首页> 外国专利> 3.6 - substituted 5 - arylamino - 1h - pyidin 2 on derivatives and related compounds as poly (adp ribose) polymerase (parp) inhibitors in the treatment of nekose or apoptosis caused tissue damage or disorders

3.6 - substituted 5 - arylamino - 1h - pyidin 2 on derivatives and related compounds as poly (adp ribose) polymerase (parp) inhibitors in the treatment of nekose or apoptosis caused tissue damage or disorders

机译:3.6-取代的5-芳基氨基-1h-吡啶2在衍生物和相关化合物上作为聚(adp核糖)聚合酶(parp)抑制剂在治疗中枢或细胞凋亡引起的组织损伤或疾病中

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

相似文献

  • 专利
  • 外文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号