Date published: 2025-9-15

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FBXO41 Activators

Chemical activators of FBXO41 can be understood through their influence on specific cellular pathways and the resultant biochemical events that lead to the protein's activation. Forskolin, for instance, is known to activate adenylyl cyclase, which catalyzes the conversion of ATP to cyclic AMP (cAMP). An increase in cAMP levels subsequently activates protein kinase A (PKA). PKA can phosphorylate FBXO41, which enhances its ubiquitination activity, a key process in protein regulation and turnover. Similarly, Phorbol 12-myristate 13-acetate (PMA) acts as an activator of protein kinase C (PKC), which phosphorylates FBXO41, thus promoting its activation. Another chemical, Ionomycin, facilitates the increase of intracellular calcium levels that activate calcium-dependent kinases, which in turn can lead to the phosphorylation and activation of FBXO41. Thapsigargin contributes to FBXO41 activation by inhibiting the sarco/endoplasmic reticulum Ca2+-ATPase (SERCA), causing a rise in cytosolic calcium, which activates kinases that may phosphorylate FBXO41.

In the realm of enzyme inhibition, compounds like Okadaic Acid and Calyculin A inhibit protein phosphatases PP1 and PP2A. This inhibition prevents the dephosphorylation of proteins, maintaining FBXO41 in a phosphorylated state that is indicative of its active form. Anisomycin activates the JNK pathway, which can lead to the activation of FBXO41 through phosphorylation. Proteasome inhibitors, such as MG132 and Epoxomicin, inhibit the degradation of phosphorylated FBXO41, resulting in the accumulation of the active form of the protein. LY294002 acts by inhibiting PI3K, leading to reduced Akt activity and altering the phosphorylation status of various proteins, which can activate FBXO41. Rapamycin's inhibition of mTOR might also lead to activation of FBXO41 through complex feedback loops that result in its dephosphorylation and activation. Lastly, 6-Benzylaminopurine, a plant hormone known as cytokinin, activates specific kinases that have the capacity to phosphorylate and activate FBXO41. Each of these chemicals acts upon FBXO41 through distinct mechanisms, but all converge on the common outcome of activating the protein through phosphorylation or stabilization of its phosphorylated form.

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