Date published: 2025-12-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

Dimethyl Arg Symmetric Inhibitors

Dimethyl 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 dimethylation of arginine residues in proteins. These inhibitors exert their effects by interfering with the enzymatic process of arginine methylation, thereby inhibiting Dimethyl Arg Symmetric. For instance, compounds like EPZ031686, DS-437, and GSK3368715 specifically target PRMT6, the primary enzyme responsible for symmetric arginine dimethylation. They bind to the active site of PRMT6 and disrupt its catalytic activity, preventing the transfer of methyl groups to arginine residues and inhibiting the generation of dimethylated arginine residues.

Similarly, inhibitors such as EPZ020411, AMI-5, and EPT-103084 selectively target PRMT6 and interfere with its methyltransferase activity, leading to inhibition of Dimethyl Arg Symmetric. These inhibitors offer valuable tools for investigating the role of symmetric arginine dimethylation in cellular processes and may have implications in diseases where dysregulation of this process is implicated. Overall, Dimethyl Arg Symmetric Inhibitors hold promise as agents and research probes for studying the biological significance of symmetric arginine methylation.

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

TC-H 106

937039-45-7sc-362801
sc-362801A
10 mg
50 mg
$155.00
$620.00
(0)

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 Dimethyl Arg Symmetric.

MS023

1831110-54-3sc-507463
5 mg
$165.00
(0)

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.