Substituted 2-pyridone derivatives, method for their...

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

C514S277000, C514S340000, C514S345000, C544S333000, C546S255000, C546S256000, C546S261000

Reexamination Certificate

active

07863280

ABSTRACT:
This invention relates to compounds of formula (I),wherein R1 and R3 independently represent fluorine, methoxy, —OCF3, C2-C3-alkenyl or C1-C4-alkyl which is optionally substituted by chlorine, methoxy or one, two or three fluorine atoms; R2 represents hydrogen, fluorine, methoxy, —OCF3, C2-C3-alkenyl or C1-C4-alkyl which is optionally substituted by chlorine, methoxy or one, two or three fluorine atoms; X represents O, S, NH or N(C1-C3-alkyl); and Ar represents an unsubstituted or at least monosubstituted aryl or heteroaryl. Said compounds are inhibitors of poly(ADP-ribose) polymerase (PARP), and may be used for the treatment of a variety of disorders.

REFERENCES:
patent: 2005/0080096 (2005-04-01), Ishida et al.
patent: 0109628 (1984-05-01), None
patent: WO 93/07137 (1993-04-01), None

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