RASA4 Activators are diverse chemical compounds that influence various signaling pathways, culminating in the enhanced activity of RASA4. Forskolin, by elevating cAMP levels, indirectly potentiates RASA4's function by stimulating PKA, which can phosphorylate substrates impacting RASA4's signaling domain. Similarly, IBMX and Rolipram both raise intracellular cAMP levels, leading to PKA activation and the subsequent enhancement of RASA4 activity. FTY720, after in vivo phosphorylation, activates sphingosine-1-phosphate receptors and modulates RASA4's function by altering lipid signaling pathways that RASA4 is involved in. Lithium Chloride, through GSK-3 inhibition, may enhance RASA4 activity by affecting components of the Wnt signaling cascade, which is linked to RASA4's regulatory mechanisms. Compounds like Epigallocatechin Gallate exert their influence by inhibiting kinases, thereby potentially reducing negative regulation on pathways that RASA4 operates within, leading to its enhanced activity.
Continuing with the theme of pathway modulation, Sphingosine-1-phosphate and A23187 both work through lipid and calcium signaling, respectively, which are crucial for the proper functioning of RASA4. While sphingosine-1-phosphate activates G-protein-coupled receptors impacting RASA4, A23187 raises intracellular calcium levels that can enhance RASA4 activity through calcium-dependent signaling pathways. Additionally, the PI3K inhibitor LY294002 and the PKC activator PMA, may indirectly enhance RASA4 by altering the PI3K/Akt pathway and related signaling processes that RASA4 is a part of. The MEK inhibitors U0126 and PD98059 could shift signaling dynamics in the MAPK pathway, thus indirectly enhancing the activity of RASA4.
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