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566313 SIRT1 Activator II - CAS 374922-43-7 - Calbiochem

The SIRT1 Activator II, also referenced under CAS 374922-43-7, modulates the biological activity of SIRT1. This small molecule/inhibitor is primarily used for Biochemicals applications.

SIRT1 Activator II - CAS 374922-43-7 - 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: 3-(Benzenesulfonyl)-1-(4-fluorophenyl)pyrrolo[4,5-b]quinoxalin-2-amine , CAY10602, SIRT1 Activator II

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566313
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概要

Replacement Information

主要スペック表

CAS #Empirical Formula
374922-43-7C₂₂H₁₅FN₄O₂S

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566313-10MGCN
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      		 ｶﾞﾗｽﾋﾞﾝ 10 mg
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      Description
      OverviewA cell-permeable pyrroloquinoxaline compound that acts as a reversible SIRT1 activator (10 µM causes ~2.3-fold fluorescent enhancement in a fluorescent assay using hrSIRT1) and enhances fat mobilization in fully differentiated 3T3L1 fibroblasts. Shown to inhibit LPS-induced TNF-α release in THP-1 cells by ~10-fold more potent than resveratrol (Cat. No. 554325).
      Catalogue Number566313
      Brand Family Calbiochem®
      Synonyms3-(Benzenesulfonyl)-1-(4-fluorophenyl)pyrrolo[4,5-b]quinoxalin-2-amine , CAY10602, SIRT1 Activator II
      References
      ReferencesLavu, S., et al. 2008. Nat. Rev. Drug Discov. 7, 841.
      Nayagam, V.M., et al. 2006. J. Biomol. Screen. 11, 959.
      Product Information
      CAS number374922-43-7
      FormOff-white powder
      Hill FormulaC₂₂H₁₅FN₄O₂S
      Chemical formulaC₂₂H₁₅FN₄O₂S
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      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 Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
      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 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
      566313-10MGCN 04055977191363

      Documentation

      SIRT1 Activator II - CAS 374922-43-7 - Calbiochem (M)SDS

      タイトル

      英語版製品安全データシート（(M)SDS） 

      SIRT1 Activator II - CAS 374922-43-7 - Calbiochem 試験成績書（CoA）

      タイトルロット番号
      566313

      参考資料

      参考資料の概要
      Lavu, S., et al. 2008. Nat. Rev. Drug Discov. 7, 841.
      Nayagam, V.M., et al. 2006. J. Biomol. Screen. 11, 959.
      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.

      Revision15-November-2021 JSW
      Synonyms3-(Benzenesulfonyl)-1-(4-fluorophenyl)pyrrolo[4,5-b]quinoxalin-2-amine , CAY10602, SIRT1 Activator II
      DescriptionA cell-permeable pyrroloquinoxaline compound that acts as a reversible SIRT1 activator (10 µM causes ~2.3-fold fluorescent enhancement in a fluorescent assay using hrSIRT1) and enhances fat mobilization in fully differentiated 3T3L1 fibroblasts. Shown to inhibit LPS-induced TNF-α release in THP-1 cells by ~10-fold more potent than resveratrol (Cat. No. 554325).
      FormOff-white powder
      Intert gas (Yes/No) Packaged under inert gas
      CAS number374922-43-7
      Chemical formulaC₂₂H₁₅FN₄O₂S
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (100 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 3 months at -20°C.
      Toxicity Standard Handling
      ReferencesLavu, S., et al. 2008. Nat. Rev. Drug Discov. 7, 841.
      Nayagam, V.M., et al. 2006. J. Biomol. Screen. 11, 959.