Date published: 2026-5-5

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p120 Inhibitors

Common p120 Inhibitors include, but are not limited to Wortmannin CAS 19545-26-7, Y-27632 dihydrochloride monohydrate CAS 129830-38-2, PD173074 CAS 219580-11-7, U-0126 CAS 109511-58-2 and SB 203580 CAS 152121-47-6.

p120-catenin, also know as p120 or CTNND1 (Catenin Delta 1), is a pivotal protein with multifaceted roles within the cellular milieu. As part of the catenin family, p120-catenin primarily functions as an anchor, latching onto the cytoplasmic tails of classical cadherins, which are cell-cell adhesion molecules. This binding helps stabilize cadherin-based cell-cell junctions, known as adherens junctions. These junctions are crucial for maintaining tissue architecture and cellular arrangement. Moreover, p120-catenin is not just a passive scaffolding protein; it actively partakes in intracellular signaling. One of its noteworthy roles is the modulation of the Rho family of GTPases, a group of enzymes known to dictate the organization and dynamics of the actin cytoskeleton. Through such interactions, p120-catenin can influence cellular behaviors like migration, proliferation, and morphology.

The realm of p120-catenin inhibitors encompasses chemical compounds designed to temper the activity of p120-catenin. These inhibitors predominantly work by disrupting p120-catenin's ability to bind to its various partners, whether it be cadherins or other signaling molecules. Given the protein's central role in stabilizing cell-cell adhesions, inhibitors that target p120-catenin may influence the robustness of adherens junctions and, consequently, the structural integrity of tissues. Furthermore, by regulating p120-catenin's interactions within various signaling cascades, these inhibitors could reshape a plethora of cellular responses and behaviors. The mode of action for these inhibitors can vary-some might focus on hindering the interaction interface between p120-catenin and cadherins, while others might aim to block its interactions with signaling entities. As scientific endeavors further unravel the multifunctionality of p120-catenin in cellular dynamics, the study and characterization of its inhibitors offer a profound lens into the intricate web of molecular interactions that orchestrate cellular cohesion and communication.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Wortmannin

19545-26-7sc-3505
sc-3505A
sc-3505B
1 mg
5 mg
20 mg
$67.00
$223.00
$425.00
97
(3)

Wortmannin is a PI3K inhibitor that can affect downstream signaling pathways. Its inhibition may lead to reduced p120 levels due to decreased stabilization or synthesis.

Y-27632, free base

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$186.00
$707.00
88
(1)

This is a Rho-associated protein kinase (ROCK) inhibitor. Since ROCK pathways can influence cell adhesion dynamics, inhibition might down-regulate p120 indirectly.

PD173074

219580-11-7sc-202610
sc-202610A
sc-202610B
1 mg
5 mg
50 mg
$47.00
$143.00
$680.00
16
(1)

PD173074 is an FGFR1 inhibitor. Since FGFR signaling can be associated with cell adhesion dynamics, this compound might indirectly reduce p120 levels.

SB 203580

152121-47-6sc-3533
sc-3533A
1 mg
5 mg
$90.00
$349.00
284
(5)

By inhibiting p38 MAPK, SB203580 could alter signaling pathways associated with cell adhesion, potentially leading to reduced p120 levels.

PP 2

172889-27-9sc-202769
sc-202769A
1 mg
5 mg
$94.00
$227.00
30
(1)

As a Src family kinase inhibitor, PP2 might influence cell-cell adhesion dynamics, possibly down-regulating p120.

ZM-447439

331771-20-1sc-200696
sc-200696A
1 mg
10 mg
$153.00
$356.00
15
(1)

This Aurora kinase inhibitor could impact cell cycle and adhesion dynamics, potentially reducing p120 levels.

XAV939

284028-89-3sc-296704
sc-296704A
sc-296704B
1 mg
5 mg
50 mg
$36.00
$117.00
$525.00
26
(1)

As a Wnt/β-catenin pathway inhibitor, XAV-939 might indirectly down-regulate p120 through affected adhesion dynamics.

MLN 4924

905579-51-3sc-484814
1 mg
$286.00
1
(0)

MLN4924 inhibits the NEDD8-activating enzyme. It might impact protein degradation pathways, potentially leading to reduced p120 levels.