N-[1,3,4]-thiadiazol-2-yl-benzene sulfonamides,...

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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Details

C514S363000, C546S268700, C548S138000

Reexamination Certificate

active

07858647

ABSTRACT:
The present invention comprises N-[1,3,4]-thiadiazol-2-yl-benzene sulfonamides, their physiologically acceptable salts and functional derivatives that exhibit peroxisome proliferator activated receptor (PPAR) PPARdelta and PPARgamma agonist activity. The structure of the compounds of the invention are defined by Formula I below,And the isomers thereof wherein the various substituents are defined herein, including their physiologically acceptable salts. Processes for the compounds preparation are also disclosed. The compounds are suitable for the treatment of fatty acid metabolism and glucose utilization disorders, disorders relating to insulin resistance are involved as well as demyelinating and other neurodegenerative disorders of the central and peripheral nervous system.

REFERENCES:
patent: 1277729 (2003-01-01), None
patent: WO 2005/005421 (2005-01-01), None
Khlaponina et al., Synthesis and Hypoglycemic Activity of 4-(Beta-Acylamidoethyl) Benzenesulfamides, Pharmaceutical Chemistry Journal, vol. 21, No. 8, pp. 588-591 (1987).
Khlaponina, L.N., et. al., Synthesis and Hypoglycemic Activity of 4-(Beta-Acylamidoethyl) Benzenesulfonamides, Pharmaceutical Chemistry Journal, vol. 21, No. 8, pp. 588-591, (1987).

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