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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...

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Detalles Bibliográficos
Autores principales: Cui, Jian, Hu, Le’An, Shi, Wei, Cui, Guozhen, Zhang, Xumu, Zhang, Qing-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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.
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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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