Date published: 2026-4-1

1-800-457-3801

SCBT Portrait Logo
Seach Input

PRAMEF22 Inhibitors

PRAMEF22 inhibitors belong to a class of molecules that specifically interact with and inhibit the activity of the PRAMEF22 protein, which is part of the PRAME family of proteins. PRAME, or "Preferentially Expressed Antigen in Melanoma," family members are generally characterized by their involvement in a variety of cellular processes, including gene regulation, protein-protein interactions, and cellular differentiation. The PRAMEF22 protein is a lesser-known member of this family, and inhibitors of PRAMEF22 are designed to modulate its activity, typically through direct binding or by preventing its interaction with other cellular components. These inhibitors may vary in structure, ranging from small molecules to more complex compounds, with specific configurations allowing them to interact with the active or regulatory sites of the PRAMEF22 protein. Such inhibitors are often categorized based on their binding affinity, specificity, and molecular structure.

From a chemical perspective, PRAMEF22 inhibitors are synthesized through various organic chemistry techniques that allow for the precise assembly of functional groups tailored to interact with the target protein. These compounds typically feature hydrophobic, hydrophilic, or charged regions that can complement the structure of PRAMEF22, ensuring effective binding and inhibition. The synthesis of PRAMEF22 inhibitors involves a detailed understanding of both the protein's structure and the specific molecular interactions required to disrupt its function. Additionally, the chemical stability, solubility, and binding kinetics of these inhibitors are key factors that influence their ability to interact with PRAMEF22 in various environments.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Retinoic Acid, all trans

302-79-4sc-200898
sc-200898A
sc-200898B
sc-200898C
500 mg
5 g
10 g
100 g
$66.00
$325.00
$587.00
$1018.00
28
(1)

May modulate gene expression through its interaction with retinoic acid receptors, affecting transcriptional activity.

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)

An HDAC inhibitor that might upregulate gene expression by increasing histone acetylation, promoting a more open chromatin state.

β-Estradiol

50-28-2sc-204431
sc-204431A
500 mg
5 g
$63.00
$182.00
8
(1)

Interacts with estrogen receptors and could modulate gene transcription through estrogen response elements.

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)

As an HDAC inhibitor, it could promote gene expression by enhancing histone acetylation.

Dexamethasone

50-02-2sc-29059
sc-29059B
sc-29059A
100 mg
1 g
5 g
$91.00
$139.00
$374.00
36
(1)

A glucocorticoid receptor agonist that may regulate the transcription of various genes through glucocorticoid response elements.

Dimethyl Sulfoxide (DMSO)

67-68-5sc-202581
sc-202581A
sc-202581B
100 ml
500 ml
4 L
$31.00
$117.00
$918.00
136
(6)

Often used as a solvent, DMSO can permeate cell membranes and might influence gene expression and cellular differentiation.

Tunicamycin

11089-65-9sc-3506A
sc-3506
5 mg
10 mg
$172.00
$305.00
66
(3)

Induces stress in the endoplasmic reticulum, which can lead to changes in gene expression through the unfolded protein response.