首页> 外国专利> 3,6-SUBSTITUTED 5-ARYLAMINO-1H-PYRIDINE-2-ONE DERIVATIVES AND RELATED COMPOUNDS AS POLY(ADP-RIBOSE)POLYMERASE (PARP) INHIBITORS IN THE TREATMENT OF TISSUE DAMAGE OR DISEASE CAUSED BY NECROSIS OR APOPTOSIS

3,6-SUBSTITUTED 5-ARYLAMINO-1H-PYRIDINE-2-ONE DERIVATIVES AND RELATED COMPOUNDS AS POLY(ADP-RIBOSE)POLYMERASE (PARP) INHIBITORS IN THE TREATMENT OF TISSUE DAMAGE OR DISEASE CAUSED BY NECROSIS OR APOPTOSIS

机译:3,6-取代的5-芳基氨基-1H-吡啶-2-酮衍生物及相关化合物,作为多聚(ADP-核糖)聚合物酶(PARP)抑制剂,用于治疗因神经衰弱或凋亡引起的组织损伤或疾病

摘要

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.
机译:本发明涉及式(I)的化合物,其中R 1和R 3独立地代表氟,甲氧基,OCF 3,C 2 -C 3烯基或C 1 -C 4烷基,其任选地被氯,甲氧基或一个,两个或三个氟原子取代; R 2代表氢,氟,甲氧基,OCF 3,C 2 -C 3链烯基或C 1 -C 4烷基,其任选地被氯,甲氧基或一个,两个或三个氟原子取代; X代表O,S,NH或N(C1-C3-烷基); Ar表示未取代或至少单取代的芳基或杂芳基。所述化合物是聚(ADP-核糖)聚合酶(PARP)的抑制剂,并且可以用于治疗多种疾病。

著录项

  • 公开/公告号IL182093A

    专利类型

  • 公开/公告日2011-02-28

    原文格式PDF

  • 申请/专利权人 SANOFI-AVENTIS DEUTSCHLAND GMBH;

    申请/专利号IL20070182093

  • 发明设计人

    申请日2007-03-21

  • 分类号C07D;

  • 国家 IL

  • 入库时间 2022-08-21 18:06:22

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