Dyrk3 Activators are a group of chemicals that can enhance the functional activity of Dyrk3, a protein involved in various cellular processes. These compounds primarily work by influencing the adenylate cyclase-cAMP-PKA pathway, a critical cell signaling pathway that Dyrk3 is directly involved in. Forskolin and IBMX, for example, enhance the functional activity of Dyrk3 by activating adenylate cyclase and inhibiting phosphodiesterases respectively, leading to an increase in cAMP levels. The elevated cAMP activates PKA, which can phosphorylate and activate Dyrk3.
On the other hand, PGE2, Epinephrine, Isoproterenol, Dopamine, Glucagon, Histamine, Serotonin, Adenosine, and Bimatoprost act by binding to specific receptors. The binding stimulates adenylate cyclase, leading to increased cAMP levels. This series of events, in turn, activates PKA, which can phosphorylate and activate Dyrk3. Rolipram, on the other hand, acts by inhibiting phosphodiesterase 4 (PDE4), resulting in an increase in cAMP levels. This ultimately leads to the activation of PKA and subsequently Dyrk3. The specific receptors involved for these compounds include EP receptors, β-adrenergic receptors, D1-like receptors, glucagon receptors, H2 receptors, 5-HT4, 5-HT6, and 5-HT7 receptors, A2A and A2B receptors, and prostaglandin receptors. The commonality among these Dyrk3 Activators is their ability to influence the adenylate cyclase-cAMP-PKA pathway, leading to the phosphorylation and activation of Dyrk3.
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