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Diterpenoid Alkaloids from the Chinese Traditional Herbal “Fuzi” and Their Cytotoxic Activity

Ten diterpenoid alkaloids, including eight aconitine-type C(19)-diterpenoid alkaloids and two hetisine-type C(20)-diterpenoid alkaloids, were isolated from the secondary roots of Aconitum carmichaeli Debx., known as “Fuzi” in Chinese traditional herbal medicine. Their structures were established on...

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Detalles Bibliográficos
Autores principales: Gao, Feng, Li, Yuan-Yuan, Wang, Dan, Huang, Xing, Liu, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268201/
https://www.ncbi.nlm.nih.gov/pubmed/22628040
http://dx.doi.org/10.3390/molecules17055187
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author Gao, Feng
Li, Yuan-Yuan
Wang, Dan
Huang, Xing
Liu, Qian
author_facet Gao, Feng
Li, Yuan-Yuan
Wang, Dan
Huang, Xing
Liu, Qian
author_sort Gao, Feng
collection PubMed
description Ten diterpenoid alkaloids, including eight aconitine-type C(19)-diterpenoid alkaloids and two hetisine-type C(20)-diterpenoid alkaloids, were isolated from the secondary roots of Aconitum carmichaeli Debx., known as “Fuzi” in Chinese traditional herbal medicine. Their structures were established on the basis of their spectroscopic data and comparison with those of the literature. Among these alkaloids, chasmanine, oxonitine and 15-acetylsongoramine were isolated for the first time from this medicinal plant. The cytotoxic activity of the alkaloids were tested against several cell lines by the MTT method in which aconitine, hypaconitine, mesaconitne and oxonitine were found to strongly inhibit the growth of the HePG2 cell line, which showed that the existence and quantity of the ester groups have a significant influence on the cytotoxicity of the diterpenoid alkaloids.
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spelling pubmed-62682012018-12-20 Diterpenoid Alkaloids from the Chinese Traditional Herbal “Fuzi” and Their Cytotoxic Activity Gao, Feng Li, Yuan-Yuan Wang, Dan Huang, Xing Liu, Qian Molecules Article Ten diterpenoid alkaloids, including eight aconitine-type C(19)-diterpenoid alkaloids and two hetisine-type C(20)-diterpenoid alkaloids, were isolated from the secondary roots of Aconitum carmichaeli Debx., known as “Fuzi” in Chinese traditional herbal medicine. Their structures were established on the basis of their spectroscopic data and comparison with those of the literature. Among these alkaloids, chasmanine, oxonitine and 15-acetylsongoramine were isolated for the first time from this medicinal plant. The cytotoxic activity of the alkaloids were tested against several cell lines by the MTT method in which aconitine, hypaconitine, mesaconitne and oxonitine were found to strongly inhibit the growth of the HePG2 cell line, which showed that the existence and quantity of the ester groups have a significant influence on the cytotoxicity of the diterpenoid alkaloids. MDPI 2012-05-04 /pmc/articles/PMC6268201/ /pubmed/22628040 http://dx.doi.org/10.3390/molecules17055187 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Gao, Feng
Li, Yuan-Yuan
Wang, Dan
Huang, Xing
Liu, Qian
Diterpenoid Alkaloids from the Chinese Traditional Herbal “Fuzi” and Their Cytotoxic Activity
title Diterpenoid Alkaloids from the Chinese Traditional Herbal “Fuzi” and Their Cytotoxic Activity
title_full Diterpenoid Alkaloids from the Chinese Traditional Herbal “Fuzi” and Their Cytotoxic Activity
title_fullStr Diterpenoid Alkaloids from the Chinese Traditional Herbal “Fuzi” and Their Cytotoxic Activity
title_full_unstemmed Diterpenoid Alkaloids from the Chinese Traditional Herbal “Fuzi” and Their Cytotoxic Activity
title_short Diterpenoid Alkaloids from the Chinese Traditional Herbal “Fuzi” and Their Cytotoxic Activity
title_sort diterpenoid alkaloids from the chinese traditional herbal “fuzi” and their cytotoxic activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268201/
https://www.ncbi.nlm.nih.gov/pubmed/22628040
http://dx.doi.org/10.3390/molecules17055187
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