Date published: 2025-9-23

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ZNF470 Inhibitors

Chemical inhibitors of ZNF470 can disrupt the protein's function through various molecular pathways. Triptolide and MG132, for instance, exert their inhibitory action by targeting the NF-κB pathway, which is crucial for the transcriptional regulation that ZNF470 is involved in. Triptolide does this by directly inhibiting the transcription factor NF-κB itself, while MG132 impedes the proteasomal degradation of IκB, the inhibitor of NF-κB. This results in the suppression of NF-κB's transcriptional activity, which can impact the regulatory roles of ZNF470 if it is involved in the NF-κB pathway. Similarly, IKK-16 also targets the NF-κB pathway but does so by inhibiting IκB kinase, thereby preventing the activation of NF-κB and possibly affecting ZNF470's function in transcriptional regulation.

Other inhibitors disrupt pathways that could intersect with ZNF470's role in transcriptional regulation. LY294002 and Wortmannin both inhibit PI3K, a key component of the signaling pathways that regulate numerous cellular functions, including transcription. The inhibition of PI3K can decrease transcriptional activities that ZNF470 regulates. Apigenin impedes the activity of protein kinase C, which can modulate the activity of various transcription factors, potentially altering ZNF470's interaction with other proteins in transcriptional regulation. U0126 and PD98059 are both MEK inhibitors and would inhibit the MEK/ERK signaling that may be necessary for ZNF470's regulatory functions. Inhibition of this pathway can impair the activities of transcription factors or cofactors that work in concert with ZNF470. SB203580 and SP600125 target the p38 MAPK and JNK pathways, respectively, both of which are involved in regulating transcription factors and their cofactors. By inhibiting these kinases, the chemical inhibitors can disrupt the regulatory processes in which ZNF470 is known to function. Lastly, rapamycin inhibits mTOR, which can impact the translation of proteins essential for transcriptional regulation, potentially affecting ZNF470 if it interacts with such proteins.

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