A patent review of BRD4 inhibitors (2020-present)

被引:0
|
作者
Chen, Yanfang [1 ]
Zhou, Huanmin [2 ]
Yu, Jiamin [3 ,4 ]
Gao, Jing [1 ]
Xue, Shengyu [3 ,4 ]
Ding, Hong [4 ]
Lin, Hua [1 ]
Luo, Cheng [2 ,3 ,4 ,5 ]
机构
[1] Fujian Normal Univ, Key Lab Microbial Pathogenesis & Intervent Fujian, Coll Life Sci, Biomed Res Ctr South China,Key Lab Innate Immune B, Fuzhou, Peoples R China
[2] Fujian Med Univ, Sch Pharm, Fuzhou, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Chinese Mat Med, Nanjing, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai, Peoples R China
[5] Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Pharmaceut Sci & Technol, Hangzhou, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
BET; BRD4; inhibitor; cancer treatment; selectivity; BROMODOMAIN PROTEIN BRD4; CANCER-CELLS; P-TEFB; BET; TARGET; MYC; DEGRADATION; IDENTIFICATION; DROSOPHILA; CARCINOMA;
D O I
10.1080/13543776.2025.2463150
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
IntroductionBromodomain-containing protein 4 (BRD4) stands as a pivotal member within the Bromodomain and Extra-Terminal Domain (BET) family, contributing significantly to epigenetic control and gene expression. Given its association with various cancers, BRD4 emerges as a promising therapeutic target, suggesting a substantial role in the treatment of diverse pathological conditions.Areas coveredThe present review is centered on patent applications concerning inhibitors targeting BRD4's bromodomain site, published from 2020 to present. A comprehensive evaluation was conducted on a total of 70 applications. The latest patented studies of BRD4 are summarized by using the keywords 'BRD4' in SciFinder, PubMed, and The lens Patents and databases in the year from 2020 to present.Expert opinionDespite the substantial progress achieved in the clinical research of numerous BET bromodomain inhibitors, their development remains fraught with challenges. To mitigate the dose-limiting toxicity (DLT) and other clinical adverse effects associated with pan-BET inhibitors, current research efforts are increasingly focus on the development of selective BRD4-BD1 or -BD2 inhibitors. These selective inhibitors exhibit considerable potential as more efficacious candidate drugs, thereby paving the way for novel avenues in both fundamental and translational research within this domain.
引用
收藏
页码:371 / 386
页数:16
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