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Development of Orally Active Thrombin Inhibitors for the Treatment of Thrombotic Disorder Diseases

Thrombotic disorders represent the major share of the various cardiovascular diseases, and significant progress has been made in the development of synthetic thrombin inhibitors as new anticoagulants. In addition to the development of highly potent and selective inhibitors with improved safety and s...

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Autores principales: He, Li-Wei, Dai, Wei-Chen, Li, Nian-Guang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272601/
https://www.ncbi.nlm.nih.gov/pubmed/26083038
http://dx.doi.org/10.3390/molecules200611046
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author He, Li-Wei
Dai, Wei-Chen
Li, Nian-Guang
author_facet He, Li-Wei
Dai, Wei-Chen
Li, Nian-Guang
author_sort He, Li-Wei
collection PubMed
description Thrombotic disorders represent the major share of the various cardiovascular diseases, and significant progress has been made in the development of synthetic thrombin inhibitors as new anticoagulants. In addition to the development of highly potent and selective inhibitors with improved safety and suitable half-life, several allosteric inhibitors have been designed and synthesized, that did not fully nullify the procoagulant signal and thus could result in reduced bleeding complications. Furthermore, natural products with thrombin inhibitory activity have been isolated, and some natural products have been modified in order to improve their inhibitory activity and metabolic stability. This review summarizes the development of orally active thrombin inhibitors for the treatment of thrombotic disorder diseases, which could serve as a reference for the interested researchers.
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spelling pubmed-62726012018-12-31 Development of Orally Active Thrombin Inhibitors for the Treatment of Thrombotic Disorder Diseases He, Li-Wei Dai, Wei-Chen Li, Nian-Guang Molecules Review Thrombotic disorders represent the major share of the various cardiovascular diseases, and significant progress has been made in the development of synthetic thrombin inhibitors as new anticoagulants. In addition to the development of highly potent and selective inhibitors with improved safety and suitable half-life, several allosteric inhibitors have been designed and synthesized, that did not fully nullify the procoagulant signal and thus could result in reduced bleeding complications. Furthermore, natural products with thrombin inhibitory activity have been isolated, and some natural products have been modified in order to improve their inhibitory activity and metabolic stability. This review summarizes the development of orally active thrombin inhibitors for the treatment of thrombotic disorder diseases, which could serve as a reference for the interested researchers. MDPI 2015-06-15 /pmc/articles/PMC6272601/ /pubmed/26083038 http://dx.doi.org/10.3390/molecules200611046 Text en © 2015 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 Review
He, Li-Wei
Dai, Wei-Chen
Li, Nian-Guang
Development of Orally Active Thrombin Inhibitors for the Treatment of Thrombotic Disorder Diseases
title Development of Orally Active Thrombin Inhibitors for the Treatment of Thrombotic Disorder Diseases
title_full Development of Orally Active Thrombin Inhibitors for the Treatment of Thrombotic Disorder Diseases
title_fullStr Development of Orally Active Thrombin Inhibitors for the Treatment of Thrombotic Disorder Diseases
title_full_unstemmed Development of Orally Active Thrombin Inhibitors for the Treatment of Thrombotic Disorder Diseases
title_short Development of Orally Active Thrombin Inhibitors for the Treatment of Thrombotic Disorder Diseases
title_sort development of orally active thrombin inhibitors for the treatment of thrombotic disorder diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272601/
https://www.ncbi.nlm.nih.gov/pubmed/26083038
http://dx.doi.org/10.3390/molecules200611046
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