Date published: 2025-9-11

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TMC6 Activators

TMC6 Activators encompass a range of chemical compounds that indirectly enhance the functional activity of TMC6 through diverse cellular signaling pathways. For instance, Forskolin, Isoproterenol, 8-Br-cAMP, and Dibutyryl cAMP all raise intracellular cAMP levels, subsequently activating protein kinase A (PKA), which is known to phosphorylate a variety of proteins. This activation cascade may increase TMC6 activity by phosphorylating it directly or by altering the cellular environment to support TMC6's role in cellular processes. Similarly, Phorbol 12-myristate 13-acetate (PMA) and Epigallocatechin gallate (EGCG) target protein kinase C (PKC) and various protein kinases respectively. PMA's activation of PKC may lead to the phosphorylation of TMC6 or its regulatory proteins, enhancing TMC6's functional activity, while EGCG, by inhibiting certain kinases, may reduce competitive phosphorylation events, thereby creating a favorable context for TMC6 activation.

Calcium ionophores like A23187 and Ionomycin increase intracellular calcium, which activates calcium-dependent kinases that could phosphorylate TMC6 or modulate its activity indirectly. Sphingosine-1-phosphate engages G protein-coupled receptors to initiate signaling events that may culminate in the enhancement of TMC6 function, potentially through the modulation of its interaction with cellular components. LY294002's inhibition of PI3K alters AKT signaling, which could indirectly affect TMC6 activity by modifying membrane dynamics and signaling pathways that TMC6 is implicated in. Genistein, by inhibiting tyrosine kinases, may diminish competitive phosphorylation or alter signaling pathways, thus indirectly enhancing TMC6's functional activity in processes such as ion transport or membrane potential regulation.

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