Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10594330 | Bioorganic & Medicinal Chemistry Letters | 2012 | 5 Pages |
Abstract
A series of novel 3-amino-N-(4-aryl-1,1-dioxothian-4-yl)butanamides were investigated as dipeptidyl peptidase IV (DPP-4) inhibitors. Introduction of a 4-phenylthiazol-2-yl group showed highly potent DPP-4 inhibitory activity. Among various derivatives, (3R)-3-amino-N-(4-(4-phenylthiazol-2-yl)-tetrahydro-2H-thiopyran-4-yl)-4-(2,4,5-trifluorophenyl)butanamide 1,1-dioxide (30) reduced blood glucose excursion in an oral glucose tolerance test by oral administration.
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Authors
Aiko Nitta, Hideaki Fujii, Satoshi Sakami, Mikiya Satoh, Junko Nakaki, Shiho Satoh, Hiroki Kumagai, Hideki Kawai,