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Amide derivatives useful as inhibitors of the production of cytokines

机译:酰胺衍生物可用作细胞因子产生的抑制剂

摘要

The invention concerns amide derivatives of formula (I): wherein RSUP3 /SUPis (1-6C)alkyl or halogeno; QSUP1 /SUPis heteroaryl which is optionally substituted with 1, 2, 3, or 4 substituents such as hydroxy, halogeno, trifluoromethyl, (1-6C)alkyl, (1-6C)alkoxy, hydroxy-(1-6C)alkyl, (1-6C)alkoxy-(1-6C)alkyl, hydroxy-(2-6C)alkoxy, amino-(2-6C)alkylamino, N-(1-6C)alkyl-(1-6C)alkylamino-(2-6C)alkylamino, aryl, heteroaryl and heterocyclyl; p is 0-2 and RSUP2 /SUPis a substituent such as hydroxy and halogeno; q is 0-4; and QSUP2 /SUPincludes optionally substituted aryl, cycloalkyl, heteroaryl and heterocyclyl; or pharmaceutically-acceptable salts or in vivo-cleavable esters thereof; processes for their preparation, pharmaceutical compositions containing them and their use in the treatment of diseases or medical conditions mediated by cytokines.
机译:本发明涉及式(I)的酰胺衍生物:其中R 3 =(1-6C)烷基或卤素。 Q 1 是杂芳基,可选地被1、2、3或4个取代基取代,例如羟基,卤代,三氟甲基,(1-6C)烷基,(1-6C)烷氧基,羟基-( 1-6C)烷基,(1-6C)烷氧基-(1-6C)烷基,羟基-(2-6C)烷氧基,氨基-(2-6C)烷基氨基,N-(1-6C)烷基-(1- 6C)烷基氨基-(2-6C)烷基氨基,芳基,杂芳基和杂环基; p为0-2,R 2 为取代基,如羟基和卤代基; q是0-4; Q 2 包括任选取代的芳基,环烷基,杂芳基和杂环基;或其药学上可接受的盐或体内可裂解的酯;的制备方法,含有它们的药物组合物及其在治疗细胞因子介导的疾病或医学状况中的用途。

著录项

  • 公开/公告号AU753741B2

    专利类型

  • 公开/公告日2002-10-24

    原文格式PDF

  • 申请/专利权人 ASTRAZENECA AB;

    申请/专利号AU5178899A

  • 申请日1999-07-29

  • 分类号C07D213/82;C07D241/44;C07D215/48;C07D261/18;C07D277/68;C07D239/74;C07D333/38;C07D401/12;C07D401/14;C07D413/12;C07D213/81;A61K31/44;A61K31/47;A61K31/495;

  • 国家 AU

  • 入库时间 2022-08-22 00:39:10

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