يعرض 1 - 19 نتائج من 19 نتيجة بحث عن '"Due-Hansen, Maria E"', وقت الاستعلام: 0.48s تنقيح النتائج
  1. 1
    Academic Journal

    المصدر: Due-Hansen , M E , Pandey , S K , Christiansen , E , Andersen , R , Hansen , S V F & Ulven , T 2016 , ' A protocol for amide bond formation with electron deficient amines and sterically hindered substrates ' , Organic & Biomolecular Chemistry , vol. 14 , no. 2 , pp. 430-433 . https://doi.org/10.1039/c5ob02129d

    وصف الملف: application/pdf

  2. 2
    Academic Journal
  3. 3
    Academic Journal

    المصدر: Hudson , B D , Due-Hansen , M E , Christiansen , E , Hansen , A M , Mackenzie , A E , Murdoch , H , Pandey , S K , Ward , R J , Marquez , R , Tikhonova , I G , Ulven , T & Milligan , G 2013 , ' Defining the molecular basis for the first potent and selective orthosteric agonists of the FFA2 free fatty acid receptor ' , Journal of Biological Chemistry , vol. 288 , no. 24 , pp. 17296-17312 . https://doi.org/10.1074/jbc.M113.455337

    وصف الملف: application/pdf

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  5. 5
    Academic Journal
  6. 6
    Academic Journal

    المصدر: Hansen , S V F , Christiansen , E , Urban , C , Hudson , B D , Stocker , C J , Due-Hansen , M E , Wargent , E T , Shimpukade , B , Almeida , R , Ejsing , C S , Cawthorne , M A , Kassack , M U , Milligan , G & Ulven , T 2016 , ' Discovery of a Potent Free Fatty Acid 1 Receptor Agonist with Low Lipophilicity, Low Polar Surface Area and Robust in Vivo Efficacy ' , Journal of Medicinal Chemistry , vol. 59 , ....

  7. 7
    Academic Journal
  8. 8
    Academic Journal

    المصدر: Christiansen , E , Due-Hansen , M E , Urban , C , Grundmann , M , Schmidt , J , Hansen , S V F , Hudson , B D , Zaibi , M , Markussen , S B , Hagesaether , E , Milligan , G , Cawthorne , M A , Kostenis , E , Kassack , M U & Ulven , T 2013 , ' Discovery of a potent and selective free fatty acid receptor 1 agonist with low lipophilicity and high oral bioavailability ' , Journal of Medicinal Chemistry , vol. 56 , no. ....

  9. 9
    Academic Journal

    المصدر: Christiansen , E , Due-Hansen , M E , Urban , C , Grundmann , M , Schröder , R , Hudson , B D , Milligan , G , Cawthorne , M A , Kostenis , E , Kassack , M U & Ulven , T 2012 , ' Free Fatty Acid Receptor 1 (FFA1/GPR40) Agonists : Mesylpropoxy Appendage Lowers Lipophilicity and Improves ADME Properties ' , Journal of Medicinal Chemistry , vol. 55 , no. 14 , pp. 6624-8 . https://doi.org/10.1021/jm3002026

  10. 10
    Academic Journal
  11. 11
    Academic Journal

    المصدر: Christiansen , E , Due-Hansen , M E & Ulven , T 2010 , ' A Rapid and Efficient Sonogashira Protocol and Improved Synthesis of Free Fatty Acid 1 (FFA1) Receptor Agonists ' , Journal of Organic Chemistry , vol. 75 , no. 4 , pp. 1301-4 . https://doi.org/10.1021/jo902533p

  12. 12
    Academic Journal

    المصدر: Christiansen , E , Due-Hansen , M E , Urban , C , Merten , N , Pfleiderer , M , Karlsen , K K , Rasmussen , S S , Steensgaard , M , Hamacher , A , Schmidt , J , Drewke , C , Petersen , R K , Kristiansen , K , Ullrich , S , Kostenis , E , Kassack , M U & Ulven , T 2010 , ' Structure−Activity Study of Dihydrocinnamic Acids and Discovery of the Potent FFA1 (GPR40) Agonist TUG-469 ' , ACS Medicinal Chemistry Letters , vol. 1 , ....

  13. 13
    Electronic Resource

    المصدر: Christiansen , E , Due-Hansen , M E , Urban , C , Merten , N , Pfleiderer , M , Karlsen , K K , Rasmussen , S S , Steensgaard , M , Hamacher , A , Schmidt , J , Drewke , C , Petersen , R K , Kristiansen , K , Ullrich , S , Kostenis , E , Kassack , M U & Ulven , T 2010 , ' Structure-activity study of dihydrocinnamic acids and discovery of the potent FFA1 (GPR40) agonist TUG-469 ' , ACS Medicinal Chemistry Letters , vol. 1 , no. 7 , pp. 345-349 .

    مصطلحات الفهرس: Diabetes, FFA1, FFAR1, GPR40, fatty acids, drug discovery, article

  14. 14
    Academic Journal
  15. 15
    Academic Journal
  16. 16
    Academic Journal
  17. 17
    Academic Journal
  18. 18
    Academic Journal
  19. 19

    المؤلفون: Due-Hansen, Maria E.

    المصدر: Due-Hansen , M E 2013 , ' Development of potent and selective modulators of the free fatty acid 1 (FFA1/GPR40) receptor ' .