ERAL1 Activators encompass a diverse array of compounds that indirectly modulate cellular metabolism and phospholipid synthesis pathways to potentially increase the activity of ERAL1. These activators primarily involve substances that can stimulate lipid metabolism, either through direct agonism of peroxisome proliferator-activated receptors (PPARs), such as Bezafibrate, Pioglitazone, Clofibrate, and Fenofibrate, or through the activation of AMP-activated protein kinase (AMPK), as seen with AICAR and Metformin. These pathways lead to an increased demand for the components of cell membrane synthesis, wherein ERAL1 plays a key role.
Additionally, molecules like Resveratrol, which activates SIRT1, and Nicotinamide mononucleotide (NMN), a precursor to NAD+, support cellular energy homeostasis and biosynthetic processes, thereby potentially enhancing ERAL1 activity. Compounds like Coenzyme Q10 contribute to mitochondrial function and cellular bioenergetics, which can indirectly influence the activity of ERAL1 by increasing the cell's metabolic capacity. Furthermore, substances like Spermidine and the amino acid Leucine are known to induce autophagy and activate mTOR signaling respectively, processes that can also lead to an upregulation of lipid biosynthesis and indirectly stimulate the functional demand for ERAL1.
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