Date published: 2026-4-1

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ZNF563 Activators

Compounds like Zinc Chloride directly contribute to the structural integrity of ZNF563, enhancing its DNA-binding capability and thus increasing its regulatory function in gene transcription. Trichostatin A and Sodium Butyrate can alter chromatin structure, thereby impacting ZNF563's role in gene expression regulation. Similarly, 5-Azacytidine, by affecting DNA methylation patterns, can influence the binding and regulatory functions of ZNF563.

Furthermore, compounds targeting various signaling pathways such as Genistein, LY294002, PD98059, and SP600125, through their actions on tyrosine kinase signaling, PI3K/Akt, MAPK/ERK, and JNK pathways respectively, can indirectly impact the cellular context in which ZNF563 operates. This includes its involvement in processes like signal transduction, proliferation, and stress responses. Additionally, Resveratrol, Curcumin, SB431542, and Rapamycin, by modulating sirtuin activity, multiple signaling pathways, TGF-β signaling, and mTOR inhibition, respectively, could indirectly influence the role of ZNF563 in the cellular environment, particularly in pathways related to inflammation, oxidative stress, and cell growth.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Zinc

7440-66-6sc-213177
100 g
$48.00
(0)

Zinc is essential for the structural integrity of zinc finger proteins like ZNF563. Zinc chloride can enhance the binding affinity of ZNF563 to DNA, thereby potentially increasing its functional activity in gene regulation.

Trichostatin A

58880-19-6sc-3511
sc-3511A
sc-3511B
sc-3511C
sc-3511D
1 mg
5 mg
10 mg
25 mg
50 mg
$152.00
$479.00
$632.00
$1223.00
$2132.00
33
(3)

A histone deacetylase inhibitor. By altering chromatin structure, it can influence gene expression patterns, potentially affecting the regulatory roles of ZNF563 in gene transcription.

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

A DNA methyltransferase inhibitor. It can alter DNA methylation patterns, which might impact the binding and regulatory functions of ZNF563 in gene expression.

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)

A tyrosine kinase inhibitor. By modulating tyrosine kinase signaling pathways, Genistein might influence the cellular context in which ZNF563 operates, particularly in signal transduction.

Sodium Butyrate

156-54-7sc-202341
sc-202341B
sc-202341A
sc-202341C
250 mg
5 g
25 g
500 g
$31.00
$47.00
$84.00
$222.00
19
(3)

A histone deacetylase inhibitor. Similar to Trichostatin A, it affects chromatin structure and gene expression, potentially influencing ZNF563's activity in transcriptional regulation.

Resveratrol

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

Known to modulate various signaling pathways including sirtuin activity. It may indirectly affect the activity of ZNF563 by altering the cellular environment and gene expression patterns.

LY 294002

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

A PI3K inhibitor. By influencing the PI3K/Akt pathway, it could indirectly affect ZNF563's function in cellular processes such as proliferation and survival.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

An ERK inhibitor, affecting the MAPK/ERK pathway. This modulation might indirectly impact ZNF563's role in cell signaling and transcription regulation.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$40.00
$150.00
257
(3)

A JNK inhibitor. By modulating the JNK signaling pathway, it could influence cellular processes where ZNF563 might be involved, particularly in stress responses and apoptosis.

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)

Known to affect multiple signaling pathways. It may indirectly influence ZNF563's activity by altering the cellular context, particularly in inflammation and oxidative stress.