ST271

Catalog No.: A18329

PTK inhibitor

ST271

ST271 Chemical Structure

CAS NO. 106392-48-7

ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.7 and 9 μM, respectively.

Availability: In stock

Package Price Qty
5 mg
$120.00
10 mg
$170.00
50 mg
$550.00
100 mg
$850.00
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Biological Activity

ST271 is a potent inhibitor of protein tyrosine kinase (PTK), inhibits phospholipase D activation stimulated by fMet-Leu-Phe and PAF, with IC50s of 6.7 and 9 μM, respectively.
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
0.1 mM 36.72 mL 183.59 mL 367.19 mL
0.5 mM 7.34 mL 36.72 mL 73.44 mL
1 mM 3.67 mL 18.36 mL 36.72 mL
5 mM 0.73 mL 3.67 mL 7.34 mL

*The above data is based on the productmolecular weight 272.34. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.

Catalog Num A18329
Actions Inhibitor
M. Wt 272.34
Formula C16H20N2O2
Solubility DMSO
Purity >98%
Storage at -20°C 3 years Powder
CAS No. 106392-48-7
Synonyms ST 271, ST-271
SMILES O=C(N)/C(C#N)=C/C1=CC(C(C)C)=C(O)C(C(C)C)=C1

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