Date published: 2025-9-18

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7530422B04Rik Activators

Chemical activators of DNA methyltransferase 3B, opposite strand can engage with the enzyme in various ways to modulate its activity. S-Adenosylmethionine serves as a direct substrate, providing a methyl group that is vital for the enzyme's methylation activity. RG108 interacts with the catalytic domain, ensuring that DNA methyltransferase 3B, opposite strand remains unobstructed in its active state. Procaine, while known for its DNA demethylating properties, can indirectly enhance the activity of DNA methyltransferase 3B, opposite strand by altering the methylation landscape, which may necessitate increased enzyme activity for maintenance of methylation status. Caffeine, through the inhibition of phosphodiesterases, leads to an increase in intracellular cAMP levels. This elevation can activate protein kinase A (PKA), which in turn can phosphorylate and activate DNA methyltransferase 3B, opposite strand. Azacytidine, after being incorporated into nucleic acids, might instigate a response that upregulates the activity of DNA methyltransferase 3B, opposite strand to counterbalance demethylation. Quercetin's antioxidant properties reduce oxidative DNA damage, creating an environment that supports the methylation functions of DNA methyltransferase 3B, opposite strand. Genistein's ability to inhibit tyrosine kinases can modify signaling pathways, potentially leading to increased activation of the enzyme. Resveratrol's activation of sirtuins, involved in cellular stress responses, may also promote the activity of DNA methyltransferase 3B, opposite strand in DNA repair processes.

Curcumin interacts with various signaling pathways, potentially leading to an increase in the activity of DNA methyltransferase 3B, opposite strand to maintain genomic stability. Similarly, 5-Aza-2'-deoxycytidine incorporation during DNA replication can trap the enzyme on the DNA, possibly resulting in increased activation as part of a cellular response to the trapped enzyme. Sinefungin, though an inhibitor, may also activate DNA methyltransferase 3B, opposite strand through binding interactions that induce allosteric changes. Finally, epigallocatechin gallate's modulation of cellular signaling pathways can lead to adjustments in the enzyme's activity as the cell responds to signaling alterations.

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