Boehringer Ingelheim Pharmaceuticals, Department of Medicinal Chemistry, Inc., 900 Ridgebury Rd. Ridgefield, CT 06801-0368, USA.
Expert Opin Ther Pat. 2010 Feb;20(2):193-212. doi: 10.1517/13543770903496442.
Pim kinases have recently emerged as targets of interest in oncology and immune regulation. Ongoing studies have identified a role for these proteins in cell survival and proliferation, both functionally and mechanistically, and overexpression has been observed in a number of human cancers and inflammatory states.
This report reviews the patent literature for Pim kinase inhibitors identified from a search of the Thomson patent databases from 1970 through July 2009. Full analyses are provided for publications reporting Pim kinases as primary targets, and a cursory description is given for those disclosing Pim as one of a limited number of secondary targets.
Readers will gain an overview of the various inhibitor series including coverage, potency, selectivity, protein binding features and therapeutic focus, and an appreciation for which scaffolds and structural features have been most highly exploited.
A greater understanding of pathological mechanisms for Pim kinases has stimulated the recent development of a variety of inhibitor classes with one compound advancing into the clinic earlier this year. Ongoing studies will help define applications for these inhibitors in the treatment of Pim-associated human diseases.
Pim 激酶已成为肿瘤学和免疫调节的研究热点。正在进行的研究已经确定了这些蛋白质在细胞存活和增殖中的作用,无论是在功能上还是在机制上,并且在许多人类癌症和炎症状态中都观察到了它们的过度表达。
这篇综述涵盖了从 1970 年到 2009 年 7 月通过汤姆森专利数据库搜索到的 Pim 激酶抑制剂的专利文献。对报道 Pim 激酶为主要靶点的出版物进行了全面分析,并对那些仅将 Pim 作为少数次要靶点之一披露的出版物进行了简要描述。
读者将获得对各种抑制剂系列的概述,包括覆盖范围、效力、选择性、蛋白质结合特性和治疗重点,并了解哪些支架和结构特征得到了最充分的利用。
对 Pim 激酶病理机制的更深入了解刺激了各种抑制剂类别的近期发展,其中一种化合物今年早些时候进入临床。正在进行的研究将有助于确定这些抑制剂在治疗与 Pim 相关的人类疾病中的应用。