LOC100041341 inhibitors contain compounds like LY294002 and Rapamycin disrupt the PI3K/Akt/mTOR signaling pathway, which is central to controlling cell growth and proliferation. By impeding this pathway, these inhibitors alter the activity of LOC100041341 if it is associated with or affected by this cascade. Similarly, SB203580, PD98059, and SP600125 are selective inhibitors for components of the MAPK pathways, which are pivotal in managing cellular stress responses, apoptosis, and cell division. These inhibitors adjust the phosphorylation and activity of proteins like LOC100041341, presuming it operates within these signaling frameworks.
Bortezomib, by inhibiting the 26S proteasome, affects the degradation of proteins, potentially altering the stability and quantity of LOC100041341 in the cell. Kinase inhibitors such as Sorafenib, PP2, and Dasatinib target tyrosine kinases and could thereby regulate the phosphorylation and functionality of LOC100041341 if it is a substrate or influenced by these enzymes. Thapsigargin and U73122 disturb calcium homeostasis and phospholipase C signaling, respectively, which could lead to modifications in proteins regulated by calcium or by inositol triphosphate and diacylglycerol, molecules produced by phospholipase C activity. Go6983 inhibits protein kinase C, which can also affect the phosphorylation state and activity of LOC100041341 if it is regulated by PKC-mediated pathways.
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