Date published: 2025-9-12

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PHF20L1 Activators

PHF20L1 Activators encompass a variety of chemical compounds that indirectly enhance PHF20L1 activity by modulating epigenetic mechanisms and chromatin remodeling processes. Compounds like Resveratrol, Nicotinamide, and S-Adenosylmethionine influence the activity of enzymes such as sirtuins and methyltransferases, which are critical in histone modification processes that PHF20L1 is associated with. Resveratrol, specifically, modulates sirtuin pathways, particularly SIRT1, impacting the methylation status of histones and non-histone proteins, thereby influencing PHF20L1's function. Similarly, Nicotinamide, a sirtuin inhibitor, affects histone deacetylation, a process interlinked with PHF20L1's role in chromatin regulation. S-Adenosylmethionine, by serving as a methyl donor, potentially enhances PHF20L1's activity in histone and DNA methylation, pivotal in gene expression regulation.

Moreover, histone deacetylase inhibitors like Trichostatin A, SAHA (Vorinostat), and other compounds such as 5-Aza-2'-deoxycytidine, Methylstat, Disulfiram, Genistein, Curcumin, BIX-01294, and JIB-04 alter the chromatin landscape by influencing histone acetylation and methylation patterns. Trichostatin A and SAHA, for instance, modify chromatin structure and histone acetylation, indirectly affecting PHF20L1's role in gene expression regulation. 5-Aza-2'-deoxycytidine, as a DNA methyltransferase inhibitor, alters DNA methylation patterns, which is significant for PHF20L1's involvement in epigenetic regulation. Methylstat and JIB-04, targeting histone demethylases, influence histone methylation status, thereby affecting gene expression patterns where PHF20L1 plays a regulatory role. Collectively, these activators, through their targeted effects on chromatin structure and epigenetic mechanisms, facilitate the enhancement of PHF20L1's function in gene regulation and chromatin remodeling.

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