CW-3308 is a cereblon-recruiting BRD9 PROTAC degrader developed through optimization of BRD9-directed degrader scaffolds. Public literature describes it as a potent, selective, and orally bioavailable BRD9 degrader with high selectivity over BRD7 and BRD4 in reported cellular systems. The BRD9-recognition element binds the bromodomain target, while the cereblon ligand recruits CRL4-cereblon; the linker organizes the target and E3 ligase into a ternary complex that enables ubiquitination. Mechanistically, CW-3308 induces BRD9 degradation through cereblon-dependent ubiquitination and proteasomal removal, thereby perturbing BRD9-associated chromatin-regulatory functions. It is valuable for studying BRD9 biology, SWI/SNF-associated bromodomain function, rhabdoid tumor and synovial sarcoma research models, BRD9 versus BRD7 selectivity, orally active degrader optimization, and the design of cereblon-based probes for epigenetic reader proteins.
Structure of 3055592-99-6
* For research and manufacturing use only. Not for human or clinical use.
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Target: CW-3308 selectively targets BRD9, a SWI/SNF-associated bromodomain protein.
Binding site: Its BRD9 ligand binds the bromodomain acetyl-lysine recognition pocket.
Mechanism of action: CW-3308 is a cereblon-recruiting BRD9 PROTAC optimized for potent and selective BRD9 degradation. It contains a BRD9 bromodomain ligand, a linker, and a thalidomide-derived CRBN ligand, allowing BRD9 recruitment to CRL4CRBN ubiquitin ligase machinery. Productive ternary-complex formation drives BRD9 ubiquitination and proteasome-dependent depletion while maintaining selectivity over related bromodomain proteins such as BRD7 and BRD4 in reported studies. CW-3308 is useful for studying BRD9-dependent chromatin regulation, SWI/SNF-associated transcriptional programs, degradation selectivity, and cellular responses in BRD9-dependent tumor models.
Applications• PROTAC-Mediated Kinase Degradation: CW-3308 is designed for the targeted degradation of specific kinases, allowing researchers to dissect kinase signaling pathways and their roles in cellular processes. This application aids in elucidating the mechanisms of kinase-related diseases and developing novel therapeutic strategies.
• Targeted Degradation in Cancer Research: By employing CW-3308, researchers can selectively degrade oncogenic proteins, providing insights into cancer cell biology and potential vulnerabilities. This approach facilitates the identification of new drug targets and the development of innovative cancer treatments.
• Studying Protein-Protein Interactions: CW-3308 enables the targeted degradation of proteins involved in critical protein-protein interactions. This application helps uncover the functional relevance of these interactions in various biological contexts, advancing our understanding of cellular dynamics and disease mechanisms.
• Investigating Protein Stability: Utilizing CW-3308 allows scientists to explore the stability and turnover of target proteins. This application is essential for studying protein homeostasis and its impact on cellular function, offering valuable information for drug discovery and development.
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
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