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.

PubMed
Abstract

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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