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504316 CP-55940 - CAS 83002-04-4 - Calbiochem

CP-55940 - CAS 83002-04-4 - Calbiochem : FDS (Fiches de données de sécurité), certificats d’analyse (CoA) et de qualité (CoQ), dossiers, brochures et autres documents disponibles.

Synonymes: 5-(1,1-Dimethylheptyl)-2-[5-hydroxy-2-(3-hydroxypropyl)cyclohexyl]phenol, CP 55,940, CP55940

Primary Target: CB receptors
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      Aperçu

      Replacement Information

      Tableau de caractéristiques principal

      CAS #Empirical Formula
      83002-04-4C₂₄H₄₀O₃
      Description
      Overview

      This product has been discontinued.



      A potent, non-selective agonist for cannabinoid (CB) receptors (Ki = 0.6 - 5.0 and 0.7 - 2.6 nM for CB1 and CB2 respectively; EC50 = 0.2, 0.3 and 5 nM for CB1, CB2 and GRP55 respectively). Often used in reference or control trials in CB research and the effects are robust in both behavioral tests and receptor binding assays.
      Catalogue Number504316
      Brand Family Calbiochem®
      Synonyms5-(1,1-Dimethylheptyl)-2-[5-hydroxy-2-(3-hydroxypropyl)cyclohexyl]phenol, CP 55,940, CP55940
      References
      ReferencesWiley, J., et al. 1995. Neuropharmacology. 34, 669.
      Griffin, G., et al. 1998. J. Pharmacol. Exp. Ther. 285, 553.
      Thomas, B., et al. 1998. J. Pharmacol. Exp. Ther. 285, 285.
      Avdesh, A., et al. 2012. Psychopharmacology (Berl). 220, 405.
      Product Information
      CAS number83002-04-4
      FormClear, colorless liquid
      FormulationSupplied in methanol.
      Hill FormulaC₂₄H₄₀O₃
      Chemical formulaC₂₄H₄₀O₃
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetCB receptors
      Primary Target K<sub>i</sub>0.6 - 5.0 and 0.7 - 2.6 nM for CB₁ and CB₂ respectively.
      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
      Global Trade Item Number
      Référence GTIN
      504316 0

      Documentation

      CP-55940 - CAS 83002-04-4 - Calbiochem FDS

      Titre

      Fiche de données de sécurité des matériaux (FDS) 

      Références bibliographiques

      Aperçu de la référence bibliographique
      Wiley, J., et al. 1995. Neuropharmacology. 34, 669.
      Griffin, G., et al. 1998. J. Pharmacol. Exp. Ther. 285, 553.
      Thomas, B., et al. 1998. J. Pharmacol. Exp. Ther. 285, 285.
      Avdesh, A., et al. 2012. Psychopharmacology (Berl). 220, 405.
      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.

      Revision21-June-2013 JSW
      Synonyms5-(1,1-Dimethylheptyl)-2-[5-hydroxy-2-(3-hydroxypropyl)cyclohexyl]phenol, CP 55,940, CP55940
      DescriptionA potent, non-selective agonist for cannabinoid (CB) receptors (Ki = 0.6 - 5.0 and 0.7 - 2.6 nM for CB1 and CB2 respectively; EC50 = 0.2, 0.3 and 5 nM for CB1, CB2 and GRP55 respectively). Often used in reference or control trials in CB research and the effects are robust in both behavioral tests and receptor binding assays.
      FormClear, colorless liquid
      FormulationSupplied in methanol.
      CAS number83002-04-4
      Chemical formulaC₂₄H₄₀O₃
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (30 mg/ml)
      Storage Protect from light
      -20°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
      ReferencesWiley, J., et al. 1995. Neuropharmacology. 34, 669.
      Griffin, G., et al. 1998. J. Pharmacol. Exp. Ther. 285, 553.
      Thomas, B., et al. 1998. J. Pharmacol. Exp. Ther. 285, 285.
      Avdesh, A., et al. 2012. Psychopharmacology (Berl). 220, 405.