首页> 外国专利> INDOLE DERIVATIVE OR PHARMACOLOGICALLY ACCEPTABLE SALT THEREOF, AS EP1 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF LOWER URINARY TRACT DYSFUNCTION

INDOLE DERIVATIVE OR PHARMACOLOGICALLY ACCEPTABLE SALT THEREOF, AS EP1 RECEPTOR ANTAGONISTS FOR THE TREATMENT OF LOWER URINARY TRACT DYSFUNCTION

机译:吲哚衍生物或药理学上可接受的盐,作为治疗下尿道功能障碍的EP1受体拮抗剂

摘要

Disclosed is a compound represented by general formula (I), which has EP1 receptor antagonist activity, or a pharmacologically acceptable salt thereof. (In general formula (I), A represents a benzene ring or the like; Y represents a C1-6 alkylene group or the like; RN represents a hydrogen atom or a C1-6 alkyl group; R1 represents a hydrogen atom, a C1-6 alkyl group or the like; R2 represents an optionally substituted phenyl group, an optionally substituted five-membered aromatic heterocyclic group, an optionally substituted six-membered aromatic heterocyclic group or the like; R3 represents a halogen atom, a C1-6 alkoxy group or the like; R4 represents a hydrogen atom or the like; and R5 represents a hydrogen atom or the like.) The compound of general formula (I) is able to be used as an agent for treatment or prevention of LUTS, in particular symptoms of OABS.
机译:公开了具有EP1受体拮抗剂活性的通式(I)表示的化合物或其药理学上可接受的盐。 (通式(I)中,A表示苯环等; Y表示C 1-6亚烷基等; RN表示氢原子或C 1-6烷基; R 1表示氢原子,C 1 -6烷基等; R 2表示任选取代的苯基,任选取代的五元芳族杂环基,任选取代的六元芳族杂环基等; R 3表示卤素原子,C 1-6烷氧基通式(I)的化合物能够用作治疗或预防LUTS的试剂,特别是R 5为氢原子等; R 4为氢原子等; R 5为氢原子等。 OABS的症状。

著录项

  • 公开/公告号NZ597810A

    专利类型

  • 公开/公告日2013-03-28

    原文格式PDF

  • 申请/专利权人 KISSEI PHARMACEUTICAL CO. LTD.;

    申请/专利号NZ20100597810

  • 申请日2010-07-26

  • 分类号A61P13/02;A61K31/404;A61K31/422;A61K31/427;A61K31/4439;A61P43;C07D209/18;C07D401/04;C07D401/06;C07D401/14;C07D405/04;C07D405/06;C07D405/14;C07D409/04;C07D409/06;C07D409/14;C07D413/14;C07D417/06;C07D417/14;

  • 国家 NZ

  • 入库时间 2022-08-21 16:40:28

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