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Synthesis of Indole Derived Protease-Activated Receptor 4 Antagonists and Characterization in Human Platelets

Protease activated receptor-4 (PAR4) is one of the thrombin receptors on human platelets and is a potential target for the management of thrombotic disorders. We sought to develop potent, selective, and novel PAR4 antagonists to test the role of PAR4 in thrombosis and hemostasis. Development of an e...

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Autores principales: Young, Summer E., Duvernay, Matthew T., Schulte, Michael L., Lindsley, Craig W., Hamm, Heidi E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679140/
https://www.ncbi.nlm.nih.gov/pubmed/23776495
http://dx.doi.org/10.1371/journal.pone.0065528
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author Young, Summer E.
Duvernay, Matthew T.
Schulte, Michael L.
Lindsley, Craig W.
Hamm, Heidi E.
author_facet Young, Summer E.
Duvernay, Matthew T.
Schulte, Michael L.
Lindsley, Craig W.
Hamm, Heidi E.
author_sort Young, Summer E.
collection PubMed
description Protease activated receptor-4 (PAR4) is one of the thrombin receptors on human platelets and is a potential target for the management of thrombotic disorders. We sought to develop potent, selective, and novel PAR4 antagonists to test the role of PAR4 in thrombosis and hemostasis. Development of an expedient three-step synthetic route to access a novel series of indole-based PAR4 antagonists also necessitated the development of a platelet based high-throughput screening assay. Screening and subsequent structure activity relationship analysis yielded several selective PAR4 antagonists as well as possible new scaffolds for future antagonist development.
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spelling pubmed-36791402013-06-17 Synthesis of Indole Derived Protease-Activated Receptor 4 Antagonists and Characterization in Human Platelets Young, Summer E. Duvernay, Matthew T. Schulte, Michael L. Lindsley, Craig W. Hamm, Heidi E. PLoS One Research Article Protease activated receptor-4 (PAR4) is one of the thrombin receptors on human platelets and is a potential target for the management of thrombotic disorders. We sought to develop potent, selective, and novel PAR4 antagonists to test the role of PAR4 in thrombosis and hemostasis. Development of an expedient three-step synthetic route to access a novel series of indole-based PAR4 antagonists also necessitated the development of a platelet based high-throughput screening assay. Screening and subsequent structure activity relationship analysis yielded several selective PAR4 antagonists as well as possible new scaffolds for future antagonist development. Public Library of Science 2013-06-11 /pmc/articles/PMC3679140/ /pubmed/23776495 http://dx.doi.org/10.1371/journal.pone.0065528 Text en © 2013 Young et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Young, Summer E.
Duvernay, Matthew T.
Schulte, Michael L.
Lindsley, Craig W.
Hamm, Heidi E.
Synthesis of Indole Derived Protease-Activated Receptor 4 Antagonists and Characterization in Human Platelets
title Synthesis of Indole Derived Protease-Activated Receptor 4 Antagonists and Characterization in Human Platelets
title_full Synthesis of Indole Derived Protease-Activated Receptor 4 Antagonists and Characterization in Human Platelets
title_fullStr Synthesis of Indole Derived Protease-Activated Receptor 4 Antagonists and Characterization in Human Platelets
title_full_unstemmed Synthesis of Indole Derived Protease-Activated Receptor 4 Antagonists and Characterization in Human Platelets
title_short Synthesis of Indole Derived Protease-Activated Receptor 4 Antagonists and Characterization in Human Platelets
title_sort synthesis of indole derived protease-activated receptor 4 antagonists and characterization in human platelets
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3679140/
https://www.ncbi.nlm.nih.gov/pubmed/23776495
http://dx.doi.org/10.1371/journal.pone.0065528
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