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Updated: Apr 15, 2026

Fluorescence-based Monitoring of PAD4 Activity via a Pro-fluorescence Substrate Analog
Published on: November 5, 2014
An updated patent review of BRD4 degraders
Zonghui Ma1, Cun Zhang1, Andrew A Bolinger1
1Chemical Biology Program, Department of Pharmacology and Toxicology, University of Texas Medical Branch (UTMB), Galveston, TX, USA.
Introduction:
Bromodomain-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 Covered:
The 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 Opinion:
BRD4 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.
Insights
Small molecule degraders targeting Bromodomain-containing protein 4 (BRD4) offer a promising therapeutic strategy for various diseases, including cancer. These degraders show superior efficacy and selectivity compared to inhibitors, with one candidate in clinical trials.
Area of Science:
- Epigenetics
- Molecular Biology
- Drug Discovery
Background:
- Bromodomain-containing protein 4 (BRD4) is implicated in diseases like cancer and inflammation.
- Targeting BRD4 through inhibition or degradation is a key therapeutic strategy.
Purpose of the Study:
- To summarize recent advances in patented BRD4 degraders.
- To discuss challenges, opportunities, and future directions for novel BRD4 degrader development.
Main Methods:
- Patents for BRD4 degraders were identified using SciFinder and Cortellis Drug Discovery Intelligence databases.
Main Results:
- BRD4 degraders demonstrate enhanced efficacy and selectivity over BRD4 inhibitors due to their protein degradation mechanism.
- A BRD4 degrader, RNK05047, is currently undergoing Phase I/II clinical trials.
Conclusions:
- Selective BRD4 protein degradation represents a viable therapeutic approach, especially for cancer treatment.
- Small-molecule BRD4 degraders hold potential for overcoming therapeutic resistance in BRD4-associated diseases.
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