Date published: 2026-1-12

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CRP3 Activators

CRP3 activators consist of a variety of chemical compounds that indirectly influence the activity of CCAAT/enhancer-binding protein delta. These activators work through several cellular mechanisms and pathways. For instance, Dexamethasone, a glucocorticoid receptor agonist, can enhance glucocorticoid receptor-mediated signaling, leading to the upregulation of CRP3 expression. Similarly, compounds like Cyclic AMP and Forskolin elevate cAMP levels, which activate protein kinase A (PKA). PKA activation can lead to enhanced CREB activity, a transcription factor that can upregulate CRP3.

Other chemicals in this class include IBMX, a non-selective phosphodiesterase inhibitor that raises cAMP and cGMP levels, potentially enhancing CRP3 activation through PKA pathways. Phorbol 12-myristate 13-acetate (PMA) activates protein kinase C (PKC), which can modulate transcription factors influencing CRP3 expression. Additionally, Retinoic acid and β-estradiol work through receptor-mediated mechanisms, modulating gene expression patterns that can include CRP3 upregulation. Epidermal Growth Factor (EGF) and Insulin are examples of compounds that activate specific receptor signaling pathways, leading to downstream signaling that affects CRP3 expression. Lastly, Sodium Butyrate and 5-Azacytidine, a histone deacetylase inhibitor and a DNA methyltransferase inhibitor, respectively, can alter chromatin structure and DNA methylation, potentially enhancing CRP3 expression.

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