,8-dihydroxyl-2,5-dimethoxy-xanthone-6-O-β-D-glucoside (1), along with two known xanthone glycosides and two flavonoid glycosides were isolated from the aerial parts of Lomatogonium rotatum (L.) Fries es Nym. The structure of 1 was elucidated by analysis of its spectroscopic data, including UV, IR, HR-ESI-MS and extensive 1 D and 2 D NMR techniques. In vitro test, compound 1 behaved similarity to swertianolin against α‑glucosidase and more potent inhibitory effects than the positive control, acarbose.

Keywords: Lomatogonium rotatum; Spectroscopic method; Xanthone glycoside; α‑glucosidase inhibitory activity.

MeSH terms

  • Cardiac Glycosides*
  • Gentianaceae* / chemistry
  • Glycosides / chemistry
  • Glycosides / pharmacology
  • Molecular Structure
  • Xanthones* / chemistry
  • Xanthones* / pharmacology
  • alpha-Glucosidases

Substances

  • Cardiac Glycosides
  • Glycosides
  • Xanthones
  • alpha-Glucosidases