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Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review
Esculetin, synonymous with 6,7-dihydroxycoumarin, is the main active ingredient of the traditional Chinese medicine Cortex Fraxini. The twig skin or trunk bark of Cortex Fraxini are used by herb doctors as a mild, bitter liver and gallbladder meridians’ nontoxic drug as well as dietary supplement. R...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155195/ https://www.ncbi.nlm.nih.gov/pubmed/28257115 http://dx.doi.org/10.3390/molecules22030387 |
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author | Liang, Chengyuan Ju, Weihui Pei, Shaomeng Tang, Yonghong Xiao, Yadong |
author_facet | Liang, Chengyuan Ju, Weihui Pei, Shaomeng Tang, Yonghong Xiao, Yadong |
author_sort | Liang, Chengyuan |
collection | PubMed |
description | Esculetin, synonymous with 6,7-dihydroxycoumarin, is the main active ingredient of the traditional Chinese medicine Cortex Fraxini. The twig skin or trunk bark of Cortex Fraxini are used by herb doctors as a mild, bitter liver and gallbladder meridians’ nontoxic drug as well as dietary supplement. Recently, with a variety of novel esculetin derivatives being reported, the molecular mechanism research as well as clinical application of Cortex Fraxini and esculetin are becoming more attractive. This mini-review will consolidate what is known about the biological activities, the mechanism of esculetin and its synthetic derivatives over the past decade in addition to providing a brief synopsis of the properties of esculetin. |
format | Online Article Text |
id | pubmed-6155195 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61551952018-11-13 Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review Liang, Chengyuan Ju, Weihui Pei, Shaomeng Tang, Yonghong Xiao, Yadong Molecules Review Esculetin, synonymous with 6,7-dihydroxycoumarin, is the main active ingredient of the traditional Chinese medicine Cortex Fraxini. The twig skin or trunk bark of Cortex Fraxini are used by herb doctors as a mild, bitter liver and gallbladder meridians’ nontoxic drug as well as dietary supplement. Recently, with a variety of novel esculetin derivatives being reported, the molecular mechanism research as well as clinical application of Cortex Fraxini and esculetin are becoming more attractive. This mini-review will consolidate what is known about the biological activities, the mechanism of esculetin and its synthetic derivatives over the past decade in addition to providing a brief synopsis of the properties of esculetin. MDPI 2017-03-02 /pmc/articles/PMC6155195/ /pubmed/28257115 http://dx.doi.org/10.3390/molecules22030387 Text en © 2017 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 Liang, Chengyuan Ju, Weihui Pei, Shaomeng Tang, Yonghong Xiao, Yadong Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review |
title | Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review |
title_full | Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review |
title_fullStr | Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review |
title_full_unstemmed | Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review |
title_short | Pharmacological Activities and Synthesis of Esculetin and Its Derivatives: A Mini-Review |
title_sort | pharmacological activities and synthesis of esculetin and its derivatives: a mini-review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6155195/ https://www.ncbi.nlm.nih.gov/pubmed/28257115 http://dx.doi.org/10.3390/molecules22030387 |
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