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1.Ortho substituted aromatic compounds useful as antagonists of the pain enhancing effects of E-type prostaglandins 失效
标题翻译: 可用作E型前列腺素疼痛增强作用拮抗剂的正交取代芳族化合物公开(公告)号:US5811459A
公开(公告)日:1998-09-22
申请号:US647977
申请日:1996-06-04
申请人: Gloria Ann Breault , John Oldfield , Howard Tucker , Peter Warner
发明人: Gloria Ann Breault , John Oldfield , Howard Tucker , Peter Warner
IPC分类号: C07D295/12 , A61K31/165 , A61K31/17 , A61K31/19 , A61K31/215 , A61K31/27 , A61K31/275 , A61K31/40 , A61K31/415 , A61K31/4166 , A61K31/44 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4412 , A61K31/4418 , A61K31/4425 , A61K31/4427 , A61K31/4433 , A61K31/495 , A61K31/505 , A61K31/535 , A61K31/5375 , A61P25/04 , A61P29/00 , A61P43/00 , C07C45/41 , C07C45/71 , C07C51/347 , C07C65/21 , C07C65/24 , C07C65/40 , C07C69/94 , C07C205/34 , C07C205/44 , C07C205/59 , C07C233/25 , C07C233/54 , C07C235/34 , C07C235/42 , C07C237/32 , C07C257/04 , C07C275/28 , C07C275/34 , C07C275/42 , C07C311/21 , C07C317/44 , C07C317/46 , C07C323/25 , C07C323/56 , C07C323/62 , C07D207/09 , C07D213/30 , C07D213/38 , C07D213/40 , C07D213/50 , C07D213/56 , C07D213/64 , C07D213/65 , C07D213/75 , C07D213/79 , C07D213/80 , C07D213/82 , C07D213/89 , C07D233/54 , C07D233/61 , C07D233/64 , C07D233/78 , C07D233/90 , C07D237/08 , C07D237/24 , C07D239/26 , C07D239/34 , C07D239/36 , C07D241/12 , C07D241/24 , C07D249/10 , C07D257/04 , C07D257/06 , C07D263/32 , C07D277/56 , C07D307/42 , C07D333/16 , C07D333/38 , C07D401/04 , C07D401/12 , C07D409/12 , C07D417/12 , C07D521/00 , C07C63/04 , C07C239/42
CPC分类号: C07D213/30 , C07C205/34 , C07C205/44 , C07C205/59 , C07C275/34 , C07C311/21 , C07C317/46 , C07C323/25 , C07C323/56 , C07C323/62 , C07C45/41 , C07C45/71 , C07C65/24 , C07C65/40 , C07C69/94 , C07D207/09 , C07D213/38 , C07D213/40 , C07D213/50 , C07D213/56 , C07D213/64 , C07D213/65 , C07D213/75 , C07D213/80 , C07D213/82 , C07D213/89 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/78 , C07D233/90 , C07D237/24 , C07D239/26 , C07D239/34 , C07D239/36 , C07D241/12 , C07D241/24 , C07D249/08 , C07D249/10 , C07D257/04 , C07D257/06 , C07D263/32 , C07D277/56 , C07D307/42 , C07D333/16 , C07D333/38 , C07D401/04 , C07D401/12 , C07D417/12 , C07C2101/02 , C07C2101/14 , C07C2102/10
摘要: The invention relates to compounds of the formula (I): ##STR1## wherein A, B and D are various ring systems such as phenyl, R.sup.1 includes carboxy, R.sup.3 is hydrogen or C.sub.1-4 alkyl and Z is a linking group such as --(CH(R.sup.5)).sub.m -- wherein m is 2, 3 or 4, and R.sub.5 includes hydrogen and methyl; and pharmaceutically acceptable salts and in vivo hydrolysable esters or amides thereof, processes for preparing these compounds, pharmaceutical compositions comprising them, and their use in the treatment of pain.
摘要翻译: PCT No.PCT / GB95 / 02417 371日期1996年6月4日 102(e)日期1996年6月4日PCT提交1995年10月12日PCT公布。 公开号WO96 / 11902 日期:1996年04月25日本发明涉及式(I)化合物:其中A,B和D是各种环系,如苯基,R 1包括羧基,R 3是氢或C 1-4烷基,Z 是连接基团,例如 - (CH(R 5))m - ,其中m是2,3或4,并且R 5包括氢和甲基; 和其药学上可接受的盐和体内可水解的酯或酰胺,制备这些化合物的方法,包含它们的药物组合物及其在治疗疼痛中的用途。