Date published: 2025-9-10

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MLL Activators

The class of MLL activators encompasses a diverse range of chemical compounds that indirectly influence the activity of the Mixed Lineage Leukemia (MLL) protein. This protein is primarily involved in the methylation of histone H3 at lysine 4 (H3K4), a crucial process in the regulation of gene expression. MLL activators function through various mechanisms, including the modulation of chromatin structure, inhibition of competing histone modifying enzymes, and alteration of cellular signaling pathways. The primary mechanism through which these activators function is by influencing the chromatin environment, making it more conducive to MLL's histone methyltransferase activity. Compounds like anacardic acid, garcinol, and curcumin exert their effects by inhibiting histone acetyltransferases or modulating other histone-modifying enzymes. This alteration in the histone modification landscape indirectly enhances MLL's ability to methylate H3K4. Additionally, some compounds, like 5'-azacytidine, act by demethylating DNA, leading to an upregulation of genes that are targets of MLL, thereby influencing its functional pathways.

Another significant aspect of these activators is their role in modulating cellular signaling pathways that intersect with MLL's regulatory network. For example, disulfiram and parthenolide affect NF-kB signaling, a pathway known to interact with MLL-regulated gene expression. Similarly, compounds like resveratrol and quercetin exert their effects through pathways involving sirtuins and histone deacetylases, respectively. These pathways, though not directly altering MLL's enzymatic activity, create a cellular context that can enhance or complement MLL's functional role in gene regulation. MLL activators represent a unique class of compounds that, while not directly interacting with MLL, play a pivotal role in modulating its activity and the broader epigenetic landscape in which it operates. Their diverse mechanisms of action, ranging from chromatin remodeling to the alteration of key signaling pathways, highlight the intricate interplay between various cellular components in regulating gene expression.

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