Date published: 2026-4-1

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ZNF589 Inhibitors

ZNF589 inhibitors belong to a distinct chemical class that primarily focuses on modulating the activity of the zinc finger protein 589 (ZNF589). Zinc finger proteins, in general, are characterized by their ability to bind to specific DNA sequences, thereby exerting regulatory control over gene expression. ZNF589, a member of this protein family, plays a crucial role in transcriptional regulation, acting as a transcription factor. The development of ZNF589 inhibitors is grounded in the aim of selectively targeting and suppressing the function of this protein, potentially offering a means to manipulate gene expression patterns in a controlled manner.

The chemical entities classified as ZNF589 inhibitors typically demonstrate a high degree of specificity for the ZNF589 protein, often involving interactions with key residues within its zinc finger domains. These inhibitors may function through various mechanisms, such as blocking the binding sites essential for ZNF589-DNA interactions or disrupting the protein's structural integrity. By interfering with the normal functioning of ZNF589, these inhibitors have the potential to influence downstream molecular events related to gene transcription. Research in this chemical class is actively exploring the design and optimization of molecules that exhibit favorable pharmacokinetic properties and enhanced selectivity for ZNF589. Understanding the structural intricacies of ZNF589 and its interaction with inhibitors is crucial for advancing the development of this chemical class, shedding light on the intricate molecular pathways that govern gene expression regulation.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Chelerythrine chloride

3895-92-9sc-3547
sc-3547A
5 mg
25 mg
$90.00
$317.00
17
(1)

A benzo[c]phenanthridine alkaloid that can intercalate into DNA and potentially disrupt the DNA binding of zinc finger proteins such as ZNF589.

1,10-Phenanthroline

66-71-7sc-255888
sc-255888A
2.5 g
5 g
$23.00
$32.00
(0)

A metal chelator that can bind to zinc ions, possibly leading to the disruption of the zinc finger domains crucial for the structure of ZNF589.

Disulfiram

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

An inhibitor of aldehyde dehydrogenase that also can chelate zinc ions, which might alter the conformation of ZNF589 and its binding capabilities.

Pyrrolidinedithiocarbamic acid ammonium salt

5108-96-3sc-203224
sc-203224A
5 g
25 g
$33.00
$64.00
11
(1)

A metal chelator and antioxidant that can bind zinc ions, potentially affecting the structural integrity of ZNF589.

Quinomycin A

512-64-1sc-202306
1 mg
$166.00
4
(1)

A quinoxaline antibiotic that intercalates into DNA and could prevent ZNF589 from accessing its DNA binding sites.

Clioquinol

130-26-7sc-201066
sc-201066A
1 g
5 g
$45.00
$115.00
2
(1)

An antifungal drug that chelates zinc and could alter the structure and function of zinc finger proteins like ZNF589.

TPEN

16858-02-9sc-200131
100 mg
$130.00
10
(3)

A zinc chelator that can strip essential zinc ions from zinc finger motifs, potentially disrupting the function of ZNF589.

Mithramycin A

18378-89-7sc-200909
1 mg
$55.00
6
(1)

An anticancer antibiotic that binds to G-C rich sequences in DNA, potentially blocking the DNA binding sites of ZNF589.

Zinc

7440-66-6sc-213177
100 g
$48.00
(0)

A competitive inhibitor of heme, which can bind to zinc and might interfere with ZNF589's zinc finger domains.

Phenylarsine oxide

637-03-6sc-3521
250 mg
$41.00
4
(1)

A trivalent arsenic compound that can bind to vicinal dithiols and might modify the cysteine-rich regions of ZNF589.