CHD9, a member of the chromodomain helicase DNA-binding (CHD) family, is involved in chromatin remodeling, a crucial process that allows the alteration of chromatin structure and the regulation of gene expression. Chromatin remodeling is instrumental in various cellular processes, including DNA replication, repair, and transcription. CHD9, like other members of the CHD family, possesses DNA-binding domains and helicase domains, enabling it to bind to nucleosomes and use ATP hydrolysis to modify the structure of the chromatin. By modulating chromatin structure, CHD9 can influence the accessibility of specific DNA regions to transcriptional machinery, effectively acting as a regulator of gene expression. The precise roles of CHD9 in cellular and developmental processes are still under investigation, but its association with chromatin remodeling highlights its potential importance in maintaining cellular homeostasis and ensuring proper gene regulation.
CHD9 inhibitors are compounds that specifically target and inhibit the function of CHD9. These molecules can modulate the chromatin remodeling activity of CHD9, thereby influencing gene expression patterns in the cell. The mechanism by which these inhibitors function can vary: some may bind directly to CHD9, prevent its interaction with chromatin, while others might inhibit its ATPase activity, essential for chromatin remodeling. By blocking CHD9 activity, these inhibitors can provide invaluable tools for researchers aiming to understand the specific roles of CHD9 in cellular processes. Studying CHD9 inhibitors can also shed light on the broader mechanisms of chromatin remodeling and how alterations in this process can impact cell function and potentially lead to disease states.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $87.00 | 9 | |
Valproic acid is a histone deacetylase (HDAC) inhibitor. By altering the acetylation status of histones, it might influence the binding efficiency of CHD9 to chromatin, potentially reducing its expression or activity. | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $133.00 $275.00 | 37 | |
SAHA is another HDAC inhibitor. By modulating chromatin compaction, it could indirectly affect CHD9 expression or its chromatin remodeling function. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
This compound is a DNA methyltransferase inhibitor. Changes in DNA methylation could impact the recruitment of CHD9 to certain genomic loci. | ||||||
RGFP966 | 1357389-11-7 | sc-507300 | 5 mg | $115.00 | ||
RGFP966 is a specific HDAC3 inhibitor. Alterations in histone acetylation might influence the chromatin interaction of CHD9. | ||||||
Mocetinostat | 726169-73-9 | sc-364539 sc-364539B sc-364539A | 5 mg 10 mg 50 mg | $214.00 $247.00 $1463.00 | 2 | |
As an HDAC inhibitor, mocetinostat might influence the chromatin environment, potentially affecting CHD9 expression or activity. | ||||||
GSK126 | 1346574-57-9 | sc-490133 sc-490133A sc-490133B | 1 mg 5 mg 10 mg | $92.00 $243.00 $306.00 | ||
GSK126 is an EZH2 inhibitor. By inhibiting histone methylation, it might impact the chromatin recruitment of CHD9. | ||||||
JIB 04 | 199596-05-9 | sc-397040 | 20 mg | $177.00 | ||
JIB-04 is a pan-Jumonji inhibitor affecting histone demethylases. It might indirectly modulate CHD9 activity or expression through changes in chromatin methylation. | ||||||
PFI-1 | 1403764-72-6 | sc-478504 | 5 mg | $98.00 | ||
PFI-1 is a BET bromodomain inhibitor. By modulating bromodomain-containing protein interactions with chromatin, it could influence CHD9's chromatin association. | ||||||
UNC1999 | 1431612-23-5 | sc-475314 | 5 mg | $142.00 | 1 | |
UNC1999 is an inhibitor of EZH1/2 methyltransferases. Changes in histone methylation might affect the chromatin binding of CHD9. | ||||||
EPZ6438 | 1403254-99-8 | sc-507456 | 1 mg | $66.00 | ||
By inhibiting the EZH2 methyltransferase, EPZ-6438 might modulate chromatin methylation states, indirectly affecting CHD9 activity. | ||||||