发明名称 TRIZYKLISCHE INDOL-2-CARBONSÄURE DERIVATE ALS SELEKTIVE NMDA REZEPTOR ANTAGONISTEN
摘要 <p>A tricyclic indole-2-carboxylic acid derivative represented by the formula 1: <CHEM> wherein X represents alkyl, halogen or cyano; R<1> represents hydrogen, or a protecting group of carboxyl group; W represents hydrogen, -CO2R<3i>, -CONR<3i>R<4i>, -A-CO2R<3i> or -A-CONR<3i>R<4i>, wherein -A- represents alkylene and R<3i> and R<4i> independently represent hydrogen, alkyl, aryl or substituted aryl, or a pharmaceutically acceptable salt thereof, these compounds are selective antagonists of glycine binding site of the NMDA receptor.</p>
申请公布号 AT219486(T) 申请公布日期 2002.07.15
申请号 AT19940117956T 申请日期 1994.11.14
申请人 SUMITOMO PHARMACEUTICALS COMPANY, LIMITED 发明人 NAGATA, RYU;TANNO, NORIHIKO;AE, NOBUYUKI
分类号 C07D209/90;(IPC1-7):C07D209/90;A61K31/405;A61K31/19;C07D209/18;C07D209/30 主分类号 C07D209/90
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