Recent advances in the discovery of Src kinase inhibitors

被引:27
|
作者
Parang, K [1 ]
Sun, GQ
机构
[1] Univ Rhode Isl, Dept Biomed & Pharmaceut Sci, Kingston, RI 02881 USA
[2] Univ Rhode Isl, Coll Pharm, Dept Cell & Mol Biol, Kingston, RI 02881 USA
基金
美国国家卫生研究院;
关键词
cancer; drug discovery; inhibitor; myocardial infarction; osteoporosis; protein kinase; SH2; domain; Src; Src family kinase; tyrosine kinase;
D O I
10.1517/13543776.15.9.1183
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Src family kinases are involved in the regulation of a wide variety of normal cellular signal transcluction pathways, such as cell growth, differentiation, survival, adhesion and migration. Considerable evidence implicates elevated expression and/or activity of Src kinases in many human cancers, osteoporosis, cardiovascular disorders and immune system dysfunction; thus, this family of protein tyrosine kinases now exists as intriguing targets for both basic research and drug discovery. Herein, a number of examples of currently developed Src family kinase inhibitors in selected patents from 2002 - 2005 will be described. Special attention will be made to the chemical diversity of ATP binding site inhibitors, potency, selectivity and therapeutic application of the compounds.
引用
收藏
页码:1183 / 1207
页数:25
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