WBSCR19 inhibitors are a class of chemical compounds that specifically target and inhibit the function of the WBSCR19 protein. The acronym WBSCR19 stands for Williams-Beuren Syndrome Chromosomal Region 19, indicating that the gene encoding this protein is located within a region that is commonly deleted in individuals with Williams-Beuren Syndrome, a complex developmental disorder. The WBSCR19 protein itself is involved in multiple cellular processes, although its precise biological functions are not fully elucidated. Inhibitors of this protein may alter various molecular pathways by interfering with its normal activity. The chemical structure and properties of WBSCR19 inhibitors can vary widely, but they share the common feature of being able to bind to the WBSCR19 protein in some capacity, affecting its interaction with other cellular components.
The development and study of WBSCR19 inhibitors involve sophisticated chemical and biological techniques to ensure specificity and efficacy. Researchers often utilize high-throughput screening methods to identify potential inhibitors from large libraries of compounds, followed by iterative cycles of optimization through medicinal chemistry. Binding assays, X-ray crystallography, and computational modeling are commonly employed to explore the interaction between the inhibitors and the WBSCR19 protein at the molecular level. These studies help to refine the inhibitors' chemical structures to improve their ability to interact with the protein's active site or allosteric sites. As with any class of protein inhibitors, the stability, solubility, and selectivity of WBSCR19 inhibitors are critical parameters that are rigorously assessed during the development process to ensure that these molecules can effectively reach their target within the complex cellular environment.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Thalidomide | 50-35-1 | sc-201445 sc-201445A | 100 mg 500 mg | $109.00 $350.00 | 8 | |
Thalidomide, through its cereblon-binding, affects the ubiquitin ligase activity of the E3 complex. This can lead to altered protein degradation pathways, which may indirectly influence WBSCR19 activity if it is subject to regulation by ubiquitination. | ||||||