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Total Synthesis and Anti-Viral Activities of an Extract of Radix isatidis
Radix isatidis (Banlangen), a famous traditional Chinese medicine, has been used for thousands of years in China due to its anti-viral activity. Through our research, we inferred that the anti-viral activity of Radix isatidis depended on the water-soluble part. Among the components of this extract,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271997/ https://www.ncbi.nlm.nih.gov/pubmed/25514229 http://dx.doi.org/10.3390/molecules191220906 |
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author | He, Li-Wei Liu, Hua-Qing Chen, Yu-Qing Yang, Jing-Yan Wang, Tian-Lin Li, Wei |
author_facet | He, Li-Wei Liu, Hua-Qing Chen, Yu-Qing Yang, Jing-Yan Wang, Tian-Lin Li, Wei |
author_sort | He, Li-Wei |
collection | PubMed |
description | Radix isatidis (Banlangen), a famous traditional Chinese medicine, has been used for thousands of years in China due to its anti-viral activity. Through our research, we inferred that the anti-viral activity of Radix isatidis depended on the water-soluble part. Among the components of this extract, the isoquinoline derivative 1 was isolated for the first time and has shown better anti-viral activity than other constituents. In this study, to solve the problem of sourcing sufficient quantities of compound 1, a total synthesis route is described, and several analogues are also evaluated for their anti-viral activities. Among them, compound 8 shown potent anti-viral activity with an IC(50) value of 15.3 µg/mL. The results suggested that isoquinoline derivatives possessed potent anti-viral activity and are worthy further development. |
format | Online Article Text |
id | pubmed-6271997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62719972018-12-28 Total Synthesis and Anti-Viral Activities of an Extract of Radix isatidis He, Li-Wei Liu, Hua-Qing Chen, Yu-Qing Yang, Jing-Yan Wang, Tian-Lin Li, Wei Molecules Article Radix isatidis (Banlangen), a famous traditional Chinese medicine, has been used for thousands of years in China due to its anti-viral activity. Through our research, we inferred that the anti-viral activity of Radix isatidis depended on the water-soluble part. Among the components of this extract, the isoquinoline derivative 1 was isolated for the first time and has shown better anti-viral activity than other constituents. In this study, to solve the problem of sourcing sufficient quantities of compound 1, a total synthesis route is described, and several analogues are also evaluated for their anti-viral activities. Among them, compound 8 shown potent anti-viral activity with an IC(50) value of 15.3 µg/mL. The results suggested that isoquinoline derivatives possessed potent anti-viral activity and are worthy further development. MDPI 2014-12-12 /pmc/articles/PMC6271997/ /pubmed/25514229 http://dx.doi.org/10.3390/molecules191220906 Text en © 2014 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/4.0/). |
spellingShingle | Article He, Li-Wei Liu, Hua-Qing Chen, Yu-Qing Yang, Jing-Yan Wang, Tian-Lin Li, Wei Total Synthesis and Anti-Viral Activities of an Extract of Radix isatidis |
title | Total Synthesis and Anti-Viral Activities of an Extract of Radix isatidis |
title_full | Total Synthesis and Anti-Viral Activities of an Extract of Radix isatidis |
title_fullStr | Total Synthesis and Anti-Viral Activities of an Extract of Radix isatidis |
title_full_unstemmed | Total Synthesis and Anti-Viral Activities of an Extract of Radix isatidis |
title_short | Total Synthesis and Anti-Viral Activities of an Extract of Radix isatidis |
title_sort | total synthesis and anti-viral activities of an extract of radix isatidis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271997/ https://www.ncbi.nlm.nih.gov/pubmed/25514229 http://dx.doi.org/10.3390/molecules191220906 |
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