IFI-27 Activators are primarily composed of DNA methyltransferase inhibitors, histone deacetylase inhibitors, and bromodomain inhibitors. The DNA methyltransferase inhibitors, such as 5-Azacytidine and Decitabine, function by reducing DNA methylation levels, potentially leading to the demethylation of the IFI-27 gene promoter. This demethylation can enhance the gene expression of IFI-27, leading to increased functional activity of the protein.
Histone deacetylase inhibitors, including Vorinostat, Entinostat, Romidepsin, and Trichostatin A, promote the acetylation of histones. This acetylation leads to a more relaxed chromatin state and enhanced gene expression. This process can enhance IFI-27 functional activity by promoting its gene expression. Bromodomain inhibitors such as JQ1, I-BET151, GSK525762, I-BET762, PFI-1, and CPI-0610 disrupt the binding of bromodomain proteins to acetylated histones. This disruption can lead to changes in gene expression, potentially enhancing the functional activity of IFI-27. These diverse compounds offer various means to enhance the functional activity of IFI-27, demonstrating the interconnectivity of cellular signaling networks and the potential influence these activators can exert on the functionality of IFI-27.
Items 11 to 11 of 11 total
Display:
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
---|---|---|---|---|---|---|
CPI-0610 | 1380087-89-7 | sc-507490 | 10 mg | $495.00 | ||
CPI-0610 is another bromodomain inhibitor. Its action can disrupt the binding of bromodomain proteins to acetylated histones, potentially enhancing IFI-27 functional activity. |