Wortmannin and LY294002 both act as PI3K inhibitors, thereby disrupting the PI3K/AKT signaling pathway, which is central to many cellular processes including cell growth, survival, and metabolism. Triciribine further inhibits the AKT pathway by directly targeting AKT, preventing its activation. Dasatinib inhibits Src family kinases, which are part of a larger signaling network that regulates various cellular processes, and can thereby alter the function of LOC729979. PD 0332991 hydrochloride, by inhibiting CDK4/6, halts cell cycle progression, which can reduce the cellular context in which LOC729979 may act. PD98059 and SP600125, inhibitors of MEK and JNK respectively, interfere with the MAPK/ERK pathway and AP-1 transcription factor activity, both of which can play roles in the regulation of numerous proteins, including LOC729979.
Thapsigargin disrupts calcium homeostasis by inhibiting the SERCA pump, which is crucial for maintaining intracellular calcium levels, thereby affecting proteins sensitive to calcium signaling such as LOC729979. MG132 targets the ubiquitin-proteasome system, altering the degradation pathway of proteins and potentially stabilizing or destabilizing LOC729979. Go6983 acts to inhibit PKC, disrupting various signal transduction pathways, which can lead to changes in the activity of LOC729979. Y-27632, as a ROCK inhibitor, affects cytoskeletal dynamics and cell morphology, which can have downstream effects on the function of LOC729979. ZM-447439, an Aurora kinase inhibitor, disrupts mitosis and cell division processes, which can modify the cellular environment and indirectly influence the activity of LOC729979.
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