Smad4 inhibitors belong to a category of compounds that play a crucial role in regulating cellular signaling pathways associated with various cellular processes. These inhibitors target the Smad4 protein, a key component of the Smad family of proteins involved in the transforming growth factor-beta (TGF-β) signaling pathway. The TGF-β pathway is integral to numerous cellular functions, including cell growth, differentiation, and apoptosis. Smad4, also known as DPC4 (Deleted in Pancreatic Cancer 4), acts as a central mediator in transmitting signals from cell surface receptors to the nucleus, where it influences gene expression. The modulation of Smad4 activity is of significant interest in biological research due to its involvement in developmental processes and homeostasis.
Smad4 inhibitors exert their effects by disrupting the normal function of the Smad4 protein, thereby altering downstream signaling events. These compounds typically interfere with the interaction between Smad4 and other proteins within the signaling pathway, inhibiting the translocation of Smad4 to the nucleus. This disruption can lead to the modification of gene expression patterns, influencing various cellular responses. The intricate regulation of Smad4's activity is essential for maintaining cellular balance, and the development of inhibitors targeting this protein provides a valuable tool for researchers to dissect the intricacies of the TGF-β signaling pathway and its associated cellular effects. By modulating the activity of Smad4, these inhibitors allow researchers to unravel the complex mechanisms underlying cellular processes.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
A 83-01 | 909910-43-6 | sc-203791 sc-203791A | 10 mg 50 mg | $198.00 $650.00 | 16 | |
Blocks TGF-β signaling by inhibiting the activin receptor-like kinase (ALK) receptors, preventing phosphorylation of SMAD2 and SMAD3. | ||||||
5-[6-[4-(1-Piperazinyl)phenyl]pyrazolo[1,5-a]pyrimidin-3-yl]quinoline | 1432597-26-6 | sc-476318 | 5 mg | $380.00 | ||
Inhibits TGF-β type I receptor, reducing phosphorylation of R-SMADs and suppressing TGF-β pathway activation. | ||||||
EW-7197 | 1352608-82-2 | sc-507465 | 5 mg | $345.00 | ||
Selectively inhibits TGF-β type I receptor kinase activity, preventing SMAD2/3 phosphorylation. | ||||||
LY2157299 | 700874-72-2 | sc-391123 sc-391123A | 5 mg 10 mg | $209.00 $352.00 | 3 | |
Blocks TGF-β type I receptor kinase and downstream signaling, reducing SMAD2/3 phosphorylation. | ||||||
ALK5 Inhibitor II | 446859-33-2 | sc-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 | |
Inhibits ALK5 and ALK4 kinases, impeding phosphorylation of SMAD2/3 and TGF-β pathway activation. | ||||||
SIS3 hydrochloride | 521984-48-5 | sc-253565 | 5 mg | $334.00 | 2 | |
Specifically inhibits SMAD3 phosphorylation, attenuating TGF-β-mediated gene expression. | ||||||
TGF-β RI Kinase Inhibitor V | 627536-09-8 | sc-203294 | 2 mg | $86.00 | 3 | |
Selectively inhibits TGF-β type I receptor kinase activity, leading to reduced SMAD2/3 phosphorylation and signaling. | ||||||
4-(6-(4-(Piperazin-1-yl)phenyl)pyrazolo[1,5-a]pyrimidin-3-yl)quinoline | 1062368-24-4 | sc-476297 | 5 mg | $240.00 | ||
Blocks ALK2 and ALK3 kinases, affecting BMP signaling and SMAD1/5/8 phosphorylation. | ||||||
LY 364947 | 396129-53-6 | sc-203122 sc-203122A | 5 mg 10 mg | $105.00 $153.00 | 4 | |
Inhibits TGF-β type I receptor kinase, attenuating SMAD2/3 phosphorylation and downstream signaling. | ||||||
ITD 1 | 1099644-42-4 | sc-507349 | 10 mg | $220.00 | ||
Disrupts TGF-β/SMAD signaling by preventing formation of the active receptor complex. | ||||||