发明名称 BLOCKADE OF SODIUM CHANNELS BY PHENOL DERIVATIVES
摘要 The invention relates to a pharmaceutical composition comprising at least one phenol derivative represented by formula (I), wherein R<1> represents a hydrogen atom, a halogen atom or a hydrocarbon group containing up to 12 carbon atoms; R<2> represents a hydrogen atom or a C1-C7 alkyl group; wherein R<1> and R<2> may optionally form a carbocyclic 5- or 6-membered ring; R<3> represents a hydrogen atom, a halogen atom or a C1-C7 alkyl group; R<4> represents a hydrogen atom, a C1-C7 alkyl group or a halogen atom; R<5> represents hydrogen atom, a halogen atom or a C1-C7 alkyl group; and R<6> represents a hydrogen atom, a C1-C7 alkyl group or a C2 or C3 alkenyl group, under the proviso that R<2> and R<4> can only both represent a hydrogen atom if both R<1> and R<5> represent a C1-C7 alkyl group and R<3> represents a halogen atom. The composition is particularly useful for the blockade of sodium channels and/or influencing the kinetics of sodium channels and thus can be used as local anesthetic, antidysrhythmic, anticonvulsant/antiepileptic and spasmolytic.
申请公布号 WO0240005(A2) 申请公布日期 2002.05.23
申请号 WO2001EP13081 申请日期 2001.11.13
申请人 B. BRAUN MELSUNGEN AG;HAESELER, GERTRUD;LEUWER, MARTIN 发明人 HAESELER, GERTRUD;LEUWER, MARTIN
分类号 A61K8/34;A61K8/49;A61K31/045;A61K31/05;A61K31/055;A61K31/075;A61K31/35;A61K31/352;A61P1/06;A61P9/00;A61P9/06;A61P21/02;A61P23/02;A61P25/08;A61P43/00;A61Q19/00 主分类号 A61K8/34
代理机构 代理人
主权项
地址