research use only

SB431542 TGF-beta/Smad inhibitor

Cat.No.S1067

SB431542 is a potent and selective inhibitor of ALK5 with IC50 of 94 nM in a cell-free assay, 100-fold more selective for ALK5 than p38 MAPK and other kinases.

Quality Control

Batch: Purity: 99.99%
99.99

Solubility in DMSO or Water

In vitro
Batch:

DMSO : 77 mg/mL (200.31 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Ethanol : 3 mg/mL

Water : Insoluble

The solubility data above are all experimental results (not literature values).

Molarity Calculator

Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

mg/kg
g
μL

Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO
%
% Tween 80
% ddH2O
% DMSO
+
%

Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Read more about SB431542 solubility in DMSO or water

Working Concentrations for Cell Culture Treatment

Step 1: Select a research area to find working concentrations, or search directly for a cell line

Read more about SB431542 working concentrations for cell culture treatment

Working Concentrations for Animal Model Treatment

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Mechanism of Action

Information SB431542 is a potent, highly selective, and ATP-competitive TGF-beta type I receptor kinase (ALK4/5/7) inhibitor. It works by blocking the receptor kinase activity, preventing the phosphorylation of Smad2/3 and disrupting downstream TGF-beta/Smad signaling. This effectively suppresses epithelial-mesenchymal transition, fibrosis, and cancer metastasis, showing significant application value in stem cell differentiation and regenerative medicine.
Primary Applications and Mechanism of Action

Read more about SB431542 Mechanism of Action

Chemical Information, Storage & Stability

Molecular Weight 384.39 Formula

C22H16N4O3

Storage (From the date of receipt)
CAS No. 301836-41-9 Download SDF Storage of Stock Solutions

Synonyms N/A Smiles C1OC2=C(O1)C=C(C=C2)C3=C(NC(=N3)C4=CC=C(C=C4)C(=O)N)C5=CC=CC=N5

Read more about storage & stability

SB431542 VS RepSox (E-616452) | Galunisertib (LY2157299) | A-83-01

Read more comparative analysis about SB431542

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Tech Support

Handling Instructions

Tel: +1-832-582-8158 Ext:3

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Frequently Asked Questions

Question 1:
I would appreciate it if you can help me in figuring out the formulation for it in vivo experiments.

Answer:
S1067 in 1% DMSO+30% polyethylene glycol+1% Tween 80 at 30 mg/ml is a suspension for oral gavage. It can also be dissolved in 2% DMSO+30% PEG 300+ddH2O at 5 mg/ml as a clear solution for IP injection.