Date published: 2025-9-12

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Olfr251 Activators

Chemical activators of Olfr251 can enact their enhancing effects through various biochemical interactions and pathways. Zinc Chloride and Magnesium Chloride can activate Olfr251 by directly binding to the receptor, which likely induces a conformational shift, leading to the activation of the olfactory signaling cascade. This direct binding can alter the receptor's structure, thus initiating signal transduction. Sodium Fluoride, by promoting protein phosphorylation within the olfactory signaling pathway, facilitates the activation of Olfr251 as it participates in this cascade. The chemical Forskolin increases the levels of intracellular cAMP, which in turn activates protein kinase A. The phosphorylation activity of protein kinase A can then target Olfr251, leading to its activation. Similarly, Phorbol Myristate Acetate directly activates protein kinase C, which is known to phosphorylate and subsequently activate Olfr251.

In addition, Ionomycin acts by increasing intracellular calcium concentration, which can trigger a series of downstream effects resulting in the phosphorylation and activation of Olfr251. Hydrogen Peroxide serves as a signaling molecule that activates kinases that can phosphorylate Olfr251, leading to its activation. The inhibition of protein phosphatases by Okadaic Acid prevents dephosphorylation, thus keeping proteins such as Olfr251 in an activated state. 4-Phenylbutyric Acid supports the proper folding of proteins, which is essential for Olfr251 to achieve the structural conformation necessary for activation. Chloroquine can activate Olfr251 by inducing changes in the intracellular pH that affect the receptor's structure, leading to its activation. Nicotine can activate Olfr251 through a process that involves an increase in intracellular calcium, which activates kinases capable of phosphorylating the receptor. Lastly, Lithium Chloride inhibits GSK-3β, and this inhibition can activate signaling pathways that involve the activation of Olfr251, ensuring that the receptor is functionally active.

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