ZDBF2 inhibitors refer to a class of chemical compounds that specifically target and inhibit the function of a genetic regulator known as ZDBF2, which is short for Zinc Finger, DBF-Type Containing 2. This regulator is a transcription factor that plays a role in the expression of various genes. Transcription factors are proteins that bind to specific DNA sequences and regulate the transcription of genetic information from DNA to messenger RNA. By controlling the activity of certain genes, transcription factors like ZDBF2 can influence a wide array of biological processes. ZDBF2 inhibitors, therefore, are designed to modulate the activity of this transcription factor through direct interaction, which can lead to changes in the expression of genes under its control.
The development of ZDBF2 inhibitors stems from a deepening understanding of the molecular mechanisms of gene regulation. Inhibition of ZDBF2 can be accomplished through various means, typically involving small molecules that can bind to the ZDBF2 protein, altering its shape or function and preventing it from interacting with DNA. The design of these inhibitors is a complex process that often requires the integration of structural biology, computational chemistry, and biochemical assays to identify compounds with the desired specificity and activity. These molecules are typically characterized by their ability to bind to the ZDBF2 protein with high affinity and specificity, which is crucial to ensure the selectivity of their action and to minimize effects on other zinc finger transcription factors.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine might demethylate DNA and alter the expression of various proteins. It could potentially inhibit the expression of DZF2 by changing its promoter methylation status. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
TSA is a histone deacetylase inhibitor. By affecting histone acetylation, it can change the chromatin structure and potentially downregulate DZF2 expression. | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
Valproic acid, like TSA, is a histone deacetylase inhibitor. It may modulate the chromatin structure to inhibit DZF2 transcription. | ||||||
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 | |
Sodium butyrate is another histone deacetylase inhibitor. It may play a role in chromatin remodeling to suppress DZF2 expression. | ||||||
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 | |
Similar to 5-Azacytidine, decitabine can demethylate DNA. It might influence DZF2 expression by modulating DNA methylation. | ||||||
RG 108 | 48208-26-0 | sc-204235 sc-204235A | 10 mg 50 mg | $128.00 $505.00 | 2 | |
RG108 is a DNA methyltransferase inhibitor. By inhibiting DNA methylation, it might impact the transcription of genes like DZF2. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
Mithramycin A is a DNA-binding that can inhibit SP1 transcription factor, potentially leading to reduced DZF2 expression if SP1 is involved in its transcription. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
Y-27632 inhibits ROCK, which has roles in various cellular processes. It could indirectly impact signaling pathways that modulate DZF2 expression. | ||||||
BIX01294 hydrochloride | 1392399-03-9 | sc-293525 sc-293525A sc-293525B | 1 mg 5 mg 25 mg | $36.00 $110.00 $400.00 | ||
BIX-01294 inhibits G9a histone methyltransferase. By affecting histone methylation, it might alter chromatin states and downregulate DZF2 expression. | ||||||
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
Disulfiram can inhibit various enzymes and might impact pathways that lead to DZF2 expression, making it a potential indirect inhibitor. | ||||||