LYAR activators encompass a variety of molecular entities that indirectly influence the activity of the LYAR protein. Forskolin functions by raising intracellular cAMP, which activates PKA and can lead to phosphorylation of proteins that influence LYAR activity, particularly in the context of cell growth and proliferation. PMA, through activation of PKC, also impacts cell cycle regulation and may enhance LYAR's role in these processes. Ionomycin, by altering intracellular calcium levels, has the potential to activate calcium-dependent signaling pathways, which could subsequently upregulate LYAR's activity if it is responsive to such signals.
Lithium chloride, by inhibiting GSK-3, could modulate LYAR's activity through alterations in gene expression regulation. Sodium orthovanadate acts as a phosphatase inhibitor, preserving phosphorylation states of proteins and enhancing LYAR function within those pathways. Increased levels of NAD⁺ can modulate sirtuin activity, impacting cellular stress responses and possibly LYAR's activity in managing cellular homeostasis. Retinoic acid, by engaging with nuclear receptors, could enhance LYAR activity through gene expression regulation. Curcumin and resveratrol, through their modulation of NF-κB, Wnt/β-catenin, and AMPK pathways, could influence LYAR's activity, particularly if it is involved in these signaling pathways. Rapamycin's inhibition of the mTOR pathway could also indirectly enhance LYAR activity, especially in the context of growth and protein synthesis.
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