Date published: 2025-11-5

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1110028C15Rik Inhibitors

Chemical inhibitors of 1110028C15Rik include a diverse array of compounds that target various kinases and enzymes involved in signal transduction pathways, which are crucial for the protein's function. Staurosporine, for instance, is a potent kinase inhibitor that can disrupt protein phosphorylation processes. Given that 1110028C15Rik activity is likely regulated by phosphorylation, staurosporine can directly impede its function. Similarly, rapamycin forms a complex with FKBP12 and specifically inhibits the mTOR pathway, a cellular mechanism potentially essential for the functional activity of 1110028C15Rik in processes such as cell growth and metabolism. LY294002 and wortmannin both target PI3K, a pivotal enzyme in the PI3K/AKT/mTOR pathway. By inhibiting PI3K, these compounds can prevent the activation of downstream components that may govern 1110028C15Rik's role within the cell.

Continuing with the theme of kinase inhibition, PD98059 and U0126 selectively inhibit MEK1 and MEK2, enzymes that participate in the MAPK/ERK pathway, possibly involved in the post-translational modification of 1110028C15Rik, thereby reducing its activity. SB203580 and SP600125 are inhibitors of p38 MAP kinase and JNK, respectively, and both compounds can disrupt signaling cascades that regulate 1110028C15Rik activity. ZM-447439, which inhibits Aurora kinases, can affect cell cycle regulation pathways in which 1110028C15Rik may be implicated. Venetoclax, a Bcl-2 inhibitor, can lead to disruptions in cell survival pathways, and since survival pathways often involve regulatory proteins, 1110028C15Rik's function can also be inhibited. Lastly, Dasatinib and PP2 are Src family kinase inhibitors, which by hindering these kinases, can impede the activation of pathways involving 1110028C15Rik. Each of these inhibitors acts on specific signaling pathways or molecular processes that are known to be associated with the function of 1110028C15Rik, thus leading to its inhibition.

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