Fused heterocyclic compounds as peptidase inhibitors

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C546S173000

Reexamination Certificate

active

07547710

ABSTRACT:
A compound represented by the formula wherein ring A is an optionally substituted 5- to 10-membered aromatic ring; R1and R2are the same or different and each is an optionally substituted hydrocarbon group or an optionally substituted heterocyclic group; X and Y are the same or different and each is a bound, —O—, —S—, —SO—, —SO?2#191- or —NR3— (R3is a hydrogen atom or an optionally substituted hydrocarbon group); and L is a divalent hydrocarbon group, or a salt thereof shows a superior peptidase-inhibitory activity and is useful as a prophylactic or therapeutic agent of diabetes and the like.

REFERENCES:
patent: 98/19998 (1998-05-01), None
patent: 01/82925 (2001-11-01), None
patent: 02/062764 (2002-08-01), None
patent: 03/068748 (2003-08-01), None
Sakurai et al., Bull. Chem. Soc. Japan, (1969), vol. 42(1), pp. 220-223.
G. M. Coppola et al.,“1-Aminomethylisoquinoline-4-carboxylates as Novel Dipeptidylpeptidase IV Inhibitors”, Bioorganic & Medicinal Chemistry Letters, vol. 10, 2000, pp. 1555-1558.
K. Augustyns et al., “The Unique Properties of Dipeptidyl-peptidase IV (DPP IV/CD26) and the Therapeutic Potential of DPP IV Inhibitors”, Current Medicinal Chemistry, vol. 6, 1999, pp. 311-327.

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