Millipore Sigma Vibrant Logo

371725 GPR43 (FFA2) Agonist - CAS 1208552-99-1 - Calbiochem

GPR43 (FFA2) Agonist is an allosteric agonist of FFA2 (GPR43). Displays a left-shifted acetate dose response (IC50 = 0.7 µM) & 111% efficacy relative to acetate in hFFA2 forskolin-induced cAMP assays.

GPR43 (FFA2) Agonist - CAS 1208552-99-1 - Calbiochem: のSDS（安全データシート）、CoA（試験成績書）およびCoQ（品質証明書）、カタログなど製品関連の技術資料を入手いただけます。

同義語: (S)-2-(4-chlorophenyl)-3,3-dimethyl-N-(5-phenylthiazol-2-yl)butanamide

View This Product on Sigma-Aldrich
371725
価格＆在庫状況を照会

概要

Replacement Information

主要スペック表

CAS #Empirical Formula
1208552-99-1C₂₁H₂₁ClN₂OS

価格＆在庫状況

カタログ番号 在庫状況包装 Qty/Pk 価格 数量
371725-10MGCN
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

      		 ｶﾞﾗｽﾋﾞﾝ 10 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 phenylacetamide compound that acts as an allosteric agonist of FFA2 (GPR43), demonstrating a left-shifted acetate dose response (IC50 = 0.7 µM) and 111% efficacy relative to acetate in hFFA2 forskolin-induced cAMP assays.
      Catalogue Number371725
      Brand Family Calbiochem®
      Synonyms(S)-2-(4-chlorophenyl)-3,3-dimethyl-N-(5-phenylthiazol-2-yl)butanamide
      References
      ReferencesWang, Y., et al. 2009. Bioorg. Med. Chem. Lett. 20, 493.
      Product Information
      CAS number1208552-99-1
      FormWhite solid
      Hill FormulaC₂₁H₂₁ClN₂OS
      Chemical formulaC₂₁H₂₁ClN₂OS
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      ApplicationGPR43 (FFA2) Agonist is an allosteric agonist of FFA2 (GPR43). Displays a left-shifted acetate dose response (IC50 = 0.7 µM) & 111% efficacy relative to acetate in hFFA2 forskolin-induced cAMP assays.
      Biological Information
      Purity>98% 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
      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
      371725-10MGCN 04055977213270

      Documentation

      GPR43 (FFA2) Agonist - CAS 1208552-99-1 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート（(M)SDS） 

      GPR43 (FFA2) Agonist - CAS 1208552-99-1 - Calbiochem 試験成績書（CoA）

      タイトルロット番号
      371725

      参考資料

      参考資料の概要
      Wang, Y., et al. 2009. Bioorg. Med. Chem. Lett. 20, 493.
      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.

      Revision06-June-2015 JSW
      Synonyms(S)-2-(4-chlorophenyl)-3,3-dimethyl-N-(5-phenylthiazol-2-yl)butanamide
      DescriptionA phenylacetamide compound that acts as an allosteric agonist of FFA2 (GPR43), demonstrating a left-shifted acetate dose response (IC50 = 0.7 µM) and 111% efficacy relative to acetate in hFFA2 forskolin-induced cAMP assays.
      FormWhite solid
      CAS number1208552-99-1
      Chemical formulaC₂₁H₂₁ClN₂OS
      Structure formulaStructure formula
      Purity>98% by HPLC
      SolubilityDMSO (50 mg/ml)
      Storage +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 3 months at -20°C.
      Toxicity Standard Handling
      ReferencesWang, Y., et al. 2009. Bioorg. Med. Chem. Lett. 20, 493.