Date published: 2025-10-30

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Olr437 Activators

Chemical activators of Olr437 include a variety of compounds that influence different biochemical pathways leading to the activation of this protein. Forskolin, known for its ability to activate adenylate cyclase, results in an increased production of cyclic AMP (cAMP). The elevated cAMP levels activate protein kinase A (PKA), which can phosphorylate Olr437, thereby activating it. Similarly, Phorbol 12-myristate 13-acetate (PMA) is a potent activator of protein kinase C (PKC), a kinase that can also phosphorylate Olr437 as part of its signaling cascade. Ionomycin, a calcium ionophore, raises the intracellular calcium concentration, which can activate proteins sensitive to calcium, including Olr437 if it is part of the calcium signaling pathway. In the same vein, Thapsigargin functions by inhibiting the SERCA pump, leading to an increase in cytosolic calcium levels, which could activate Olr437 if it is responsive to calcium.

BAY K8644, an L-type calcium channel agonist, increases calcium influx, which can activate Olr437 if the protein is calcium-dependent. Zinc pyrithione elevates intracellular zinc levels, which can activate zinc-responsive proteins, potentially including Olr437. Okadaic acid and Calyculin A, both protein phosphatase inhibitors, lead to a general increase in phosphorylated proteins within the cell, which could result in the activation of Olr437 through increased phosphorylation. Anisomycin activates stress-activated protein kinases, which may phosphorylate and activate Olr437 within cellular stress response pathways. Ouabain disrupts ion gradients by inhibiting the Na+/K+ ATPase pump, which could trigger signal transduction pathways involving the activation of Olr437. Veratridine opens sodium channels, causing depolarization that may initiate signaling pathways involving Olr437. Lastly, H-89 dihydrochloride, a PKA inhibitor, can lead to the compensatory activation of proteins regulated by PKA, which may include Olr437 through complex feedback and regulatory mechanisms within the cell.

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