Wortmannin and LY294002 both act as PI3K inhibitors, which can suppress pathways critical for protein activity, including AKT signaling. Trametinib, as a MEK inhibitor, and Sorafenib, a RAF inhibitor, target the MAPK/ERK pathway, which is a key regulator of cell division and proliferation. If LOC730198 functions within this pathway, its activity would be impacted. Sunitinib, a receptor tyrosine kinase inhibitor, has the ability to disrupt various signal transduction processes, which can affect proteins that are regulated by or dependent on these pathways. Rapamycin inhibits mTOR, a central protein in cellular growth and metabolism, which could influence LOC730198 if it is linked to these pathways. ABT-199 targets BCL-2, a family of proteins that regulate cell death, and could therefore alter the activity of LOC730198 if it plays a role in apoptotic processes.
Crizotinib inhibits ALK, a tyrosine kinase involved in cell growth signaling pathways, potentially affecting LOC730198 if it interacts with those pathways. PD0332991, a CDK4/6 inhibitor, halts cell cycle progression and could impact LOC730198 if it is involved in the regulation of the cell cycle. SP600125 inhibits JNK, affecting both apoptosis and inflammatory pathways, which can influence LOC730198 if it has a role in these processes. ZM-447439, an Aurora kinase inhibitor, disrupts the process of mitosis, potentially affecting LOC730198 if its activity is related to cell division. Lastly, Olaparib, a PARP inhibitor, influences DNA repair mechanisms, which can impact LOC730198 if it is involved in the maintenance of genomic integrity.
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