Date published: 2025-9-16

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C1orf167 Inhibitors

C1orf167 inhibitors encompass a diverse array of chemical compounds that attenuate the protein's activity. Staurosporine, a broad-spectrum kinase inhibitor, and chelerythrine, a specific inhibitor ofProtein Kinase C, diminish the functional activity of C1orf167 by interfering with kinase-related signaling, which is crucial for phosphorylation events that C1orf167 may depend on. If C1orf167's functionality is intertwined with the phosphoinositide 3-kinase (PI3K)/AKT pathway, the use of LY 294002 and Wortmannin, both PI3K inhibitors, would result in a decreased AKT phosphorylation, thereby indirectly reducing C1orf167's activity. Similarly, compounds like PD 98059, U0126, and SB 203580 inhibit different nodes within the MAPK signaling cascade; PD 98059 and U0126 target MEK, while SB 203580 specifically inhibits p38 MAPK. If C1orf167 functions within this cascade, these inhibitors would disrupt the pathway, leading to a decrease in C1orf167 activity. Rapamycin, targeting mTOR signaling, would also downregulate C1orf167 if it is reliant on mTORC1's role in protein synthesis modulation.

Moreover, Sunitinib's role as a receptor tyrosine kinase (RTK) inhibitor suggests that if C1orf167's activity is connected to RTK signaling, blocking these kinases would result in suppressed C1orf167 function. Bortezomib operates through proteasome inhibition, which could decrease C1orf167's activity by altering the degradation rates of proteins that regulate C1orf167's function or by maintaining proteins that act as C1orf167 suppressors. Triciribine, targeting AKT, would impede any downstream signaling related to C1orf167, assuming there is a regulatory relationship. Lastly, SP600125's inhibition of c-Jun N-terminal kinase (JNK) might lower C1orf167 activity by reducing AP-1 transcription factor activity, which could be essential for C1orf167's expression or function. Collectively, these inhibitors work through distinct but interrelated mechanisms to diminish the functional activity of C1orf167 by impacting signaling pathways and molecular processes that are potentially pivotal for its role in cellular physiology.

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