ZNF12 inhibitors are a class of compounds that specifically target and modulate the activity of zinc finger protein 12 (ZNF12), a transcription factor known for its role in gene expression regulation. ZNF12 is part of a larger family of zinc finger proteins, which are characterized by their zinc finger domains-structural motifs stabilized by zinc ions that facilitate the binding of proteins to specific DNA sequences. ZNF12, like other zinc finger proteins, plays a crucial role in transcriptional regulation by interacting with promoter regions of target genes. By inhibiting ZNF12, these compounds can disrupt the normal regulatory pathways that this protein oversees, resulting in altered expression of downstream genes. The precise binding of ZNF12 inhibitors to their target is often achieved through interactions with the zinc finger motifs, which can lead to changes in the protein's ability to bind DNA or affect its interaction with other transcriptional machinery.
The inhibition of ZNF12 can lead to wide-ranging effects on cellular processes, as zinc finger proteins are often involved in the regulation of multiple genes that control various cellular functions, such as differentiation, growth, and apoptosis. ZNF12 is particularly interesting because of its involvement in pathways related to cellular stress responses and developmental regulation. The design and study of ZNF12 inhibitors often involve structural analysis of the protein, identification of its binding sites, and exploration of the conformational changes that occur upon inhibition. These inhibitors can be used as molecular tools to dissect the role of ZNF12 in cellular networks and to study how modulation of transcription factors can influence complex biological systems. Researchers often rely on crystallography, molecular modeling, and other biophysical techniques to characterize the interactions between ZNF12 and its inhibitors, thereby gaining insights into their molecular mechanisms and regulatory potential.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $53.00 $89.00 | 7 | |
Alters zinc finger protein structures by binding to zinc ions. | ||||||
α-Amanitin | 23109-05-9 | sc-202440 sc-202440A | 1 mg 5 mg | $269.00 $1050.00 | 26 | |
Inhibitor of RNA polymerase II, affecting transcription processes. | ||||||
Flavopiridol | 146426-40-6 | sc-202157 sc-202157A | 5 mg 25 mg | $78.00 $259.00 | 41 | |
Cyclin-dependent kinase (CDK) inhibitor affecting transcription initiation. | ||||||
Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $74.00 $243.00 $731.00 $2572.00 $21848.00 | 53 | |
Intercalates DNA, preventing the binding of transcription factors and other DNA-binding proteins. | ||||||
Plumbagin | 481-42-5 | sc-253283 sc-253283A | 100 mg 250 mg | $52.00 $62.00 | 6 | |
Generates reactive oxygen species (ROS) which can cause oxidative stress and impact DNA-binding proteins. | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | $231.00 $863.00 | 1 | |
Bromodomain inhibitor affecting transcription regulation by binding to bromodomains besides acetylated lysines. | ||||||
Ibrutinib | 936563-96-1 | sc-483194 | 10 mg | $156.00 | 5 | |
Inhibits Bruton's tyrosine kinase (BTK), which plays a role in B cell receptor signaling affecting transcription. | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $45.00 $164.00 $200.00 $402.00 $575.00 $981.00 $2031.00 | 46 | |
Tyrosine kinase inhibitor that can affect various pathways including transcription regulation. | ||||||