The chemicals identified as Tra-2α Activators are an ensemble of compounds that function primarily through the elevation of intracellular cAMP levels or the inhibition of cAMP degradation, leading to enhanced protein kinase A (PKA) activity. These compounds, ranging from neurotransmitters and hormones like epinephrine and dopamine to phosphodiesterase inhibitors such as IBMX and theophylline, converge on the activation of PKA. PKA is a key signaling molecule that phosphorylates a variety of substrates within the cell, influencing numerous cellular processes. The activation of PKA by these chemicals can result in the phosphorylation of target proteins that either directly or indirectly modulate the activity of Tra-2α. This modulation could be due to changes in the phosphorylation status of Tra-2α itself or alterations in the activity of proteins that interact with or regulate Tra-2α.
The broad spectrum of these compounds reflects the wide-ranging mechanisms through which cAMP-PKA signaling can be modulated. For instance, forskolin directly stimulates adenylate cyclase to produce cAMP, while IBMX and rolipram prevent the breakdown of cAMP, thereby sustaining its signaling capabilities.
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