Department of Chemistry, Technical University of Denmark, DK-2800 Kgs. Lyngby, Denmark.
Protein and Peptide Chemistry, Novo Nordisk A/S, DK-2760 Måløv, Denmark.
Trends Pharmacol Sci. 2015 Jul;36(7):422-39. doi: 10.1016/j.tips.2015.04.005. Epub 2015 May 12.
Kinases have emerged as one of the most intensively pursued targets in current pharmacological research, especially for cancer, due to their critical roles in cellular signaling. To date, the US FDA has approved 28 small-molecule kinase inhibitors, half of which were approved in the past 3 years. While the clinical data of these approved molecules are widely presented and structure-activity relationship (SAR) has been reported for individual molecules, an updated review that analyzes all approved molecules and summarizes current achievements and trends in the field has yet to be found. Here we present all approved small-molecule kinase inhibitors with an emphasis on binding mechanism and structural features, summarize current challenges, and discuss future directions in this field.
激酶已成为当前药理学研究中最受关注的靶点之一,尤其是在癌症领域,因为它们在细胞信号转导中起着关键作用。迄今为止,美国 FDA 已批准了 28 种小分子激酶抑制剂,其中一半是在过去 3 年内批准的。虽然这些已批准分子的临床数据已广泛呈现,并且针对个别分子的构效关系 (SAR) 已有报道,但尚未发现对所有已批准分子进行分析并总结该领域当前成就和趋势的更新综述。在这里,我们重点介绍了所有已批准的小分子激酶抑制剂,包括其结合机制和结构特征,总结了当前的挑战,并讨论了该领域的未来发展方向。