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Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud

Diterpenoids are the focus of natural product drug discovery because of their great structural diversity and pronounced biological activities. Euphorbia fischeriana Steud is a Chinese traditional medicinal herb for curing edema, ascites, and cancer. This plant contains rich diterpenoids. Based on th...

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Detalles Bibliográficos
Autores principales: Jian, Baiyu, Zhang, Hao, Liu, Jicheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017929/
https://www.ncbi.nlm.nih.gov/pubmed/29669996
http://dx.doi.org/10.3390/molecules23040935
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author Jian, Baiyu
Zhang, Hao
Liu, Jicheng
author_facet Jian, Baiyu
Zhang, Hao
Liu, Jicheng
author_sort Jian, Baiyu
collection PubMed
description Diterpenoids are the focus of natural product drug discovery because of their great structural diversity and pronounced biological activities. Euphorbia fischeriana Steud is a Chinese traditional medicinal herb for curing edema, ascites, and cancer. This plant contains rich diterpenoids. Based on the carbon skeleton and substituents, it can be classified into thirteen subtypes: ent-abietane, daphnane, tigliane, ingenane, ent-atisane, ent-rosane, ent-kaurene, ent-kaurane, secotigliane, lathyrane, ent-pimarene, isopimarene and dimeric. In this paper, we reviewed the chemical structures and biological activities of 90 diterpenoids isolated from this medicinal herb. We hope that this work can serve as a reference for further research of these diterpenoids and lay the foundation for drug discovery.
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spelling pubmed-60179292018-11-13 Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud Jian, Baiyu Zhang, Hao Liu, Jicheng Molecules Review Diterpenoids are the focus of natural product drug discovery because of their great structural diversity and pronounced biological activities. Euphorbia fischeriana Steud is a Chinese traditional medicinal herb for curing edema, ascites, and cancer. This plant contains rich diterpenoids. Based on the carbon skeleton and substituents, it can be classified into thirteen subtypes: ent-abietane, daphnane, tigliane, ingenane, ent-atisane, ent-rosane, ent-kaurene, ent-kaurane, secotigliane, lathyrane, ent-pimarene, isopimarene and dimeric. In this paper, we reviewed the chemical structures and biological activities of 90 diterpenoids isolated from this medicinal herb. We hope that this work can serve as a reference for further research of these diterpenoids and lay the foundation for drug discovery. MDPI 2018-04-18 /pmc/articles/PMC6017929/ /pubmed/29669996 http://dx.doi.org/10.3390/molecules23040935 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jian, Baiyu
Zhang, Hao
Liu, Jicheng
Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud
title Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud
title_full Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud
title_fullStr Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud
title_full_unstemmed Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud
title_short Structural Diversity and Biological Activities of Diterpenoids Derived from Euphorbia fischeriana Steud
title_sort structural diversity and biological activities of diterpenoids derived from euphorbia fischeriana steud
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017929/
https://www.ncbi.nlm.nih.gov/pubmed/29669996
http://dx.doi.org/10.3390/molecules23040935
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