发明名称 NEW INTERMEDIATE COMPOUND
摘要 This invention relates to novel 3-substituted-2-oxindole derivatives which are inhibitors of prostaglandin H2 synthase, 5-lipoxygenase and interleukin-1 biosynthesis. The compounds of the invention are useful as inhibitors of prostaglandin H2 synthase and interleukin-1 biosynthesis, per se, and as analgesic, antiinflammatory and antiarthritic agents in the treatment of chronic inflammatory diseases. This invention also relates to pharmaceutical compositions comprising said 3-substituted-2-oxindole derivatives; to methods of inhibiting prostaglandin H2 synthase and biosynthesis of interleukin-1; and to treating chronic inflammatory diseases in a mammal with said compounds. Further, this invention relates to certain novel carboxylic acids useful as intermediates in the preparation of the 3-substituted-2-oxindole derivatives of this invention and to a process for the preparation of the 3-substituted-2-oxindole derivatives.
申请公布号 JPH07118261(A) 申请公布日期 1995.05.09
申请号 JP19940186078 申请日期 1994.08.08
申请人 PFIZER INC 发明人 FUREDERITSUKU JIEIKOBU EEGOTSUTO;KAARU JIYOSEFU GOTSUDAADO;GEIRII RICHIYAADO SHIYURUTE
分类号 C07D333/40;A61K31/38;A61K31/381;A61K31/40;A61K31/403;A61K31/404;A61K31/41;A61K31/425;A61K31/44;A61K31/4427;A61K31/443;A61K31/4433;A61K31/445;A61K31/495;A61P3/00;A61P9/06;A61P19/02;A61P25/04;A61P29/00;A61P43/00;C07D;C07D209/12;C07D209/26;C07D209/34;C07D333/38;C07D401/06;C07D403/04;C07D403/06;C07D405/06;C07D407/06;C07D409/06;C07D413/04;C07D413/06;C07D417/04;C07D417/06;C07D417/14;C07F9/547;C07F9/6561;(IPC1-7):C07D333/40 主分类号 C07D333/40
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