首页> 外国专利> 3,6-substituted 5-arylamino-1H-pyridin-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-pyridin-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-酮衍生物和相关化合物作为聚(ADP-核糖)聚合酶(PARP)抑制剂,用于治疗坏死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。

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