HDA1 inhibitors belong to a chemical class that exerts their influence on a specific group of enzymes called histone deacetylase 1 (HDA1). These inhibitors function by modulating the activity of HDA1, which is responsible for the removal of acetyl groups from histone proteins. HDA1 inhibitors are compounds that reduce the enzymatic activity of the histone deacetylase HDA1, a protein implicated in the removal of acetyl groups from histone proteins, which plays a pivotal role in the regulation of chromatin structure and gene expression. By inhibiting HDA1, these chemicals can lead to an increase in the acetylation levels of histones, thereby promoting a more open chromatin conformation and potentially enhancing the transcriptional activity of certain genes.
The inhibition of HDA1 can occur through direct or indirect mechanisms. Direct inhibitors interact with the active site of HDA1 or with critical regions of the enzyme that are necessary for its deacetylase function. Such binding can block substrate access, interfere with the catalytic mechanism, or alter the enzyme's structure in a way that diminishes its activity. These inhibitors often mimic the structure of HDA1 substrates or cofactors, competing with them and thus preventing the normal deacetylation reaction from occurring. Indirect inhibitors may not bind to HDA1 directly but can affect its activity by altering cellular pathways that modulate the enzyme's function. This could involve the inhibition of upstream signals that activate HDA1 or the enhancement of pathways that lead to its degradation. In addition, indirect inhibitors might modulate the expression levels of HDA1 by affecting the transcription or translation of its gene or by destabilizing the mRNA, resulting in reduced synthesis of the enzyme.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $133.00 $275.00 | 37 | |
Vorinostat was the first HDAC inhibitor used in the research of cutaneous T-cell lymphoma. It works by binding to the active site of HDAC enzymes, including HDAC1, leading to the accumulation of acetylated histones and subsequent gene expression changes. | ||||||
Romidepsin | 128517-07-7 | sc-364603 sc-364603A | 1 mg 5 mg | $218.00 $634.00 | 1 | |
Romidepsin is another HDAC inhibitor used in the research of cutaneous T-cell lymphoma. It primarily targets HDAC1 and HDAC2 and induces cell cycle arrest and apoptosis in cancer cells. | ||||||
Panobinostat | 404950-80-7 | sc-208148 | 10 mg | $200.00 | 9 | |
Panobinostat is a potent pan-HDAC inhibitor that inhibits several HDAC enzymes, including HDACIt has been investigated for multiple myeloma in combination with other drugs. | ||||||
MS-275 | 209783-80-2 | sc-279455 sc-279455A sc-279455B | 1 mg 5 mg 25 mg | $24.00 $90.00 $212.00 | 24 | |
Entinostat is a selective HDAC1 inhibitor that has shown potential in various cancers. It exerts its effects by modulating gene expression and promoting anti-tumor immune responses. | ||||||
Belinostat | 414864-00-9 | sc-269851 sc-269851A | 10 mg 100 mg | $156.00 $572.00 | ||
Belinostat is an HDAC inhibitor that targets multiple HDAC enzymes, including HDACIt has been investigated for peripheral T-cell lymphoma. | ||||||
SB939 | 929016-96-6 | sc-364610 sc-364610A | 5 mg 50 mg | $209.00 $851.00 | ||
SB939 is an investigational HDAC1 inhibitor that has shown promise for acute myeloid leukemia and myelodysplastic syndrome. | ||||||
Chidamide | 743420-02-2 | sc-364462 sc-364462A sc-364462B | 1 mg 5 mg 25 mg | $62.00 $250.00 $1196.00 | ||
Chidamide is an HDAC1-selective inhibitor that has been approved in China for peripheral T-cell lymphoma. It exhibits anti-cancer effects by inducing cell cycle arrest and apoptosis. | ||||||
Mocetinostat | 726169-73-9 | sc-364539 sc-364539B sc-364539A | 5 mg 10 mg 50 mg | $214.00 $247.00 $1463.00 | 2 | |
Mocetinostat is a selective HDAC1 inhibitor that has shown potential for various solid tumors and hematological malignancies. | ||||||
PI3K/HDAC Inhibitor | 1339928-25-4 | sc-364584 sc-364584A | 5 mg 10 mg | $347.00 $471.00 | ||
Fimepinostat is a dual inhibitor of HDAC and phosphoinositide 3-kinase (PI3K). It targets HDAC1, among other HDAC enzymes, and has shown activity against lymphoma and other cancers. | ||||||
CI 994 | 112522-64-2 | sc-205245 sc-205245A | 10 mg 50 mg | $99.00 $536.00 | 1 | |
CI-994 is an HDAC1 inhibitor that has demonstrated anti-cancer effects in research studies. It modulates gene expression and induces cell cycle arrest and apoptosis in cancer cells. | ||||||