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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...

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Autores principales: He, Xiaoyan, Abulizi, Xiatiguli, Li, Xiaowan, Ma, Guoxu, Sun, Zhaocui, Wei, Hongyan, Xu, Xudong, Shi, Leiling, Zhang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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).
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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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