PD 173074
Tocris Bioscience | Catalog # 3044
Product Description
PD 173074 is a selective FGFR1 and FGFR3 inhibitor (IC50 values are 5, 21.5, ~100, 17600 and 19800 nM for FGFR3, FGFR1, VEGFR2, PDGFR and c-Src respectively, and > 50000 nM for EGFR, InsR, MEK and PKC). Inhibits VEGF- and FGF-induced angiogenesis in the mouse cornea model of angiogenesis. Inhibits proliferation and differentiation of oligodendrocyte progenitors. Also promotes mESC self-renewal, facilitates the conversion of mouse epiblast stem cells to an earlier pluripotency state and inhibits differentiation of miPSCs to cardiomyocytes. Suppresses cell proliferation in cell lines expressing mutated FGFR3 protein. Blocks tumor growth in H510 and H69 SCLC xenograft models.Licensing Information
Sold for research purposes under agreement from Pfizer Inc.
Product Specifications for PD 173074
Molecular Weight
Formula
Storage
Purity
Chemical Name
CAS Number
PubChem ID
InChI Key
SMILES
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 | 52.37 | 100 | |
| Ethanol | 52.37 | 100 |
Preparing Stock Solutions for PD 173074
The following data is based on the product molecular weight 523.67.
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 | 1.91 mL | 9.55 mL | 19.10 mL |
| 5 mM | 0.38 mL | 1.91 mL | 3.82 mL |
| 10 mM | 0.19 mL | 0.95 mL | 1.91 mL |
| 50 mM | 0.04 mL | 0.19 mL | 0.38 mL |
Calculators
Background References
References are publications that support the biological activity of the product. See our Citations tab to view 100 publications citing the usage of this product.
- Buehr Capture of authentic embryonic stem cells from rat blastocysts. Cell 2008 PMID: 19109897
- Chan PLoS One
- Zhou Conversion of mouse epiblast stem cells to an earlier pluripotency state by small molecules. J.Biol.Chem. 2010 PMID: 20705612
- Pardo The fibroblast growth factor receptor inhibitor PD173074 blocks small cell lung cancer growth in vitro and in vivo. Cancer Res. 2010 PMID: 19903855
- Trudel Inhibition of fibroblast growth factor receptor 3 induces differentiation and apoptosis in t(4;14) myeloma. Neoplasia 2004 PMID: 14715624
- Miyake 1-tert-butyl-3-[6-(3,5-dimethoxy-phenyl)-2-(4-diethylamino-butylamino)-pyrido[2,3-d]pyrimidin-7-yl]-urea (PD173074), a selective tyrosine kinase inhibitor of fibroblast growth factor receptor-3 (FGFR3), inhibits cell proliferation of bla J.Pharmacol.Exp.Ther. 2010 PMID: 19955487
- Bansal Specific inhibitor of FGF receptor signaling: FGF-2-mediated effects on proliferation, differentiation, and MAPK activation are inhibited by PD173074 in oligodendrocyte-lineage cells. J.Neurosci.Res. 2003 PMID: 14598292
Product Documents for PD 173074
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Product Specific Notices for PD 173074
For research use only
Related Research Areas
Citations for PD 173074
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Species: MouseAssay Type: In VivoCell Line/Tissue: skinVerified Customer | Posted 06/29/2020Mouse primary fibroblasts also treat with PD173074 2 μM, vehicle: DMSO.Mice received a dose of 25 mg per kg body weight PD173074 dissolved in acetone or vehicle only topically onto the back skin.
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