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508316 CTAP - CAS 103429-32-9 - Calbiochem

CTAP - CAS 103429-32-9 - Calbiochem: SDB (Sicherheitsdatenblätter), Analysenzertifikate und Qualitätszertifikate, Dossiers, Broschüren und andere verfügbare Dokumente.

Synonyme: µ opioid receptor antagonist, CTAP

Primary Target: u Opioid receptpr
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508316
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Übersicht

Replacement Information

Key Spec Table

CAS #Empirical Formula
103429-32-9C₅₁H₆₉N₁₃O₁₁S₂

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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
      Quality LevelMQ100
      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
      Global Trade Item Number
      Bestellnummer GTIN
      5083160001 04055977261844

      Documentation

      CTAP - CAS 103429-32-9 - Calbiochem SDB

      Titel

      Sicherheitsdatenblatt (SDB) 

      CTAP - CAS 103429-32-9 - Calbiochem Analysenzertifikate

      TitelChargennummer
      508316

      Literatur

      Übersicht
      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.
      Datenblatt

      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 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
      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.