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566324 SIRT2 Inhibitor, AGK2 - CAS 304896-28-4 - Calbiochem

概述

Replacement Information

重要规格表

CAS #Empirical Formula
304896-28-4C₂₃H₁₃Cl₂N₃O₂

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566324-5MGCN
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      Description
      OverviewA cell-permeable quinoline compound that targets the nicotinamide-binding site and acts as a reversible sirtuin 2- (SIRT2) selective inhibitor (IC50 = 3.5 µM) with little activity against SIRT1/3 (IC50 >50 µM). Prevents cellular α-tubulin deacetylation in HeLa cells in a dose-dependent manner and with little cytotoxic effect. Shown to rescue α-Synuclein-mediated toxicity both in primary rat embryo midbrain cultures in vitro and in a Drosophila PD model in vivo. The inactive isomer AGK7 (Cat. No. 566326) can be used as a negative control.
      Catalogue Number566324
      Brand Family Calbiochem®
      Synonyms2-Cyano-3-(5-(2,5-dichlorophenyl)-2-furanyl)-N-5-quinolinyl-2-propenamide, Sirtuin 2 Inhibitor, SIRT2 Inhibitor I, SIRT1 Inhibitor IV
      References
      ReferencesOuterio, T.F., et al. 2007. Science 317, 516.
      Product Information
      CAS number304896-28-4
      FormYellow solid
      Hill FormulaC₂₃H₁₃Cl₂N₃O₂
      Chemical formulaC₂₃H₁₃Cl₂N₃O₂
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥95% 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 Ambient Temperature Only
      Toxicity Standard Handling
      Storage +2°C to +8°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 6 months at -20°C.
      Packaging Information
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      产品目录编号 GTIN
      566324-5MGCN 04055977191417

      Documentation

      SIRT2 Inhibitor, AGK2 - CAS 304896-28-4 - Calbiochem MSDS

      职位

      物料安全数据表 (MSDS) 

      SIRT2 Inhibitor, AGK2 - CAS 304896-28-4 - Calbiochem 分析证书

      标题批号
      566324

      参考

      参考信息概述
      Outerio, T.F., et al. 2007. Science 317, 516.

      数据表

      标题
      SIRTainty™ Class III HDAC Assay
      数据表

      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.

      Revision26-March-2008 RFH
      Synonyms2-Cyano-3-(5-(2,5-dichlorophenyl)-2-furanyl)-N-5-quinolinyl-2-propenamide, Sirtuin 2 Inhibitor, SIRT2 Inhibitor I, SIRT1 Inhibitor IV
      DescriptionA cell-permeable quinoline compound that targets the nicotinamide-binding site and acts as a reversible sirtuin 2- (SIRT2) selective inhibitor (IC50 = 3.5 µM) with little activity against SIRT1/3 (IC50 >50 µM). Prevents cellular α-tubulin deacetylation in HeLa cells in a dose-dependent manner and with little cytotoxic effect. Shown to rescue α-Synuclein-mediated toxicity both in primary rat embryo midbrain cultures in vitro and in a Drosophila PD model in vivo. The inactive isomer AGK7 (Cat. No. 566326) can be used as a negative control.
      FormYellow solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number304896-28-4
      Chemical formulaC₂₃H₁₃Cl₂N₃O₂
      Structure formulaStructure formula
      Purity≥95% by HPLC
      SolubilityDMSO (2.5 mg/ml). Slight warming may be required for complete solubilization.
      Storage Protect from light
      +2°C to +8°C
      Do Not Freeze Ok to freeze
      Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
      Toxicity Standard Handling
      ReferencesOuterio, T.F., et al. 2007. Science 317, 516.