Date published: 2025-9-10

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ZNF529 Inhibitors

ZNF529 inhibitors are a class of chemical compounds specifically designed to target and modulate the activity of the ZNF529 protein, a member of the zinc finger protein family. Zinc finger proteins, including ZNF529, are characterized by their zinc finger motifs, which are structural domains that facilitate binding to DNA, RNA, or other proteins. ZNF529, like many other zinc finger proteins, is believed to function as a transcription factor, playing a crucial role in the regulation of gene expression. By binding to specific DNA sequences, ZNF529 likely influences the transcription of target genes involved in various cellular processes, including development, differentiation, and cellular response to environmental stimuli. Inhibitors of ZNF529 are developed to disrupt its ability to bind to DNA or interact with other transcriptional machinery, allowing researchers to study its specific role in gene regulation and the broader impact it may have on cellular function.

The development of ZNF529 inhibitors involves a detailed understanding of the protein's structure, particularly its zinc finger domains, which are critical for its DNA-binding capability. Structural biology techniques such as X-ray crystallography, cryo-electron microscopy, and nuclear magnetic resonance (NMR) spectroscopy are employed to determine the three-dimensional configuration of ZNF529. This structural information is essential for identifying potential binding sites where inhibitors can effectively target and block the protein's function. Computational tools like molecular docking and virtual screening are then used to identify small molecules that can specifically bind to these key regions, effectively inhibiting ZNF529's activity. Once potential inhibitors are identified, they are synthesized and subjected to rigorous in vitro testing to evaluate their binding properties, specificity, and inhibitory potency. These compounds are further refined through iterative cycles of chemical optimization to enhance their effectiveness and stability. The study of ZNF529 inhibitors not only provides valuable insights into the specific functions of this transcription factor but also contributes to a broader understanding of the molecular mechanisms that regulate gene expression and the role of zinc finger proteins in cellular biology.

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Tozasertib

639089-54-6sc-358750
sc-358750A
25 mg
50 mg
$61.00
$85.00
4
(1)

As an Aurora kinase inhibitor, VX-680 could prevent cell-cycle-related phosphorylation events, potentially inhibiting ZNF529 function if ZNF529 is involved in cell cycle regulation or progression.

Palbociclib

571190-30-2sc-507366
50 mg
$315.00
(0)

Palbociclib inhibits CDK4/6, which could inhibit the phosphorylation of retinoblastoma protein, ultimately inhibiting E2F-target genes and other regulatory mechanisms that ZNF529 may be part of for cell cycle control.