首页> 外国专利> Bicyclic carbamoylpyridone derivatives having HIV integrase inhibitory activity

Bicyclic carbamoylpyridone derivatives having HIV integrase inhibitory activity

机译:具有HIV整合酶抑制活性的双环氨基甲酰基吡啶酮衍生物

摘要

[Object] Is to provide a novel compound having an anti-viral activity, particularly a HIV integrase inhibitory activity, and an agent, particularly an anti-HIV agent. [Solving means] A compound represented by the formula: (wherein Z 1 is NR 4 (R 4 is hydrogen, optionally substituted lower alkyl etc.), O or CH 2 ; Z 2 is optionally substituted lower alkylene or optionally substituted lower alkenylene, each may be intervened by a heteroatom group selected from group consisting O, S, SO, SO 2 , NR 5 (R 5 is selected independently from the same substituent group of R 4 ) -N= and =N-; R 1 is hydrogen or lower alkyl; X is a single bond, a heteroatom group selected from O, S, SO, SO 2 and NH, or lower alkylene or lower alkenylene each may be intervened by the heteroatom group; R 2 is optionally substituted aryl; R 3 is hydrogen, halogen, hydroxy, optionally substituted alkyl group etc.)
机译:目的是提供一种具有抗病毒活性,特别是HIV整合酶抑制活性的新型化合物,以及一种试剂,特别是抗HIV试剂。 [解决方案]由下式表示的化合物:(其中Z 1为NR 4(R 4为氢,任选取代的低级烷基等),O或CH 2;Z 2是任选取代的低级亚烷基或任选取代的低级亚烯基,它们各自可被选自O,S,SO,SO 2,NR 5的杂原子基团介入(R 5独立地选自R 4的相同取代基)-N =和= N-;R 1为氢或低级烷基;X为单键,选自O,S,SO,SO 2和NH的杂原子基团,或低级亚烷基或低级亚烯基可被杂原子基团插入;R 2是任选取代的芳基;R 3为氢,卤素,羟基,任选取代的烷基等)

著录项

  • 公开/公告号JP5317257B2

    专利类型

  • 公开/公告日2013-10-16

    原文格式PDF

  • 申请/专利权人 塩野義製薬株式会社;

    申请/专利号JP20070503763

  • 发明设计人 吉田 弘志;川筋 孝;垰田 善之;

    申请日2006-02-20

  • 分类号C07D471/04;A61K31/4985;A61P31/18;A61P43;

  • 国家 JP

  • 入库时间 2022-08-21 16:58:53

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