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504467 L-CCG-I - CAS 117857-93-9 - Calbiochem

L-CCG-I - CAS 117857-93-9 - Calbiochem: Ficha de datos de seguridad (MSDS o SDS), certificado de análisis y de calidad (CoA y CoQ), expedientes, folletos y otros documentos disponibles.
Primary Target: mGlu₂ & mGlu₃
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      Descripción

      Replacement Information

      Tabla espec. clave

      CAS #Empirical Formula
      117857-93-9C₆H₉NO₄
      Description
      Overview

      This product has been discontinued.



      A potent agonist for group II metabotropic glutamate receptors (EC50 = 0.49 µM and 0.44 µM for mGlu2 and mGlu3, respectively). Higher level of activity than glutamate or (±)-trans-ACPD. Widely used in studies related to neurotransmissions mediated via group II mGlu receptors.
      Catalogue Number504467
      Brand Family Calbiochem®
      References
      ReferencesShinozaki, H., et al. 1989. Br. J. Pharmacol. 98, 1213.
      Hayashi, Y., et al. 1992. Br. J. Pharmacol. 107, 539.
      Nakanishi,S. 1992. Science. 258, 597.
      Watkins, J., et al. 1994. Trends Pharmacol Sci. 15, 333.
      Schoepp, D.D., et al. 1999. Neuropharmacology. 38, 1431.
      Product Information
      CAS number117857-93-9
      FormWhite solid
      Hill FormulaC₆H₉NO₄
      Chemical formulaC₆H₉NO₄
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetmGlu₂ & mGlu₃
      Purity≥97% 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 Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
      Toxicity Standard Handling
      Storage +2°C to +8°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 3 months at -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      Número de referencia GTIN
      504467 0

      Documentation

      L-CCG-I - CAS 117857-93-9 - Calbiochem Ficha datos de seguridad (MSDS)

      Título

      Ficha técnica de seguridad del material (MSDS) 

      L-CCG-I - CAS 117857-93-9 - Calbiochem Certificados de análisis

      CargoNúmero de lote
      504467

      Referencias bibliográficas

      Visión general referencias
      Shinozaki, H., et al. 1989. Br. J. Pharmacol. 98, 1213.
      Hayashi, Y., et al. 1992. Br. J. Pharmacol. 107, 539.
      Nakanishi,S. 1992. Science. 258, 597.
      Watkins, J., et al. 1994. Trends Pharmacol Sci. 15, 333.
      Schoepp, D.D., et al. 1999. Neuropharmacology. 38, 1431.

      Folleto

      Cargo
      New Products Flyer- Feb 2014 - Vol 1
      Pathways and Biomarkers of Glutamatergic Synapse Flyer
      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.

      Revision20-September-2013 JSW
      DescriptionA potent agonist for group II metabotropic glutamate receptors (EC50 = 0.49 µM and 0.44 µM for mGlu2 and mGlu3, respectively). Higher level of activity than glutamate or (±)-trans-ACPD. Widely used in studies related to neurotransmissions mediated via group II mGlu receptors.
      FormWhite solid
      CAS number117857-93-9
      Chemical formulaC₆H₉NO₄
      Structure formulaStructure formula
      Purity≥97% by HPLC
      SolubilityAqueous basic solutions
      Storage Protect from light
      +2°C to +8°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
      Toxicity Standard Handling
      ReferencesShinozaki, H., et al. 1989. Br. J. Pharmacol. 98, 1213.
      Hayashi, Y., et al. 1992. Br. J. Pharmacol. 107, 539.
      Nakanishi,S. 1992. Science. 258, 597.
      Watkins, J., et al. 1994. Trends Pharmacol Sci. 15, 333.
      Schoepp, D.D., et al. 1999. Neuropharmacology. 38, 1431.