Date published: 2025-12-21

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PRAME like-3 Activators

The class of compounds designated as PRAMEL3 Activators encompasses a range of chemicals known to influence gene expression and epigenetic states within cells. These activators typically work by targeting the intricate machinery that regulates DNA and histone modifications, thereby controlling the transcriptional status of genes. For instance, certain members of this chemical class inhibit the activity of DNA methyltransferases, enzymes responsible for adding methyl groups to DNA, which usually serves to repress gene expression. By inhibiting these enzymes, these compounds can lead to a decrease in DNA methylation, which in turn can result in the reactivation of gene transcription. In the context of PRAMEL3, this means that genes normally silenced could be expressed again under the influence of these activators.

Similarly, other members of this class function by hindering histone deacetylases (HDACs). Histone acetylation is a process that typically correlates with an active chromatin state and gene expression. HDAC inhibitors, therefore, can increase the acetylation of histones, which can relax the chromatin structure and make it more accessible for transcription factors and the transcriptional machinery, potentially leading to an increase in gene expression. By altering the epigenetic landscape, these compounds can induce a state that favors transcriptional activity. In addition to epigenetic modulation, certain chemicals within this class can affect the stability and expression of proteins by inhibiting the proteasome and NF-kB pathway, which are involved in protein degradation and critical cellular signaling pathways, respectively. Through these diverse but interconnected mechanisms, the compounds classified as PRAMEL3 Activators can play a significant role in modulating the expression and function of genes such as PRAMEL3.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$214.00
$316.00
$418.00
7
(1)

Inhibits DNA methyltransferases, which leads to DNA hypomethylation and could possibly activate PRAMEL3 by upregulating its gene expression.

Suberoylanilide Hydroxamic Acid

149647-78-9sc-220139
sc-220139A
100 mg
500 mg
$130.00
$270.00
37
(2)

A histone deacetylase inhibitor that promotes acetylation of histones, which could possibly activate PRAMEL3 by facilitating transcriptional activation.

Trichostatin A

58880-19-6sc-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
(3)

Another histone deacetylase inhibitor that could possibly activate PRAMEL3 by enhancing the acetylation of histones and promoting gene expression.

Panobinostat

404950-80-7sc-208148
10 mg
$196.00
9
(1)

This broad-spectrum HDAC inhibitor could possibly activate PRAMEL3 by altering chromatin structure and modulating gene expression patterns.

Romidepsin

128517-07-7sc-364603
sc-364603A
1 mg
5 mg
$214.00
$622.00
1
(1)

An HDAC inhibitor that could possibly activate PRAMEL3 through chromatin relaxation and subsequent activation of gene expression.

MS-275

209783-80-2sc-279455
sc-279455A
sc-279455B
1 mg
5 mg
25 mg
$24.00
$88.00
$208.00
24
(2)

Acts as an HDAC inhibitor and could possibly activate PRAMEL3 by modifying histone acetylation, influencing gene transcription.

5-Azacytidine

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

By incorporating into RNA and DNA, it could possibly activate PRAMEL3 by causing demethylation and activation of silenced genes.

Mocetinostat

726169-73-9sc-364539
sc-364539B
sc-364539A
5 mg
10 mg
50 mg
$210.00
$242.00
$1434.00
2
(1)

An HDAC inhibitor that could possibly activate PRAMEL3 by affecting chromatin structure and gene expression.

Valproic Acid

99-66-1sc-213144
10 g
$85.00
9
(1)

An HDAC inhibitor which could possibly activate PRAMEL3 by inducing hyperacetylation of histones and affecting gene expression.

Disulfiram

97-77-8sc-205654
sc-205654A
50 g
100 g
$52.00
$87.00
7
(1)

Proteasome and NF-kB pathway inhibitor that could possibly activate PRAMEL3 by affecting protein stability and gene expression.