106392-48-7

ST271 Chemical Structure
106392-48-7

Chemical Structure

ST271

  • CAS No.: 106392-48-7
  • Formula:C16H20N2O2
  • Molecular Weight:272.34

IUPAC Name: (E)-2-cyano-3-(4-hydroxy-3,5-diisopropylphenyl)acrylamide

InChIKey: HMLQHJRJKQDTKW-LFYBBSHMSA-N

SMILES: O=C(N)/C(C#N)=C/C1=CC(C(C)C)=C(O)C(C(C)C)=C1

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.

Cat. No. Product Name Purity Description Pricing
HY-103097
ST271 98.00% 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.
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HY-103097R
ST271 (Standard) ≥98% ST271 (Standard) is the analytical standard of ST271 (HY-103097). This product is intended for research and analytical applications. 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.
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USD 0.00

This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

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