Date published: 2025-9-12

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SNX10 Activators

SNX10 activators are a diverse class of chemical compounds that work by influencing the cAMP-PKA pathway to enhance the endosomal trafficking process that SNX10 is directly involved in. Forskolin, Rolipram, Epinephrine, Caffeine, Dopamine, Histamine, Serotonin, Norepinephrine, IBMX, Isoproterenol, Salbutamol, and Terbutaline all enhance the levels of cAMP, a second messenger that activates PKA. PKA phosphorylates Rab GTPases, proteins that are crucial for the regulation of endosomal trafficking, a key process that SNX10 facilitates. The mechanism by which these chemicals activate SNX10 is by promoting the phosphorylation of Rab GTPases, a critical step in the endosomal trafficking process. By enhancing cAMP levels, these chemicals activate PKA, which then phosphorylates Rab GTPases, promoting their activity. This leads to an enhancement of the endosomal trafficking process, in which SNX10 plays a direct role. In this way,these chemicals indirectly enhance the functional activity of SNX10. It's important to note that while these chemicals don't directly interact with SNX10, their influence on cAMP-PKA pathway and Rab GTPases provides a mechanism for indirectly enhancing the activity of SNX10.

Most of these compounds, such as Forskolin and Rolipram, interact with enzymes like adenylyl cyclase and phosphodiesterase-4 respectively to enhance the level of cAMP. Others, like Epinephrine, Dopamine, and Norepinephrine, bind to specific receptors that trigger the production of cAMP via G-protein activation of adenylyl cyclase. Compounds like Caffeine and IBMX inhibit phosphodiesterase enzymes, impeding the breakdown of cAMP, and thus enhancing its levels. Regardless of their specific mechanisms, all these compounds ultimately lead to increased cAMP levels, resulting in the activation of PKA. The activated PKA then phosphorylates Rab GTPases, which play a crucial role in the endosomal trafficking process that SNX10 facilitates. This series of events indirectly leads to the enhanced functional activity of SNX10.

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