Sir3 inhibitors belong to a chemical class of compounds specifically designed to target and inhibit the activity of the Silent Information Regulator 3 (Sir3) protein. Sir3 is a critical component of the Sir complex, which plays a key role in gene silencing and chromatin organization in certain organisms, such as yeast. By interfering with the function of Sir3, these inhibitors may disrupt the formation of repressive chromatin structures and impact gene expression patterns. Sir3 inhibitors can encompass a range of natural and synthetic compounds, each with its specific mechanism of action. Some inhibitors may work by directly binding to the Sir3 protein, preventing its association with other components of the Sir complex or inhibiting its interaction with specific chromatin regions. Others may modulate post-translational modifications of Sir3, affecting its localization and activity within the cell. Additionally, certain inhibitors may interfere with the recruitment of Sir3 to specific genomic loci, thereby influencing gene silencing processes.
Researchers employ various approaches, such as rational drug design, high-throughput screening, and structural studies, to identify and develop Sir3 inhibitors. These inhibitors serve as valuable tools in studying the mechanisms of gene silencing, chromatin remodeling, and epigenetic regulation in cells and organisms. Moreover, the discovery of Sir3 inhibitors contributes to a deeper understanding of chromatin biology and gene regulation, offering insights into the role of Sir3 in maintaining genome stability and modulating gene expression. These inhibitors provide researchers with means to investigate the intricate processes of epigenetic regulation, which can have far-reaching implications in various biological contexts. It's important to acknowledge that the field of Sir3 inhibitors is an area of ongoing research and development, and specific details on individual compounds may vary.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Nicotinamide | 98-92-0 | sc-208096 sc-208096A sc-208096B sc-208096C | 100 g 250 g 1 kg 5 kg | $44.00 $66.00 $204.00 $831.00 | 6 | |
Nicotinamide is a derivative of vitamin B3 and has been shown to inhibit the activity of SIR3 by interfering with the enzymatic activity of the SIR complex. | ||||||
Splitomicin | 5690-03-9 | sc-358701 | 5 mg | $48.00 | ||
Splitomicin is a natural product that has been found to inhibit SIR3 by interfering with its interaction with other components of the SIR complex. | ||||||
Sirtinol | 410536-97-9 | sc-205976 sc-205976A | 1 mg 5 mg | $38.00 $113.00 | 14 | |
Sirtinol is a synthetic compound known to inhibit the activity of SIR3 and other sirtuin proteins, which are a family of NAD+-dependent histone deacetylases. | ||||||
SIRT1/2 Inhibitor IV, Cambinol | 14513-15-6 | sc-204280 | 5 mg | $145.00 | 4 | |
Cambinol is another synthetic compound that has been shown to inhibit SIR3 and other sirtuins, thereby affecting gene silencing and chromatin modifications. | ||||||
Salermide | 1105698-15-4 | sc-224276 sc-224276A | 5 mg 10 mg | $70.00 $105.00 | 3 | |
Salermide is a small molecule that has been identified as a SIR3 inhibitor, potentially disrupting SIR complex function and gene silencing. | ||||||
EX 527 | 49843-98-3 | sc-203044 | 5 mg | $87.00 | 32 | |
EX-527 is a selective inhibitor of SIRT1, a sirtuin protein closely related to SIR3, and may also impact SIR3 activity. | ||||||
SIRT2 Inhibitor, AGK2 | 304896-28-4 | sc-202813A sc-202813 sc-202813B sc-202813C | 1 mg 5 mg 10 mg 25 mg | $46.00 $148.00 $316.00 $490.00 | 5 | |
AGK2 is another selective SIRT1 inhibitor with potential effects on SIR3 function. | ||||||
Tenovin-6 | 1011557-82-6 | sc-224296 sc-224296A | 1 mg 5 mg | $272.00 $1214.00 | 9 | |
Tenovin-6 is a small molecule that inhibits the activity of SIRT1 and may also affect SIR3-mediated gene silencing. | ||||||
1-Benzoyl-3-phenyl-2-thiourea | 4921-82-8 | sc-258614A sc-258614 | 1 g 5 g | $43.00 $129.00 | ||
This compound, also called TM-2-51, is a compound with reported SIR3 inhibitory activity, potentially interfering with its function in chromatin remodeling. | ||||||