Date published: 2025-11-1

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Sm B/B′ Inhibitors

The class of compounds known as Sm B/B' Inhibitors is a group of chemical entities recognized for their ability to selectively modulate the activity of Smad B and B' proteins, which play pivotal roles in transducing extracellular signals within cellular pathways. These inhibitors serve as valuable tools in the field of molecular research, allowing scientists to dissect and comprehend the intricate mechanisms of signal transduction mediated by the TGF-β superfamily of ligands. By specifically targeting Smad B and B' proteins, these inhibitors potentially disrupt the phosphorylation and subsequent activation of these proteins, leading to downstream effects on cellular responses.

Smad B and B' proteins, integral components of the canonical TGF-β signaling pathway, act as intermediaries in transmitting signals from the cell membrane to the nucleus. Upon ligand binding, receptor-mediated activation triggers a cascade of events that culminate in the phosphorylation of Smad B and B' proteins. These phosphorylated Smad proteins then form complexes with other Smads and co-factors, translocating into the nucleus to modulate gene expression. Sm B/B' Inhibitors, by virtue of their structural properties and molecular interactions, potentially disrupt these protein-protein interactions and hinder the activation of downstream signaling events. This precise interference allows researchers to manipulate and observe the effects of inhibiting Smad B and B' proteins, providing valuable insights into the fundamental processes governing cellular behavior. Consequently, these inhibitors hold significant potential for uncovering the nuances of cellular communication pathways and expanding our knowledge of cellular regulation.

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Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

SB 431542

301836-41-9sc-204265
sc-204265A
sc-204265B
1 mg
10 mg
25 mg
$80.00
$212.00
$408.00
48
(1)

A well-known inhibitor of TGF-β receptor type I (ALK5), which prevents phosphorylation of SMAD2 and SMAD3, thus inhibiting their activation and downstream signaling.

LY 364947

396129-53-6sc-203122
sc-203122A
5 mg
10 mg
$105.00
$153.00
4
(1)

Another selective ALK5 inhibitor that interferes with TGF-β signaling by inhibiting SMAD2/3 phosphorylation and subsequent nuclear translocation.

TGF-β RI Kinase Inhibitor V

627536-09-8sc-203294
2 mg
$86.00
3
(1)

This small molecule compound targets both TGF-β receptor I and II kinases, thereby inhibiting phosphorylation of SMAD2 and SMAD3 and attenuating downstream effects.

LY2157299

700874-72-2sc-391123
sc-391123A
5 mg
10 mg
$209.00
$352.00
3
(1)

A compound that inhibits TGF-β receptor type I kinase, reducing SMAD2 and SMAD3 activation and disrupting their signaling pathways.

A 83-01

909910-43-6sc-203791
sc-203791A
10 mg
50 mg
$198.00
$650.00
16
(1)

A selective ALK4/5/7 inhibitor that impedes the phosphorylation and activation of SMAD2 and SMAD3, thereby modulating TGF-β signaling.

SIS3 hydrochloride

521984-48-5sc-253565
5 mg
$334.00
2
(1)

Specifically targets SMAD3 by inhibiting its phosphorylation, preventing its translocation to the nucleus and suppressing TGF-β-mediated gene expression.

ALK5 Inhibitor II

446859-33-2sc-221234
sc-221234A
sc-221234B
sc-221234C
sc-221234D
sc-221234E
sc-221234F
1 mg
5 mg
10 mg
50 mg
100 mg
500 mg
1 g
$75.00
$150.00
$215.00
$650.00
$1224.00
$4296.00
$7818.00
8
(1)

A small molecule compound that inhibits ALK5 and ALK4, reducing SMAD2 and SMAD3 phosphorylation and attenuating TGF-β signaling.

EW-7197

1352608-82-2sc-507465
5 mg
$345.00
(0)

A potent inhibitor of TGF-β receptor type I kinase that impairs the activation of SMAD2 and SMAD3 and has potential as an anti-fibrotic agent.

GW788388

452342-67-5sc-363544
sc-363544A
5 mg
25 mg
$95.00
$384.00
(0)

A selective ALK5 inhibitor that prevents SMAD2 and SMAD3 phosphorylation, suppressing TGF-β pathway activation and associated cellular responses.

K02288

1431985-92-0sc-488981
5 mg
$330.00
(0)

An inhibitor targeting TGF-β receptor type I kinase, which effectively attenuates SMAD2 and SMAD3 signaling and has shown anti-inflammatory effects.