Report for Fuchs H

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References (3)

Title : Binding to dipeptidyl peptidase-4 determines the disposition of linagliptin (BI 1356)--investigations in DPP-4 deficient and wildtype rats - Retlich_2009_Biopharm.Drug.Dispos_30_422
Author(s) : Retlich S , Withopf B , Greischel A , Staab A , Jaehde U , Fuchs H
Ref : Biopharmaceutics & Drug Disposition , 30 :422 , 2009
Abstract : Retlich_2009_Biopharm.Drug.Dispos_30_422
ESTHER : Retlich_2009_Biopharm.Drug.Dispos_30_422
PubMedSearch : Retlich_2009_Biopharm.Drug.Dispos_30_422
PubMedID: 19771584

Title : Concentration-dependent plasma protein binding of the novel dipeptidyl peptidase 4 inhibitor BI 1356 due to saturable binding to its target in plasma of mice, rats and humans - Fuchs_2009_J.Pharm.Pharmacol_61_55
Author(s) : Fuchs H , Tillement JP , Urien S , Greischel A , Roth W
Ref : J Pharm Pharmacol , 61 :55 , 2009
Abstract : Fuchs_2009_J.Pharm.Pharmacol_61_55
ESTHER : Fuchs_2009_J.Pharm.Pharmacol_61_55
PubMedSearch : Fuchs_2009_J.Pharm.Pharmacol_61_55
PubMedID: 19126297

Title : 8-(3-(R)-aminopiperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylme thyl)-3,7-dihydropurine-2,6-dione (BI 1356), a highly potent, selective, long-acting, and orally bioavailable DPP-4 inhibitor for the treatment of type 2 diabetes - Eckhardt_2007_J.Med.Chem_50_6450
Author(s) : Eckhardt M , Langkopf E , Mark M , Tadayyon M , Thomas L , Nar H , Pfrengle W , Guth B , Lotz R , Sieger P , Fuchs H , Himmelsbach F
Ref : Journal of Medicinal Chemistry , 50 :6450 , 2007
Abstract : Eckhardt_2007_J.Med.Chem_50_6450
ESTHER : Eckhardt_2007_J.Med.Chem_50_6450
PubMedSearch : Eckhardt_2007_J.Med.Chem_50_6450
PubMedID: 18052023
Gene_locus related to this paper: human-DPP4