Inhibitors like Wortmannin and Triciribine act on PI3K and AKT, respectively, key components in the PI3K/AKT/mTOR signaling pathway that governs critical aspects of cell growth and survival. Disruption of this pathway through these inhibitors can lead to altered cellular outcomes that may intersect with the activities of LOC644978. Rapamycin and GSK2126458, target the mTOR complex, a central regulator of cellular metabolism and growth. By inhibiting mTOR, these compounds can significantly reduce the synthesis of proteins and impede cellular proliferation, potentially influencing any regulatory roles that LOC644978 may have on these processes.
Further tailoring the cellular communication network, compounds such as PD0325901, Sorafenib, and GW5074, inhibit key kinases within the MAPK/ERK pathway, which is pivotal for the regulation of gene expression, cell division, and differentiation. The inhibition of these kinases can lead to a cascade of effects that potentially affect the functional dynamics of LOC644978. The compound SB203580 targets p38 MAPK, an important mediator of inflammatory responses and apoptosis. By inhibiting this kinase, SB203580 can influence pathological states and stress responses within cells, which may intersect with the biological roles of LOC644978. NSC 23766 and BAY 11-7082 disrupt cellular processes such as cytoskeletal reorganization and the immune response, respectively, by targeting Rac1 activation and NF-κB activation, illustrating the diverse range of cellular functions that can be modulated to influence the function of proteins like LOC644978. Lastly, MG132 and LY3214996, by targeting the proteasome and ERK1/2 respectively, can impact protein turnover and MAPK signaling pathways, affecting diverse cellular processes including cell cycle progression and apoptosis. These inhibitors serve to illustrate the broad scope of cellular processes that can be modulated to influence the function of proteins like LOC644978.
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