Two New α-Glucosidase Inhibitory Depsidones from the Lichen Parmotrema cristiferum (Taylor) Hale

Chem Biodivers. 2023 Mar;20(3):e202201213. doi: 10.1002/cbdv.202201213. Epub 2023 Mar 8.

Abstract

A bioactivity-guided investigation of the lichen Parmotrema cristiferum (Taylor) Hale (Parmeliaceae) led to the isolation of two new depsidones, cristifones A and B (1 and 2). The structures of the isolated compounds were identified by spectroscopic methods and comparison with the literature data. Compound 1 showed the initial combined structures of depsidone and depside cores. The two isolated compounds were then evaluated for α-glucosidase inhibition. Compounds 1 and 2 were confirmed as potent, with IC50 values of 21.5 and 18.4 μM, respectively. Compound 2 was a non-competitive inhibitor against α-glucosidase, as indicated by the intersect in the second quadrant of each respective plot.

Keywords: Parmotrema cristiferum; cristifones A and B; depside; depsidone; α-glucosidase inhibition.

MeSH terms

  • Glycoside Hydrolase Inhibitors* / pharmacology
  • Lichens* / chemistry
  • Parmeliaceae* / chemistry
  • alpha-Glucosidases / chemistry
  • alpha-Glucosidases / metabolism

Substances

  • alpha-Glucosidases
  • depsidone
  • Glycoside Hydrolase Inhibitors

Supplementary concepts

  • Parmotrema cristiferum