Date published: 2026-2-14

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Zfp663 Activators

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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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

IBMX

28822-58-4sc-201188
sc-201188B
sc-201188A
200 mg
500 mg
1 g
$260.00
$350.00
$500.00
34
(1)

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

16561-29-8sc-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
(6)

Activator of protein kinase C which can phosphorylate proteins that associate with GlyCAM1, enhancing its functional activity.

Ionomycin

56092-82-1sc-3592
sc-3592A
1 mg
5 mg
$78.00
$270.00
80
(4)

Calcium ionophore that increases intracellular calcium levels, activating calcium-dependent kinases that can phosphorylate proteins interacting with GlyCAM1, leading to its functional enhancement.

AICAR

2627-69-2sc-200659
sc-200659A
sc-200659B
50 mg
250 mg
1 g
$65.00
$280.00
$400.00
48
(2)

Activates AMP-activated protein kinase, which can phosphorylate proteins that interact with GlyCAM1, potentially enhancing its activity.

Genistein

446-72-0sc-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
(1)

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

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$123.00
$400.00
148
(1)

PI3K inhibitor that can lead to the activation of downstream targets that interact with and enhance the functional activity of GlyCAM1.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$90.00
$349.00
284
(5)

p38 MAPK inhibitor that can modulate the stress response, impacting proteins that associate with and enhance the activity of GlyCAM1.

Caffeine

58-08-2sc-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
(1)

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

458-37-7sc-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
(1)

Modulator of transcription factors and kinases that can lead to the activation of proteins which enhance the functional activity of GlyCAM1.

Resveratrol

501-36-0sc-200808
sc-200808A
sc-200808B
100 mg
500 mg
5 g
$80.00
$220.00
$460.00
64
(2)

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.