Research Advances in Kinase Enzymes and Inhibitors for Cardiovascular Disease Treatment
Author(s) -
Rand Shahin,
Omar Shaheen,
Faris ElDahiyat,
Maha Habash,
Sana Saffour
Publication year - 2017
Publication title -
future science oa
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 23
ISSN - 2056-5623
DOI - 10.4155/fsoa-2017-0010
Subject(s) - medicine , staurosporine , pharmacology , kinase , disease , context (archaeology) , drug discovery , protein kinase a , drug , bioinformatics , biology , biochemistry , paleontology
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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