The chemical class known as Zfp663 Activators encompasses a range of substances that target the molecular pathways influencing the activity of the Zinc finger protein 663 (Zfp663), a member of the zinc finger protein family. These activators are not direct agonists in the classical sense; rather, they work by modulating the cellular environment or affecting signaling pathways that indirectly increase the functional activity of Zfp663. The activation of Zfp663 involves enhancing its DNA-binding affinity, transcriptional activity, or its interaction with other proteins. The diversity in the chemical structures of these activators is broad, ranging from small organic molecules to larger bioactive compounds, each with a unique mode of action that ultimately converges on the upregulation of Zfp663 activity. Some compounds in this class work by altering the chromatin state, such as histone deacetylase inhibitors, which lead to a more transcriptionally active chromatin conformation, facilitating greater access for Zfp663 to its DNA binding sites. Others may influence the phosphorylation status of proteins within the cell, thereby modifying the interaction landscape in which Zfp663 operates, or affect the cellular concentration of metal ions, such as zinc, which are crucial for the structural integrity of Zfp663's DNA-binding domains.
Moreover, the Zfp663 Activators class includes compounds that may alter gene expression patterns or the stability of mRNA transcripts, indirectly influencing Zfp663 protein levels and activity. For example, some molecules in this class may inhibit enzymes involved in the modification of DNA or histones, leading to an epigenetic landscape more favorable to the transcription of genes under the regulatory domain of Zfp663. Others may bind to allosteric sites on regulatory proteins, inducing conformational changes that propagate through signaling cascades and impact the activity of Zfp663. It is essential to note that the actions of these activators are subject to cellular context, including the presence of co-factors, the expression levels of Zfp663, and the specific cell type in which they are operating. The regulatory mechanisms affected by these activators are intricate and can involve multiple feedback loops and interactions with diverse cellular pathways.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
IBMX | 28822-58-4 | sc-201188 sc-201188B sc-201188A | 200 mg 500 mg 1 g | $260.00 $350.00 $500.00 | 34 | |
Non-specific inhibitor of phosphodiesterases, leading to increased cAMP levels and prolonged protein kinase A activation, which can enhance the functional activity of GlyCAM1 through phosphorylation of associated proteins. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $41.00 $132.00 $214.00 $500.00 $948.00 | 119 | |
Activator of protein kinase C which can phosphorylate proteins that associate with GlyCAM1, enhancing its functional activity. | ||||||
Ionomycin | 56092-82-1 | sc-3592 sc-3592A | 1 mg 5 mg | $78.00 $270.00 | 80 | |
Calcium ionophore that increases intracellular calcium levels, activating calcium-dependent kinases that can phosphorylate proteins interacting with GlyCAM1, leading to its functional enhancement. | ||||||
AICAR | 2627-69-2 | sc-200659 sc-200659A sc-200659B | 50 mg 250 mg 1 g | $65.00 $280.00 $400.00 | 48 | |
Activates AMP-activated protein kinase, which can phosphorylate proteins that interact with GlyCAM1, potentially enhancing its activity. | ||||||
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 upregulate the activity of proteins which, when less phosphorylated, may interact with and enhance the function of GlyCAM1. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
PI3K inhibitor that can lead to the activation of downstream targets that interact with and enhance the functional activity of GlyCAM1. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
p38 MAPK inhibitor that can modulate the stress response, impacting proteins that associate with and enhance the activity of GlyCAM1. | ||||||
Caffeine | 58-08-2 | sc-202514 sc-202514A sc-202514B sc-202514C sc-202514D | 50 g 100 g 250 g 1 kg 5 kg | $33.00 $67.00 $97.00 $192.00 $775.00 | 13 | |
Adenosine receptor antagonist that can increase cAMP levels, leading to the activation of protein kinase A and subsequent phosphorylation of proteins that enhance the functional activity of GlyCAM1. | ||||||
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 | $37.00 $69.00 $109.00 $218.00 $239.00 $879.00 $1968.00 | 47 | |
Modulator of transcription factors and kinases that can lead to the activation of proteins which enhance the functional activity of GlyCAM1. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $80.00 $220.00 $460.00 | 64 | |
Activates sirtuins and modulates several kinases and transcription factors, which can lead to the activation of proteins that interact with and enhance the functional activity of GlyCAM1. | ||||||