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Cytotoxic constituents and a new hydroxycinnamic acid derivative from Leontodon saxatilis (Asteraceae, Cichorieae)
In our ongoing research for the discovery of new constituents with antimyeloma activity, we investigated 15 compounds present in the aerial parts of Leontodon saxatilis for their cytotoxic potential against NCI-H929, U266, and OPM2 cell lines. One of the isolated compounds displayed a new natural pr...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695733/ https://www.ncbi.nlm.nih.gov/pubmed/35423597 http://dx.doi.org/10.1039/d0ra10973h |
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author | Ҫiҫek, Serhat Sezai Willer, Johanna Preziuso, Francesca Sönnichsen, Frank Greil, Richard Girreser, Ulrich Zidorn, Christian Jöhrer, Karin |
author_facet | Ҫiҫek, Serhat Sezai Willer, Johanna Preziuso, Francesca Sönnichsen, Frank Greil, Richard Girreser, Ulrich Zidorn, Christian Jöhrer, Karin |
author_sort | Ҫiҫek, Serhat Sezai |
collection | PubMed |
description | In our ongoing research for the discovery of new constituents with antimyeloma activity, we investigated 15 compounds present in the aerial parts of Leontodon saxatilis for their cytotoxic potential against NCI-H929, U266, and OPM2 cell lines. One of the isolated compounds displayed a new natural product and was identified as 5-feruloyl-2α-hydroxyquinic acid after LC-MS and NMR experiments. Of the remaining compounds, cichoric acid and three flavone glycosides, apigenin 4′-O-β-d-glucoside, luteolin 7-O-β-d-glucoside and luteolin 4′-O-β-d-glucoside, showed moderate cytotoxic activity, whereas the effects of two aglyones apigenin and luteolin were more pronounced. Though the cytotoxic potential of the two aglycones (against other cell lines) was reported in various studies, our work moreover showed that cooccurrence of these two compounds with similar components of lower activity led to comparable results and at the same time minimized the damage of healthy fibroblast cells. Thus, our work could be a starting point for additional studies on the synergistic effect of similar components against myeloma cell lines. |
format | Online Article Text |
id | pubmed-8695733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-86957332022-04-13 Cytotoxic constituents and a new hydroxycinnamic acid derivative from Leontodon saxatilis (Asteraceae, Cichorieae) Ҫiҫek, Serhat Sezai Willer, Johanna Preziuso, Francesca Sönnichsen, Frank Greil, Richard Girreser, Ulrich Zidorn, Christian Jöhrer, Karin RSC Adv Chemistry In our ongoing research for the discovery of new constituents with antimyeloma activity, we investigated 15 compounds present in the aerial parts of Leontodon saxatilis for their cytotoxic potential against NCI-H929, U266, and OPM2 cell lines. One of the isolated compounds displayed a new natural product and was identified as 5-feruloyl-2α-hydroxyquinic acid after LC-MS and NMR experiments. Of the remaining compounds, cichoric acid and three flavone glycosides, apigenin 4′-O-β-d-glucoside, luteolin 7-O-β-d-glucoside and luteolin 4′-O-β-d-glucoside, showed moderate cytotoxic activity, whereas the effects of two aglyones apigenin and luteolin were more pronounced. Though the cytotoxic potential of the two aglycones (against other cell lines) was reported in various studies, our work moreover showed that cooccurrence of these two compounds with similar components of lower activity led to comparable results and at the same time minimized the damage of healthy fibroblast cells. Thus, our work could be a starting point for additional studies on the synergistic effect of similar components against myeloma cell lines. The Royal Society of Chemistry 2021-03-10 /pmc/articles/PMC8695733/ /pubmed/35423597 http://dx.doi.org/10.1039/d0ra10973h Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Ҫiҫek, Serhat Sezai Willer, Johanna Preziuso, Francesca Sönnichsen, Frank Greil, Richard Girreser, Ulrich Zidorn, Christian Jöhrer, Karin Cytotoxic constituents and a new hydroxycinnamic acid derivative from Leontodon saxatilis (Asteraceae, Cichorieae) |
title | Cytotoxic constituents and a new hydroxycinnamic acid derivative from Leontodon saxatilis (Asteraceae, Cichorieae) |
title_full | Cytotoxic constituents and a new hydroxycinnamic acid derivative from Leontodon saxatilis (Asteraceae, Cichorieae) |
title_fullStr | Cytotoxic constituents and a new hydroxycinnamic acid derivative from Leontodon saxatilis (Asteraceae, Cichorieae) |
title_full_unstemmed | Cytotoxic constituents and a new hydroxycinnamic acid derivative from Leontodon saxatilis (Asteraceae, Cichorieae) |
title_short | Cytotoxic constituents and a new hydroxycinnamic acid derivative from Leontodon saxatilis (Asteraceae, Cichorieae) |
title_sort | cytotoxic constituents and a new hydroxycinnamic acid derivative from leontodon saxatilis (asteraceae, cichorieae) |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695733/ https://www.ncbi.nlm.nih.gov/pubmed/35423597 http://dx.doi.org/10.1039/d0ra10973h |
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