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Design, Synthesis and Anti-Platelet Aggregation Activity Study of Ginkgolide-1,2,3-triazole Derivatives
Ginkgolides are the major active component of Ginkgo biloba for inhibition of platelet activating factor receptor. An azide-alkyne Huisgen cycloaddition reaction was used to introduce a triazole nucleus into the target ginkgolide molecules. A series of ginkgolide-1,2,3-triazole conjugates with varie...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600273/ https://www.ncbi.nlm.nih.gov/pubmed/31181694 http://dx.doi.org/10.3390/molecules24112156 |
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author | Cui, Jian Hu, Le’An Shi, Wei Cui, Guozhen Zhang, Xumu Zhang, Qing-Wen |
author_facet | Cui, Jian Hu, Le’An Shi, Wei Cui, Guozhen Zhang, Xumu Zhang, Qing-Wen |
author_sort | Cui, Jian |
collection | PubMed |
description | Ginkgolides are the major active component of Ginkgo biloba for inhibition of platelet activating factor receptor. An azide-alkyne Huisgen cycloaddition reaction was used to introduce a triazole nucleus into the target ginkgolide molecules. A series of ginkgolide-1,2,3-triazole conjugates with varied functional groups including benzyl, phenyl and heterocycle moieties was thus synthesized. Many of the designed derivatives showed potent antiplatelet aggregation activities with IC(50) values of 5~21 nM. |
format | Online Article Text |
id | pubmed-6600273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66002732019-07-16 Design, Synthesis and Anti-Platelet Aggregation Activity Study of Ginkgolide-1,2,3-triazole Derivatives Cui, Jian Hu, Le’An Shi, Wei Cui, Guozhen Zhang, Xumu Zhang, Qing-Wen Molecules Article Ginkgolides are the major active component of Ginkgo biloba for inhibition of platelet activating factor receptor. An azide-alkyne Huisgen cycloaddition reaction was used to introduce a triazole nucleus into the target ginkgolide molecules. A series of ginkgolide-1,2,3-triazole conjugates with varied functional groups including benzyl, phenyl and heterocycle moieties was thus synthesized. Many of the designed derivatives showed potent antiplatelet aggregation activities with IC(50) values of 5~21 nM. MDPI 2019-06-07 /pmc/articles/PMC6600273/ /pubmed/31181694 http://dx.doi.org/10.3390/molecules24112156 Text en © 2019 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 Cui, Jian Hu, Le’An Shi, Wei Cui, Guozhen Zhang, Xumu Zhang, Qing-Wen Design, Synthesis and Anti-Platelet Aggregation Activity Study of Ginkgolide-1,2,3-triazole Derivatives |
title | Design, Synthesis and Anti-Platelet Aggregation Activity Study of Ginkgolide-1,2,3-triazole Derivatives |
title_full | Design, Synthesis and Anti-Platelet Aggregation Activity Study of Ginkgolide-1,2,3-triazole Derivatives |
title_fullStr | Design, Synthesis and Anti-Platelet Aggregation Activity Study of Ginkgolide-1,2,3-triazole Derivatives |
title_full_unstemmed | Design, Synthesis and Anti-Platelet Aggregation Activity Study of Ginkgolide-1,2,3-triazole Derivatives |
title_short | Design, Synthesis and Anti-Platelet Aggregation Activity Study of Ginkgolide-1,2,3-triazole Derivatives |
title_sort | design, synthesis and anti-platelet aggregation activity study of ginkgolide-1,2,3-triazole derivatives |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6600273/ https://www.ncbi.nlm.nih.gov/pubmed/31181694 http://dx.doi.org/10.3390/molecules24112156 |
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