Date published: 2025-9-13

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C10orf83 Inhibitors

Chemical inhibitors of C10orf83 include a range of compounds that target various signaling pathways and cellular processes, which are essential for the protein's function. Palbociclib, a CDK4/6 inhibitor, can disrupt cell cycle progression that C10orf83 may be involved in, leading to an inhibition of its function. Similarly, Staurosporine, a broad-spectrum kinase inhibitor, can impede numerous phosphorylation-dependent signaling pathways, potentially including those that C10orf83 participates in, thus inhibiting its activity. The PI3K inhibitors LY294002 and Wortmannin can obstruct the PI3K/Akt pathway, which is often crucial for the survival and function of proteins like C10orf83. Rapamycin, an mTOR inhibitor, can disrupt downstream signaling that C10orf83 may rely on for its function.

Further, the p38 MAP kinase inhibitor SB203580 and the MEK1/2 inhibitor PD98059 can block the MAPK signaling pathway, which is pivotal for many proteins' activities, including potentially C10orf83. The proteasome inhibitor MG132 can lead to an accumulation of cellular proteins, including possibly C10orf83, which may be inhibited if it relies on proteasomal degradation for regulation. Another proteasome inhibitor, Bortezomib, can similarly lead to an accumulation of C10orf83, thus inhibiting its function. SP600125 inhibits JNK, and PP2 inhibits Src family tyrosine kinases, both potentially disrupting distinct signaling pathways crucial for C10orf83's activity. Lastly, Y-27632, a ROCK inhibitor, can interfere with the Rho/ROCK pathway, which may play a role in C10orf83's function within the cell. Each of these chemicals targets specific pathways or processes that are essential for C10orf83's activity, leading to its functional inhibition.

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