Date published: 2026-5-9

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ZNF38 Inhibitors

ZNF38 inhibitors belong to a specific chemical class of compounds that are designed to interact with and modulate the activity of the zinc finger protein 38 (ZNF38). ZNF38 is a transcription factor that plays a role in regulating gene expression and is involved in various cellular processes. The inhibitors targeting ZNF38 are designed to interfere with its function through various mechanisms. One common approach is to target the bromodomain, a conserved structural domain present in ZNF38, which recognizes and binds to acetylated histones, thereby regulating gene expression. These inhibitors are often small molecules that can bind to the bromodomain, disrupting its interaction with acetylated histones and thereby affecting the transcriptional regulation mediated by ZNF38. In addition to targeting the bromodomain, some ZNF38 inhibitors may act on other domains or regions of the protein, interfering with its binding to other proteins or DNA elements involved in transcriptional regulation. The chemical structures of these inhibitors can vary widely, and they are often designed and optimized through structure-activity relationship studies to improve their potency and specificity. Researchers and drug developers have employed various computational and experimental techniques to identify and synthesize ZNF38 inhibitors, aiming to better understand the biological functions of ZNF38 and its involvement in disease processes.

Due to their ability to modulate gene expression, ZNF38 inhibitors have attracted significant interest in the scientific community. Studies involving these inhibitors have provided valuable insights into the regulatory mechanisms of gene expression, contributing to a deeper understanding of cellular biology. The development of selective and potent ZNF38 inhibitors has the potential to be an essential tool for researchers to investigate the role of ZNF38 in cellular processes and unravel its functional significance in various biological contexts.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

C646

328968-36-1sc-364452
sc-364452A
10 mg
50 mg
$265.00
$944.00
5
(1)

C646 is a inhibitor of the bromodomain and extra-terminal (BET) family of proteins, including ZNF3It functions by disrupting protein-protein interactions and inhibiting the binding of BET proteins to acetylated histones.

I-BET 151 Hydrochloride

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

I-BET151 is a synthetic small molecule that also inhibits BET proteins, including ZNF38, by binding to their bromodomains.

PFI 3

1819363-80-8sc-507340
10 mg
$300.00
(0)

PFI-3 is a selective inhibitor of the ZNF38-associated polycomb repressive complex 1 (PRC1) E3 ubiquitin ligase activity.

4-[(1E)-2-(2-Amino-4-hydroxy-5-methylphenyl)diazenyl]-N-2-pyridinylbenzenesulfonamide

1395084-25-9sc-480120
5 mg
$300.00
(0)

MS436 is a chemical compound that has been found to inhibit ZNF38.

UNC 1215

1415800-43-9sc-475020
10 mg
$380.00
(0)

UNC1215 is a potent and selective inhibitor of the BRPF1 bromodomain, which is closely related to ZNF38 and part of the same protein complex.

RVX 208

1044870-39-4sc-472700
10 mg
$340.00
(0)

RVX-208 is a small molecule that has been reported to inhibit BET proteins, which may include ZNF38.

GSK 525762A

1260907-17-2sc-490339
sc-490339A
sc-490339B
sc-490339C
sc-490339D
5 mg
10 mg
50 mg
100 mg
1 g
$300.00
$540.00
$940.00
$1680.00
$5900.00
(0)

I-BET762 is a BET inhibitor that can target ZNF38 and other BET family members to alter gene expression and cellular functions.