Millipore Sigma Vibrant Logo

508015 CTOP - CAS 103429-31-8 - Calbiochem

View This Product on Sigma-Aldrich
508015
価格&在庫状況を照会

概要

Replacement Information

主要スペック表

CAS #Empirical Formula
103429-31-8C₅₀H₆₇N₁₁O₁₁S₂

価格&在庫状況

カタログ番号 在庫状況包装 Qty/Pk 価格 数量
5.08015.0001
在庫状況検索中…
現在国内在庫なし
現在国内在庫なし
現在国内在庫有り 
販売中止
在庫僅少
現在国内在庫あり
    Remaining : Will advise
      Remaining : Will advise
      注文対象外
      お問合せください
      Contact Customer Service

      ガラスビン 1 mg
      価格を検索中…
      価格が見つかりません
      Minimum Quantity needs to be mulitiple of
      Maximum Quantity is
      弊社照会 詳細を表示 
      値引
      ()
       
      弊社照会
      Description
      OverviewA potent antagonist highly selective for µ opioid receptor (Ki = 0.96 nM for µ receptor and > 10,000 nM for δ receptors). Often used for studying the functional roles of µ opioid receptors in both central and peripheral nervous systems.
      Catalogue Number508015
      Brand Family Calbiochem®
      Synonymsµ Opioid Receptor Antagonist, CTOP
      References
      ReferencesFeng, Y., et al. 2012. Curr Drug Targets. 13, 230.
      Hawkins, N., et al. 1989. J. Pharmacol. Exp. Ther. 248, 73.
      Gulya, K., et al. 1988. Eur. J. Pharmacol. 150, 355.
      Product Information
      CAS number103429-31-8
      FormWhite solid
      FormulationSupplied as trifluoracetate salt
      Hill FormulaC₅₀H₆₇N₁₁O₁₁S₂
      Chemical formulaC₅₀H₆₇N₁₁O₁₁S₂
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary Targetmu opioid
      Primary Target K<sub>i</sub>0.96 nM
      Purity≥95% by HPLC
      Physicochemical Information
      Peptide SequenceD-Phe-Cys-Tyr-D-Trp-Orn-Thr-Pen-Thr-NH2 (Orn: ornithine; Pen: penicillamine; SS bond: 2-7)
      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
      カタログ番号 GTIN
      5.08015.0001 04055977242751

      Documentation

      CTOP - CAS 103429-31-8 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート((M)SDS) 

      CTOP - CAS 103429-31-8 - Calbiochem 試験成績書(CoA)

      タイトルロット番号
      508015

      参考資料

      参考資料の概要
      Feng, Y., et al. 2012. Curr Drug Targets. 13, 230.
      Hawkins, N., et al. 1989. J. Pharmacol. Exp. Ther. 248, 73.
      Gulya, K., et al. 1988. Eur. J. Pharmacol. 150, 355.
      データシート

      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.

      Revision13-September-2024 JSW
      Synonymsµ Opioid Receptor Antagonist, CTOP
      DescriptionA potent antagonist highly selective for µ opioid receptor (Ki = 0.96 nM for µ receptor and > 10,000 nM for δ receptors). Often used for studying the functional roles of µ opioid receptors in both central and peripheral nervous systems.
      FormWhite solid
      FormulationSupplied as trifluoracetate salt
      CAS number103429-31-8
      Chemical formulaC₅₀H₆₇N₁₁O₁₁S₂
      Peptide SequenceD-Phe-Cys-Tyr-D-Trp-Orn-Thr-Pen-Thr-NH2 (Orn: ornithine; Pen: penicillamine; SS bond: 2-7)
      Structure formulaStructure formula
      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
      ReferencesFeng, Y., et al. 2012. Curr Drug Targets. 13, 230.
      Hawkins, N., et al. 1989. J. Pharmacol. Exp. Ther. 248, 73.
      Gulya, K., et al. 1988. Eur. J. Pharmacol. 150, 355.