Salazinic Acid-Derived Depsidones and Diphenylethers with α-Glucosidase Inhibitory Activity from the Lichen Parmotrema dilatatum

Planta Med. 2020 Nov;86(16):1216-1224. doi: 10.1055/a-1203-0623. Epub 2020 Aug 20.

Abstract

Three new depsidones, parmosidones F - G (1 - 2), and 8'-O-methylsalazinic acid (3), and 3 new diphenylethers, parmetherines A - C (4 - 6), together with 2 known congeners were isolated from the whole thalli of Parmotrema dilatatum, a foliose chlorolichen. Their structures were unambiguously determined by extensive spectroscopic analyses and comparison with literature data. The isolated polyphenolics were assayed for their α-glucosidase inhibitory activities. Newly reported benzylated depsidones 1: and 2: in particular inhibited α-glucosidase with IC50 values of 2.2 and 4.3 µM, respectively, and are thus more potent than the positive control, acarbose.

MeSH terms

  • Depsides
  • Glycoside Hydrolase Inhibitors / pharmacology
  • Lactones
  • Lichens*
  • Plant Extracts / pharmacology
  • Salicylates
  • alpha-Glucosidases*

Substances

  • Depsides
  • Glycoside Hydrolase Inhibitors
  • Lactones
  • Plant Extracts
  • Salicylates
  • salazinic acid
  • depsidone
  • alpha-Glucosidases