Novel heterocyclic DPP-4 inhibitors for the treatment of type 2 diabetes-Reference-Cited by-同舟云学术

Novel heterocyclic DPP-4 inhibitors for the treatment of type 2 diabetes

Published:2012-02 Issue:3 Volume:22 Page:1464-1468
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Sutton Jon M.,Clark David E.,Dunsdon Stephen J.,Fenton Garry,Fillmore Amanda,Harris Neil V.,Higgs Chris,Hurley Chris A.,Krintel Sussie L.,MacKenzie Robert E.,Duttaroy Alokesh,Gangl Eric,Maniara Wiesia,Sedrani Richard,Namoto Kenji,Ostermann Nils,Gerhartz Bernd,Sirockin Finton,Trappe Jörg,Hassiepen Ulrich,Baeschlin Daniel K.

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference24 articles.

1. Long-Term Treatment With the Dipeptidyl Peptidase IV Inhibitor P32/98 Causes Sustained Improvements in Glucose Tolerance, Insulin Sensitivity, Hyperinsulinemia, and β-Cell Glucose Responsiveness in VDF (fa/fa) Zucker Rats

2. Glucagon-Like Peptide-1 and the Islet β-Cell: Augmentation of Cell Proliferation and Inhibition of Apoptosis

3. Endocrine Regulation of Human Fetal Growth: The Role of the Mother, Placenta, and Fetus

4. Dipeptidyl-peptidase IV hydrolyses gastric inhibitory polypeptide, glucagon-like peptide-1(7-36)amide, peptide histidine methionine and is responsible for their degradation in human serum

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