发明名称 Phenyl derivatives useful as blockers of chloride channels
摘要 The present invention relates to a method for the treatment of a disorder or disease of a living animal body, including a human, which disorder or disease is responsive to the blockade of chloride channels, comprising administering to a living animal body in need thereof a therapeutically effective amount of a compound having formula (I) or a pharmaceutically acceptable salt thereof wherein R<2>, R<3>, R<4> and R<5> are each independently selected from hydrogen, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, alkoxy, hydroxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro, amino, and aryl, aralkyl, arylamino, aryloxy, aryl-CO-, or heteroaryl, wherein the aryl or heteroaryl group may be substituted one or more times with substituents selected from alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, hydroxy, alkoxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro and amino; or R<3> and R<4> or R<4> and R<5> together form a fused 4 to 7 membered carbocyclic ring which may be unsaturated, or partially or fully saturated while the other substituents R<2>, R<3>, R<4> and R<5> is as defined above; Y is -CO-, -CS-, -SO2-, or -C(=N-R<8>)-, wherein R<8> is hydrogen, alkyl, or cyano; X is -NH-, -CH2-NH-, -SO2-NH-, or -CH2-; Z is -NR<6>-, -O-, -CH=CH-, -N=CH-, -CH=N-, or -NR<6>-CH2-, wherein R<6> is hydrogen, or alkyl; R<11>, R<12>, R<13>, R<14> and R<15> are each independently selected from hydrogen, alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, alkoxy, hydroxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro, amino, and aryl, aralkyl, arylamino, aryloxy, aryl-CO-, or heteroaryl, wherein the aryl or heteroaryl group may be substituted one or more times with substituents selected from alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, hydroxy, alkoxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro and amino; or one of R<11> and R<12>, R<12> and R<13>, R<13> and R<14> or R<14> and R<15> together form a fused 4 to 7 membered carbocyclic ring which may be unsaturated, or partially or fully saturated while the other substituents R<11>, R<12>, R<13>, R<14> and R<15> is as defined above.
申请公布号 AU2962297(A) 申请公布日期 1998.01.05
申请号 AU19970029622 申请日期 1997.05.26
申请人 NEUROSEARCH A/S 发明人 PALLE CHRISTOPHERSEN;OVE PEDERSEN
分类号 A61K31/00;A61K31/155;A61K31/165;A61K31/17;A61K31/19;A61K31/235;A61K31/24;A61P1/00;A61P1/04;A61P1/12;A61P7/00;A61P7/06;A61P9/00;A61P9/10;A61P9/12;A61P27/00;A61P27/06;A61P29/00;A61P37/00;A61P37/08;C07C233/55;C07C271/58;C07C275/40;C07C309/51;C07C311/08;C07C311/21;C07C311/47;C07C311/60;C07C335/22 主分类号 A61K31/00
代理机构 代理人
主权项
地址