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371724 GPR119 Agonist, AS1269574 - CAS 330981-72-1 - Calbiochem

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371724
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概要

Replacement Information

主要スペック表

CAS #Empirical Formula
330981-72-1C₁₃H₁₄BrN₃O

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371724-10MGCN
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      ガラスビン 10 mg
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      Description
      OverviewA pyrimidine compound that acts as an effective GPR119 agonist (EC50 = 2.5 µM in stimulating cAMP in hGPR119-expressing HEK293 cells) and reportedly exhibits no activity toward β-adrenergic or GLP-1 receptors. Shown to enhance 16.8 mM glucose-induced insulin secretion from murine MIN-6 β-cells (mU/20 min = 0.44 and 0.22, respectively, with or without 10 µM AS1269574) in vitro and improve glucose tolerance in normal mice (100 mg/kg; p.o.) without any significant hypoglycemic effect in vivo.
      Catalogue Number371724
      Brand Family Calbiochem®
      Synonyms2-((2-(4-Bromophenyl)-6-methylpyrimidin-4-yl)amino)ethanol, G-Protein Coupled Receptor 119 Agonist, GPCR2 Agonist, MGC119957 Agonist, SNORF25 Agonist
      References
      ReferencesYoshida, S., et cl. 2010. Biochem. Biophys. Res. Commun. 400, 437.
      Product Information
      CAS number330981-72-1
      FormAmber solid
      Hill FormulaC₁₃H₁₄BrN₃O
      Chemical formulaC₁₃H₁₄BrN₃O
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Purity≥99% 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 at Ambient Temperature or with Blue Ice or with Dry Ice
      Toxicity Regulatory Review
      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
      カタログ番号 GTIN
      371724-10MGCN 04055977213263

      Documentation

      GPR119 Agonist, AS1269574 - CAS 330981-72-1 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート((M)SDS) 

      GPR119 Agonist, AS1269574 - CAS 330981-72-1 - Calbiochem 試験成績書(CoA)

      タイトルロット番号
      371724

      参考資料

      参考資料の概要
      Yoshida, S., et cl. 2010. Biochem. Biophys. Res. Commun. 400, 437.
      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.

      Revision24-September-2012 JSW
      Synonyms2-((2-(4-Bromophenyl)-6-methylpyrimidin-4-yl)amino)ethanol, G-Protein Coupled Receptor 119 Agonist, GPCR2 Agonist, MGC119957 Agonist, SNORF25 Agonist
      DescriptionA pyrimidine compound that acts as an effective GPR119 agonist (EC50 = 2.5 µM in stimulating cAMP in hGPR119-expressing HEK293 cells) and reportedly exhibits no activity toward β-adrenergic or GLP-1 receptors. Shown to enhance 16.8 mM glucose-induced insulin secretion from murine MIN-6 β-cells (mU/20 min = 0.22, 0.29, 0.44, respectively, with 0, 1, 10 µM AS1269574) in vitro and improve glucose tolerance in normal mice (26% decrease and 60% increase, respectively, of control blood glucose and insulin AUC0-1h in OGTT; 100 mg/kg; p.o.) without affecting basal blood glucose level in either fed or fasting mice in vivo.
      FormAmber solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number330981-72-1
      Chemical formulaC₁₃H₁₄BrN₃O
      Structure formulaStructure formula
      Purity≥99% by HPLC
      SolubilityDMSO (>10 mg/ml)
      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 Regulatory Review
      ReferencesYoshida, S., et cl. 2010. Biochem. Biophys. Res. Commun. 400, 437.