Date published: 2025-9-18

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HSCARG_NMRAL1 Activators

Nicotinamide, a form of vitamin B3, plays a critical role by enhancing cellular levels of NAD+, a cofactor that is pivotal for the activity of NAD+-dependent enzymes, including HSCARG_NMRAL1. The presence of higher NAD+ levels can lead to a facilitation of HSCARG_NMRAL1's enzymatic functions, which are essential for maintaining cellular homeostasis. Compounds such as resveratrol and 1,1-Dimethylbiguanide, Hydrochloride have been shown to impact cellular energy balance through their respective pathways. Resveratrol activates SIRT1, which may lead to the deacetylation and subsequent activation of proteins like HSCARG_NMRAL1. On the other hand, metformin activates AMPK, a master regulator of cellular energy status, which can then influence NAD+ metabolism and, consequently, the activity of HSCARG_NMRAL1.

Quercetin and sulforaphane engage with the cellular redox systems, potentially altering the redox state within cells, which can have a downstream effect on redox-sensitive proteins such as HSCARG_NMRAL1. By modulating the oxidative environment, these compounds may indirectly affect the protein's conformation and activity. Curcumin is known to modulate the NF-kB signaling pathway, which has widespread effects on cellular function, including potentially affecting the activity of HSCARG_NMRAL1. Similarly, epigallocatechin gallate (EGCG) impacts methylation pathways, which may influence the expression and activity of this protein. Ademetionine, as a methyl donor, could also play a role in the methylation status of HSCARG_NMRAL1 or its related pathways, thus modulating its activity. Other activators, such as butyrate, act as histone deacetylase inhibitors, influencing gene expression patterns that could lead to upregulated expression of HSCARG_NMRAL1. Zinc is an essential mineral that plays a critical role in NAD+ synthesis, a substrate necessary for HSCARG_NMRAL1's function. Alpha-ketoglutarate, a key component of the TCA cycle, can impact the redox balance, which might affect HSCARG_NMRAL1 as well. N-acetylcysteine (NAC) acts as an antioxidant, restoring cellular redox balance and potentially impacting the function of HSCARG_NMRAL1.

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