Date published: 2025-9-19

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ZNF697 Inhibitors

ZNF697 inhibitors form a diverse group of compounds that each take a unique approach to downregulate the functional activity of the ZNF697 protein. Histone deacetylase inhibitors like Trichostatin A, and DNA methyltransferase inhibitors such as 5-Azacytidine, target epigenetic mechanisms. They modify chromatin architecture and DNA methylation patterns, respectively, which can lead to reduced ZNF697 binding to DNA and a consequent decrease in its regulatory influence on gene expression. Similarly, proteasome inhibitors like MG-132 and Bortezomib can indirectly diminish ZNF697 function by stabilizing proteins that regulate its activity, or by overwhelming the protein degradation pathways, including those that might manage ZNF697 levels. This modulation of proteostasis is critical for maintaining the balance of intracellular protein levels and can lead to decreased ZNF697 activity when perturbed.

Compounds suchas PD 98059, LY 294002, and Rapamycin act on specific signaling pathways and protein synthesis processes to indirectly reduce ZNF697 activity. PD 98059 suppresses the MAPK/ERK pathway, which may downregulate transcription factors controlling ZNF697 expression, leading to less ZNF697 function. LY 294002 inhibits the PI3K/AKT signaling cascade, potentially affecting the stability and activity of ZNF697 by targeting proteins downstream in this pathway. Rapamycin, an mTOR pathway inhibitor, can lower the production of proteins, including ZNF697, thus impeding its regulatory role. Other inhibitors, such as SB 431542, Triptolide, Chetomin, JQ1, and Alisertib, leverage diverse mechanisms involving TGF-β receptor signaling, transcriptional repression, disruption of HIF-1 function, interference with BET bromodomains, and alteration of cell cycle-related protein phosphorylation to decrease the expression or activity of ZNF697. These inhibitors collectively employ a multifaceted approach to reducing ZNF697's influence on gene regulation, thereby achieving functional inhibition through interference at various biological levels.

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