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119126 Adenosine Triphosphate, 2-Methylthio-, Tetrasodium Salt - CAS 43170-89-4 - Calbiochem

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      Descripción

      Replacement Information

      Tabla espec. clave

      CAS #Empirical Formula
      43170-89-4C₁₁H₁₄N₅O₁₃P₃SNa₄•xH2O
      Description
      Overview

      This product has been discontinued.



      An ATP analog that induces aortic smooth muscle relaxation in rat (EC50 = 240 nM).

      Catalogue Number119126
      Brand Family Calbiochem®
      Synonyms2-Methylthio ATP, 4Na, 2-MeS-ATP, Adenosine Triphosphate, 2-Methylthio-, Tetrasodium Salt
      References
      ReferencesJankowski, M., et al. 2001. J. Physiol. 530, 123.
      Hansmann, G., et al. 1997. Naunyn Schmiedebergs Arch Pharmacol. 356, 641.
      Burnstock, G., et al. 1983. Br. J. Pharmacol. 79, 907.
      Cusack, N.J., and Hourani, S.M. 1982. Br. J. Pharmacol. 75, 397.
      Product Information
      CAS number43170-89-4
      FormWhite solid
      Hill FormulaC₁₁H₁₄N₅O₁₃P₃SNa₄•xH2O
      Chemical formulaC₁₁H₁₄N₅O₁₃P₃SNa₄•xH2O
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥90% by HPLC
      Physicochemical Information
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Dry Ice Only
      Toxicity Standard Handling
      Storage ≤ -70°C
      Do not freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-70°C). Stock solutions are stable for up to 3 months at -70°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Número de referencia GTIN
      119126 0

      Documentation

      Licencias necesarias

      Título
      PRODUCTO REGULADO POR LA SECRETARÍA DE SALUD

      Adenosine Triphosphate, 2-Methylthio-, Tetrasodium Salt - CAS 43170-89-4 - Calbiochem Certificados de análisis

      CargoNúmero de lote
      119126

      Referencias bibliográficas

      Visión general referencias
      Jankowski, M., et al. 2001. J. Physiol. 530, 123.
      Hansmann, G., et al. 1997. Naunyn Schmiedebergs Arch Pharmacol. 356, 641.
      Burnstock, G., et al. 1983. Br. J. Pharmacol. 79, 907.
      Cusack, N.J., and Hourani, S.M. 1982. Br. J. Pharmacol. 75, 397.

      Citas

      Título
    • Hana Zemkova, et al. (2006) Roles of Purinergic P2X Receptors as Pacemaking Channels and Modulators of Calcium-Mobilizing Pathway in Pituitary Gonadotrophs. Molecular Endocrinology In press,.
    • Ficha técnica

      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.

      Revision18-July-2014 JSW
      Synonyms2-Methylthio ATP, 4Na, 2-MeS-ATP, Adenosine Triphosphate, 2-Methylthio-, Tetrasodium Salt
      DescriptionAn ATP analog that acts as a P2Y purinoreceptor agonist. Induces aortic smooth muscle relaxation in rat (EC50 = 240 nM). Inhibits ADP-induced platelet aggregation.
      FormWhite solid
      CAS number43170-89-4
      Chemical formulaC₁₁H₁₄N₅O₁₃P₃SNa₄•xH2O
      Structure formulaStructure formula
      Purity≥90% by HPLC
      SolubilityH₂O (5 mg/ml)
      Storage ≤ -70°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-70°C). Stock solutions are stable for up to 3 months at -70°C.
      Toxicity Standard Handling
      ReferencesJankowski, M., et al. 2001. J. Physiol. 530, 123.
      Hansmann, G., et al. 1997. Naunyn Schmiedebergs Arch Pharmacol. 356, 641.
      Burnstock, G., et al. 1983. Br. J. Pharmacol. 79, 907.
      Cusack, N.J., and Hourani, S.M. 1982. Br. J. Pharmacol. 75, 397.
      Citation
    • Hana Zemkova, et al. (2006) Roles of Purinergic P2X Receptors as Pacemaking Channels and Modulators of Calcium-Mobilizing Pathway in Pituitary Gonadotrophs. Molecular Endocrinology In press,.