TM4SF4 Activators comprise a diverse range of chemical compounds that influence the functional activity of TM4SF4 through various indirect mechanisms. Forskolin, by elevating cAMP levels, activates PKA, leading to the phosphorylation of substrates in TM4SF4-associated pathways, enhancing TM4SF4's role in cell signaling and membrane dynamics. Genistein, as a tyrosine kinase inhibitor, reduces competitive signaling, thus favoring TM4SF4-associated pathways in cellular adhesion and signal transduction. Similarly, Sphingosine-1-phosphate modulates lipid signaling pathways, thereby enhancing TM4SF4's role in these processes. Thapsigargin and A23187, by increasing intracellular calcium, activate calcium-dependent pathways, crucial for TM4SF4's role in cellular adhesion and migration. Additionally, PMA, as a PKC activator, and kinase inhibitors like Epigallocatechin gallate, influence signaling pathways to indirectly augment TM4SF4's activity in cell proliferation and survival.
Continuing this modulation, LY294002 and Wortmannin, as PI3K inhibitors, alter the PI3K/Akt signaling pathway, impacting TM4SF4's involvement in cell migration and survival. SB203580 and U0126, targeting the MAPK signaling pathways, influence TM4SF4's activity in cellular stress responses, apoptosis, differentiation, and proliferation. These compounds, by modulating these specific pathways, indirectly enhance TM4SF4's functional role in these processes. Staurosporine, despite its broad-spectrum kinase inhibition, selectively activates TM4SF4 pathways by lifting the inhibition exerted by specific kinases on TM4SF4-related processes. Collectively, these TM4SF4 Activators, through their targeted effects on cellular signaling, facilitate the enhancement of TM4SF4-mediated functions, particularly in areas of cell signaling, membrane dynamics, adhesion, and migration, without the need for upregulating its expression or direct activation.
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