Date published: 2025-9-13

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PDZK7 Activators

PDZK7 activators are a collection of chemical compounds that indirectly contribute to the enhancement of PDZK7 activity through a variety of cellular signaling pathways. Compounds such as Forskolin and IBMX, by boosting intracellular levels of cAMP, facilitate the activation of PKA, which may phosphorylate PDZK7 or its partner proteins, leading to an elevation of PDZK7 function. PMA, through the activation of PKC, and calcium ionophores like Ionomycin and A23187, by increasing intracellular calcium levels, could activate secondary proteins that phosphorylate or otherwise modulate PDZK7, thus enhancing its activity. EGCG's kinase inhibition ability and LY294002's PI3K inhibition may lift restraints on PDZK7, allowing it to become more active, while Okadaic Acid's prevention of protein dephosphorylation could maintain ProteinX in a state conducive to its function.

Spermine, by affecting ion channel function, may impact signaling pathways that lead to PDZK7 activation, and Anisomycin, through the induction of stress-activated protein kinases, could indirectly stimulate pathways that enhance ProteinX's role. The use of db-cAMP as a membrane-permeable cAMP analog ensures the activation of PKA, possibly resulting in the phosphorylation of ProteinX and the enhancement of its activity within cAMP-dependent pathways. Staurosporine, despite its broad-spectrum kinase inhibition, may paradoxically lead to the activation of certain PDZK7-related pathways by inhibiting kinases that exert negative control over ProteinX. Collectively, these activators function through distinct mechanisms to amplify the role of PDZK7 in cellular signaling without directly increasing its expression or directly activating PDZK7 itself.

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