The chemical class known as BAHD1 Inhibitors refers to a group of compounds designed to modulate the activity of BAHD1, a protein integral to chromatin remodeling and transcriptional repression. The primary mechanism of these inhibitors is to interfere with the functional dynamics of BAHD1 within the chromatin structure. This interference can occur through various molecular pathways, each targeting different aspects of BAHD1's role in epigenetic regulation. One key approach involves altering the epigenetic landscape to which BAHD1 responds, such as modifying the methylation or acetylation patterns of histones. These changes can impact BAHD1's ability to recognize, bind, and modulate chromatin, thereby influencing its role in gene silencing and chromatin compaction. By modulating these epigenetic marks, the inhibitors can effectively alter the interaction dynamics between BAHD1 and the chromatin, leading to changes in gene expression patterns and chromatin architecture.
In addition to targeting the epigenetic interface, some inhibitors in this class focus on disrupting the interactions between BAHD1 and other proteins involved in chromatin remodeling and transcriptional regulation. This approach includes inhibiting the protein-protein interactions that facilitate the recruitment of BAHD1 to specific chromatin sites or its collaboration with other chromatin-modifying enzymes. By hindering these interactions, these inhibitors can reduce the efficacy of BAHD1 in establishing repressive chromatin environments, thereby affecting the overall transcriptional landscape. Moreover, some inhibitors work by influencing the broader regulatory mechanisms of chromatin structure and gene expression, indirectly affecting the functional capacity of BAHD1. This includes modulating the cellular mechanisms that govern the accessibility and compaction of chromatin, which are essential for BAHD1's activity in transcriptional repression. Overall, the development of BAHD1 inhibitors represents an advanced approach to understanding and modulating chromatin dynamics and gene expression. These inhibitors serve as crucial tools for probing the complex interplay between chromatin structure and gene regulation, offering insights into the sophisticated mechanisms of epigenetic control. By targeting both the direct chromatin-binding activity of BAHD1 and the wider chromatin regulatory network, these inhibitors highlight the multifaceted strategies required for effective modulation of key components in gene expression regulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
Could possibly inhibit BAHD1 by altering DNA methylation patterns, impacting its chromatin-binding sites. | ||||||
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 | |
Could possibly inhibit BAHD1 by modifying histone acetylation, affecting chromatin structure and interaction. | ||||||
Ademetionine | 29908-03-0 | sc-278677 sc-278677A | 100 mg 1 g | $180.00 $655.00 | 2 | |
Could possibly inhibit BAHD1 by altering histone and DNA methylation, impacting its binding to chromatin. | ||||||
Mocetinostat | 726169-73-9 | sc-364539 sc-364539B sc-364539A | 5 mg 10 mg 50 mg | $210.00 $242.00 $1434.00 | 2 | |
Could possibly inhibit BAHD1 by changing histone acetylation states, affecting chromatin accessibility. | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
Could possibly inhibit BAHD1 by impacting chromatin structure and its ability to bind. | ||||||
MS-275 | 209783-80-2 | sc-279455 sc-279455A sc-279455B | 1 mg 5 mg 25 mg | $24.00 $88.00 $208.00 | 24 | |
Could possibly inhibit BAHD1 by modifying chromatin compaction. | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $128.00 $505.00 | 2 | |
Could possibly inhibit BAHD1 by affecting DNA methylation and chromatin structure. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Could possibly inhibit BAHD1 by affecting acetylation levels of histones. | ||||||
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 | |
Could possibly inhibit BAHD1 by altering DNA methylation states. | ||||||
Panobinostat | 404950-80-7 | sc-208148 | 10 mg | $196.00 | 9 | |
Could possibly inhibit BAHD1 by changing the histone modification landscape on chromatin. | ||||||