Date published: 2026-2-14

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BAGE3 Inhibitors

BAGE3 inhibitors are a class of chemical compounds that specifically target the BAGE3 (B melanoma antigen family member 3) protein, which is part of a larger group of proteins involved in various cellular processes, including gene regulation and intracellular signaling. BAGE3 is expressed primarily in certain types of cells, playing a role in regulating cell cycle progression, transcriptional control, and other key cellular functions. Inhibitors of BAGE3 work by directly binding to the protein or its associated molecular partners, blocking its normal function within the cell. This interference can disrupt the normal signaling or regulatory pathways in which BAGE3 is involved, leading to altered cellular behavior such as changes in protein expression, reduced cell proliferation, or modifications in cellular metabolism.

BAGE3 inhibitors tend to be small molecules, carefully designed for high specificity and strong affinity to the BAGE3 protein or its functional domains. The structure of these inhibitors can vary, but they typically feature chemical groups that allow them to engage in specific interactions, such as hydrogen bonding or hydrophobic contacts, with key residues in the BAGE3 protein. Researchers often focus on optimizing the chemical stability, solubility, and permeability of these inhibitors to enhance their performance in experimental systems. Structural variations among BAGE3 inhibitors may also contribute to differences in their potency or selectivity, making some inhibitors more effective at modulating BAGE3-related processes than others. By studying the effects of these inhibitors, scientists can gain insights into the biochemical functions of the BAGE3 protein and its broader role in cellular dynamics.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Azacytidine

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

This agent may demethylate the BAGE3 gene promoter, leading to transcriptional silencing and thus decrease in BAGE3 expression.

5-Aza-2′-Deoxycytidine

2353-33-5sc-202424
sc-202424A
sc-202424B
25 mg
100 mg
250 mg
$218.00
$322.00
$426.00
7
(1)

By inducing hypomethylation at the BAGE3 gene locus, 5-Aza-2′-Deoxycytidine could repress the initiation of transcription, resulting in lowered BAGE3 levels.

Suberoylanilide Hydroxamic Acid

149647-78-9sc-220139
sc-220139A
100 mg
500 mg
$133.00
$275.00
37
(2)

Suberoylanilide Hydroxamic Acid may lead to hyperacetylation of histones at the BAGE3 promoter, creating a condensed chromatin state that hinders gene transcription.

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)

This compound could prevent histone deacetylase from removing acetyl groups on histones near the BAGE3 gene, reducing its expression.

Romidepsin

128517-07-7sc-364603
sc-364603A
1 mg
5 mg
$218.00
$634.00
1
(1)

Romidepsin may cause an increase in acetylated histones at the BAGE3 gene, leading to a compact chromatin structure and diminished gene expression.

MS-275

209783-80-2sc-279455
sc-279455A
sc-279455B
1 mg
5 mg
25 mg
$24.00
$90.00
$212.00
24
(2)

MS-275's inhibition of class I histone deacetylases could lead to a decrease in BAGE3 expression through chromatin remodeling at the gene site.

(±)-JQ1

1268524-69-1sc-472932
sc-472932A
5 mg
25 mg
$231.00
$863.00
1
(0)

JQ1 might disrupt the recognition of acetylated histones by bromodomain-containing proteins at the BAGE3 locus, leading to reduced expression levels.

I-BET 151 Hydrochloride

1300031-49-5 (non HCl Salt)sc-391115
10 mg
$450.00
2
(0)

I-BET151 may prevent bromodomain proteins from binding to acetylated histones at the BAGE3 promoter, resulting in decreased transcription.

RG 108

48208-26-0sc-204235
sc-204235A
10 mg
50 mg
$131.00
$515.00
2
(1)

By inhibiting DNA methyltransferases, RG 108 could decrease methylation levels of the BAGE3 gene, resulting in transcriptional repression.

Disulfiram

97-77-8sc-205654
sc-205654A
50 g
100 g
$53.00
$89.00
7
(1)

Disulfiram could alter the ubiquitin-proteasome pathway, leading to stabilization of repressive transcription factors and downregulation of BAGE3.