Date published: 2025-9-13

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GPATCH8 Activators

Forskolin is a well-known compound that can elevate intracellular cAMP levels, leading to the activation of PKA, which is critical for phosphorylation events within the cell. By boosting cAMP, Forskolin can indirectly influence the activity of proteins that are involved in the same pathways as GPATCH8, perhaps altering its activity or the activity of proteins that interact with it. Ionomycin, a calcium ionophore, increases calcium concentrations within the cell, which can trigger a host of calcium-dependent signaling mechanisms. These mechanisms are often integral to processes such as transcription, translation, and post-translational modifications, potentially impacting the function of proteins like GPATCH8. Phorbol 12-myristate 13-acetate, or PMA, is another activator that targets protein kinase C (PKC). PKC is involved in a variety of cellular responses, and its activation can lead to the phosphorylation of substrates that could modify the function of GPATCH8 or its regulatory proteins.

Epidermal Growth Factor (EGF) interacts with its receptor to initiate a signaling cascade that could intersect with GPATCH8's pathways. This growth factor can modulate a wide array of cellular functions, possibly including those associated with GPATCH8. Insulin, through its receptor-mediated signaling pathway, influences numerous cellular processes, including those associated with RNA processing and splicing, and could potentially modulate the activity or regulation of GPATCH8. 5-Azacytidine and Trichostatin A are compounds that affect the epigenetic landscape of the cell. 5-Azacytidine inhibits DNA methyltransferase, altering gene expression patterns, which may influence GPATCH8's expression or function. Trichostatin A, a histone deacetylase inhibitor, can change chromatin structure and gene expression, potentially impacting GPATCH8. The inhibitors LY294002, PD98059, rapamycin, SB203580, and SP600125 target various kinases and signaling molecules such as PI3K, MEK, mTOR, p38 MAPK, and JNK. Inhibition of these molecules can suppress or alter signaling pathways and cellular processes, which might involve GPATCH8 either directly or indirectly.

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