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Protostane and Fusidane Triterpenes: A Mini-Review
Protostane triterpenes belong to a group of tetracyclic triterpene that exhibit unique structural characteristics. Their natural distribution is primarily limited to the genus Alisma of the Alismataceae family, but they have also been occasionally found in other plant genera such as Lobelia, Garcini...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901436/ https://www.ncbi.nlm.nih.gov/pubmed/23563857 http://dx.doi.org/10.3390/molecules18044054 |
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author | Zhao, Ming Gödecke, Tanja Gunn, Jordan Duan, Jin-Ao Che, Chun-Tao |
author_facet | Zhao, Ming Gödecke, Tanja Gunn, Jordan Duan, Jin-Ao Che, Chun-Tao |
author_sort | Zhao, Ming |
collection | PubMed |
description | Protostane triterpenes belong to a group of tetracyclic triterpene that exhibit unique structural characteristics. Their natural distribution is primarily limited to the genus Alisma of the Alismataceae family, but they have also been occasionally found in other plant genera such as Lobelia, Garcinia, and Leucas. To date, there are 59 known protostane structures. Many of them have been reported to possess biological properties such as improving lipotropism, hepatoprotection, anti-viral activity against hepatitis B and HIV-I virus, anti-cancer activity, as well as reversal of multidrug resistance in cancer cells. On the other hand, fusidanes are fungal products characterized by 29-nor protostane structures. They possess antibiotic properties against staphylococci, including the methicillin-resistant Staphylococcus aureus (MRSA). Fusidic acid is a representative member which has found clinical applications. This review covers plant sources of the protostanes, their structure elucidation, characteristic structural and spectral properties, as well as biological activities. The fungal sources, structural features, biological activities of fusidanes are also covered in this review. Additionally, the biogenesis of these two types of triterpenes is discussed and a refined pathway is proposed. |
format | Online Article Text |
id | pubmed-3901436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-39014362014-01-24 Protostane and Fusidane Triterpenes: A Mini-Review Zhao, Ming Gödecke, Tanja Gunn, Jordan Duan, Jin-Ao Che, Chun-Tao Molecules Review Protostane triterpenes belong to a group of tetracyclic triterpene that exhibit unique structural characteristics. Their natural distribution is primarily limited to the genus Alisma of the Alismataceae family, but they have also been occasionally found in other plant genera such as Lobelia, Garcinia, and Leucas. To date, there are 59 known protostane structures. Many of them have been reported to possess biological properties such as improving lipotropism, hepatoprotection, anti-viral activity against hepatitis B and HIV-I virus, anti-cancer activity, as well as reversal of multidrug resistance in cancer cells. On the other hand, fusidanes are fungal products characterized by 29-nor protostane structures. They possess antibiotic properties against staphylococci, including the methicillin-resistant Staphylococcus aureus (MRSA). Fusidic acid is a representative member which has found clinical applications. This review covers plant sources of the protostanes, their structure elucidation, characteristic structural and spectral properties, as well as biological activities. The fungal sources, structural features, biological activities of fusidanes are also covered in this review. Additionally, the biogenesis of these two types of triterpenes is discussed and a refined pathway is proposed. MDPI 2013-04-05 /pmc/articles/PMC3901436/ /pubmed/23563857 http://dx.doi.org/10.3390/molecules18044054 Text en © 2013 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 license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Zhao, Ming Gödecke, Tanja Gunn, Jordan Duan, Jin-Ao Che, Chun-Tao Protostane and Fusidane Triterpenes: A Mini-Review |
title | Protostane and Fusidane Triterpenes: A Mini-Review |
title_full | Protostane and Fusidane Triterpenes: A Mini-Review |
title_fullStr | Protostane and Fusidane Triterpenes: A Mini-Review |
title_full_unstemmed | Protostane and Fusidane Triterpenes: A Mini-Review |
title_short | Protostane and Fusidane Triterpenes: A Mini-Review |
title_sort | protostane and fusidane triterpenes: a mini-review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901436/ https://www.ncbi.nlm.nih.gov/pubmed/23563857 http://dx.doi.org/10.3390/molecules18044054 |
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