BRD7 inhibitors represent a class of small molecules designed to specifically target and modulate the activity of Bromodomain-containing protein 7 (BRD7). BRD7 is a member of the bromodomain and extra-terminal (BET) protein family, which plays a crucial role in regulating gene expression through its interaction with acetylated histones. These proteins are known to be involved in various cellular processes, including transcriptional regulation, cell cycle control, and chromatin remodeling. BRD7, in particular, has gained attention in recent years due to its implication in several diseases.
The mechanism of BRD7 inhibitors revolves around their ability to bind to the bromodomain pocket of BRD7. This interaction disrupts the binding of BRD7 to acetylated histones, leading to a downstream effect on gene expression. By inhibiting BRD7, these compounds can modulate the transcription of genes associated with diseases, offering a novel avenue for drug discovery and development. Researchers have been actively investigating various small molecules, peptides, and compounds with the aim of optimizing their binding affinity and selectivity for BRD7. Understanding the structural and functional aspects of BRD7 inhibitors is essential for elucidating their applications in various contexts, such as cancer research and other diseases linked to dysregulated gene expression.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
4-[(1E)-2-(2-Amino-4-hydroxy-5-methylphenyl)diazenyl]-N-2-pyridinylbenzenesulfonamide | 1395084-25-9 | sc-480120 | 5 mg | $300.00 | ||
Also called MS436, this compound is another small molecule inhibitor of BRD7 that has shown activity against BRD7-dependent cancer cells | ||||||
MS417 | 916489-36-6 | sc-507505 | 5 mg | $228.00 | ||
MS417 is a BRD7 inhibitor that has been explored for its role in modulating BRD7-mediated gene expression, particularly in the context of cancer. | ||||||