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

Asshaima Paramita DeviThuc-Huy DuongSolenn FerronMehdi A BeniddirMinh-Hiep DinhVan-Kieu NguyenNguyen-Kim-Tuyen PhamDinh-Hung MacJoël BoustieWarinthorn ChavasiriPierre Le Pogam
Published in: Planta medica (2020)
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.
Keyphrases
  • molecular docking
  • molecular dynamics simulations
  • systematic review
  • electronic health record
  • anti inflammatory