发明名称 GUANIDINE DERIVATIVES, METHOD OF PREPARATION THEREOF, AND METHOD FOR INHIBITING Na<SP>+</SP>/H EXCHANGE IN CELLS
摘要 FIELD: pharmaceutical chemistry. SUBSTANCE: new guanidine derivatives with formula I: &lt;EMI ID=0.313 HE=27 WI=36 TI=CHI&gt; (I) are provided where Y is nitrogen or group C-R (R is hydrogen, lower alkyl, hydroxyl, etc.); R is hydrogen, optionally substituted aryl, aryloxy group, etc.; R hydrogen, lower alkoxy, hydroxyl, etc.; Z nitrogen or C-R (R is hydrogen, halogen, hydroxyl, lower alkyl, etc. ); and W nitrogen or C-R (R is hydrogen) and their pharmaceutical acceptable salts. Compound of invention are useful as drugs in treatment and/or prophylactics of cardiac infarction or ischemic disease. Method of preparing these compounds is also provided. EFFECT: extended choice of cardiovascular medicines. 15 cl, 1 tbl, 34 ex
申请公布号 RU2141946(C1) 申请公布日期 1999.11.27
申请号 RU19950122558 申请日期 1994.05.12
申请人 FUDZISAVA FARMAS'JUTIKAL KO., LTD. 发明人 ATSUSI KUNO;JOSIKAZU INOU;KHISASI TAKASUGI;KHIROAKI MIZUNO;KUMI JAMASAKI
分类号 C07D237/10;A61K31/155;A61K31/34;A61K31/341;A61K31/38;A61K31/381;A61K31/40;A61K31/41;A61K31/415;A61K31/425;A61K31/426;A61K31/44;A61K31/4427;A61K31/455;A61K31/495;A61K31/53;A61K31/535;A61P9/00;A61P9/08;A61P9/10;A61P13/02;A61P15/00;C07C279/10;C07C279/22;C07D207/32;C07D207/325;C07D207/327;C07D207/333;C07D207/335;C07D207/34;C07D213/56;C07D231/12;C07D231/38;C07D239/26;C07D239/28;C07D257/04;C07D277/28;C07D277/30;C07D307/52;C07D333/24;C07D401/04;C07D401/10;C07D403/10;C07D403/14;C07D413/04;C07D413/12;C07D498/04;C07D521/00;(IPC1-7):C07D207/32 主分类号 C07D237/10
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