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Daphnane-Type Diterpenes from Stelleropsis tianschanica and Their Antitumor Activity
Four new daphnane-type diterpenes named tianchaterpenes C-F (1–4) and six known ones were isolated from Stelleropsis tianschanica. Their structures were elucidated based on chemical and spectral analyses. The comparisons of calculated and experimental electronic circular dichroism (ECD) methods were...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458044/ https://www.ncbi.nlm.nih.gov/pubmed/36080468 http://dx.doi.org/10.3390/molecules27175701 |
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author | He, Xiaoyan Abulizi, Xiatiguli Li, Xiaowan Ma, Guoxu Sun, Zhaocui Wei, Hongyan Xu, Xudong Shi, Leiling Zhang, Jing |
author_facet | He, Xiaoyan Abulizi, Xiatiguli Li, Xiaowan Ma, Guoxu Sun, Zhaocui Wei, Hongyan Xu, Xudong Shi, Leiling Zhang, Jing |
author_sort | He, Xiaoyan |
collection | PubMed |
description | Four new daphnane-type diterpenes named tianchaterpenes C-F (1–4) and six known ones were isolated from Stelleropsis tianschanica. Their structures were elucidated based on chemical and spectral analyses. The comparisons of calculated and experimental electronic circular dichroism (ECD) methods were used to determine the absolute configurations of new compounds. Additionally, compounds 1–10 were evaluated for their cytotoxic activities against HGC-27 cell lines; the results demonstrate that compound 2 had strong cytotoxic activities with IC(50) values of 8.8 µM, for which activity was better than that of cisplatin (13.2 ± 0.67 µM). |
format | Online Article Text |
id | pubmed-9458044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94580442022-09-09 Daphnane-Type Diterpenes from Stelleropsis tianschanica and Their Antitumor Activity He, Xiaoyan Abulizi, Xiatiguli Li, Xiaowan Ma, Guoxu Sun, Zhaocui Wei, Hongyan Xu, Xudong Shi, Leiling Zhang, Jing Molecules Article Four new daphnane-type diterpenes named tianchaterpenes C-F (1–4) and six known ones were isolated from Stelleropsis tianschanica. Their structures were elucidated based on chemical and spectral analyses. The comparisons of calculated and experimental electronic circular dichroism (ECD) methods were used to determine the absolute configurations of new compounds. Additionally, compounds 1–10 were evaluated for their cytotoxic activities against HGC-27 cell lines; the results demonstrate that compound 2 had strong cytotoxic activities with IC(50) values of 8.8 µM, for which activity was better than that of cisplatin (13.2 ± 0.67 µM). MDPI 2022-09-04 /pmc/articles/PMC9458044/ /pubmed/36080468 http://dx.doi.org/10.3390/molecules27175701 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article He, Xiaoyan Abulizi, Xiatiguli Li, Xiaowan Ma, Guoxu Sun, Zhaocui Wei, Hongyan Xu, Xudong Shi, Leiling Zhang, Jing Daphnane-Type Diterpenes from Stelleropsis tianschanica and Their Antitumor Activity |
title | Daphnane-Type Diterpenes from Stelleropsis tianschanica and Their Antitumor Activity |
title_full | Daphnane-Type Diterpenes from Stelleropsis tianschanica and Their Antitumor Activity |
title_fullStr | Daphnane-Type Diterpenes from Stelleropsis tianschanica and Their Antitumor Activity |
title_full_unstemmed | Daphnane-Type Diterpenes from Stelleropsis tianschanica and Their Antitumor Activity |
title_short | Daphnane-Type Diterpenes from Stelleropsis tianschanica and Their Antitumor Activity |
title_sort | daphnane-type diterpenes from stelleropsis tianschanica and their antitumor activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458044/ https://www.ncbi.nlm.nih.gov/pubmed/36080468 http://dx.doi.org/10.3390/molecules27175701 |
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