Chemical inhibitors of OTTMUSG00000010009 function by disrupting various signaling pathways that are crucial for the protein's activity. Rapamycin, a well-known inhibitor of the mTOR pathway, directly binds to and inhibits mTOR, a central regulator of cell growth and proliferation which is essential for the function of OTTMUSG00000010009. Similarly, Wortmannin and LY294002 focus on the PI3K/Akt/mTOR signaling pathway, with Wortmannin irreversibly inhibiting PI3K and LY294002 selectively targeting the same kinase, resulting in diminished phosphorylation and activation of downstream elements that are vital for OTTMUSG00000010009's role in the cell. PD98059 and U0126 both act as selective inhibitors of MEK1/2, thereby preventing the activation of the MAPK/ERK pathway, a pathway known to influence cell growth and survival, and consequently, the function of OTTMUSG00000010009. SB203580 and SP600125 each target specific MAP kinase pathways, with SB203580 inhibiting p38 MAP kinase and SP600125 inhibiting JNK, both of which are important for regulating cell cycle and stress response pathways that affect OTTMUSG00000010009 activity.
Continuing the inhibition profile, PP2 disrupts the signaling by Src family tyrosine kinases, which are involved in various cellular processes including cell adhesion, growth, and differentiation, thereby altering the signaling context in which OTTMUSG00000010009 operates. GF109203X targets protein kinase C (PKC), which is crucial for phosphorylation events that control cell cycle progression and apoptosis, hence affecting OTTMUSG00000010009 function. BAY 11-7082 inhibits the activation of NF-κB, a factor involved in regulating immune and inflammatory responses, thereby influencing the signaling environment pertinent to OTTMUSG00000010009. Lastly, LY3214996 provides a more targeted approach, specifically inhibiting ERK1/2 within the MAPK/ERK pathway.
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