Erlotinib, by inhibiting EGFR, can alter pathways that are crucial for cell survival and division, thus affecting any regulatory role LOC729355 may have in these processes. LY294002, through its inhibition of PI3K, can disrupt the AKT pathway, leading to changes in cell survival signals that LOC729355 may be a part of. Sorafenib, with its multi-kinase inhibition profile, can broadly affect cell proliferation and angiogenesis, potentially modulating any contributory role of LOC729355 in these pathways.
U0126 and PD98059 are both inhibitors of the MEK enzyme, acting on the MAPK/ERK pathway, which is central to cell growth and differentiation, and any involvement of LOC729355 in this pathway can be regulated by these inhibitors. Staurosporine and SP600125 broadly target protein kinases and JNK, respectively, impacting numerous cellular functions including those potentially influenced by LOC729355. SB431542 disrupts the TGF-beta signaling, which can influence cell differentiation and proliferation, processes where LOC729355 may play a part. Rapamycin's inhibition of mTOR has profound effects on cell growth and proliferation, which can alter the functional state of LOC729355 if it is involved in these processes. Dasatinib acts on Src family kinases that are integral to cell migration and invasion, potentially affecting LOC729355's regulation of these processes. Thapsigargin disrupts calcium homeostasis by inhibiting SERCA pumps, affecting cellular signaling and function, including any role of LOC729355. Lastly, Z-VAD-FMK's inhibition of caspases affects the apoptosis pathway, which can alter the activity of LOC729355 if it is part of this process.
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