mSin3A9 inhibitors are a class of small molecules that target the mSin3A9 protein, a component of the mSin3A co-repressor complex. This complex is highly conserved and plays a pivotal role in transcriptional repression across various species. mSin3A9 is a key subunit that mediates interactions with histone deacetylases (HDACs), leading to chromatin condensation and transcriptional silencing. Through these interactions, the mSin3A9-containing complexes help regulate gene expression in response to diverse signaling pathways. These complexes are responsible for fine-tuning cellular responses by modulating the transcriptional landscape, often functioning as mediators of epigenetic changes. Inhibitors targeting mSin3A9 disrupt its role in these processes, offering a means to perturb the balance of chromatin modifications and the associated gene repression.
The biochemical mechanism by which mSin3A9 inhibitors operate typically involves blocking the protein-protein interactions between mSin3A9 and other components of the co-repressor complex. This interference hinders the formation of stable repressive complexes and impairs their ability to recruit HDACs or other chromatin-modifying enzymes. Consequently, histone acetylation levels may increase locally at specific promoters or gene loci, leading to an open chromatin structure that allows for enhanced transcriptional activity. Given the critical involvement of mSin3A9 in maintaining transcriptional homeostasis, these inhibitors provide valuable tools for studying gene regulation and chromatin dynamics at a molecular level. Moreover, by controlling the recruitment of chromatin modifiers, mSin3A9 inhibitors enable researchers to explore the broader implications of chromatin remodeling in various biological processes such as development, differentiation, and stress responses.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
An antifungal antibiotic that inhibits HDAC, leading to increased acetylation of histones and reduced interaction with mSin3A. | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
It inhibits HDAC activity and can disrupt mSin3A-associated complexes. | ||||||
Romidepsin | 128517-07-7 | sc-364603 sc-364603A | 1 mg 5 mg | $214.00 $622.00 | 1 | |
A cyclic peptide that inhibits HDAC, altering chromatin structure and potentially affecting mSin3A recruitment to target genes. | ||||||
Belinostat | 414864-00-9 | sc-269851 sc-269851A | 10 mg 100 mg | $153.00 $561.00 | ||
Inhibits HDAC activity, impacting histone acetylation and the function of associated corepressor complexes including mSin3A. | ||||||
Panobinostat | 404950-80-7 | sc-208148 | 10 mg | $196.00 | 9 | |
A potent HDAC inhibitor that leads to hyperacetylation of histones and can perturb mSin3A-mediated repression. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
A short-chain fatty acid with HDAC inhibitory activity, affecting histone acetylation and mSin3A interaction with chromatin. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 19 | |
A dietary fatty acid that acts as an HDAC inhibitor, potentially disrupting the function of mSin3A in chromatin remodeling. | ||||||
MS-275 | 209783-80-2 | sc-279455 sc-279455A sc-279455B | 1 mg 5 mg 25 mg | $24.00 $88.00 $208.00 | 24 | |
A synthetic benzamide derivative that selectively inhibits class I HDACs, influencing mSin3A's role in gene repression. | ||||||
Mocetinostat | 726169-73-9 | sc-364539 sc-364539B sc-364539A | 5 mg 10 mg 50 mg | $210.00 $242.00 $1434.00 | 2 | |
A benzamide HDAC inhibitor that can affect mSin3A activity by modulating histone acetylation. | ||||||
Chidamide | 743420-02-2 | sc-364462 sc-364462A sc-364462B | 1 mg 5 mg 25 mg | $61.00 $245.00 $1173.00 | ||
A benzamide chemical that inhibits HDAC, impacting histone acetylation and mSin3A's corepressor activity. | ||||||