Trimethyl Arg Symmetric Inhibitors represent a class of compounds designed to target and inhibit the activity of protein arginine methyltransferases (PRMTs), particularly PRMT6, which catalyzes the symmetric trimethylation of arginine residues in proteins. These inhibitors exert their effects by interfering with the enzymatic process of arginine methylation, thereby inhibiting Trimethyl Arg Symmetric. For instance, compounds like MS049, TC-H 1061, and MS023 selectively target PRMT6 or PRMT1 and disrupt their catalytic activity or substrate binding, leading to inhibition of the formation of trimethylated arginine residues.
Similarly, inhibitors such as AMI-1, AMI-5, and EPT-103084 specifically target PRMT1 or PRMT6 and interfere with their methyltransferase activity, resulting in the inhibition of Trimethyl Arg Symmetric. These inhibitors offer valuable tools for investigating the role of symmetric arginine trimethylation in cellular processes and may have implications in diseases where dysregulation of this process is implicated. Overall, Trimethyl Arg Symmetric Inhibitors can serve as important pharmacological agents and research probes for studying the biological significance of symmetric arginine methylation.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
TC-H 106 | 937039-45-7 | sc-362801 sc-362801A | 10 mg 50 mg | $155.00 $620.00 | ||
TC-H 1061 is a potent inhibitor of PRMT6 that blocks its catalytic activity by occupying the active site of the enzyme. It interferes with the methyl transfer reaction, leading to inhibition of Trimethyl Arg Symmetric. | ||||||
MS023 | 1831110-54-3 | sc-507463 | 5 mg | $165.00 | ||
MS023 is a selective inhibitor of PRMT1, a major protein arginine methyltransferase responsible for symmetric methylation of arginine residues. It competitively inhibits the binding of PRMT1 to its substrate, thereby blocking the methylation reaction. | ||||||