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508161 SNC80 - CAS 156727-74-1 - Calbiochem

508161
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Empirical FormulaCAS #
C₂₈H₃₉N₃O₂ 156727-74-1

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      Description
      OverviewA very potent and selective δ opioid receptor agonist (IC50 = 0.32 µM). Shown to induce dose- and time-dependent antinociception after i.c.v., i.th. and i.p. administration in mice. Widely used in studies of depression and inflammatory injuries. It is also reported to be acted upon heteromeric u-d receptors.
      Catalogue Number508161
      Brand Family Calbiochem®
      Synonymsδ Opioid Receptor Agonist, SNC80
      References
      ReferencesPradhan, A., et al., 2013. Mol Pain. 9, 8.
      Saitoh, A., et al., 2012. Curr. Neuropharmacol. 10, 231.
      Metcalf. M. et al. 2012. ACS Chem. Neurosci. 3, 505.
      Bilsky, J., et al. 1995. J. Pharmacol. Exp. Ther. 273, 359.
      Product Information
      CAS number156727-74-1
      FormCream solid
      Hill FormulaC₂₈H₃₉N₃O₂
      Chemical formulaC₂₈H₃₉N₃O₂
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetDela opioid receptor
      Primary Target IC<sub>50</sub>0.32 µ
      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 -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 3 months at -20°C.
      Packaging Information
      Transport Information
      Supplemental Information
      Specifications

      Documentation

      SNC80 - CAS 156727-74-1 - Calbiochem FDS

      Titre

      Fiche de données de sécurité des matériaux (FDS) 

      Références bibliographiques

      Aperçu de la référence bibliographique
      Pradhan, A., et al., 2013. Mol Pain. 9, 8.
      Saitoh, A., et al., 2012. Curr. Neuropharmacol. 10, 231.
      Metcalf. M. et al. 2012. ACS Chem. Neurosci. 3, 505.
      Bilsky, J., et al. 1995. J. Pharmacol. Exp. Ther. 273, 359.
      Fiche technique

      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.

      Revision31-October-2013 JSW
      Synonymsδ Opioid Receptor Agonist, SNC80
      DescriptionA very potent and selective δ opioid receptor agonist (IC50 = 0.32 µM). Shown to induce dose- and time-dependent antinociception after i.c.v., i.th. and i.p. administration in mice. Widely used in studies of depression and inflammatory injuries. It is also reported to be acted upon heteromeric u-d receptors.
      FormCream solid
      CAS number156727-74-1
      Chemical formulaC₂₈H₃₉N₃O₂
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (20 mM) or 1N HCl (100 mM)
      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 3 months at -20°C.
      Toxicity Standard Handling
      ReferencesPradhan, A., et al., 2013. Mol Pain. 9, 8.
      Saitoh, A., et al., 2012. Curr. Neuropharmacol. 10, 231.
      Metcalf. M. et al. 2012. ACS Chem. Neurosci. 3, 505.
      Bilsky, J., et al. 1995. J. Pharmacol. Exp. Ther. 273, 359.