CHRAC17 inhibitors belong to a distinctive class of chemical compounds specifically designed to modulate the activity of CHRAC17, a chromatin accessibility complex subunit. The CHRAC (chromatin accessibility complex) is a multi-subunit complex crucial for the regulation of chromatin structure and accessibility, playing a pivotal role in various cellular processes such as transcription, DNA repair, and replication. CHRAC17, one of the subunits of this complex, is recognized for its involvement in facilitating chromatin remodeling by promoting nucleosome sliding, a process vital for the dynamic regulation of gene expression.
CHRAC17 are meticulously designed molecules that interfere with the normal functioning of CHRAC17, thus influencing the chromatin remodeling processes in which this subunit is involved. These inhibitors typically exert their effects through mechanisms such as competitive binding, disrupting the interactions between CHRAC17 and its substrates, or by altering the conformation of CHRAC17, thereby hindering its enzymatic activity. The modulation of CHRAC17 activity by these inhibitors holds promise for unraveling the intricacies of chromatin dynamics, shedding light on the fundamental mechanisms governing gene expression, DNA repair, and other essential cellular functions. As researchers delve deeper into the structural and functional aspects of CHRAC17 inhibitors, a more comprehensive understanding of chromatin biology and its implications in cellular processes is anticipated, potentially paving the way for innovative insights into the molecular basis of gene regulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $87.00 | 9 | |
Inhibits histone deacetylases, causing hyperacetylation which can disrupt CHRAC17 chromatin remodeling. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $31.00 $47.00 $84.00 $222.00 | 19 | |
Histone deacetylase inhibitor that could alter the chromatin state, impacting CHRAC17 activity. | ||||||
M 344 | 251456-60-7 | sc-203124 sc-203124A | 1 mg 5 mg | $109.00 $322.00 | 8 | |
Inhibits histone deacetylases, potentially altering CHRAC17-mediated chromatin remodeling. | ||||||
Panobinostat | 404950-80-7 | sc-208148 | 10 mg | $200.00 | 9 | |
Potent histone deacetylase inhibitor which may disrupt CHRAC17's role in chromatin architecture. | ||||||
Chidamide | 743420-02-2 | sc-364462 sc-364462A sc-364462B | 1 mg 5 mg 25 mg | $62.00 $250.00 $1196.00 | ||
Inhibits histone deacetylases, possibly influencing CHRAC17's chromatin remodeling activity. | ||||||
Romidepsin | 128517-07-7 | sc-364603 sc-364603A | 1 mg 5 mg | $218.00 $634.00 | 1 | |
Binds to and inhibits histone deacetylases, could alter the function of CHRAC17 in chromatin structure. | ||||||
Belinostat | 414864-00-9 | sc-269851 sc-269851A | 10 mg 100 mg | $156.00 $572.00 | ||
Inhibits histone deacetylases, which could affect the chromatin remodeling activity of CHRAC17. | ||||||
JNJ-26481585 | 875320-29-9 | sc-364515 sc-364515A | 5 mg 50 mg | $321.00 $1224.00 | ||
Histone deacetylase inhibitor that may impact CHRAC17's role in modifying chromatin accessibility. | ||||||