Sch-66336 (Sarasar®) and other benzocycloheptapyridyl farnesyl protein transferase inhibitors:: Discovery, biology and clinical observations

被引:36
作者
Taveras, AG
Kirschmeier, P
Baum, CM
机构
[1] Schering Plough Res Inst, Dept Med Chem, Kenilworth, NJ 07033 USA
[2] Schering Plough Res Inst, Dept Oncol Biol, Kenilworth, NJ 07033 USA
[3] Schering Plough Res Inst, Dept Biol Clin, Kenilworth, NJ 07033 USA
关键词
D O I
10.2174/1568026033452104
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Farnesyl Protein Transferase as a target for therapeutic intervention is currently under investigation in human clinical trials. Sch-66336 (sarasar(R)), a benzocycloheptapyridyl Farnesyl Transferase Inhibitor (FTI), has been found to be effective in cellular proliferation assays and in in vivo oncology models both as a single agent and in combination with other anti-cancer agents. Clinically, early evidence is being generated that suggests efficacy in humans, particularly in patients with leukemia. Herein, we review the biology of FPT, the discovery of Sch-66336 and other benzocycloheptapyridyl FTIs, and the clinical evaluation of Sch-66336 for the treatment of leukemia and solid tumors.
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页码:1103 / 1114
页数:12
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