Dumas Jacques, Smith Roger A, Lowinger Timothy B
Bayer Research Center, Bayer Pharmaceutical Corporation, West Haven, CT 06516, USA.
Curr Opin Drug Discov Devel. 2004 Sep;7(5):600-16.
With two compounds on the market (Gleevec and Iressa), and a number of drug candidates in late-stage clinical trials, small-molecule kinase inhibitors hold great potential as novel therapies for cancer and inflammatory disorders. Inhibitors from the urea class were first reported in 1996 and have emerged as an important compound class for medicinal chemists due to their unique binding mode and kinase inhibition profile. Currently, five members of this class are undergoing clinical trials, BIRB-796 (Boehringer Ingelheim Pharmaceuticals Inc), BAY-43-9006 (Bayer AG/Onyx Pharmaceuticals Inc), CP-547632 (Pfizer Inc), MLN-518 (Millennium Pharmaceuticals Inc) and KRN-951 (Kirin Brewery Co Ltd). This review focuses on the most recent developments in the discovery of urea-based protein kinase inhibitors.
随着两种药物(格列卫和易瑞沙)上市,以及一些候选药物进入后期临床试验阶段,小分子激酶抑制剂作为癌症和炎症性疾病的新型疗法具有巨大潜力。脲类抑制剂于1996年首次报道,由于其独特的结合模式和激酶抑制谱,已成为药物化学家的一类重要化合物。目前,该类别的五种药物正在进行临床试验,分别是BIRB - 796(勃林格殷格翰制药公司)、BAY - 43 - 9006(拜耳公司/安进制药公司)、CP - 547632(辉瑞公司)、MLN - 518(千年制药公司)和KRN - 951(麒麟啤酒株式会社)。本综述重点关注基于脲的蛋白激酶抑制剂发现方面的最新进展。