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An updated patent review of BRD4 degraders
被引:3
|作者:
Ma, Zonghui
[1
]
Zhang, Cun
[1
]
Bolinger, Andrew A.
[1
]
Zhou, Jia
[1
]
机构:
[1] Univ Texas Med Branch UTMB, Dept Pharmacol & Toxicol, Chem Biol Program, Galveston, TX 77555 USA
基金:
美国国家卫生研究院;
关键词:
Bromodomain-containing protein 4 (BRD4);
epigenetic regulation;
disease therapeutics;
inhibitors;
degraders;
proteolysis-targeting chimera (PROTAC);
molecular glue (MG);
protein degradation;
BET BROMODOMAIN INHIBITORS;
P-TEFB;
HISTONE ACETYLTRANSFERASE;
TARGETING BROMODOMAIN;
PROTEIN-DEGRADATION;
THERAPEUTIC TARGET;
STRUCTURAL BASIS;
DRUG DISCOVERY;
CHROMATIN;
CANCER;
D O I:
10.1080/13543776.2024.2400166
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
IntroductionBromodomain-containing protein 4 (BRD4), an important epigenetic reader, is closely associated with the pathogenesis and development of many diseases, including various cancers, inflammation, and infectious diseases. Targeting BRD4 inhibition or protein elimination with small molecules represents a promising therapeutic strategy, particularly for cancer therapy.Areas coveredThe recent advances of patented BRD4 degraders were summarized. The challenges, opportunities, and future directions for developing novel potent and selective BRD4 degraders are also discussed. The patents of BRD4 degraders were searched using the SciFinder and Cortellis Drug Discovery Intelligence database.Expert opinionBRD4 degraders exhibit superior efficacy and selectivity to BRD4 inhibitors, given their unique mechanism of protein degradation instead of protein inhibition. Excitingly, RNK05047 is now in phase I/II clinical trials, indicating that selective BRD4 protein degradation may offer a viable therapeutic strategy, particularly for cancer. Targeting BRD4 with small-molecule degraders provides a promising approach with the potential to overcome therapeutic resistance for treating various BRD4-associated diseases.
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页码:929 / 951
页数:23
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