Wortmannin and LY294002, for instance, exert their effects by targeting the PI3K pathway, a critical signaling route that governs cell growth and metabolism. Their inhibition of PI3K can lead to downstream effects, potentially including the modulation of LOC729688 activity. Similarly, Rapamycin acts on the mTOR pathway, a pivotal regulator of cellular growth and proliferation, which may also affect LOC729688 function if it is linked to this pathway. In the context of the MAPK pathway, both SB203580 and PD98059 are selective inhibitors of different kinases within this signaling cascade. SB203580 targets p38 MAP kinase, while PD98059 inhibits MEK1, both potentially altering the signaling events that could determine the activity of LOC729688. The compound SP600125, which inhibits JNK, and the MEK1/2 inhibitor U0126, also function within the MAPK pathway and are capable of modulating the protein's activity, provided that LOC729688 is a downstream target of these pathways.
Further branching into the realm of kinase inhibition, PP2 specifically targets Src family kinases, which are integral to a multitude of cellular processes. The inhibition of Src kinases by PP2 can thus influence the activity of LOC729688. On the other hand, PD0325901, another MEK inhibitor with enhanced bioavailability compared to PD98059, and Ku-55933, an ATM kinase inhibitor, act on the cell cycle and DNA damage response, respectively. These inhibitors could impact LOC729688 function if it is involved in these cellular responses. Lastly, the proteasome inhibitor MG132 and the Aurora kinase inhibitor ZM447439 play roles in protein degradation and mitotic progression, respectively.
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