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Two Novel Quassinoid Glycosides with Antiviral Activity from the Samara of Ailanthus altissima

Phytochemistry investigations on Ailanthus altissima (Mill.) Swingle, a Simaroubaceae plant that is recognized as a traditional herbal medicine, have afforded various natural products, among which C(20) quassinoid is the most attractive for their significant and diverse pharmacological and biologica...

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Autores principales: Tan, Qing-Wei, Ni, Jian-Cheng, Shi, Jian-Ting, Zhu, Jian-Xuan, Chen, Qi-Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730543/
https://www.ncbi.nlm.nih.gov/pubmed/33276431
http://dx.doi.org/10.3390/molecules25235679
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author Tan, Qing-Wei
Ni, Jian-Cheng
Shi, Jian-Ting
Zhu, Jian-Xuan
Chen, Qi-Jian
author_facet Tan, Qing-Wei
Ni, Jian-Cheng
Shi, Jian-Ting
Zhu, Jian-Xuan
Chen, Qi-Jian
author_sort Tan, Qing-Wei
collection PubMed
description Phytochemistry investigations on Ailanthus altissima (Mill.) Swingle, a Simaroubaceae plant that is recognized as a traditional herbal medicine, have afforded various natural products, among which C(20) quassinoid is the most attractive for their significant and diverse pharmacological and biological activities. Our continuous study has led to the isolation of two novel quassinoid glycosides, named chuglycosides J and K, together with fourteen known lignans from the samara of A. altissima. The new structures were elucidated based on comprehensive spectra data analysis. All of the compounds were evaluated for their anti-tobacco mosaic virus activity, among which chuglycosides J and K exhibited inhibitory effects against the virus multiplication with half maximal inhibitory concentration (IC(50)) values of 56.21 ± 1.86 and 137.74 ± 3.57 μM, respectively.
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spelling pubmed-77305432020-12-12 Two Novel Quassinoid Glycosides with Antiviral Activity from the Samara of Ailanthus altissima Tan, Qing-Wei Ni, Jian-Cheng Shi, Jian-Ting Zhu, Jian-Xuan Chen, Qi-Jian Molecules Article Phytochemistry investigations on Ailanthus altissima (Mill.) Swingle, a Simaroubaceae plant that is recognized as a traditional herbal medicine, have afforded various natural products, among which C(20) quassinoid is the most attractive for their significant and diverse pharmacological and biological activities. Our continuous study has led to the isolation of two novel quassinoid glycosides, named chuglycosides J and K, together with fourteen known lignans from the samara of A. altissima. The new structures were elucidated based on comprehensive spectra data analysis. All of the compounds were evaluated for their anti-tobacco mosaic virus activity, among which chuglycosides J and K exhibited inhibitory effects against the virus multiplication with half maximal inhibitory concentration (IC(50)) values of 56.21 ± 1.86 and 137.74 ± 3.57 μM, respectively. MDPI 2020-12-02 /pmc/articles/PMC7730543/ /pubmed/33276431 http://dx.doi.org/10.3390/molecules25235679 Text en © 2020 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 Article
Tan, Qing-Wei
Ni, Jian-Cheng
Shi, Jian-Ting
Zhu, Jian-Xuan
Chen, Qi-Jian
Two Novel Quassinoid Glycosides with Antiviral Activity from the Samara of Ailanthus altissima
title Two Novel Quassinoid Glycosides with Antiviral Activity from the Samara of Ailanthus altissima
title_full Two Novel Quassinoid Glycosides with Antiviral Activity from the Samara of Ailanthus altissima
title_fullStr Two Novel Quassinoid Glycosides with Antiviral Activity from the Samara of Ailanthus altissima
title_full_unstemmed Two Novel Quassinoid Glycosides with Antiviral Activity from the Samara of Ailanthus altissima
title_short Two Novel Quassinoid Glycosides with Antiviral Activity from the Samara of Ailanthus altissima
title_sort two novel quassinoid glycosides with antiviral activity from the samara of ailanthus altissima
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730543/
https://www.ncbi.nlm.nih.gov/pubmed/33276431
http://dx.doi.org/10.3390/molecules25235679
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