Date published: 2025-9-11

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FAHD2B Activators

Forskolin, a well-described diterpene, serves as a catalyst for adenylyl cyclase, resulting in elevated cAMP levels and subsequent activation of protein kinase A. This kinase phosphorylates various substrates, potentially influencing proteins that govern the activity of FAHD2B. Ionomycin, another activator, disrupts intracellular calcium balance, which activates calcium-dependent kinases. These kinases then go on to phosphorylate a host of proteins, some of which may be involved in modulating FAHD2B activity. Phorbol esters, such as PMA, stimulate protein kinase C, a pivotal player in cellular signaling. PKC phosphorylates a spectrum of proteins, and this action can extend to those interacting with FAHD2B, affecting its activity. In contrast, compounds like U0126 and PD98059 specifically inhibit MEK1/2, crucial components in the MAPK/ERK pathway, leading to an altered phosphorylation landscape that could impact FAHD2B activity.

Protein phosphatase inhibitors like Okadaic Acid and Calyculin A prevent dephosphorylation, thereby maintaining proteins in a phosphorylated state that can influence FAHD2B's function. Flavonoids such as Epigallocatechin Gallate and stilbenoids like Resveratrol engage with various signaling pathways, possibly altering the activity of proteins associated with FAHD2B. Polyamines, represented by spermine, regulate cellular homeostasis and could indirectly affect FAHD2B. Furthermore, Lithium Chloride acts on GSK-3, a kinase with multiple substrates, and Sodium Butyrate, a histone deacetylase inhibitor, changes gene expression patterns, both of which can lead to changes in FAHD2B activity.

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