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Pyrazolopyridine derivatives as selective cox-2 inhibitors

机译:吡唑并吡啶衍生物作为选择性cox-2抑制剂

摘要

The invention provides the compounds of formula (I) embedded imageand pharmaceutically acceptable derivatives thereof wherein:R0 and R1 are independently selected from the group consisting of H, halogen, C1-6alkyl, C1-6alkoxy, and C1-6alkoxy substituted by one or more fluorine atoms;R2 is selected from the group consisting of H, C1-6alkyl, C1-6alkyl substituted by one or more fluorine atoms, C1-6alkoxy, C1-6hydroxyalkyl, SC1-6alkyl, C(O)H, C(O)C1-6alkyl, C1-6alkylsulphonyl, and C1-6alkoxy substituted by one or more fluorine atoms; andR3 is C1-6alkyl or NH2.;Compounds of formula (I) are potent and selective inhibitors of COX-2 and are of use in the treatment of the pain, fever, inflammation of a variety of conditions and diseases.
机译:本发明提供式(I)的化合物 <图像alt =“嵌入式图像” file =“ US07223772-20070529-C00001.GIF” he =“ 34.21mm” imgContent =“ chem” imgFormat =“ GIF” wi =“ 61.30mm“ /> 及其药学上可接受的衍生物,其中: R 0 和R 1 独立选自H,卤素,C 1-6 烷基, C 1-6 烷氧基和C 1-6 烷氧基被一个或多个氟原子取代; R 2 选自由H,C 1-6 烷基,被一个或多个取代的C 1-6 烷基组成的组。更多氟原子,C 1-6 烷氧基,C 1-6 羟烷基,SC 1-6 烷基,C(O)H,C被一个或多个氟原子取代的(O)C 1-6 烷基,C 1-6 烷基磺酰基和C 1-6 烷氧基;并且 R 3 是C 1-6 烷基或NH 2 ;式(I)的化合物是COX-2的有效和选择性抑制剂,可用于治疗疼痛,发烧,炎症各种状况和疾病。

著录项

  • 公开/公告号US7223772B1

    专利类型

  • 公开/公告日2007-05-29

    原文格式PDF

  • 申请/专利权人 IAN BAXTER CAMPBELL;ALAN NAYLOR;

    申请/专利号US19990830836

  • 发明设计人 IAN BAXTER CAMPBELL;ALAN NAYLOR;

    申请日1999-11-01

  • 分类号A61K31/415;A61K31/44;C07D231/56;C07D471/02;

  • 国家 US

  • 入库时间 2022-08-21 21:00:47

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