Stilbenes in Carex acuta and Carex lepidocarpa

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

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Publication Details

Journal
Molecules
Published
2024-08-13
DOI
https://doi.org/10.3390/molecules29163840
Citations
2
Primary Topic
Metabolomics and Mass Spectrometry Studies
Type
article
Field-Weighted Citation Impact
0.47

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article

Stilbenes in Carex acuta and Carex lepidocarpa

Štěpán Horník, Jan Třı́ska, Andrea Kučerová, Ján Sýkora et al.
2 citations
Molecules
Metabolomics and Mass Spectrometry Studies
0.47
article

Stilbenes in Carex acuta and Carex lepidocarpa

Štěpán Horník, Jan Třı́ska, Andrea Kučerová, Ján Sýkora, Naděžda Vrchotová
article en
2 citations

Abstract

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

MoleculesVol. 29(16)
Czech Academy of Sciences (CZ), Czech Academy of Sciences, Global Change Research Institute (CZ), Czech Academy of Sciences, Institute of Chemical Process Fundamentals (CZ), Czech Academy of Sciences, Institute of Botany (CZ), University of Chemistry and Technology, Prague (CZ)
Akademie Věd České Republiky
Life in Land
Openalex Percentile: Top 36%
Metabolomics and Mass Spectrometry Studies
0.47
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