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567790 ST638

567790
  
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      Overview

      Replacement Information

      Key Spec Table

      Empirical FormulaCAS #
      C₁₉H₁₈N₂O₃S107761-24-0
      Description
      Overview

      This product has been discontinued.





      A cell-permeable, reversible, and substrate competitive protein tyrosine kinase inhibitor (IC50 = 370 nM) that also inhibits HGF-induced MAP kinase activation in hepatocytes. Also shown to inhibit phospholipase D activity in human neutrophils. Decreases the O2· production induced by pervanadate in guinea pig neutrophils.
      Catalogue Number567790
      Brand Family Calbiochem®
      Synonymsα-Cyano-(3-ethoxy-4-hydroxy-5-phenylthiomethyl)cinnamide
      References
      ReferencesAdachi, T., et al. 1996. Hepatology 23, 1244.
      Yamaguchi, M., et al. 1995. Arch. Biochem. Biophys. 323, 382.
      Uings, I., et al. 1992. Biochem. J. 281, 597.
      Shiraishi, T., et al. 1988. Chem. Pharm. Bull. 36, 974.
      Product Information
      CAS number107761-24-0
      ATP CompetitiveY
      FormPale yellow solid
      Hill FormulaC₁₉H₁₈N₂O₃S
      Chemical formulaC₁₉H₁₈N₂O₃S
      ReversibleY
      Structure formula ImageStructure formula Image
      Applications
      Biological Information
      Primary Targetprotein tyrosine kinase
      Primary Target IC<sub>50</sub>370 nM against protein tyrosine kinase
      Purity≥98% by HPLC
      Physicochemical Information
      Cell permeableY
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      RTECSUC6316200
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      Toxicity Standard Handling
      Storage -20°C
      Protect from Light Protect from light
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications

      Documentation

      ST638 SDS

      Title

      Safety Data Sheet (SDS) 

      ST638 Certificates of Analysis

      TitleLot Number
      567790

      References

      Reference overview
      Adachi, T., et al. 1996. Hepatology 23, 1244.
      Yamaguchi, M., et al. 1995. Arch. Biochem. Biophys. 323, 382.
      Uings, I., et al. 1992. Biochem. J. 281, 597.
      Shiraishi, T., et al. 1988. Chem. Pharm. Bull. 36, 974.
      Data Sheet

      Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

      Revision04-May-2011 RFH
      Synonymsα-Cyano-(3-ethoxy-4-hydroxy-5-phenylthiomethyl)cinnamide
      DescriptionA cell-permeable, reversible, and substrate competitive protein tyrosine kinase inhibitor (IC50 = 370 nM) that also inhibits HGF-induced MAP kinase activation in hepatocytes. Also shown to inhibit phospholipase D activity in human neutrophils. Decreases the O2· production induced by pervanadate in guinea pig neutrophils.
      FormPale yellow solid
      CAS number107761-24-0
      RTECSUC6316200
      Chemical formulaC₁₉H₁₈N₂O₃S
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMF or DMSO (100 mg/ml)
      Storage -20°C
      Protect from light
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 1 month at -20°C.
      Toxicity Standard Handling
      ReferencesAdachi, T., et al. 1996. Hepatology 23, 1244.
      Yamaguchi, M., et al. 1995. Arch. Biochem. Biophys. 323, 382.
      Uings, I., et al. 1992. Biochem. J. 281, 597.
      Shiraishi, T., et al. 1988. Chem. Pharm. Bull. 36, 974.