Date published: 2026-5-16

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Histone cluster 1 H4H Inhibitors

Histone cluster 1 H4H Inhibitors represent a specialized category of chemical compounds designed to selectively inhibit the activity of histone cluster 1, with a specific focus on the H4H subtype. Histones play a crucial role in the organization of DNA within the nucleus, forming nucleosomes that serve as the structural foundation for chromatin. The H4H designation refers to a variant of histone H4, one of the core histones essential for nucleosome assembly. As a specific variant within histone cluster 1, H4H becomes a target for researchers seeking to unravel the complexities of chromatin dynamics and gene regulation.

The development of Histone cluster 1 H4H Inhibitors requires a comprehensive understanding of the structural characteristics of histone H4H and its specific role within chromatin organization. These inhibitors are intricately designed for specificity, aiming to selectively bind to key regions of Histone cluster 1 H4H and disrupt its normal functions. By employing these inhibitors in experimental contexts, researchers can explore the consequences of inhibiting this particular histone variant, providing valuable insights into chromatin remodeling and the intricate regulation of gene expression. The study of histones, including variants like H4H, significantly contributes to advancing our understanding of epigenetic mechanisms, offering crucial insights into the dynamic processes governing gene regulation and the complex orchestration of cellular functions at the chromatin level.

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Items 1 to 10 of 12 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
$218.00
$322.00
$426.00
7
(1)

Decitabine is a DNA methyltransferase inhibitor that can cause DNA demethylation, potentially leading to altered gene expression profiles, which may include the expression of histone genes.

Suberoylanilide Hydroxamic Acid

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

Vorinostat is an HDAC inhibitor known to influence histone acetylation and can affect transcription of a wide range of genes, potentially including those for histones.

Mocetinostat

726169-73-9sc-364539
sc-364539B
sc-364539A
5 mg
10 mg
50 mg
$214.00
$247.00
$1463.00
2
(1)

Mocetinostat is an HDAC inhibitor that can change the acetylation state of histones, potentially influencing gene expression, which could include the expression of histone genes.

Belinostat

414864-00-9sc-269851
sc-269851A
10 mg
100 mg
$156.00
$572.00
(1)

Belinostat is an HDAC inhibitor that may affect chromatin structure and gene expression, potentially including the regulation of histone gene transcription.

Chidamide

743420-02-2sc-364462
sc-364462A
sc-364462B
1 mg
5 mg
25 mg
$62.00
$250.00
$1196.00
(1)

Chidamide is an HDAC inhibitor that can alter histone acetylation, potentially affecting gene expression, including histone genes.

ITF2357

732302-99-7sc-364513
sc-364513A
5 mg
50 mg
$340.00
$1950.00
(0)

Givinostat is an HDAC inhibitor that can impact gene expression by altering histone and protein acetylation, which may include effects on histone gene expression.

Valproic Acid

99-66-1sc-213144
10 g
$87.00
9
(1)

Valproic acid is an HDAC inhibitor that can affect gene expression by changing the acetylation state of histones, potentially influencing the transcription of histone genes.

Romidepsin

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

Romidepsin is an HDAC inhibitor that can modify the acetylation levels of histones, potentially affecting the expression of a wide array of genes, including histone genes.

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)

Trichostatin A is an HDAC inhibitor that can affect gene expression by altering histone acetylation, which may influence the transcription of histone genes.

Sirtinol

410536-97-9sc-205976
sc-205976A
1 mg
5 mg
$38.00
$113.00
14
(1)

Sirtinol is an inhibitor of the sirtuin family of NAD+-dependent deacetylases, which can influence histone acetylation and gene expression, potentially affecting histone gene expression.