Date published: 2025-9-16

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ZNF416 Inhibitors

Chemical inhibitors of ZNF416 act through a variety of cellular signaling pathways to achieve functional inhibition. Wortmannin and LY294002 are both inhibitors of phosphatidylinositol 3-kinase (PI3K), a vital component of the PI3K/AKT pathway, which is central to various cellular processes including proliferation and survival. Inhibition of PI3K leads to a downstream reduction in AKT activity, a kinase that, when active, can influence the function of ZNF416. Triciribine targets AKT directly, preventing its activation and subsequent signaling events that would otherwise contribute to the functional activity of ZNF416. By inhibiting this pathway, these chemicals limit the cellular context in which ZNF416 can operate, thereby inhibiting its function.

In addition, the MAPK pathway, which includes a cascade of proteins such as MEK, ERK, JNK, and p38, can be targeted by chemicals such as PD98059, SP600125, U0126, and SB203580 to inhibit ZNF416. PD98059 and U0126 specifically inhibit MEK1/2, which effectively reduces ERK activation, a protein kinase that can be involved in pathways where ZNF416 has a role, leading to ZNF416 inhibition. SP600125 and SB203580 target the JNK and p38 MAP kinases, respectively, which are also part of the MAPK pathway and whose inhibition can disrupt the signaling that may be necessary for ZNF416 function. Src family kinases, which are upstream regulators of various signaling pathways, can be inhibited by chemicals like PP2 and PD173955. By inhibiting Src family kinases, these chemicals disrupt the regulatory pathways that could contribute to the normal function of ZNF416. Another Src kinase inhibitor, Dasatinib, also serves to dampen the activity of kinases that are part of signaling cascades related to the function of ZNF416. Finally, Palbociclib, a CDK4/6 inhibitor, can halt the progression of the cell cycle, which is a process that ZNF416 may influence. The inhibition of CDK4/6 by Palbociclib disrupts the cell cycle-dependent signaling pathways, leading to the inhibition of ZNF416 function.

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