504375 (S)-3,4-DCPG - CAS 201730-11-2 - Calbiochem

(S)-3,4-DCPG - CAS 201730-11-2 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: (S)-3,4-Dicarboxyphenylglycine

Primary Target: mGlu8a
504375
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      Overview

      Replacement Information

      Key Specifications Table

      Empirical FormulaCAS #
      C₁₀H₉NO₆ 201730-11-2

      Pricing & Availability

      Catalog Number AvailabilityPackaging Qty/Pack Price Quantity
      5.04375.0001
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          		 Glass bottle 10 mg
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          Description
          OverviewA highly potent and selective mGlu8a agonist (EC50 = 31 nM, a value of 100-fold lower those for mGlu1-7). Negligible activation at NMDA and kainate receptors. Exerts an amygdala mediated angiogenic-effect and evokes neuronal activities in stress-related brain areas following systemic administration in mice in vivo. A potent anticonvulsant in mice in vivo.
          Catalogue Number504375
          Brand Family Calbiochem®
          Synonyms(S)-3,4-Dicarboxyphenylglycine
          References
          ReferencesDobia, A., et al. 2013. Neuropharmacology. 66, 274.
          Thomas, N., et al. 1997. Eur. J. Pharmacol. 338 , 111.
          Moldrich, R., et al. 2001. Neuropharmacology. 40, 732.
          Thomas, N., et al, 2001. Neuropharmacology. 40, 311.
          Linden, A., et al, 2003. Neuropharmacology. 45, 473.
          Product Information
          CAS number201730-11-2
          FormWhite solid
          Hill FormulaC₁₀H₉NO₆
          Chemical formulaC₁₀H₉NO₆
          Structure formula ImageStructure formula Image
          Applications
          Biological Information
          Primary TargetmGlu8a
          Purity≥98% 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 +15°C to +30°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

          Documentation

          References

          Reference overview
          Dobia, A., et al. 2013. Neuropharmacology. 66, 274.
          Thomas, N., et al. 1997. Eur. J. Pharmacol. 338 , 111.
          Moldrich, R., et al. 2001. Neuropharmacology. 40, 732.
          Thomas, N., et al, 2001. Neuropharmacology. 40, 311.
          Linden, A., et al, 2003. Neuropharmacology. 45, 473.
          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.

          Revision12-July-2013 JSW
          Synonyms(S)-3,4-Dicarboxyphenylglycine
          DescriptionA highly potent and selective mGlu8a agonist (EC50 = 31 nM, a value of 100-fold lower those for mGlu1-7). Negligible activation at NMDA and kainate receptors. Exerts an amygdala mediated angiogenic-effect and evokes neuronal activities in stress-related brain areas following systemic administration in mice in vivo. A potent anticonvulsant in mice in vivo.
          FormWhite solid
          CAS number201730-11-2
          Chemical formulaC₁₀H₉NO₆
          Structure formulaStructure formula
          Purity≥98% by HPLC
          SolubilityH₂O (100 mM)
          Storage +15°C to +30°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 3 months at -20°C.
          Toxicity Standard Handling
          ReferencesDobia, A., et al. 2013. Neuropharmacology. 66, 274.
          Thomas, N., et al. 1997. Eur. J. Pharmacol. 338 , 111.
          Moldrich, R., et al. 2001. Neuropharmacology. 40, 732.
          Thomas, N., et al, 2001. Neuropharmacology. 40, 311.
          Linden, A., et al, 2003. Neuropharmacology. 45, 473.