a Medicinal Chemistry and Pharmacology Division , CSIR - Indian Institute of Chemical Technology , Hyderabad , India.
b Chemical Science Division, Academy of Scientific & Innovative Research (AcSIR) , New Delhi , India.
Expert Opin Ther Pat. 2016;26(4):505-22. doi: 10.1517/13543776.2016.1159299. Epub 2016 Mar 15.
Inhibition of Bromodomain and Extra Terminal (BET) proteins is an emerging approach for developing advanced cancer therapeutics. In 2015, at least thirty patents have been published for developing cancer chemotherapeutics by targeting BET. Currently there are seven small molecule BET inhibitors in various stages of clinical trials for the development of anti-cancer drugs.
Important patents focusing on development of BET inhibitors as potential cancer therapeutics published in 2015 have been covered. The reports are presented together with a review of the related structural chemical space. This review mainly focuses on the therapeutic applications, chemical class and structural modifications along with the molecules currently in clinical trials.
BET sub-family proteins are one of the emerging targets to develop anti-cancer agents. Although many research groups have demonstrated the rationality of BET inhibition to combat cancer, a detailed molecular study needs to be performed to investigate the affected biological pathways. Selectivity among BET proteins should be kept in mind while developing BET inhibitors. In-silico molecular modelling studies can also provide valuable information for designing selective BET inhibitors towards anti-cancer drug discovery and development.
抑制溴结构域和末端结构域(BET)蛋白是开发先进癌症治疗方法的新兴途径。2015 年,至少有三十项专利已发表,旨在通过靶向 BET 来开发癌症化疗药物。目前,有七种小分子 BET 抑制剂处于癌症药物开发的各种临床试验阶段。
本文涵盖了 2015 年发表的针对 BET 抑制剂开发作为潜在癌症治疗药物的重要专利。报告与相关结构化学空间的综述一起呈现。该综述主要集中在治疗应用、化学类别和结构修饰以及目前正在临床试验中的分子上。
BET 亚家族蛋白是开发抗癌药物的新兴靶点之一。尽管许多研究小组已经证明 BET 抑制在对抗癌症方面的合理性,但需要进行详细的分子研究来研究受影响的生物途径。在开发 BET 抑制剂时,应注意 BET 蛋白之间的选择性。计算机分子建模研究也可以为设计针对抗癌药物发现和开发的选择性 BET 抑制剂提供有价值的信息。