Date published: 2025-9-11

1-800-457-3801

SCBT Portrait Logo
Seach Input

H2afb2 Inhibitors

H2afb2 inhibitors are a specific class of chemical compounds designed to modulate the activity of the H2afb2 protein. H2afb2, also known as histocompatibility 2, alpha-fetoprotein locus 2, is a protein found within the major histocompatibility complex (MHC) system in mice. The MHC system plays a critical role in the immune response by presenting antigenic peptides to T cells, enabling the immune system to recognize and respond to foreign pathogens effectively. H2afb2, much like other MHC molecules, is intricately involved in the complex process of antigen presentation, which is fundamental for initiating immune responses against infections. The development of H2afb2 inhibitors is primarily motivated by the goal of selectively interacting with the H2afb2 protein, potentially influencing its antigen-presenting activity and impacting immune recognition processes.

Typically, H2afb2 inhibitors consist of small molecules or chemical compounds that are precisely engineered to bind to H2afb2, targeting either its active site or allosteric sites. This interaction has the potential to modulate H2afb2's behavior, potentially affecting its ability to present antigenic peptides to T cells and, consequently, influencing the immune response against foreign antigens. Researchers are dedicated to unraveling the molecular mechanisms and functions of H2afb2 within the MHC system, with the aim of gaining profound insights into the complex immune recognition processes. The development of H2afb2 inhibitors represents an ongoing and dynamic area of research within the fields of immunology and molecular pharmacology, contributing significantly to our understanding of the immune system's functioning and its role in detecting and responding to foreign antigens.

SEE ALSO...

Items 1 to 10 of 12 total

Display:

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Azacytidine

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

A cytosine analog that inhibits DNA methyltransferases, potentially leading to changes in chromatin structure and downregulation of histone gene expression.

RG 108

48208-26-0sc-204235
sc-204235A
10 mg
50 mg
$128.00
$505.00
2
(1)

A non-nucleoside DNA methyltransferase inhibitor, RG108 may prevent methylation of histone gene promoters, potentially reducing their expression.

Histone Lysine Methyltransferase Inhibitor Inhibitor

935693-62-2 free basesc-202651
5 mg
$148.00
4
(1)

A diazepin-quinazolin-amine derivative that inhibits G9a histone methyltransferase, possibly affecting histone modification and gene expression patterns.

Mocetinostat

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

An inhibitor of histone deacetylases, which may result in hyperacetylated chromatin and altered expression of histone genes like H2afb2.

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)

Another DNA methyltransferase inhibitor that incorporates into DNA, could lead to hypomethylation of histone gene promoters, affecting their transcription.

Panobinostat

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

A potent pan-deacetylase inhibitor which may influence histone acetylation and thereby impact histone 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)

Selectively inhibits class I histone deacetylases, potentially altering chromatin structure and downregulating histone gene expression.

Parthenolide

20554-84-1sc-3523
sc-3523A
50 mg
250 mg
$79.00
$300.00
32
(2)

Known to inhibit NF-kB, a transcription factor that can regulate genes including those coding for histone proteins.

Disulfiram

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

Can modulate acetylation and other post-translational modifications of histones, potentially affecting histone gene expression.

Suberoylanilide Hydroxamic Acid

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

An HDAC inhibitor that may increase acetylation of histones, thereby altering gene expression patterns including those of histone genes.