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10.4155/fsoa-2017-0010

http://scihub22266oqcxt.onion/10.4155/fsoa-2017-0010
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C5674217!5674217!29134113
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suck abstract from ncbi


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pmid29134113      Future+Sci+OA 2017 ; 3 (4): ä
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  • Research advances in kinase enzymes and inhibitors for cardiovascular disease treatment #MMPMID29134113
  • Shahin R; Shaheen O; El-Dahiyat F; Habash M; Saffour S
  • Future Sci OA 2017[Nov]; 3 (4): ä PMID29134113show ga
  • 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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