Challenges in design of biochemical assays for the identification of small molecules to target multiple conformations of protein kinases.
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Chene, Patrick (2008) Challenges in design of biochemical assays for the identification of small molecules to target multiple conformations of protein kinases. Drug Discovery Today, 13 (11-12). pp. 522-529. ISSN 1359-6446
Abstract
Protein kinases are under intense investigation because they play an important part in human diseases. Recent advances in structural biology and medicinal chemistry show that in addition to the adenosine triphosphate binding site, other 'druggable' pockets are formed at their surface when they adopt specific conformations. These findings open up the possibility of designing compounds with new modes of binding. The identification of these new inhibitors requires assays to be designed that allow the conformational flexibility of these enzymes to be better exploited. This review describes how biochemical assays can be adopted to explore these new drug design strategies.
| Item Type: | Article |
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| Additional Information: | author can archive post-print (ie final draft post-refereeing); Publisher's version/PDF cannot be used |
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| Date Deposited: | 14 Dec 2009 13:53 |
| Last Modified: | 31 Jan 2013 01:06 |
| URI: | https://oak.novartis.com/id/eprint/788 |