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370698 GW7647 - CAS 265129-71-3 - Calbiochem

A cell-permeable urea-substituted thioisobutyric acid compound that acts as a potent and selective PPARα.

GW7647 - CAS 265129-71-3 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

Synonyms: GW647, 2-(4-(2-(1-Cyclohexanebutyl-3-cyclohexylureido)ethyl)phenylthio)-2-methylpropionic Acid, PPAR Agonist IV, PPARα Agonist II, PPARβ/δ Agonist I, PPARγ Agonist III

Primary Target: PPARα
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370698
가격 및 재고 조회

개요

Replacement Information

주요 사양표

CAS #Empirical Formula
265129-71-3C₂₉H₄₆N₂O₃S

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370698-5MGCN
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      		 Plastic ampoule 5 mg
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      Description
      OverviewA cell-permeable urea-substituted thioisobutyric acid (ureido-TiBA) compound that acts as a potent and selective PPARα agonist (PPARα, γ and δ - EC50 = 6 nM, 1.1 µM and 6.2 µM for human; 1 nM, 1.3 µM and 2.9 µM for murine, respectively). Also displays in vivo lipid-lowering activity in rats.
      Catalogue Number370698
      Brand Family Calbiochem®
      SynonymsGW647, 2-(4-(2-(1-Cyclohexanebutyl-3-cyclohexylureido)ethyl)phenylthio)-2-methylpropionic Acid, PPAR Agonist IV, PPARα Agonist II, PPARβ/δ Agonist I, PPARγ Agonist III
      References
      ReferencesMuoio, D.M., et al. 2002. J. Biol. Chem. 277, 26089.
      Brown, P.J., et al. 2001. Bioorg. Med. Chem. Lett. 11, 1225.
      Oliver, W.R. Jr., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 5306.
      Poirier, H., et al. 2001. Biochem. J. 355, 481.
      Product Information
      CAS number265129-71-3
      ATP CompetitiveN
      FormWhite solid
      Hill FormulaC₂₉H₄₆N₂O₃S
      Chemical formulaC₂₉H₄₆N₂O₃S
      ReversibleN
      Structure formula ImageStructure formula Image
      Quality LevelMQ100
      Applications
      Biological Information
      Primary TargetPPARα
      Primary Target IC<sub>50</sub>EC50 = 6 nM, 1.1 µM and 6.2 µM for human PPARα, γ and δ, respectively; EC50 = 1 nM, 1.3 µM and 2.9 µM for murine PPARα, γ and δ, respectively
      Purity≥98% by HPLC
      Physicochemical Information
      Cell permeableY
      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 Irritant
      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
      카탈로그 번호 GTIN
      370698-5MGCN 04055977191769

      Documentation

      GW7647 - CAS 265129-71-3 - Calbiochem MSDS

      타이틀

      물질안전보건자료(MSDS) 

      GW7647 - CAS 265129-71-3 - Calbiochem Certificates of Analysis

      TitleLot Number
      370698

      References

      참고문헌 보기
      Muoio, D.M., et al. 2002. J. Biol. Chem. 277, 26089.
      Brown, P.J., et al. 2001. Bioorg. Med. Chem. Lett. 11, 1225.
      Oliver, W.R. Jr., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 5306.
      Poirier, H., et al. 2001. Biochem. J. 355, 481.
      Data Sheet

      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.

      Revision07-July-2008 RFH
      SynonymsGW647, 2-(4-(2-(1-Cyclohexanebutyl-3-cyclohexylureido)ethyl)phenylthio)-2-methylpropionic Acid, PPAR Agonist IV, PPARα Agonist II, PPARβ/δ Agonist I, PPARγ Agonist III
      DescriptionA cell-permeable, urea-substituted, thioisobutyric acid (ureido-TiBA) compound that acts as a potent and selective peroxisome proliferator-activated receptor α (PPARα) agonist (EC50 = 6 nM for human PPARα, 1.1 µM for human PPARγ, and 6.2 µM human PPARδ; 1 nM for murine PPARα, 1.3 µM for murine PPARγ, and 2.9 µM murine PPARδ). Also shown to lower lipid levels in rats.
      FormWhite solid
      Intert gas (Yes/No) Packaged under inert gas
      CAS number265129-71-3
      Chemical formulaC₂₉H₄₆N₂O₃S
      Structure formulaStructure formula
      Purity≥98% by HPLC
      SolubilityDMSO (50 mg/ml) or Ethanol (12 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 Irritant
      ReferencesMuoio, D.M., et al. 2002. J. Biol. Chem. 277, 26089.
      Brown, P.J., et al. 2001. Bioorg. Med. Chem. Lett. 11, 1225.
      Oliver, W.R. Jr., et al. 2001. Proc. Natl. Acad. Sci. USA 98, 5306.
      Poirier, H., et al. 2001. Biochem. J. 355, 481.