Salazinic acid-derived depsidones and diphenylethers with α-glucosidase inhibitory activity from the lichen Parmotrema dilatatum

Author:
Devi A.P., Duong T.-H., Ferron S., Beniddir M.A., Dinh M.-H., Nguyen V.-K., Pham N.-K.-T., Mac D.-H., Boustie J., Chavasiri W. & Le Pogam P.
Year:
2020
Journal:
Planta Medica
Pages:
86(16): 1216–1224
Url:
DOI: 10.1055/a-1203-0623
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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. Key words: depsidones - Diphenylethers - α-glucosidase - Lichens - Polyphenolics - Parmotrema dilatatum,
Id:
39415
Submitter:
zpalice
Post_time:
Tuesday, 21 April 2026 10:41