Chemical inhibitors of PEBP2αA encompass a variety of compounds that target different kinases and enzymes involved in the phosphorylation and regulation of this protein. Kenpaullone and Alsterpaullone are inhibitors that target Glycogen synthase kinase 3 beta (GSK-3β), a kinase that has a role in the phosphorylation of PEBP2αA, which is a critical post-translational modification that affects the protein's activity. By inhibiting GSK-3β, these compounds prevent the phosphorylation of PEBP2αA, thus leading to a reduction in its activity. Similarly, Lithium chloride and SB 216763 also inhibit GSK-3β, thereby reducing the phosphorylation and subsequent activation of PEBP2αA. Indirubin-3'-monoxime and Roscovitine target cyclin-dependent kinases (CDKs), which are known to phosphorylate PEBP2αA. By inhibiting these CDKs, the phosphorylation and activity of PEBP2αA are diminished.
Furthermore, H-89 acts as an inhibitor of Protein kinase A (PKA), which can phosphorylate PEBP2αA. The inhibition of PKA by H-89 leads to a decrease in PEBP2αA phosphorylation and therefore its activity. Y-27632 inhibits Rho-associated protein kinase (ROCK), which is involved in actin dynamics that can influence PEBP2αA function in cellular signaling pathways. By inhibiting ROCK, Y-27632 can disrupt these actin dynamics, thereby inhibiting the activity of PEBP2αA. In the MAPK signaling cascade, PD 98059 and U0126 inhibit MEK, which is an upstream activator of ERK. ERK can phosphorylate PEBP2αA, and therefore, by inhibiting MEK, PD 98059 and U0126 effectively reduce the phosphorylation and activity of PEBP2αA. SP600125 inhibits c-Jun N-terminal kinase (JNK), another kinase that can phosphorylate PEBP2αA, leading to a decrease in PEBP2αA's activity. Lastly, LY294002 is an inhibitor of Phosphoinositide 3-kinases (PI3K), which is upstream of AKT, another kinase that can phosphorylate PEBP2αA. By inhibiting PI3K, LY294002 decreases AKT activity, which in turn reduces the phosphorylation and activity of PEBP2αA. Each of these chemicals serves as an inhibitor by disrupting the phosphorylation state of PEBP2αA, which is essential for its activation and function within the cell.
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