Design and discovery of small molecules targeting Raf-1 kinase

被引:145
作者
Lowinger, TB [1 ]
Riedl, B [1 ]
Dumas, J [1 ]
Smith, RA [1 ]
机构
[1] Bayer Corp, Div Pharmaceut, Bayer Res Ctr, West Haven, CT 06516 USA
关键词
diphenyl ureas; BAY; 43-9006; Raf-1; kinase; cancer; Ras;
D O I
10.2174/1381612023393125
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Raf kinase, an enzyme which acts downstream in the Ras signaling pathway, is involved in cancerous cell proliferation. Thus, small molecule inhibitors of Raf kinase activity may be important agents for the treatment of cancer. A novel class of Raf-1 inhibitors was discovered, using a combination of medicinal and combinatorial chemistry approaches. This effort culminated in the identification of the clinical candidate BAY 43-9006, currently undergoing Phase I clinical trials. The present review summarizes the medicinal chemistry development of ureas as highly potent inhibitors of Raf-1 kinase.
引用
收藏
页码:2269 / 2278
页数:10
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