发明名称 N-phenylarylsulfonamide compound, pharmaceutical composition comprising the compound as active ingredient, synthetic intermediate for the compound and process for its preparation
摘要 An N-phenylarylsulfonylamide compound of formula (I) (R1 is COOH etc.; R2 is hydrogen, methyl, etc.; R3 and R4 are a combination of methyl and methyl, etc.; R5 is isopropyl etc.; Ar is thiazolyl, pyridyl, 5-methyl-2-furyl each optionally substituted with methyl; n is zero or 1), a synthetic intermediate for the compound and a process for its preparation. The compound of formula (I) binds to a prostaglandin E2 receptor, especially an EP1 subtype receptor, and antagonizes it. It is less affected by protein binding, so it has a satisfactory in vivo activity. Therefore, it is considered to be useful as an analgesic, an antipyretic agent, an agent for the treatment of pollakiuria (frequent urination) and/or lower urinary tract disease syndrome or an antineoplastic agent.
申请公布号 US8088802(B2) 申请公布日期 2012.01.03
申请号 US20090603194 申请日期 2009.10.21
申请人 NAGANAWA ATSUSHI;SAITO TETSUJI;KOBAYASHI KAORU;MARUYAMA TAKAYUKI;NAKAI YOSHIHIKO;HASHIMOTO SHINSUKE;ONO PHARMACEUTICAL CO., LTD. 发明人 NAGANAWA ATSUSHI;SAITO TETSUJI;KOBAYASHI KAORU;MARUYAMA TAKAYUKI;NAKAI YOSHIHIKO;HASHIMOTO SHINSUKE
分类号 A61K31/41;C07D307/64;A61K31/34;A61K31/341;A61K31/4245;A61K31/426;A61K31/427;A61K31/4402;A61K31/4406;A61K31/4439;A61P1/04;A61P13/00;A61P13/02;A61P29/00;A61P35/00;A61P43/00;C07D213/70;C07D213/71;C07D257/04;C07D271/06;C07D277/20;C07D277/36;C07D285/08;C07D307/00;C07D401/12;C07D405/12;C07D413/00;C07D413/12;C07D417/00;C07D417/12;C07D421/00 主分类号 A61K31/41
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