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Recent Progress of Src SH2 and SH3 Inhibitors as Anticancer Agents

期刊

CURRENT MEDICINAL CHEMISTRY
卷 17, 期 12, 页码 1117-1124

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/092986710790827861

关键词

Protein tyrosine kinases; Src kinases; SH2; SH3; inhibitor; peptidomimetic; nonpeptide; progress

资金

  1. National Hi-tech RD Program [2007AA091501, 2006AA09Z416, 2006AA09Z425]

向作者/读者索取更多资源

Src family tyrosine kinases (SFKs) play key roles in regulating signal transduction in cellular processes. However, hyper-activated SFKs lead to uncontrolled cell proliferation and cancers. For both Src SH2 and SH3 domains involve in the regulation of tumorigenesis signal pathways, the SH2 and SH3 inhibition strategies are expected to block the protein-protein interactions between SFKs and their corporation proteins to abolish the signal transduction. Many inhibitors of SH2 and SH3 domain have been identified. Herein, some predominant examples of these inhibitors are reviewed.

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