Progress in the development of inhibitors of SH2 domains

被引:59
|
作者
Cody, WL [1 ]
Lin, ZW
Panek, RL
Rose, DW
Rubin, JR
机构
[1] Warner Lambert Parke Davis, Parke Davis Pharmaceut Res, Dept Chem, Ann Arbor, MI 48105 USA
[2] Warner Lambert Parke Davis, Parke Davis Pharmaceut Res, Dept Cardiovasc Therapeut, Ann Arbor, MI 48105 USA
[3] Univ Calif San Diego, Dept Med, Whittier Diabet Program, Vet Adm Res Fdn, La Jolla, CA 92093 USA
关键词
D O I
10.2174/1381612003401532
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
SH2 domains are discrete structural motifs common to a variety of critical intracellular signaling proteins. Inhibitors of specific SH2 domains have become important therapeutic targets in the treatment and/or prevention of restenosis, cancers (including small cell lung), cardiovascular disease, osteoporosis, apoptosis among others. Considering the social and economic impact of these diseases significant attention has been focused on the development of potent and selective inhibitors of specific SH2 domains. In particular, considerable research has been performed on Src, PI 3-kinase, Grb2 and more recently, Lck. In this review, we will focus on progress in the development of inhibitors for these specific SH2 domains and evaluate potential future targets.
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收藏
页码:59 / 98
页数:40
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