Date published: 2025-9-14

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C11orf57 Inhibitors

C11orf57 inhibitors are a diverse class of compounds that can affect various cellular signaling pathways and processes. Staurosporine, by inhibiting PKC, could reduce the phosphorylation of proteins that are necessary for the activity or stability of C11orf57, leading to its functional downregulation. Similarly, LY294002 and Wortmannin, both PI3K inhibitors, could decrease the phosphorylation of Akt, which may be required for the optimal functional activity of C11orf57. By reducing PI3K/Akt signaling, these compounds indirectly inhibit the activity of C11orf57.

MEK inhibitors such as U0126 and PD98059 prevent the activation of ERK1/2, which could be essential for the function of C11orf57. The inhibition of these kinases may, therefore, lead to a decrease in C11orf57 activity. Rapamycin's inhibition of mTORC1 affects protein synthesis and other processes that C11orf57 may rely on, indirectly leading to its functional inhibition. In contrast, proteasome inhibitors like Bortezomib and MG132 could lead to the accumulation of negative regulators of C11orf57, inhibiting its function.

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