Millipore Sigma Vibrant Logo

219372 Cathepsin G Inhibitor I - CAS 429676-93-7 - Calbiochem

View This Product on Sigma-Aldrich
219372
価格&在庫状況を照会

概要

Replacement Information

主要スペック表

CAS #Empirical Formula
429676-93-7C₃₆H₃₃N₂O₆P

価格&在庫状況

カタログ番号 在庫状況包装 Qty/Pk 価格 数量
219372-1MGCN
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

      樹脂アンプル 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, selective, reversible, competitive, non-peptide inhibitor of cathepsin G [IC50 = 53 nM and Ki = 63 nM]. Weakly inhibits chymotrypsin (Ki = 1.5 µM) and poorly inhibits thrombin, factor Xa, factor IXa, plasmin, trypsin, tryptase, proteinase 3, and human leukocyte elastase (IC50 > 100 µM).
      Catalogue Number219372
      Brand Family Calbiochem®
      References
      ReferencesGreco, M.N., et al. 2002. J. Am. Chem. Soc. 124, 3810.
      Product Information
      CAS number429676-93-7
      ATP CompetitiveN
      FormWhite solid
      Hill FormulaC₃₆H₃₃N₂O₆P
      Chemical formulaC₃₆H₃₃N₂O₆P
      ReversibleY
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      ApplicationCathepsin G Inhibitor I, CAS 429676-93-7, is a potent, selective, reversible, competitive, non-peptide inhibitor of cathepsin G (IC50 = 53 nM and Ki = 63 nM).
      Biological Information
      Primary Targetcathepsin G
      Primary Target IC<sub>50</sub>53 nM
      Primary Target K<sub>i</sub>63 nM for cathepsin G
      Purity≥98% by HPLC
      Physicochemical Information
      Cell permeableN
      Dimensions
      Materials Information
      Toxicological Information
      Safety Information according to GHS
      Safety Information
      Product Usage Statements
      Storage and Shipping Information
      Ship Code Ambient Temperature Only
      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
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      カタログ番号 GTIN
      219372-1MGCN 04055977202267

      Documentation

      Cathepsin G Inhibitor I - CAS 429676-93-7 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート((M)SDS) 

      Cathepsin G Inhibitor I - CAS 429676-93-7 - Calbiochem 試験成績書(CoA)

      タイトルロット番号
      219372

      参考資料

      参考資料の概要
      Greco, M.N., et al. 2002. J. Am. Chem. Soc. 124, 3810.
      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.

      Revision05-April-2011 RFH
      DescriptionA potent, selective, reversible, and competitive non-peptide inhibitor of cathepsin G (IC50 = 53 nM and Ki = 63 nM). Weakly inhibits chymotrypsin (Ki = 1.5 µM) and does not have any significant inhibitory effect on thrombin, factor Xa, factor IXa, plasmin, trypsin, tryptase, proteinase 3, and human leukocyte elastase (IC50 > 100 µM).
      FormWhite solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number429676-93-7
      Chemical formulaC₃₆H₃₃N₂O₆P
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (5 mg/ml) or Methanol
      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
      ReferencesGreco, M.N., et al. 2002. J. Am. Chem. Soc. 124, 3810.