ZFP72 inhibitors represent a class of chemical compounds that specifically target and inhibit the function of the ZFP72 protein, a member of the zinc finger protein (ZFP) family. Zinc finger proteins are characterized by their structural motifs, which bind to zinc ions and enable interaction with DNA, RNA, or other proteins. ZFP72, in particular, is a transcription factor, meaning it plays a crucial role in regulating gene expression by binding to specific DNA sequences. Inhibition of ZFP72 disrupts its ability to regulate gene transcription, potentially altering the expression of target genes associated with cellular processes such as differentiation, proliferation, and metabolic regulation. The structural complexity of ZFP72 provides a number of potential interaction sites for inhibitors, making the development of selective inhibitors an area of high interest in biochemical research.
Chemically, ZFP72 inhibitors can act through a variety of mechanisms to block the interaction between ZFP72 and its target sequences. Some inhibitors function by directly binding to the zinc finger domains, which are essential for the protein's ability to maintain its structure and bind DNA. Others may target co-factors or protein-protein interactions that are necessary for ZFP72's transcriptional activity. These inhibitors can exhibit high specificity due to the unique structural motifs within ZFP72, which differ from other members of the zinc finger protein family. Understanding the precise molecular interactions and the structural dynamics between ZFP72 and its inhibitors is a key focus in structural biology, as it sheds light on the fundamental mechanisms governing transcriptional regulation at the molecular level. This class of inhibitors contributes to broader investigations into gene regulation networks, protein-DNA interactions, and the role of zinc finger proteins in cellular function.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
Vorinostat is a histone deacetylase inhibitor that may affect ZNF72 expression by modulating the acetylation status of histones, thereby impacting gene transcription. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol is a natural polyphenol compound that has been shown to inhibit ZNF72 expression through its action on various signaling pathways involved in gene regulation. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
Curcumin, a natural compound found in turmeric, may inhibit ZNF72 expression by interfering with transcription factors or signaling pathways involved in gene regulation. | ||||||
Niclosamide | 50-65-7 | sc-250564 sc-250564A sc-250564B sc-250564C sc-250564D sc-250564E | 100 mg 1 g 10 g 100 g 1 kg 5 kg | $37.00 $77.00 $184.00 $510.00 $1224.00 $5814.00 | 8 | |
Niclosamide, an anthelmintic drug, has been found to impact ZNF72 expression possibly through modulation of Wnt/β-catenin signaling or other relevant cellular pathways. | ||||||
Triptolide | 38748-32-2 | sc-200122 sc-200122A | 1 mg 5 mg | $88.00 $200.00 | 13 | |
Triptolide, a diterpenoid epoxide, may inhibit ZNF72 expression by interfering with the activity of transcription factors or other regulatory proteins involved in gene expression. | ||||||
Betulinic Acid | 472-15-1 | sc-200132 sc-200132A | 25 mg 100 mg | $115.00 $337.00 | 3 | |
Betulinic acid, a natural compound, has been suggested to inhibit ZNF72 expression possibly through modulation of specific signaling pathways or epigenetic regulatory mechanisms. | ||||||
Etoposide (VP-16) | 33419-42-0 | sc-3512B sc-3512 sc-3512A | 10 mg 100 mg 500 mg | $32.00 $170.00 $385.00 | 63 | |
Etoposide, a chemotherapy medication, may impact ZNF72 expression by interfering with topoisomerase II activity, potentially leading to changes in gene transcription. | ||||||
Tunicamycin | 11089-65-9 | sc-3506A sc-3506 | 5 mg 10 mg | $169.00 $299.00 | 66 | |
Tunicamycin, an antibiotic, may inhibit ZNF72 expression by impacting protein glycosylation processes, leading to downstream effects on gene expression and cellular function. | ||||||
Auranofin | 34031-32-8 | sc-202476 sc-202476A sc-202476B | 25 mg 100 mg 2 g | $150.00 $210.00 $1899.00 | 39 | |
Auranofin, a gold-containing compound, has been shown to inhibit ZNF72 expression possibly through modulation of redox signaling pathways or other relevant cellular mechanisms. | ||||||
Geldanamycin | 30562-34-6 | sc-200617B sc-200617C sc-200617 sc-200617A | 100 µg 500 µg 1 mg 5 mg | $38.00 $58.00 $102.00 $202.00 | 8 | |
Geldanamycin, a benzoquinone ansamycin antibiotic, may impact ZNF72 expression by interfering with the activity of heat shock proteins or other chaperone-mediated processes. | ||||||