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J Med Chem ; 45(12): 2362-5, 2002 Jun 06.
Article in English | MEDLINE | ID: mdl-12036346

ABSTRACT

Dipeptidyl peptidase IV (DPP-IV) inhibition has the potential to become a valuable therapy for type 2 diabetes. We report the first use of solid-phase synthesis in the discovery of a new DPP-IV inhibitor class and a solution-phase synthesis that is practical up to the multikilogram scale. One compound, NVP-DPP728 (2), is profiled as a potent, selective, and short-acting DPP-IV inhibitor that has excellent oral bioavailability and potent antihyperglycemic activity.


Subject(s)
Dipeptidyl Peptidase 4/metabolism , Enzyme Inhibitors/chemical synthesis , Hypolipidemic Agents/chemical synthesis , Nitriles/chemical synthesis , Protease Inhibitors/chemical synthesis , Pyrrolidines/chemical synthesis , Administration, Oral , Animals , Biological Availability , Caco-2 Cells , Enzyme Inhibitors/pharmacology , Glucose Tolerance Test , Humans , Hypolipidemic Agents/pharmacology , Macaca fascicularis , Male , Nitriles/pharmacology , Protease Inhibitors/pharmacology , Pyrrolidines/pharmacology , Rats , Rats, Sprague-Dawley , Structure-Activity Relationship
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