Date published: 2025-9-26

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LOC643278 Inhibitors

Among LOC643278 inhibitors Staurosporine stands out as a broad-spectrum kinase inhibitor, capable of disrupting kinase-dependent signaling pathways which may control or interact with LOC643278. Inhibition of these pathways by staurosporine can affect LOC643278's phosphorylation state and subsequently its activity. LY294002, as a PI3K inhibitor, can suppress the PI3K/Akt pathway, a key signaling route for cell proliferation and survival, which may involve LOC643278. PD98059 and sorafenib, by targeting MEK and Raf kinases respectively, can attenuate the MAPK/ERK pathway, potentially affecting the phosphorylation and activity of LOC643278 if it is regulated by this pathway. SB203580 and SP600125 are inhibitors of the p38 MAP kinase and JNK pathways, respectively. These pathways are often associated with cellular stress responses, and inhibition by these compounds can modulate the activity of LOC643278 if it is part of these signaling cascades. Rapamycin, by inhibiting mTOR, can affect the mTOR signaling pathway, which is pivotal for cell growth and metabolism, potentially altering the function of LOC643278 if it is a component of this pathway.

PP2 as a selective inhibitor of Src family kinases and dasatinib as a multi-targeted kinase inhibitor can affect various signaling pathways, including those in which LOC643278 may be involved, by altering phosphorylation patterns of key proteins. Bortezomib, through proteasome inhibition, can alter the degradation of proteins, potentially causing an accumulation of regulatory proteins that may impact the stability and function of LOC643278. Thapsigargin targets SERCA, leading to disruptions in intracellular calcium levels, which can have wide-ranging effects on calcium-dependent signaling pathways that might include LOC643278. ZM-447439 inhibits Aurora kinases, which are crucial for cell cycle progression, potentially impacting LOC643278 if it is linked to the regulation of the cell cycle.

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