Chemical inhibitors such as WZB117 and Rapamycin exert influence by restricting cellular energy supply and disrupting growth signaling pathways, respectively, thereby creating an environment that can impair the protein's function. LY294002 and U0126, as PI3K and MEK inhibitors, alter the dynamics of the PI3K-Akt and MAPK/ERK pathways, pivotal conduits for signals that govern cell proliferation and survival, which in turn can impact the role of C2orf44_BC068281. Inhibition of TGF-beta receptors by compounds like SB431542, or interference with the JNK pathway by SP600125, can also reshape the protein's functional landscape by altering cellular proliferation and stress response pathways.
Furthermore, Y-27632 and ZM-447439, which inhibit ROCK and Aurora kinases, respectively, affect cytoskeletal organization and cell division, processes in which C2orf44_BC068281 might play a part. The targeting of protein degradation pathways by Bortezomib, a proteasome inhibitor, can influence the stability and turnover of the protein. Similarly, Thapsigargin's disruption of calcium homeostasis through SERCA pump inhibition and KN-93's blockade of CaMKII can modulate calcium signaling, potentially affecting C2orf44_BC068281's activity.
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