Journal
CURRENT PHARMACEUTICAL DESIGN
Volume 10, Issue 10, Pages 1083-1091Publisher
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1381612043452677
Keywords
structure-based drug design; PTK; SAR; BTK; JAK3; computational chemistry; inflammation; leukemia
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Many protein tyrosine kinases (PTK), including Janus kinase 3 (JAK3) and Bruton's tyrosine kinase (BTK), have been recently identified as potential drug targets to treat diverse diseases including inflammation and cancer. The wealth of structural information currently available for protein kinase-inhibitor complexes facilitates the structure-based design of novel kinase inhibitors. In this report, we discuss the structural basis of protein kinase inhibitor design and the common binding features of small molecule kinase inhibitors including pyridinyl imidazoles, purines, oxindoles, anilinoquinazolines and isoquinalines. The structural features of targeted kinase proteins and their inhibitor complexes are discussed with respect to their structure-and-activity relationships (SAR). We present a structural comparison of kinase inhibitors with a special emphasis on inhibitors of JAK3 and BTK.
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