Date published: 2025-11-14

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MBD3L4 Inhibitors

MBD3L4 Inhibitors are a class of compounds that influence the functional activity of MBD3L4 by primarily affecting the methylation status of DNA. The inhibitory action of these compounds is rooted in their capacity to either directly inhibit DNA methyltransferase enzymes or to incorporate into DNA and trap these enzymes, leading to reduced levels of DNA methylation. This decreased methylation can impede the ability of MBD3L4 to recognize and bind to methylated DNA, which is central to its role in the cell.

Compounds such as 5-Azacytidine, RG108, and Procainamide work by inhibiting DNA methyltransferase activity, which is expected to reduce the methylation marks that MBD3L4 typically recognizes. This could result in a decreased interaction between MBD3L4 and its DNA targets, effectively inhibiting the protein's normal activity. Other inhibitors, such as Hydralazine and Decitabine, also contribute to demethylation of DNA, further promoting the disassociation of MBD3L4 from methylated DNA regions. Additionally, compounds like SGI-1027 and Disulfiram inhibit the enzyme activity that adds methyl groups to DNA, which in turn would limit the functionality of MBD3L4. Nanaomycin A, while specifically targeting DNMT3B, along with EGCG, a natural compound from green tea, both contribute to a similar outcome by decreasing the methylated substrates available for MBD3L4

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