Yu Tao, Yang Yanyan, Yin De Qing, Hong Sungyoul, Son Young-Jin, Kim Jong-Hoon, Cho Jae Youl
a 1 Qingdao University, Medical College , Qingdao 266071, China.
b 2 Linyi Center for Disease Control and Prevention , Linyi 276000, China.
Expert Opin Ther Pat. 2015;25(12):1385-96. doi: 10.1517/13543776.2015.1081168. Epub 2015 Aug 19.
TANK-binding kinase 1 (TBK1) is a noncanonical IκB kinase family member that regulates the innate immune response. Misregulation of TBK1 activity can promote inflammatory disorders and oncogenesis; therefore, TBK1 inhibitors are considered a promising therapy for inflammation and cancer.
In this review, the authors provide information on the role of TBK1 in human health and on recently developed inhibitors from patents granted from 2011 to 2014. The reader will gain an understanding of the mechanisms of TBK1 function as well as the structure and biological activity of recently developed TBK1 inhibitors. Google and NCBI search engines were used to find relevant patents and clinical information using "TBK1 inhibitor" as the search term.
The role of TBK1 in various diseases has prompted the further investigation of significant targets. Although research on TBK1 inhibitors has increased over the last few years, only a few inhibitors of this kinase have been identified. In addition, almost all of the chemical inhibitors are modified from different scaffolds and/or chemotypes of pyrimidine. Specifically, compound BX795 is the representative one, which was first patented as a potent TBK1 inhibitor. Even though some compounds have displayed interesting potential inhibition and selectivity of TBK1 in vitro and in in vivo trials, the development of more efficient and selective TBK1 inhibitors is still required.
TANK结合激酶1(TBK1)是一种非典型的IκB激酶家族成员,可调节先天性免疫反应。TBK1活性的失调可促进炎症性疾病和肿瘤发生;因此,TBK1抑制剂被认为是治疗炎症和癌症的一种有前景的疗法。
在本综述中,作者提供了关于TBK1在人类健康中的作用以及2011年至2014年授予专利的最近开发的抑制剂的信息。读者将了解TBK1功能的机制以及最近开发的TBK1抑制剂的结构和生物活性。使用谷歌和NCBI搜索引擎,以“TBK1抑制剂”为搜索词查找相关专利和临床信息。
TBK1在各种疾病中的作用促使人们对重要靶点进行进一步研究。尽管在过去几年中对TBK1抑制剂的研究有所增加,但仅鉴定出了少数几种该激酶的抑制剂。此外,几乎所有化学抑制剂都是从嘧啶的不同支架和/或化学类型修饰而来。具体而言,化合物BX795是具有代表性的一种,它最初作为一种有效的TBK1抑制剂获得专利。尽管一些化合物在体外和体内试验中显示出对TBK1有趣的潜在抑制作用和选择性,但仍需要开发更有效和选择性更高的TBK1抑制剂。