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  • The design of potent and selective inhibitors of DPP-4: optimization of ADME properties by amide replacements.

The design of potent and selective inhibitors of DPP-4: optimization of ADME properties by amide replacements.

Bioorganic & medicinal chemistry letters (2009-10-17)
Sonja Nordhoff, Stephan Bulat, Silvia Cerezo-Gálvez, Oliver Hill, Barbara Hoffmann-Enger, Meritxell López-Canet, Claudia Rosenbaum, Christian Rummey, Meinolf Thiemann, Victor G Matassa, Paul J Edwards, Achim Feurer
ABSTRACT

For a series of beta-homophenylalanine based inhibitors of dipeptidyl peptidase IV ADME properties were improved by the incorporation of amide replacements. These efforts led to a novel series of potent and selective inhibitors of DPP-4 that exhibit an attractive pharmacokinetic profile and show excellent efficacy in an animal model of diabetes.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
DL-Homophenylalanine, 98%
Sigma-Aldrich
L-Homophenylalanine hydrochloride, 97%