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Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment

The targeting of protein kinases has great future potential for the design of new drugs against cardiovascular diseases (CVDs). Enormous efforts have been made toward achieving this aim. Unfortunately, kinase inhibitors designed to treat CVDs have suffered from numerous limitations such as poor sele...

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Autores principales: Shahin, Rand, Shaheen, Omar, El-Dahiyat, Faris, Habash, Maha, Saffour, Sana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Science Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674217/
https://www.ncbi.nlm.nih.gov/pubmed/29134113
http://dx.doi.org/10.4155/fsoa-2017-0010
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author Shahin, Rand
Shaheen, Omar
El-Dahiyat, Faris
Habash, Maha
Saffour, Sana
author_facet Shahin, Rand
Shaheen, Omar
El-Dahiyat, Faris
Habash, Maha
Saffour, Sana
author_sort Shahin, Rand
collection PubMed
description The targeting of protein kinases has great future potential for the design of new drugs against cardiovascular diseases (CVDs). Enormous efforts have been made toward achieving this aim. Unfortunately, kinase inhibitors designed to treat CVDs have suffered from numerous limitations such as poor selectivity, bad permeability and toxicity. So, where are we now in terms of discovering effective kinase targeting drugs to treat CVDs? Various drug design techniques have been approached for this purpose since the discovery of the inhibitory activity of Staurosporine against protein kinase C in 1986. This review aims to provide context for the status of several emerging classes of direct kinase modulators to treat CVDs and discuss challenges that are preventing scientists from finding new kinase drugs to treat heart disease.
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spelling pubmed-56742172017-11-13 Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment Shahin, Rand Shaheen, Omar El-Dahiyat, Faris Habash, Maha Saffour, Sana Future Sci OA Review The targeting of protein kinases has great future potential for the design of new drugs against cardiovascular diseases (CVDs). Enormous efforts have been made toward achieving this aim. Unfortunately, kinase inhibitors designed to treat CVDs have suffered from numerous limitations such as poor selectivity, bad permeability and toxicity. So, where are we now in terms of discovering effective kinase targeting drugs to treat CVDs? Various drug design techniques have been approached for this purpose since the discovery of the inhibitory activity of Staurosporine against protein kinase C in 1986. This review aims to provide context for the status of several emerging classes of direct kinase modulators to treat CVDs and discuss challenges that are preventing scientists from finding new kinase drugs to treat heart disease. Future Science Ltd 2017-08-08 /pmc/articles/PMC5674217/ /pubmed/29134113 http://dx.doi.org/10.4155/fsoa-2017-0010 Text en © 2017 Rand Shahin This work is licensed under the Creative Commons Attribution 4.0 License (http://creativecommons.org/licenses/by/4.0/)
spellingShingle Review
Shahin, Rand
Shaheen, Omar
El-Dahiyat, Faris
Habash, Maha
Saffour, Sana
Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment
title Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment
title_full Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment
title_fullStr Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment
title_full_unstemmed Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment
title_short Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment
title_sort research advances in kinase enzymes and inhibitors for cardiovascular disease treatment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674217/
https://www.ncbi.nlm.nih.gov/pubmed/29134113
http://dx.doi.org/10.4155/fsoa-2017-0010
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