NIH Chemical Genomics Center, NHGRI, National Institutes of Health, Bethesda, MD 20892-3370, USA.
Curr Top Med Chem. 2011;11(7):800-9. doi: 10.2174/156802611795165052.
Small molecule kinase inhibitors are important tools for studying cellular signaling pathways, phenotypes and are, occasionally, useful clinical agents. With stereochemistry pervasive throughout the molecules of life it is no surprise that a single stereocenter can bestow a ligand with distinct binding affinities to various protein targets. While the majority of small molecule kinase inhibitors reported to date are achiral, a number of asymmetric compounds show great utility as tools for probing kinase-associated biomolecular events as well as promising therapeutic leads. The mechanism by which chirality is introduced varies but includes screening of chiral libraries, incorporation of chiral centers during optimization efforts and the rational installation of a chiral moiety as guided by structural and modeling efforts. Here we discuss several advanced chiral small molecule kinase inhibitors where stereochemistry plays an important role in terms of potency and selectivity.
小分子激酶抑制剂是研究细胞信号通路、表型的重要工具,偶尔也可用作临床药物。由于立体化学在生命分子中无处不在,因此毫不奇怪,一个手性中心可以赋予配体与各种蛋白质靶标不同的结合亲和力。虽然迄今为止报道的大多数小分子激酶抑制剂都是无手性的,但一些不对称化合物作为研究与激酶相关的生物分子事件的工具以及有前途的治疗先导化合物具有很大的用处。引入手性的机制各不相同,但包括筛选手性库、在优化过程中引入手性中心以及在结构和建模的指导下合理安装手性部分。在这里,我们讨论了几种先进的手性小分子激酶抑制剂,其中立体化学在手性小分子激酶抑制剂的活性和选择性方面起着重要作用。