Date published: 2025-12-18

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phostensin Inhibitors

Phostensin inhibitors belong to a class of chemical compounds designed to selectively target and modulate the activity of the protein known as phostensin. Phostensin, also referred to as phosphatase 1 nuclear targeting subunit (PNUTS), is a regulatory protein that plays a critical role in cellular processes related to protein phosphorylation and dephosphorylation. Phostensin is known for its interaction with protein phosphatase 1 (PP1), a crucial enzyme that regulates a wide range of cellular functions by dephosphorylating target proteins. The interaction between phostensin and PP1 is essential for controlling the activity and substrate specificity of PP1. Phostensin inhibitors are developed through chemical synthesis and structural optimization techniques, with the primary goal of interacting with specific domains or functional motifs of the phostensin protein to influence its interactions with PP1 and other cellular processes related to protein phosphorylation.

The design of phostensin inhibitors typically involves creating molecules that can selectively bind to phostensin, potentially disrupting its interactions with PP1 or modulating its regulatory functions. By modulating phostensin activity, these inhibitors can potentially impact protein dephosphorylation and, in turn, affect various cellular processes that rely on precise protein phosphorylation states, such as cell cycle regulation, DNA repair, and signal transduction. The study of phostensin inhibitors provides valuable insights into the intricate molecular mechanisms governing protein phosphorylation and dephosphorylation, offering a deeper understanding of the fundamental processes that underlie cellular signaling and regulation. This research advances our knowledge of basic cell biology and the regulatory networks that maintain cellular homeostasis.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Azacytidine

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

Incorporated into RNA and DNA and may disrupt methylation, potentially reducing gene expression.

Fluorouracil

51-21-8sc-29060
sc-29060A
1 g
5 g
$36.00
$149.00
11
(1)

A uracil analog that interferes with nucleotide synthesis and can inhibit mRNA production.

Triptolide

38748-32-2sc-200122
sc-200122A
1 mg
5 mg
$88.00
$200.00
13
(1)

Exhibits anti-inflammatory properties and can downregulate transcription factors, possibly affecting gene expression.

Bortezomib

179324-69-7sc-217785
sc-217785A
2.5 mg
25 mg
$132.00
$1064.00
115
(2)

Proteasome inhibitor that can affect various signaling pathways and potentially downregulate gene expression.

Suberoylanilide Hydroxamic Acid

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

Inhibits histone deacetylases, affecting chromatin structure and gene expression.

(±)-JQ1

1268524-69-1sc-472932
sc-472932A
5 mg
25 mg
$226.00
$846.00
1
(0)

Inhibits BET bromodomains, possibly leading to alterations in chromatin structure and gene transcription.

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, altering gene expression.

Flavopiridol

146426-40-6sc-202157
sc-202157A
5 mg
25 mg
$78.00
$254.00
41
(3)

Inhibits cyclin-dependent kinases (CDKs) and can affect transcription regulation.

Temozolomide

85622-93-1sc-203292
sc-203292A
25 mg
100 mg
$89.00
$250.00
32
(1)

Alkylates/methylates DNA, which can lead to mismatch repair and downregulation of gene expression.

Actinomycin D

50-76-0sc-200906
sc-200906A
sc-200906B
sc-200906C
sc-200906D
5 mg
25 mg
100 mg
1 g
10 g
$73.00
$238.00
$717.00
$2522.00
$21420.00
53
(3)

Interacts with DNA and inhibits the elongation phase of RNA polymerase, decreasing gene expression.