Zfp866 inhibitors represent a class of chemical compounds that target the activity of Zfp866, a zinc finger protein. Zinc finger proteins are a large family of transcription factors characterized by the presence of zinc finger domains, which typically bind DNA, RNA, or proteins to regulate gene expression. Zfp866 is part of this family and is involved in various cellular processes, including gene transcription, chromatin remodeling, and possibly the regulation of specific signaling pathways. Zfp866 inhibitors function by interfering with the normal activity of the Zfp866 protein, potentially by preventing its binding to target nucleic acids or other molecular partners. These inhibitors can influence the downstream genetic and molecular effects that arise from Zfp866's activity, making them important for understanding the regulatory networks controlled by this specific zinc finger protein. The exact molecular mechanisms of these inhibitors often depend on their structure, which determines how they interact with the zinc finger domains or other functional regions of Zfp866.
The design and synthesis of Zfp866 inhibitors typically involve structure-based approaches, leveraging knowledge of the protein's zinc finger domains and their binding affinities. Researchers often employ techniques such as crystallography or computational modeling to predict how small molecules can disrupt these interactions. Such inhibitors may contain motifs that can mimic the natural ligands of Zfp866 or introduce steric hindrance, preventing the protein from accessing its targets. The chemical composition of these inhibitors can vary, but they often possess specific functional groups that enhance their binding specificity and affinity toward Zfp866. These compounds may also be subject to further chemical modification to improve their stability, solubility, and selectivity. Through detailed biochemical assays, researchers can evaluate how these inhibitors affect Zfp866's role in gene regulation, offering valuable insights into the protein's broader functions within cellular systems.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
XAV939 | 284028-89-3 | sc-296704 sc-296704A sc-296704B | 1 mg 5 mg 50 mg | $35.00 $115.00 $515.00 | 26 | |
XAV939, a tankyrase inhibitor, directly targets tankyrase enzymes. Inhibition of tankyrase disrupts the Wnt/β-catenin pathway, which interacts with Zfp866. XAV939 indirectly influences Zfp866 by preventing its modulation through the Wnt/β-catenin pathway. | ||||||
IWR-1-endo | 1127442-82-3 | sc-295215 sc-295215A | 5 mg 10 mg | $82.00 $132.00 | 19 | |
IWR-1, a tankyrase inhibitor, directly targets tankyrase enzymes. Inhibition of tankyrase disrupts the Wnt/β-catenin pathway, which interacts with Zfp866. IWR-1 indirectly influences Zfp866 by preventing its modulation through the Wnt/β-catenin pathway. | ||||||
G007-LK | 1380672-07-0 | sc-507467 | 1 mg | $48.00 | ||
G007-LK, a tankyrase inhibitor, directly targets tankyrase enzymes. Inhibition of tankyrase disrupts the Wnt/β-catenin pathway, which interacts with Zfp866. G007-LK indirectly influences Zfp866 by preventing its modulation through the Wnt/β-catenin pathway. | ||||||
JW 55 | 664993-53-7 | sc-364517 sc-364517A | 10 mg 50 mg | $172.00 $726.00 | ||
JW55, a tankyrase inhibitor, directly targets tankyrase enzymes. Inhibition of tankyrase disrupts the Wnt/β-catenin pathway, which interacts with Zfp866. JW55 indirectly influences Zfp866 by preventing its modulation through the Wnt/β-catenin pathway. | ||||||
WIKI4 | 838818-26-1 | sc-397021 sc-397021A | 5 mg 25 mg | $90.00 $351.00 | ||
WIKI4, a tankyrase inhibitor, directly targets tankyrase enzymes. Inhibition of tankyrase disrupts the Wnt/β-catenin pathway, which interacts with Zfp866. WIKI4 indirectly influences Zfp866 by preventing its modulation through the Wnt/β-catenin pathway. | ||||||