PRMT7 inhibitors belong to a class of chemical compounds designed to selectively target and impede the enzymatic activity of protein arginine methyltransferase 7 (PRMT7). PRMT7 is a member of the protein arginine methyltransferase (PRMT) family, which plays a crucial role in the post-translational modification of proteins by catalyzing the addition of methyl groups to arginine residues. The PRMT family is involved in various cellular processes, including gene expression, signal transduction, and the regulation of protein-protein interactions. PRMT7, in particular, has been identified as a key player in the modulation of diverse biological functions, making it an attractive target for drug discovery efforts.
PRMT7 inhibitors are designed to interact specifically with the active site of PRMT7, disrupting its catalytic function and preventing the transfer of methyl groups to target proteins. Understanding the structural features of PRMT7 and its catalytic mechanism is crucial for the rational design of these inhibitors. Researchers employ various strategies, such as structure-based drug design and high-throughput screening, to identify and optimize small molecules capable of binding to PRMT7 with high affinity and specificity. As our understanding of the role of PRMT7 in cellular processes continues to evolve, the development of PRMT7 inhibitors holds promise for elucidating the functional consequences of inhibiting this specific enzyme and may provide valuable insights for future research in the broader field of epigenetics and protein regulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Adenosine | 58-61-7 | sc-291838 sc-291838A sc-291838B sc-291838C sc-291838D sc-291838E sc-291838F | 1 g 5 g 100 g 250 g 1 kg 5 kg 10 kg | $34.00 $48.00 $300.00 $572.00 $1040.00 $2601.00 $4682.00 | 1 | |
Adenosine, a purine nucleoside, can modulate methylation processes by competing with S-adenosylmethionine, the principal methyl donor used by PRMT7. | ||||||
Sinefungin | 58944-73-3 | sc-203263 sc-203263B sc-203263C sc-203263A | 1 mg 100 mg 1 g 10 mg | $271.00 $5202.00 $40368.00 $704.00 | 4 | |
Sinefungin, a natural nucleoside analogue of S-adenosylmethionine, can inhibit PRMT7 by competing with its physiological substrate. | ||||||
3-Deazaneplanocin, HCl salt | 120964-45-6 | sc-351856 sc-351856A sc-351856B | 1 mg 5 mg 10 mg | $256.00 $612.00 $936.00 | 2 | |
DZNep can inhibit PRMT7 by reducing the intracellular concentration of S-adenosylmethionine, the principal methyl donor used by PRMT7. | ||||||
Adenosine, periodate oxidized | 34240-05-6 | sc-214510 sc-214510A | 25 mg 100 mg | $119.00 $364.00 | ||
Adenosine, periodate can inhibit PRMT7 by depleting S-adenosylmethionine levels, leading to a reduction in the protein's methyltransferase activity. | ||||||
5′-Deoxy-5′-methylthioadenosine | 2457-80-9 | sc-202427 | 50 mg | $122.00 | 1 | |
5'-Methylthioadenosine, a byproduct of polyamine biosynthesis, can inhibit PRMT7 by competing with S-adenosylmethionine. | ||||||
Quercetin | 117-39-5 | sc-206089 sc-206089A sc-206089E sc-206089C sc-206089D sc-206089B | 100 mg 500 mg 100 g 250 g 1 kg 25 g | $11.00 $17.00 $110.00 $250.00 $936.00 $50.00 | 33 | |
Quercetin, a plant flavonol, can inhibit PRMTs by interacting with the active site, potentially altering PRMT7's methylation activity. | ||||||
Fisetin | 528-48-3 | sc-276440 sc-276440A sc-276440B sc-276440C sc-276440D | 50 mg 100 mg 500 mg 1 g 100 g | $52.00 $79.00 $104.00 $156.00 $2913.00 | 7 | |
Fisetin, a flavonoid, can inhibit PRMT7 by binding to the active site and potentially altering the protein's methylation activity. | ||||||
Parthenolide | 20554-84-1 | sc-3523 sc-3523A | 50 mg 250 mg | $81.00 $306.00 | 32 | |
Parthenolide, a sesquiterpene lactone, can inhibit PRMT7 by modifying the active site cysteine residues, interfering with the protein's activity. | ||||||
Ellagic Acid, Dihydrate | 476-66-4 | sc-202598 sc-202598A sc-202598B sc-202598C | 500 mg 5 g 25 g 100 g | $58.00 $95.00 $245.00 $727.00 | 8 | |
Ellagic acid, a natural phenol antioxidant, can inhibit PRMT7 by binding to the active site, potentially altering the protein's methylation activity. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $43.00 $73.00 $126.00 $243.00 $530.00 $1259.00 | 11 | |
Epigallocatechin gallate, a type of catechin, can inhibit PRMT7 by binding to the active site, potentially altering the protein's methylation activity. | ||||||