SB 431542
Tocris Bioscience, part of Bio-Techne | Catalog # 1614
Key Product Details
Description
Product Description
SB 431542 is a potent and selective inhibitor of the transforming growth factor-β (TGF-β) type I receptor/ALK5 (IC50 = 94 nM), and its relatives ALK4 and ALK7. Suppresses TGF-β-induced proliferation of human osteosarcoma cells. Replaces SOX2 in reprogramming of fibroblasts into iPSCs. Stimulates proliferation, differentiation and sheet formation of ESC-derived endothelial cells. Inhibits TGF-β-induced EMT, migration, invasion and VEGF secretion in several human cancer cell lines. Also used in a protocol to generate brain organoids from human iPSCs. Can be used in a small molecule cocktail to generate 3D culture of lung alveolar cells, or vascular organoids. Also used in a protocol to generate cortical neurons from hiPSCs or dopaminergic neurons from hPSCs (see our protocol below).SB 431542 synthesized to cGMP guidelines also available.
For more information about how SB 431542 may be used, see our protocols: 3D Culture of Lung Alveolar Cells, Differentiation of Hematopoietic Progenitors from hPSCs, Generating Midbrain Dopaminergic Neurons from hPSCs, Generating Vascular Organoids, Accelerated Induction of Cortical Neurons from hiPSCs.
Scientific Data Images for SB 431542
Application of SB 431542 in dopaminergic neurons derived from hiPSCs.
Dopaminergic neurons derived from human induced pluripotent stem cells (hiPSC) using SB 431542, CHIR 99021 (Catalog # 4423, Tocris), DAPT (Catalog # 2634, Tocris) and Purmorphamine (Catalog # 4551, Tocris). Cells cultured in Neuronal Media supplemented with TGF-3 (Catalog # 8420-B3, R&D Systems), cAMP, GDNF (Catalog # 212-GD, R&D Systems), BDNF (Catalog # 248-BDB, R&D Systems), N21-MAX (Catalog # AR008, R&D Systems). Differentiation shown at days 55 (left) and 62 (right). Images courtesy of Kevin Flynn, Bio-Techne.Product Specifications
Molecular Weight
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The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Solubility
| Solvent | Max Conc. mg/mL | Max Conc. mM | |
|---|---|---|---|
| Solubility | |||
| DMSO | 38.44 | 100 with gentle warming | |
| Ethanol | 3.84 | 10 |
Preparing Stock Solutions
for SB 431542
The following data is based on the product molecular weight 384.39
Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which all affect the solvent volumes required to prepare stock solutions.
| Concentration / Solvent Volume / Mass | 1 mg | 5 mg | 10 mg |
|---|---|---|---|
| 1 mM | 2.60 mL | 13.01 mL | 26.02 mL |
| 5 mM | 0.52 mL | 2.60 mL | 5.20 mL |
| 10 mM | 0.26 mL | 1.30 mL | 2.60 mL |
| 50 mM | 0.05 mL | 0.26 mL | 0.52 mL |
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Background References
References are publications that support the biological activity of the product.
- Schafer An in vivo neuroimmune organoid model to study human microglia phenotypes. Cell 2023 PMID: 37172564
- Halder A specific inhibitor of TGF-beta receptor kinase, SB-431542, as a potent antitumor agent for human cancers. Neoplasia 2005 PMID: 15967103
- Watabe TGF-beta receptor kinase inhibitor enhances growth and integrity of embryonic stem cell-derived endothelial cells. J.Cell Biol. 2003 PMID: 14676305
- Matsuyama SB-431542 and Gle. inhibit transforming growth factor-β-induced proliferation of human osteosarcoma cells. Cancer Res. 2003 PMID: 14633705
- Laping Inhibition of transforming growth factor (TGF)-β1-induced extracellular matrix with a novel inhibitor of the TGF-β type I receptor kinase activity: SB-431542. Mol.Pharmacol. 2002 PMID: 12065755
- Inman SB-431542 is a potent and specific inhibitor of transforming growth factor-β superfamily type I AVNreceptor-like kinase (ALK) receptors ALK4, ALK5, and ALK7. Mol.Pharmacol. 2002 PMID: 12065756
Product Specific Notices for SB 431542
For research use only