Date published: 2025-9-14

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RNF24 Activators

RNF24 activators encompass a variety of chemical compounds that indirectly promote the functional activity of RNF24 through distinct cellular signaling pathways. Forskolin, by raising cAMP levels, indirectly augments RNF24's functional role by facilitating PKA-mediated phosphorylation events, which may stabilize RNF24 or enhance its interactions with substrates. Similarly, PMA, as an activator of PKC, contributes to the potential phosphorylation of RNF24-interacting proteins, thereby possibly increasing RNF24's E3 ubiquitin ligase activity. Ionomycin, by elevating intracellular calcium, can induce calcium-dependent protein kinases to phosphorylate RNF24 or its substrates, leading to an increase in its ubiquitination activity. The PI3K pathway inhibitor LY294002, as well as PD 98059, which targets MEK, may alter signaling branches to favor RNF24's regulatory roles, while SB 203580's inhibition of p38 and EGCG's broad kinase inhibitory effects could stabilize RNF24, thus enhancing its activity. Sildenafil, through PDE5 inhibition and subsequent cAMP and cGMP accumulation, could support PKA and PKG pathways that enhance the activity of RNF24. Additionally, phosphatase inhibitors such as Okadaic Acid and Calyculin A elevate phosphorylation within the cell, potentially maintaining or promoting phosphorylations that bolster RNF24's stability or substrate interactions.

The activity of RNF24 is further influenced by chemical inducers that modulate calcium signaling and metalloenzyme activity. Thapsigargin, by disrupting calcium homeostasis, could activate pathways that lead to the phosphorylation of RNF24, enhancing its role in ubiquitination processes. Zinc Pyrithione, by affecting metal ion balance, might alter RNF24's structure or function, thereby potentially increasing its ubiquitin ligase activity.

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