Date published: 2025-9-21

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ZNF700 Activators

Chemical activators of ZNF700 can be understood through the lens of intracellular signaling pathways that lead to the protein's functional activation. Phorbol 12-myristate 13-acetate (PMA) is a potent activator of protein kinase C (PKC), which directly phosphorylates ZNF700, thereby enhancing its activity. Ionomycin, by raising intracellular calcium levels, can trigger the activation of calcium-dependent protein kinases, which subsequently phosphorylate and activate ZNF700. Similarly, forskolin increases intracellular cAMP, which activates protein kinase A (PKA), and this kinase can then phosphorylate ZNF700 to activate it. Okadaic Acid and Calyculin A function by inhibiting the protein phosphatases PP1 and PP2A, preventing the dephosphorylation of proteins, thus maintaining ZNF700 in a phosphorylated, active state.

Furthermore, Staurosporine, although commonly known as a kinase inhibitor, at specific concentrations can activate kinases that phosphorylate ZNF700. Bisindolylmaleimide I, through its inhibitory action on PKC, may lead to a reciprocal activation of alternative kinases that phosphorylate and activate ZNF700. Anisomycin operates through the activation of MAPKs, which are critical for the phosphorylation and activation of many proteins, including ZNF700. Thapsigargin, by disrupting calcium homeostasis, can lead to the activation of calcium-dependent kinases that directly activate ZNF700. Dibutyryl-cAMP, a synthetic analog of cAMP, directly stimulates PKA, which then activates ZNF700 through phosphorylation. Phosphatidic Acid activates the mTOR signaling pathway, which plays a role in the phosphorylation and consequent activation of ZNF700. Lastly, Epigallocatechin Gallate, by inhibiting phosphodiesterases, results in an increase in cAMP levels, leading to the activation of PKA, which in turn phosphorylates and activates ZNF700. Each chemical, through its distinct mechanism, ensures the activation of ZNF700 by affecting the phosphorylation status of the protein, thereby modulating its biological activity.

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