EHZF inhibitors are a class of chemical compounds that specifically target and inhibit the activity of the enhancer of zeste homolog (EZH), a protein that plays a crucial role in gene regulation through chromatin modification. EHZF, often referred to in the context of EHZF-like proteins, is involved in the regulation of gene expression by modulating the structure of chromatin, making certain regions of the DNA more or less accessible for transcription. This modulation is critical for various cellular processes, including differentiation, development, and the maintenance of cellular identity. EHZF inhibitors interfere with these processes by blocking the enzymatic activity of EHZF proteins, thereby preventing the addition of methyl groups to histone proteins, a key mechanism by which these proteins exert their regulatory functions.
Inhibitors of EHZF are valuable tools in research aimed at understanding the complex dynamics of epigenetic regulation. By selectively inhibiting EHZF activity, researchers can study the specific roles that these proteins play in chromatin remodeling and gene expression. This can help uncover how changes in chromatin structure influence cellular behavior and contribute to the regulation of various biological processes. Additionally, EHZF inhibitors can be used to explore the broader network of interactions within the cell that are influenced by chromatin state, providing insights into how epigenetic modifications are coordinated and maintained. These inhibitors are particularly useful in experiments designed to probe the mechanisms underlying gene silencing and activation, as well as in studies focused on the long-term stability of gene expression patterns across different cell types and developmental stages. Overall, EHZF inhibitors are powerful tools for advancing our understanding of epigenetics and the intricate molecular mechanisms that regulate gene expression in eukaryotic cells.
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| Nom du produit | CAS # | Ref. Catalogue | Quantité | Prix HT | CITATIONS | Classement |
|---|---|---|---|---|---|---|
Bicalutamide | 90357-06-5 | sc-202976 sc-202976A | 100 mg 500 mg | $41.00 $143.00 | 27 | |
Cet antagoniste du récepteur des androgènes pourrait avoir des effets indirects sur l'expression de ZNF703 dans des types de cellules ou des conditions spécifiques. | ||||||
Temozolomide | 85622-93-1 | sc-203292 sc-203292A | 25 mg 100 mg | $89.00 $250.00 | 32 | |
En tant qu'agent alkylant, le témozolomide pourrait influencer les réponses aux lésions de l'ADN et moduler indirectement l'expression de ZNF703. | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
Un inhibiteur de l'ADN méthyltransférase qui peut affecter le statut de méthylation des gènes, influençant indirectement ZNF175 s'il fonctionne dans des mécanismes dépendant de la méthylation. | ||||||
Nutlin-3 | 548472-68-0 | sc-45061 sc-45061A sc-45061B | 1 mg 5 mg 25 mg | $56.00 $212.00 $764.00 | 24 | |
Inhibiteur de MDM2 qui active p53, affectant ainsi le réseau transcriptionnel auquel ZNF175 peut participer. | ||||||