Date published: 2025-9-15

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FHL-2 Activators

The class of FHL-2 activators encompasses a diverse array of chemicals that modulate the function of FHL-2, a protein involved in various cellular processes. These activators either directly target FHL-2 or act indirectly by influencing specific signaling pathways associated with FHL-2. AICAR (Acadesine), Resveratrol, Metformin, GW501516 (Cardarine), Quercetin, A769662, Oxytocin, Betaine, NAD+ (Nicotinamide adenine dinucleotide), Berberine, Epigallocatechin Gallate (EGCG), and FK866 (Apoptozole) represent a selection of chemicals with the ability to activate FHL-2 or its associated pathways. AICAR, Resveratrol, Metformin, Quercetin, and Berberine are activators of AMP-activated protein kinase (AMPK), a key player in cellular energy regulation. These chemicals can influence FHL-2-mediated processes related to energy homeostasis, cell growth, and metabolism.

GW501516 (Cardarine) is a peroxisome proliferator-activated receptor-delta (PPAR-δ) agonist, activating pathways associated with metabolism and inflammation. This chemical offers a tool to explore the impact of PPAR-δ activation on FHL-2 function. Oxytocin, a neuropeptide hormone, can activate its receptor, influencing FHL-2-mediated pathways related to social behavior and stress response. Betaine, NAD+, and FK866 (Apoptozole) operate indirectly by modulating pathways involved in methylation, redox reactions, and NAD+ availability, respectively. These chemicals can impact FHL-2 function in processes such as gene expression, aging, and stress response. The remaining chemicals, A769662, Epigallocatechin Gallate (EGCG), and FK866 (Apoptozole), contribute to FHL-2 modulation through various pathways, including AMPK, sirtuin activation, and NAD+ depletion, offering a range of tools for investigating FHL-2 dynamics in cellular processes. Researchers can leverage these activators to unravel the intricate regulatory mechanisms of FHL-2, gaining insights into its role in normal cellular physiology and disease states. The specific targeting of FHL-2 or its associated pathways allows for detailed investigations into the functional aspects of FHL-2, providing valuable tools for advancing our understanding of cellular dynamics.

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