Fused heterocyclic derivatives as PPAR modulators

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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C514S300000, C546S118000, C546S113000

Reexamination Certificate

active

07598266

ABSTRACT:
The present invention is directed to compounds represented by the following structural formula, Formula I:wherein:(a) X is selected from the group consisting of a single bond, O, S, S(O)2and N;(b) U is an aliphatic linker;(c) Y is selected from the group consisting of C, O, S, NH and a single bond;(d) E is C(R3)(R4)A or A and wherein(i) A is selected from the group consisting of carboxyl, tetrazole, C1-C6alkylnitrile, carboxamide, sulfonamide and acylsulfonamide;(e) B is selected from the group consisting of S, O, C, and N;(f) Z is selected from the group consisting of N and C; with the proviso that when B is C then Z is N.

REFERENCES:
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patent: 1 167 357 (2002-02-01), None
patent: WO 00/64876 (2000-11-01), None
patent: WO 01/00603 (2001-01-01), None
patent: WO 03/066574 (2003-08-01), None
Byrn et al. Solid-State Chemistry of Drugs, 2d, Chapter 11 Hydrates and Solvates, 233-247, 233.
Rami, H.K., et al, “Synthetic ligands for PPAR gamma—review of patent literature 1994-1999”, Expert Opinion Ther. Patents, 2000, 10(5):623-634.

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