Date published: 2025-10-26

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ZNF474 Inhibitors

ZNF474 Inhibitors encompass a range of chemical agents that exert their influence on the zinc finger protein 474 by modulating the pathways and processes to which it is connected. These compounds are not direct antagonists of ZNF474 but operate by altering the cellular context in which ZNF474 functions, thereby indirectly modulating its activity. The members of this class include kinase inhibitors, which target key signaling enzymes such as MEK1, p38 MAP kinase, and JNK. These enzymes are pivotal in the phosphorylation and activation of various proteins that can interact with ZNF474, hence affecting its role in transcriptional regulation. Another subset within this class is the PI3K inhibitors which impact nuclear signaling pathways that ZNF474 is postulated to regulate.

Additionally, the class includes agents which act on the epigenetic level to influence chromatin structure and DNA methylation, respectively. Such epigenetic modifications can change the expression patterns of genes under the regulatory domain of ZNF474. Proteasome inhibitors also form a part of this category, targeting the protein degradation machinery that could dictate the turnover of ZNF474 or its associated regulatory proteins. Lastly, compounds that function by inhibiting mTOR and modulating the degradation of transcription factors, which in turn may affect the transcriptional networks involving ZNF474.

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