Abstract
The cis-3-amino-4-(2-cyanopyrrolidide)-pyrrolidine template has been shown to afford low nanomolar inhibitors of human DPP-IV that exhibit a robust PK/PD profile. An X-ray co-crystal structure of 5 confirmed the proposed mode of binding. The potent single digit DPP-IV inhibitor 53 exhibited a preferred PK/PD profile in preclinical animal models and was selected for additional profiling.
MeSH terms
-
Amination
-
Animals
-
Benzene / chemistry*
-
Cyanides / chemistry*
-
Dipeptidyl Peptidase 4 / chemistry
-
Dipeptidyl Peptidase 4 / metabolism
-
Dipeptidyl-Peptidase IV Inhibitors*
-
Dogs
-
Drug Design
-
Humans
-
Inhibitory Concentration 50
-
Models, Molecular
-
Molecular Structure
-
Protease Inhibitors / chemical synthesis*
-
Protease Inhibitors / chemistry
-
Protease Inhibitors / pharmacology*
-
Pyrroles / chemistry*
-
Pyrroles / pharmacology*
-
Rats
-
Stereoisomerism
-
Structure-Activity Relationship
Substances
-
Cyanides
-
Dipeptidyl-Peptidase IV Inhibitors
-
Protease Inhibitors
-
Pyrroles
-
DPP4 protein, human
-
Dipeptidyl Peptidase 4
-
Benzene