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420144 JNK Inhibitor XIII - CAS 40045-50-9 - Calbiochem

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420144
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概要

Replacement Information

主要スペック表

CAS #Empirical Formula
40045-50-9C₅H₃N₅O₂S₃

価格&在庫状況

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420144-10MGCN
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      10 mg
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      Description
      OverviewA cell-permeable non-peptidyl thiazolyl-thiadiazole alternative to pepJIP1 (TI-JIP1153-163) and TAT-pepJIP1 (Cat. Nos. 420133 & 420134, respectively) as a JIP-docking site-targeting (IC50 = 239 nM against pepJIP1 binding to JNK1) and substrate-competitive JNK inhibitor (IC50 = 700 nM against ATF2 phosphorylation by JNK1), while exhibiting little activity (IC50 >50 µM) toward p38α, Akt, furin, or lethal factor. Shown to inhibit the phosphorylation of overexpressed GFP-c-Jun in HeLa cultures upon TNF-α stimulation (IC50 = 6.23 µM) in vitro and restore insulin sensitivity in a murine of type-2 diabetes model (25 mg/kg, i.p.) in vivo. Biostability analysis with rat liver microsome preparations results in a compound half-life of 27 min at 37.5°C.
      Catalogue Number420144
      Brand Family Calbiochem®
      Synonyms5-(5-Nitrothiazol-2-ylthio)-1,3,4-thiadiazol-2-amine
      References
      ReferencesDe, S.K., et al. 2009. J. Med. Chem. 52, 1943.
      Product Information
      CAS number40045-50-9
      FormPale yellow solid
      Hill FormulaC₅H₃N₅O₂S₃
      Chemical formulaC₅H₃N₅O₂S₃
      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 Shipped 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
      Packaged under inert gas Packaged under inert gas
      Transport Information
      Supplemental Information
      Specifications
      Global Trade Item Number
      カタログ番号 GTIN
      420144-10MGCN 04055977211108

      Documentation

      JNK Inhibitor XIII - CAS 40045-50-9 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート((M)SDS) 

      JNK Inhibitor XIII - CAS 40045-50-9 - Calbiochem 試験成績書(CoA)

      タイトルロット番号
      420144

      参考資料

      参考資料の概要
      De, S.K., et al. 2009. J. Med. Chem. 52, 1943.
      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-April-2011 RFH
      Synonyms5-(5-Nitrothiazol-2-ylthio)-1,3,4-thiadiazol-2-amine
      DescriptionA cell-permeable non-peptidyl thiazolyl-thiadiazole alternative to pepJIP1 (TI-JIP1153-163) and TAT-pepJIP1 (Cat. Nos. 420133 & 420134, respectively) as a JIP-docking site-targeting (IC50 = 239 nM against pepJIP1 binding to JNK1) and substrate-competitive JNK inhibitor (IC50 = 700 nM against ATF2 phosphorylation by JNK1), while exhibiting little activity (IC50 >50 µM) toward p38α, Akt, furin, or lethal factor. Shown to inhibit the phosphorylation of overexpressed GFP-c-Jun in HeLa cultures upon TNF-α stimulation (IC50 = 6.23 µM) in vitro and restore insulin sensitivity in a murine of type-2 diabetes model (25 mg/kg, i.p.) in vivo. Biostability analysis with rat liver microsome preparations results in a compound half-life of 27 min at 37.5°C.
      FormPale yellow solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number40045-50-9
      Chemical formulaC₅H₃N₅O₂S₃
      Structure formulaStructure formula
      Purity≥95% by HPLC
      SolubilityDMSO (50 mg/ml) or Ethanol (4 mg/ml)
      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
      ReferencesDe, S.K., et al. 2009. J. Med. Chem. 52, 1943.