Date published: 2025-9-19

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C12orf41 Inhibitors

Chemical inhibitors of C12orf41 can exert their inhibitory effects through various mechanisms that target different kinases and signaling pathways, which are crucial for the proper function and regulation of the protein. PD173074 acts by inhibiting FGFR1 kinase, thereby reducing the fibroblast growth factor (FGF) signaling that is essential for a variety of cellular processes, including those that may involve C12orf41. The reduced activity in this pathway can lead to the inhibition of C12orf41's function. Y-27632 targets ROCK1 kinase, and by inhibiting this kinase, it can decrease the phosphorylation of substrates that are potentially interactive with C12orf41, thus inhibiting its function. SB431542 targets the TGF-β type I receptor ALK5, leading to diminished Smad2/3 signaling; this can impact the regulation of C12orf41. SP600125 inhibits JNK, which can lead to reduced phosphorylation of c-Jun, affecting transcription factors that regulate C12orf41. LY294002, a PI3K inhibitor, can decrease AKT signaling, which is involved in the regulation of C12orf41.

In the second part of the signaling cascade, U0126 inhibits MEK1/2, potentially leading to reduced ERK pathway signaling that could inhibit downstream proteins interacting with C12orf41. Rapamycin, by inhibiting mTOR, can reduce the activity of S6K and 4E-BP1, thus potentially inhibiting proteins in signaling pathways close to C12orf41. SB203580 targets p38 MAPK, and its inhibition can decrease the activation of substrates that may interact with C12orf41. PP2, through the inhibition of Src family kinases, can reduce the activity of downstream pathways that interact with C12orf41. Dasatinib acts on Bcr-Abl and Src family kinases, and its inhibitory action can lead to reduced phosphorylation of proteins regulating C12orf41. Lapatinib inhibits EGFR and HER2, which are upstream of signaling pathways involving C12orf41, and its inhibition can lead to diminished activity of C12orf41. Lastly, Sorafenib's inhibition of multiple receptor tyrosine kinases in the MAPK pathway can lead to the inhibition of downstream proteins that interact with C12orf41, thus inhibiting its function. Each chemical inhibitor targets specific signaling pathways or kinases that, when inhibited, lead to the downregulation of activities within the cell that are necessary for the proper function of C12orf41.

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