ZNF792 activators are a class of chemicals that engage with the ZNF792 protein, a lesser-known member of the zinc finger protein family. This family is characterized by the presence of zinc finger domains, which are small, functional motifs within the protein that coordinate a zinc ion to help stabilize the protein's structure, enabling it to bind to DNA and influence gene expression. The zinc finger motifs typically consist of a combination of cysteine and histidine residues that create a unique tertiary structure essential for binding. The specific biological roles of ZNF792 are not as well documented as some other members of this family, but it is presumed to share the characteristic function of modulating transcriptional activity. ZNF792 activators are thus designed to increase the DNA-binding affinity or the transcription-modulating activity of ZNF792. The precise molecular mechanisms by which these activators function are the subject of research, and they are often uncovered through the detailed study of ZNF792's structure and interactions with other biomolecules.
The journey to identify and develop ZNF792 activators typically begins with high-throughput screening to locate molecules that have the potential to bind to and enhance ZNF792 activity. This identification process involves assaying a large library of compounds for their ability to interact with ZNF792 and facilitate its function. Once potential activators are found, they undergo a rigorous validation process that includes additional biochemical assays to ensure their effect is specific to ZNF792, avoiding unintended interactions with other zinc finger proteins or cellular components. Following the establishment of their specificity, the compounds enter an optimization phase, where their chemical structures are refined to improve their efficacy, stability, and specificity. Techniques such as X-ray crystallography, NMR spectroscopy, and computational modeling are employed to elucidate the binding mode of these activators to ZNF792. These methods provide a molecular-level view of the interactions and inform modifications to the activator structure that might enhance the desired activity. Through an iterative process of design and testing, chemists and biologists work to create a series of compounds that can reliably modulate the activity of ZNF792, advancing understanding of its role within the zinc finger protein family and its interactions within the cell.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Cholecalciferol | 67-97-0 | sc-205630 sc-205630A sc-205630B | 1 g 5 g 10 g | $70.00 $160.00 $290.00 | 2 | |
Vitamin D3, through its active metabolite, can modulate gene transcription by binding to the vitamin D receptor, potentially affecting ZNF792 expression. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
EGCG, a catechin in green tea, may modify gene expression through epigenetic mechanisms and signaling pathways, possibly influencing ZNF792. | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
It is a DNA methyltransferase inhibitor, leading to demethylation of DNA and potentially enhancing the expression of genes like ZNF792. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Forskolin activates adenylate cyclase, increasing cAMP levels, which may lead to changes in gene expression, possibly including ZNF792. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
This antitumor antibiotic binds to G-C rich DNA sequences, potentially disrupting transcription factor binding and altering gene expression. | ||||||
β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | $62.00 $178.00 | 8 | |
As a primary female sex hormone, beta-estradiol can regulate gene expression via estrogen receptors, possibly affecting ZNF792 expression. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA is a diacylglycerol analog that activates protein kinase C and can influence transcription factors and gene expression. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
A synthetic glucocorticoid that binds to the glucocorticoid receptor, potentially influencing the expression of certain genes, including ZNF792. | ||||||
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $30.00 $46.00 $82.00 $218.00 | 19 | |
As an HDAC inhibitor, it can increase the acetylation of histones, leading to a more open chromatin structure and potentially affecting gene expression. | ||||||
13-cis-Retinoic acid | 4759-48-2 | sc-205568 sc-205568A | 100 mg 250 mg | $74.00 $118.00 | 8 | |
It is a retinoid that can regulate gene expression by binding to retinoic acid receptors, potentially affecting genes like ZNF792. | ||||||