Report for Mark M

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References (4)

Title : Chronic treatment with the dipeptidyl peptidase-4 inhibitor BI 1356 [(R)-8-(3-amino-piperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-yl methyl)-3,7-dihydro-purine-2,6-dione] increases basal glucagon-like peptide-1 and improves glycemic control in diabetic rodent models - Thomas_2009_J.Pharmacol.Exp.Ther_328_556
Author(s) : Thomas L , Tadayyon M , Mark M
Ref : Journal of Pharmacology & Experimental Therapeutics , 328 :556 , 2009
Abstract : Thomas_2009_J.Pharmacol.Exp.Ther_328_556
ESTHER : Thomas_2009_J.Pharmacol.Exp.Ther_328_556
PubMedSearch : Thomas_2009_J.Pharmacol.Exp.Ther_328_556
PubMedID: 18971371

Title : (R)-8-(3-amino-piperidin-1-yl)-7-but-2-ynyl-3-methyl-1-(4-methyl-quinazolin-2-ylm ethyl)-3,7-dihydro-purine-2,6-dione (BI 1356), a novel xanthine-based dipeptidyl peptidase 4 inhibitor, has a superior potency and longer duration of action compared with other dipeptidyl peptidase-4 inhibitors - Thomas_2008_J.Pharmacol.Exp.Ther_325_175
Author(s) : Thomas L , Eckhardt M , Langkopf E , Tadayyon M , Himmelsbach F , Mark M
Ref : Journal of Pharmacology & Experimental Therapeutics , 325 :175 , 2008
Abstract : Thomas_2008_J.Pharmacol.Exp.Ther_325_175
ESTHER : Thomas_2008_J.Pharmacol.Exp.Ther_325_175
PubMedSearch : Thomas_2008_J.Pharmacol.Exp.Ther_325_175
PubMedID: 18223196

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

Title : The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment - Clark_2003_Genome.Res_13_2265
Author(s) : Clark HF , Gurney AL , Abaya E , Baker K , Baldwin D , Brush J , Chen J , Chow B , Chui C , Crowley C , Currell B , Deuel B , Dowd P , Eaton D , Foster J , Grimaldi C , Gu Q , Hass PE , Heldens S , Huang A , Kim HS , Klimowski L , Jin Y , Johnson S , Lee J , Lewis L , Liao D , Mark M , Robbie E , Sanchez C , Schoenfeld J , Seshagiri S , Simmons L , Singh J , Smith V , Stinson J , Vagts A , Vandlen R , Watanabe C , Wieand D , Woods K , Xie MH , Yansura D , Yi S , Yu G , Yuan J , Zhang M , Zhang Z , Goddard A , Wood WI , Godowski P , Gray A
Ref : Genome Res , 13 :2265 , 2003
Abstract : Clark_2003_Genome.Res_13_2265
ESTHER : Clark_2003_Genome.Res_13_2265
PubMedSearch : Clark_2003_Genome.Res_13_2265
PubMedID: 12975309
Gene_locus related to this paper: human-CES3 , human-CES4A