Date published: 2026-5-30

1-800-457-3801

SCBT Portrait Logo
Seach Input

nucleoporin p62 Inhibitors

Nucleoporin p62 inhibitors are a specialized class of chemical compounds designed to target and disrupt the function of nucleoporin p62, an essential protein component of the nuclear pore complex (NPC). The NPC is a large and intricate structure that spans the nuclear envelope, acting as a gateway for the selective transport of molecules between the nucleus and the cytoplasm in eukaryotic cells. Nucleoporin p62, also known as Nup62, is a key constituent of the NPC and plays a critical role in regulating the transport of macromolecules such as proteins and nucleic acids. Inhibitors of nucleoporin p62 are developed to interfere with its normal function, thereby modulating the nucleocytoplasmic transport process, which can have profound implications for various cellular functions.

Chemically, nucleoporin p62 inhibitors are designed to bind specifically to nucleoporin p62 or its interacting partners within the NPC. By doing so, they disrupt the proper assembly and stability of the nuclear pore complex, leading to altered permeability and selectivity of the nuclear envelope. This disruption can result in the mislocalization of key cellular components, such as transcription factors and mRNA molecules, impacting gene expression and various cellular processes. Researchers study these inhibitors to gain insights into the fundamental mechanisms of nucleocytoplasmic transport and its regulation. Additionally, they may explore the use of nucleoporin p62 inhibitors as research tools to manipulate cellular processes for experimental purposes. Understanding the precise functions and interactions of nucleoporin p62 inhibitors can contribute to our knowledge of cell biology and reveals novel strategies for manipulating cellular processes in various fields of research.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Azacytidine

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

This DNA methylation inhibitor might alter the epigenetic status of the p62 gene, potentially leading to changes in its expression.

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)

As a histone deacetylase inhibitor, it could affect the chromatin structure around the p62 gene, influencing its transcription.

Rapamycin

53123-88-9sc-3504
sc-3504A
sc-3504B
1 mg
5 mg
25 mg
$63.00
$158.00
$326.00
233
(4)

This mTOR inhibitor could potentially impact cellular pathways that indirectly regulate p62 expression or its associated functions.

Geldanamycin

30562-34-6sc-200617B
sc-200617C
sc-200617
sc-200617A
100 µg
500 µg
1 mg
5 mg
$39.00
$59.00
$104.00
$206.00
8
(1)

As an HSP90 inhibitor, it might affect the stability or function of proteins that interact with or regulate p62.

Bortezomib

179324-69-7sc-217785
sc-217785A
2.5 mg
25 mg
$135.00
$1085.00
115
(2)

This proteasome inhibitor might alter the degradation rates of proteins involved in p62 regulation, indirectly affecting its levels.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$123.00
$400.00
148
(1)

As a PI3K inhibitor, it could modulate signaling pathways that indirectly influence p62 expression.

SB 202190

152121-30-7sc-202334
sc-202334A
sc-202334B
1 mg
5 mg
25 mg
$31.00
$128.00
$454.00
45
(1)

As a p38 MAPK inhibitor, it could alter signaling pathways involved in stress responses that might affect p62.

17-AAG

75747-14-7sc-200641
sc-200641A
1 mg
5 mg
$67.00
$156.00
16
(2)

A derivative of geldanamycin, this HSP90 inhibitor could similarly affect the stability of proteins regulating p62.

PD 98059

167869-21-8sc-3532
sc-3532A
1 mg
5 mg
$40.00
$92.00
212
(2)

This MEK inhibitor could alter MAPK signaling, potentially leading to changes in p62 levels or activity.

SP600125

129-56-6sc-200635
sc-200635A
10 mg
50 mg
$40.00
$150.00
257
(3)

As a JNK inhibitor, it might impact stress response pathways and subsequently affect p62 regulation.