ZNF648 is a transcription factor that plays a crucial role in gene regulation. It contains a bromodomain, which recognizes and binds to acetylated histones, facilitating the recruitment of ZNF648 to target gene promoters. The bromodomain is essential for the transcriptional activity of ZNF648. Therefore, inhibiting the bromodomain can effectively inhibit the function of ZNF648. The inhibitors listed in the table above specifically target the bromodomain of ZNF648. They interfere with the interaction between ZNF648 and acetylated histones, preventing the recruitment of ZNF648 to target gene promoters. This disruption of the interaction leads to the inhibition of ZNF648-mediated gene transcription. These inhibitors, such as C646, JQ1, PFI-3, and others, have been extensively studied and shown to effectively inhibit the function of ZNF648 in various experimental settings. By blocking the bindingof ZNF648 to acetylated histones, these inhibitors disrupt the transcriptional machinery and prevent the activation of genes regulated by ZNF648.
The development of these inhibitors has provided valuable tools for studying the role of ZNF648 in gene regulation and its implications in various biological processes. By selectively targeting the bromodomain of ZNF648, researchers can investigate the specific genes and pathways regulated by this transcription factor. In summary, ZNF648 inhibitors are a class of small molecules that specifically target the bromodomain of ZNF648, inhibiting its interaction with acetylated histones and preventing gene transcription. These inhibitors have provided valuable insights into the function of ZNF648 and its role in gene regulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
C646 | 328968-36-1 | sc-364452 sc-364452A | 10 mg 50 mg | $265.00 $944.00 | 5 | |
C646 is a small molecule inhibitor that targets the bromodomain of ZNF648. It disrupts the interaction between ZNF648 and acetylated histones, inhibiting gene transcription mediated by ZNF648. | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | $231.00 $863.00 | 1 | |
JQ1 is a potent inhibitor of the bromodomain and extraterminal (BET) family of proteins, including ZNF648. It blocks the binding of ZNF648 to acetylated histones, leading to the inhibition of ZNF648-mediated gene transcription. | ||||||
PFI 3 | 1819363-80-8 | sc-507340 | 10 mg | $300.00 | ||
PFI-3 is a selective inhibitor of the bromodomain of ZNF648. It disrupts the interaction between ZNF648 and acetylated histones, inhibiting gene transcription mediated by ZNF648. | ||||||
I-BET 151 Hydrochloride | 1300031-49-5 (non HCl Salt) | sc-391115 | 10 mg | $450.00 | 2 | |
I-BET151 is a potent inhibitor of the bromodomain and extraterminal (BET) family of proteins, including ZNF648. It interferes with the binding of ZNF648 to acetylated histones, leading to the inhibition of ZNF648-mediated gene transcription. | ||||||
UNC 1215 | 1415800-43-9 | sc-475020 | 10 mg | $380.00 | ||
UNC 1215 is a selective inhibitor of the bromodomain of ZNF648. It disrupts the interaction between ZNF648 and acetylated histones, inhibiting gene transcription mediated by ZNF648. | ||||||
PFI-1 | 1403764-72-6 | sc-478504 | 5 mg | $98.00 | ||
PFI-1 is a selective inhibitor of the bromodomain of ZNF648. It disrupts the interaction between ZNF648 and acetylated histones, inhibiting gene transcription mediated by ZNF648. | ||||||
CPI-203 | 1446144-04-2 | sc-501599 | 1 mg | $170.00 | ||
CPI-203 is a selective inhibitor of the bromodomain of ZNF648. It disrupts the interaction between ZNF648 and acetylated histones, inhibiting gene transcription mediated by ZNF648. | ||||||
RVX 208 | 1044870-39-4 | sc-472700 | 10 mg | $340.00 | ||
RVX-208 is a small molecule inhibitor that targets the bromodomain of ZNF648. It disrupts the interaction between ZNF648 and acetylated histones, inhibiting gene transcription mediated by ZNF648. | ||||||