508316 | CTAP - CAS 103429-32-9 - Calbiochem

508316
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      Overview

      Replacement Information

      Key Specifications Table

      Empirical FormulaCAS #
      C₅₁H₆₉N₁₃O₁₁S₂ 103429-32-9

      Pricing & Availability

      Catalog NumberAvailability Packaging Qty/Pack Price Quantity
      5.08316.0001
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          Glass bottle 1 mg
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          Description
          OverviewA highly potent octapeptide that acts as a selective and brain penetrating bioavailable µ opioid receptor antagonist (IC50 = 3.5 nM). Used in studies of reward systems and additions.
          Catalogue Number508316
          Brand Family Calbiochem®
          Synonymsµ opioid receptor antagonist, CTAP
          References
          ReferencesPerry, C., et al., 2013. Behav. Neurosci. 127, 535.
          Burkett, J. et al. 2011. Neuropsychopharm. 36, 2200.
          Steinmiller, L., et al., 2008. Psychopharmacol. (Berl). 195, 497.
          Sterious, S., et al., 2003. J. Pharmacol. Exp. Ther. 304, 301.
          Abbruscato, T., et al. 1997. J. Pharmacol. 280, 402.
          Product Information
          CAS number103429-32-9
          FormOff-white solid
          Hill FormulaC₅₁H₆₉N₁₃O₁₁S₂
          Chemical formulaC₅₁H₆₉N₁₃O₁₁S₂
          Applications
          Biological Information
          Primary Targetu Opioid receptpr
          Primary Target IC<sub>50</sub>3.5 nM
          Purity≥95% by HPLC
          Physicochemical Information
          Peptide SequenceD-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 (2-7 disulfide bond)
          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

          SDS

          Title

          Safety Data Sheet (SDS) 

          References

          Reference overview
          Perry, C., et al., 2013. Behav. Neurosci. 127, 535.
          Burkett, J. et al. 2011. Neuropsychopharm. 36, 2200.
          Steinmiller, L., et al., 2008. Psychopharmacol. (Berl). 195, 497.
          Sterious, S., et al., 2003. J. Pharmacol. Exp. Ther. 304, 301.
          Abbruscato, T., et al. 1997. J. Pharmacol. 280, 402.
          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.

          Revision25-October-2013 JSW
          Synonymsµ opioid receptor antagonist, CTAP
          DescriptionA highly potent octapeptide that acts as a selective and brain penetrating bioavailable µ opioid receptor antagonist (IC50 = 3.5 nM). Used in studies of reward systems and additions.
          FormOff-white solid
          CAS number103429-32-9
          Chemical formulaC₅₁H₆₉N₁₃O₁₁S₂
          Peptide SequenceD-Phe-Cys-Tyr-D-Trp-Arg-Thr-Pen-Thr-NH2 (2-7 disulfide bond)
          Purity≥95% by HPLC
          SolubilityH₂O
          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
          ReferencesPerry, C., et al., 2013. Behav. Neurosci. 127, 535.
          Burkett, J. et al. 2011. Neuropsychopharm. 36, 2200.
          Steinmiller, L., et al., 2008. Psychopharmacol. (Berl). 195, 497.
          Sterious, S., et al., 2003. J. Pharmacol. Exp. Ther. 304, 301.
          Abbruscato, T., et al. 1997. J. Pharmacol. 280, 402.