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Chemical Constituents With Antiproliferative Activity From Pogostemon cablin (Blanco) Benth.
Two new patchoulene sesquiterpenoid glycosides (1–2), a natural patchoulane-type sesquiterpenoid (3) and a natural cadinene-type sesquiterpenoid (4), were isolated from the aerial parts of Pogostemon cablin (Blanco) Benth., together with eleven known sesquiterpenoids (5–15) and eleven known flavonoi...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334562/ https://www.ncbi.nlm.nih.gov/pubmed/35910745 http://dx.doi.org/10.3389/fchem.2022.938851 |
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author | Peng, Xingjia Ang, Song Zhang, Yizi Fan, Fenling Wu, Mengshuo Liang, Peiting Wen, Yan Gan, Lishe Zhang, Kun Li, Dongli Yue, Jianmin |
author_facet | Peng, Xingjia Ang, Song Zhang, Yizi Fan, Fenling Wu, Mengshuo Liang, Peiting Wen, Yan Gan, Lishe Zhang, Kun Li, Dongli Yue, Jianmin |
author_sort | Peng, Xingjia |
collection | PubMed |
description | Two new patchoulene sesquiterpenoid glycosides (1–2), a natural patchoulane-type sesquiterpenoid (3) and a natural cadinene-type sesquiterpenoid (4), were isolated from the aerial parts of Pogostemon cablin (Blanco) Benth., together with eleven known sesquiterpenoids (5–15) and eleven known flavonoids (16–26). Their chemical structures were elucidated on the basis of spectroscopic methods, including NMR, HRESIMS, IR, and CD spectroscopic data analysis, as well as chemical hydrolysis. The isolated compounds 1–13 and 15–26 were tested for inhibitory effects on the proliferation of HepG2 cancer cells. Among them, compounds 17 and 19 displayed anti-proliferative effects against HepG2 cells with IC(50) values of 25.59 and 2.30 μM, respectively. Furthermore, the flow cytometry analysis and Western blotting assays revealed that compound 19 significantly induced apoptosis of HepG2 cells by downregulating the ratio of Bcl-2/Bax and upregulating the expression of cleaved caspase-3 and cleaved caspase-9. Therefore, the potential pharmaceutical applications of P. cablin would be applied according to our study findings. |
format | Online Article Text |
id | pubmed-9334562 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93345622022-07-30 Chemical Constituents With Antiproliferative Activity From Pogostemon cablin (Blanco) Benth. Peng, Xingjia Ang, Song Zhang, Yizi Fan, Fenling Wu, Mengshuo Liang, Peiting Wen, Yan Gan, Lishe Zhang, Kun Li, Dongli Yue, Jianmin Front Chem Chemistry Two new patchoulene sesquiterpenoid glycosides (1–2), a natural patchoulane-type sesquiterpenoid (3) and a natural cadinene-type sesquiterpenoid (4), were isolated from the aerial parts of Pogostemon cablin (Blanco) Benth., together with eleven known sesquiterpenoids (5–15) and eleven known flavonoids (16–26). Their chemical structures were elucidated on the basis of spectroscopic methods, including NMR, HRESIMS, IR, and CD spectroscopic data analysis, as well as chemical hydrolysis. The isolated compounds 1–13 and 15–26 were tested for inhibitory effects on the proliferation of HepG2 cancer cells. Among them, compounds 17 and 19 displayed anti-proliferative effects against HepG2 cells with IC(50) values of 25.59 and 2.30 μM, respectively. Furthermore, the flow cytometry analysis and Western blotting assays revealed that compound 19 significantly induced apoptosis of HepG2 cells by downregulating the ratio of Bcl-2/Bax and upregulating the expression of cleaved caspase-3 and cleaved caspase-9. Therefore, the potential pharmaceutical applications of P. cablin would be applied according to our study findings. Frontiers Media S.A. 2022-07-15 /pmc/articles/PMC9334562/ /pubmed/35910745 http://dx.doi.org/10.3389/fchem.2022.938851 Text en Copyright © 2022 Peng, Ang, Zhang, Fan, Wu, Liang, Wen, Gan, Zhang, Li and Yue. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Peng, Xingjia Ang, Song Zhang, Yizi Fan, Fenling Wu, Mengshuo Liang, Peiting Wen, Yan Gan, Lishe Zhang, Kun Li, Dongli Yue, Jianmin Chemical Constituents With Antiproliferative Activity From Pogostemon cablin (Blanco) Benth. |
title | Chemical Constituents With Antiproliferative Activity From Pogostemon cablin (Blanco) Benth. |
title_full | Chemical Constituents With Antiproliferative Activity From Pogostemon cablin (Blanco) Benth. |
title_fullStr | Chemical Constituents With Antiproliferative Activity From Pogostemon cablin (Blanco) Benth. |
title_full_unstemmed | Chemical Constituents With Antiproliferative Activity From Pogostemon cablin (Blanco) Benth. |
title_short | Chemical Constituents With Antiproliferative Activity From Pogostemon cablin (Blanco) Benth. |
title_sort | chemical constituents with antiproliferative activity from pogostemon cablin (blanco) benth. |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334562/ https://www.ncbi.nlm.nih.gov/pubmed/35910745 http://dx.doi.org/10.3389/fchem.2022.938851 |
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