Date published: 2025-11-26

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4933426M11Rik Inhibitors

Chemical inhibitors of 4933426M11Rik include a variety of compounds that target different kinases and signaling pathways, which can lead to the functional inhibition of this protein. Staurosporine, a well-known kinase inhibitor, can inhibit a broad range of protein kinases, possibly including those that directly phosphorylate 4933426M11Rik, thereby reducing its activity. Similarly, Bisindolylmaleimide I, as a selective protein kinase C (PKC) inhibitor, can prevent PKC-mediated phosphorylation events that might be crucial for the activation or function of 4933426M11Rik. The mTOR inhibitor Rapamycin binds to mTOR complex and inhibits its activity, which can result in the inhibition of proteins in mTOR signaling pathways, including 4933426M11Rik.

Additionally, LY294002 and Wortmannin, both phosphoinositide 3-kinases (PI3K) inhibitors, can block the PI3K-dependent signaling cascades, possibly halting downstream phosphorylation events involving 4933426M11Rik. PD98059 and U0126, which are specific inhibitors of MEK1/2, can prevent the activation of the extracellular signal-regulated kinase (ERK) pathway, a process that possibly regulates the function of 4933426M11Rik. SB203580 and SP600125, inhibitors of p38 MAP kinase and c-Jun N-terminal kinase (JNK) respectively, can suppress the MAPK signaling pathway, which may include the functional regulation of 4933426M11Rik. PP2, a Src family kinase inhibitor, can inhibit the Src signaling that may lead to the functional inhibition of 4933426M11Rik. Y-27632, a selective inhibitor of the Rho-associated protein kinase (ROCK), can reduce the activity of downstream proteins in the Rho/ROCK signaling pathway, including 4933426M11Rik. Finally, PD173074, which inhibits the fibroblast growth factor receptor 1 (FGFR1) kinase, can inhibit downstream signaling pathways that regulate the activity of proteins like 4933426M11Rik.

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