首页> 外国专利> New substituted quinoline compounds as inhibitors of S-nitrosoglutathione reductase

New substituted quinoline compounds as inhibitors of S-nitrosoglutathione reductase

机译:新的取代喹啉化合物作为S-亚硝基谷胱甘肽还原酶的抑制剂

摘要

The compound of Formula I: ** Formula ** wherein m is selected from the group consisting of 0, 1, 2 or 3; R1 is independently selected from the group consisting of chlorine, fluorine, bromine, cyano and methoxy; R2b and R2c are independently selected from the group consisting of hydrogen, halogen, C1-C3 alkyl, fluorinated C1-C3 alkyl, cyano, C1-C3 alkoxy and N (CH3) 2; X is selected from the group consisting of n is selected from the group consisting of 0, 1 and 2; R3 is independently selected from the group consisting of halogen, C1-C3 alkyl, fluorinated C1-C3 alkyl, cyano, C1-C3 alkoxy and NR4R4 'where R4 and R4' are independently selected from the group consisting of C1-C3 alkyl , or R4 when taken together with R4 'forms a ring with 3 to 6 members; and A is selected from the group consisting of or a pharmaceutically acceptable salt, stereoisomer or N-oxide thereof.
机译:式I的化合物:**式**其中m选自0、1、2或3; R1独立地选自氯,氟,溴,氰基和甲氧基; R 2b和R 2c独立地选自氢,卤素,C 1 -C 3烷基,氟化的C 1 -C 3烷基,氰基,C 1 -C 3烷氧基和N(CH 3)2; X选自由n组成的组,n选自由0、1和2组成的组; R 3独立地选自卤素,C 1 -C 3烷基,氟化C 1 -C 3烷基,氰基,C 1 -C 3烷氧基和NR 4 R 4',其中R 4和R 4'独立地选自C 1 -C 3烷基,或当R4与R4一起时,形成具有3至6个成员的环; A选自其药学上可接受的盐,立体异构体或N-氧化物。

著录项

  • 公开/公告号ES2553771T3

    专利类型

  • 公开/公告日2015-12-11

    原文格式PDF

  • 申请/专利权人 NIVALIS THERAPEUTICS INC.;

    申请/专利号ES20110831651T

  • 发明设计人 SUN XICHENG;QIU JIAN;STOUT ADAM;

    申请日2011-10-07

  • 分类号C07D215/20;A61K31/47;A61K31/4709;A61P11;C07D401/04;C07D401/10;C07D409/04;C07D409/14;C07D413/10;C07D417/10;

  • 国家 ES

  • 入库时间 2022-08-21 14:22:21

相似文献

  • 专利
  • 外文文献
  • 中文文献
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