Chemical activators of T2R15 include a variety of compounds that can initiate the bitter taste sensation by directly interacting with the taste receptor. Denatonium Benzoate, known for its extreme bitterness, activates T2R15 by binding to its ligand-binding domain, which induces a structural change in the receptor, enabling it to interact with G-proteins that kick-start the intracellular signaling cascade necessary for taste perception. Similarly, Quinine, a naturally bitter compound, serves as a direct activator by binding to T2R15, leading to an interaction with signaling molecules that amplify the bitter taste signal.
Propylthiouracil, Saccharin, Sucralose, and Aspartame are artificial sweeteners that paradoxically activate T2R15, despite their primary association with sweetness. This activation process involves direct binding to the receptor, followed by the activation of signaling pathways that culminate in the perception of bitterness. Phenylthiocarbamide (PTC), another well-known bitter compound, activates T2R15 by binding directly to the receptor, subsequently activating taste cells. Acesulfame Potassium, another artificial sweetener, and Caffeine, a bitter alkaloid found in coffee and tea, both activate T2R15 through a similar mechanism, where direct receptor binding triggers the bitter taste signaling pathway. Naringin, a flavonoid found in grapefruits, and Aloin, found in aloe, both activate T2R15 by direct interaction with the receptor, resulting in the activation of downstream signaling processes that contribute to the perception of bitterness. Lastly, Magnesium Sulfate, which has a bitter taste, also activates T2R15 through receptor interaction, which leads to the signaling processes that enable bitter taste transduction. All these chemicals, by directly binding and activating T2R15, showcase the diverse nature of compounds that can trigger the bitter taste response through this specific taste receptor.
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