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
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

