Date published: 2025-10-30

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Rim3 Activators

Rim3 Activators encompass a diverse range of chemical compounds that indirectly promote the functional activity of Rim3 through modulation of various signaling pathways integral to synaptic vesicle dynamics. For example, Forskolin, by increasing cAMP, indirectly enhances Rim3's role in neurotransmitter release, while BAPTA-AM, by chelating intracellular calcium, may influence Rim3's involvement in calcium-dependent processes. Sphingosine-1-phosphate and Ionomycin both operate through different mechanisms of lipid signaling and calcium elevation, respectively, to potentiate the cellular processes that Rim3 is known to be involved in, specifically synaptic vesicle priming and exocytosis. Similarly, PMA and EGCG contribute to the activation of Rim3 by modulating protein kinase C and inhibiting various protein kinases that would otherwise negatively regulate neurotransmitter release, where Rim3 plays a crucial role.

Compounds such as LY294002 and Wortmannin, by inhibiting PI3K, alter downstream signaling that is likely to affect synaptic vesicle docking and priming processes in which Rim3 is directly involved, thereby enhancing its functional activity. MRS1845 and CPA, through their actions on G-protein-coupled receptors and adenosine receptors, respectively, have the potential to enhance Rim3's role in neurotransmitter release by modulating the cAMP pathway. In addition, Ryanodine's effect on the ryanodine receptors can lead to an increase in calcium release from intracellular stores, which is a key factor in calcium-dependent exocytosis mediated by Rim3. Lastly, Isoproterenol, through beta-adrenoreceptor activation and cAMP elevation, can indirectly enhance the functional activity of Rim3 by influencing the cAMP-dependent signaling pathways that are involved in synaptic vesicle release.

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