Date published: 2025-9-16

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AQP10 Activators

AQP10 Activators encompass a diverse array of chemical compounds that indirectly enhance the functional activity of AQP10 through modulation of intracellular signaling pathways and cellular processes that govern its trafficking and membrane localization. Forskolin, by catalyzing the conversion of ATP to cAMP, indirectly augments AQP10's water transport function by facilitating its translocation to the cell surface. Similarly, Glyburide and Ionomycin, through their respective modulation of intracellular K+ and Ca2+ concentrations, may induce the translocation of AQP10 to the plasma membrane, thereby enhancing its activity. Phorbol 12-myristate 13-acetate (PMA) stimulates PKC, which can phosphorylate substrates involved in AQP10 trafficking, while Calmodulin inhibitors and Brefeldin A disrupt intracellular signaling and Golgi apparatus function, potentially altering AQP10 distribution within the cell. Dibutyryl cyclic AMP (db-cAMP) and Isoproterenol, through their cAMP elevating effects, and Cholera toxin, by increasing cAMP via ADP-ribosylation, are thought to facilitate AQP10's membrane insertion and activity.

Epigallocatechin gallate (EGCG) and Genistein exert their effects by inhibiting kinases that may regulate proteins involved in AQP10 trafficking, suggesting a potential enhancement of AQP10 function. IBMX, by preventing the breakdown of cAMP, is believed to contribute to the same outcome by maintaining a cellular environment conducive to AQP10 membrane presence. These chemical activators, by influencing various signaling molecules and pathways.

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