LY 364947
Tocris Bioscience, part of Bio-Techne | Catalog # 2718
Selective inhibitor of TGF-βRI
Discontinued Product
2718 has been discontinued.
View all TGF-beta Receptor Inhibitors products.
Key Product Details
Description
Selective inhibitor of TGF-βRI
Alternative Names
HTS 466284
Product Description
LY 364947 is a selective inhibitor of TGF-β type-I receptor (TGF-β RI, TGFR-I, TβR-I, ALK-5) (IC50 values are 59, 400 and 1400 nM for TGR-β RI, TGF-β RII and MLK-7K respectively). Inhibits TGF-β-dependent luciferase production in mink lung cells (p3TP lux) and growth in mouse fibroblasts (NIH 3T3) (IC50 values are 47 and 89 nM respectively). Suppresses invasion of MDA-MB-231 breast cancer cells in a matrigel invasion assay.Product Specifications
Molecular Weight
272.31
Formula
C17H12N4
Storage
Store at RT
Purity
≥99% (HPLC)
Chemical Name
4-[3-(2-Pyridinyl)-1H-pyrazol-4-yl]-quinoline
CAS Number
396129-53-6
PubChem ID
447966
InChI Key
IBCXZJCWDGCXQT-UHFFFAOYSA-N
SMILES
N1C=C(C(=N1)C1=CC=CC=N1)C1=CC=NC2=CC=CC=C12
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 | 27.23 | 100 |
Preparing Stock Solutions
for LY 364947
The following data is based on the product molecular weight 272.31
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 | 3.67 mL | 18.36 mL | 36.72 mL |
| 5 mM | 0.73 mL | 3.67 mL | 7.34 mL |
| 10 mM | 0.37 mL | 1.84 mL | 3.67 mL |
| 50 mM | 0.07 mL | 0.37 mL | 0.73 mL |
Calculators
Molarity Calculator
Dilution Calculator
Reconstitution Calculator
Background References
References are publications that support the biological activity of the product.
- Li Dihydropyrrolopyrazole transforming growth factor-β type I receptor kinase domain inhibitors: a novel benzimidazole series with selectivity versus transforming growth factor-β type II receptor kinase and mixed lineage kinase 7. J.Med.Chem. 2006 PMID: 16539403
- Shiou Smad4-dependent regulation of urok. plasminogen activator secretion and RNA stability associated with invasiveness by autocrine and paracrine transforming growth factor-β. J.Biol.Chem. 2006 PMID: 16959768
- Sawyer Synthesis and activity of new aryl- and heteroaryl-substituted pyrazole inhibitors of the transforming growth factor-μ type I receptor kinase domain. J.Med.Chem. 2003 PMID: 12954047
Product Specific Notices for LY 364947
For research use only
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