Molecules (Aug 2024)

Stilbenes in <i>Carex acuta</i> and <i>Carex lepidocarpa</i>

  • Jan Tříska,
  • Naděžda Vrchotová,
  • Štěpán Horník,
  • Jan Sýkora,
  • Andrea Kučerová

DOI
https://doi.org/10.3390/molecules29163840
Journal volume & issue
Vol. 29, no. 16
p. 3840

Abstract

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Stilbenes in the roots of Carex acuta and Carex lepidocarpa were studied. Root samples were extracted with 100% methanol and analyzed by HPLC and LC-MS. In this way, trans-resveratrol dimers (m/z 455 Da [M + H]+), trimers (m/z 681 Da [M + H]+) and tetramers (m/z 907 Da [M + H]+) were identified in the extracts. Using LC-NMR in stop-flow mode, pallidol and trans-ε-viniferin as dimers were identified. After the separation of individual peaks and their measurement by 1H NMR, cis and trans-miyabenol A as a tetramer and cis-miyabenol C as a trimer were identified. In the case of miyabenol A, it is a chromatographically inseparable mixture of cis and trans isomers in the ratio of 2:3 according to 1H NMR measurement. In the case of cis-miyabenol C, the Z-trans-trans-miyabenol C configuration was confirmed. The remaining unidentified peak with a practically identical UV-VIS spectrum to that of cis-miyabenol C is most likely another isomer of miyabenol C.

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