GPR120 inhibitors are a class of chemical compounds that specifically target and modulate the activity of the G-protein coupled receptor 120 (GPR120), also known as free fatty acid receptor 4 (FFA4). GPR120 is a transmembrane protein found primarily in various tissues, including adipose tissue, the gastrointestinal tract, and immune cells, where it plays a crucial role in regulating metabolic and inflammatory processes. Inhibitors of GPR120 are designed to interfere with the receptor's signaling pathways, thereby influencing downstream cellular responses.
These inhibitors function by binding to GPR120 and altering its conformation or preventing its activation by endogenous ligands, which are typically long-chain fatty acids such as omega-3 fatty acids. By doing so, they can modulate intracellular signaling cascades associated with GPR120, including the activation of intracellular kinases and the release of secondary messengers like calcium ions. This modulation can have a wide range of effects on cellular physiology, including changes in lipid metabolism, insulin sensitivity, and inflammation. Consequently, GPR120 inhibitors have garnered significant attention in the field of metabolic research and are considered valuable tools for studying the intricate interplay between fatty acid signaling and various physiological processes.
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