C11orf71 inhibitors are a class of compounds that interfere with specific signaling pathways to indirectly decrease the functional activity of the C11orf71 protein. These inhibitors target various kinases and signaling molecules upstream of C11orf71, impacting its activity. For instance, PI3K inhibitors like LY294002 and Wortmannin obstruct the pathway leading to AKT activation. This, in turn, would abrogate downstream survival and growth signals, potentially leading to decreased C11orf71 activity if C11orf71 operates downstream of AKT. Similarly, mTOR inhibitors such as Rapamycin and PP242 can profoundly impact protein synthesis and cell growth pathways, which could translate to reduced C11orf71 activity if C11orf71 is implicated in these pathways.
Furthermore, MEK inhibitors such as U0126, PD98059,PD0325901, and GSK1120212 specifically target the MEK/ERK signaling cascade. The MEK/ERK pathway is a critical regulator of cell proliferation and survival, and if C11orf71 is a downstream effector within this pathway, its activity would be expected to decrease following MEK inhibition. The specificity of these compounds for MEK1/2 ensures that the impact on C11orf71 is due to the targeted suppression of ERK1/2 activation. In addition to the MEK/ERK pathway, p38 MAPK and JNK are part of the MAP kinase family, which responds to stress stimuli. Inhibitors such as SB203580 and SP600125 that target these kinases could attenuate the activation of transcription factors and other proteins involved in stress response and apoptosis.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Trametinib | 871700-17-3 | sc-364639 sc-364639A sc-364639B | 5 mg 10 mg 1 g | $112.00 $163.00 $928.00 | 19 | |
Also known as Trametinib, a highly specific inhibitor of MEK1/2, leading to the inhibition of ERK1/2 phosphorylation. Its action can lead to decreased C11orf71 activity if C11orf71 is regulated through the MEK/ERK axis. | ||||||