LIN-53 inhibitors refer to a class of small molecules or compounds that specifically target and modulate the activity of the LIN-53 protein. LIN-53, also known as CAF-1 p48 or RbAp48, is a highly conserved chromatin-associated protein that plays a critical role in chromatin remodeling, histone binding, and nucleosome assembly. This protein is part of several chromatin-modifying complexes, such as the nucleosome remodeling and deacetylase (NuRD) complex and the Polycomb repressive complex 2 (PRC2), where it functions in the regulation of gene expression by facilitating or inhibiting the access of transcription factors to DNA. LIN-53 is essential for maintaining epigenetic stability, and it contributes to cell fate determination, differentiation, and cellular memory.
Inhibitors of LIN-53 are designed to interfere with its ability to interact with other proteins or DNA, thereby disrupting its role in chromatin remodeling. These inhibitors can affect the assembly of nucleosomes and the deposition of histone proteins, altering chromatin architecture. By targeting LIN-53, these compounds may change the landscape of histone modifications, such as methylation or acetylation, which are critical for regulating gene expression patterns. LIN-53 inhibitors can therefore be utilized to study the underlying mechanisms of chromatin regulation, especially in contexts where LIN-53-mediated pathways play a pivotal role in cellular processes like proliferation, differentiation, and epigenetic regulation. The development and application of LIN-53 inhibitors provide a valuable tool for investigating the dynamics of chromatin structure and gene regulation.
SEE ALSO...
Items 1 to 10 of 12 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
HDAC inhibitor that can disrupt chromatin remodeling, indirectly affecting LIN-53 functions. | ||||||
Romidepsin | 128517-07-7 | sc-364603 sc-364603A | 1 mg 5 mg | $214.00 $622.00 | 1 | |
HDAC inhibitor that alters chromatin structure which can impact LIN-53 associated pathways. | ||||||
Mocetinostat | 726169-73-9 | sc-364539 sc-364539B sc-364539A | 5 mg 10 mg 50 mg | $210.00 $242.00 $1434.00 | 2 | |
Targets HDAC, potentially affecting the pathways LIN-53 is involved in. | ||||||
MS-275 | 209783-80-2 | sc-279455 sc-279455A sc-279455B | 1 mg 5 mg 25 mg | $24.00 $88.00 $208.00 | 24 | |
By inhibiting HDAC, it can influence chromatin remodeling processes associated with LIN-53. | ||||||
ITF2357 | 732302-99-7 | sc-364513 sc-364513A | 5 mg 50 mg | $340.00 $1950.00 | ||
HDAC inhibitor that can disrupt chromatin structure and processes LIN-53 is associated with. | ||||||
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 | |
Influences histone modification by HDAC inhibition, potentially affecting LIN-53 related pathways. | ||||||
Belinostat | 414864-00-9 | sc-269851 sc-269851A | 10 mg 100 mg | $153.00 $561.00 | ||
HDAC inhibitor which can impact chromatin remodeling related to LIN-53 functions. | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | $226.00 $846.00 | 1 | |
Bromodomain inhibitor that disrupts chromatin reader proteins, possibly influencing LIN-53's role. | ||||||
I-BET 151 Hydrochloride | 1300031-49-5 (non HCl Salt) | sc-391115 | 10 mg | $450.00 | 2 | |
By targeting bromodomains, it affects chromatin interactions potentially linked to LIN-53. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Acts as an HDAC inhibitor which can affect chromatin modification pathways related to LIN-53. | ||||||