Forskolin, by increasing intracellular cAMP, activates PKA, which can phosphorylate a wide range of proteins and possibly influence OR1Q1's activity. Ionomycin, through its elevation of intracellular calcium levels, can activate calcium-dependent signaling cascades, potentially affecting OR1Q1. Similarly, PMA's activation of PKC can lead to phosphorylation events that may interact with OR1Q1's signaling network.
Other members of this class, such as LY294002 and Rapamycin, target key regulatory proteins and complexes like PI3K and mTOR, respectively, which have broad effects on cell growth and metabolism, processes that OR1Q1 may be a part of. Inhibitors such as SB216763, SP600125, and PD168393 provide additional layers of modulation by targeting GSK-3, JNK, and EGFR kinase, which are involved in pathways like Wnt signaling, stress response, and growth factor signaling. These pathways can have wide-ranging implications for protein activities within the cell, including that of OR1Q1. Moreover, compounds like ZM-447439, which inhibits Aurora kinases, can affect mitotic events, while Tunicamycin and Thapsigargin induce ER stress and disrupt Ca²⁺ homeostasis, respectively. These conditions can lead to a cascade of cellular responses, potentially affecting the signaling pathways in which OR1Q1 is active.
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