发明名称 FUSED IMIDAZOLIUM DERIVATIVES
摘要 This invention relates to medicaments, particularly novel fused imidazolium derivatives useful for the treatment of cancers and novel synthetic intermediate compounds thereof having the formula: <IMG> The novel imidazolium derivatives fused with an aryl ring or heteroaryl ring, characterized in that the 1- and/or 3-position is substituted by an alkyl group etc. having a substituent selected from the group consisting of -OR a, -SR a, -prodrug-formed OH, -O-lower alkylene-OR a, -O-lower alkylene-O-lower alkylene-OR a, -O-lower alkylene-NR a R b, -O-lower alkylene-O-lower alkylene-NR a R b, -O-lower alkylene-NR c-lower alkylene-NR a R b, -OCO-NR a R b, -SOR a, -SO2R a, -SO2NR a R b, -NR a-SO2R b, -CO2H, -NR a R b, -NR c-lower alkylene-NR a R b, -N (-lower alkylene- NR a R b)2r, -RinD, -NO2, -CN, -halogen, -CO2R a, -COO-, -CONR a R b, -CONR a-O-R b, -NR a-COR b, -NR a-CO-NR b R c, -OCOR a and -CO-R a, have excellent anti-tumor activity and low toxicity and are useful as anticancer agents having wide margins of safety.
申请公布号 CA2395717(C) 申请公布日期 2008.05.20
申请号 CA20012395717 申请日期 2001.02.14
申请人 YAMANOUCHI PHARMACEUTICAL CO., LTD. 发明人 TOYOSHIMA, AKIRA;KINOYAMA, ISAO;MATSUHISA, AKIRA;NAKAHARA, TAKAHITO;TAKEUCHI, MASAHIRO;OKADA, MINORU
分类号 C07D401/06;A61K31/36;A61K31/416;A61K31/4184;A61K31/4188;A61K31/424;A61K31/4245;A61K31/427;A61K31/429;A61K31/437;A61K31/4439;A61K31/4453;A61K31/4468;A61K31/454;A61K31/47;A61K31/4709;A61K31/497;A61K31/4985;A61K31/501;A61K31/5025;A61K31/506;A61K31/519;A61K31/5375;A61K31/551;A61P35/00;C07C233/41;C07C235/14;C07C237/04;C07C255/24;C07C255/25;C07C255/58;C07C259/06;C07C271/28;C07C311/37;C07C317/28;C07C323/25;C07D209/16;C07D211/58;C07D213/38;C07D213/64;C07D213/74;C07D213/89;C07D215/12;C07D233/54;C07D235/02;C07D235/10;C07D235/14;C07D239/26;C07D241/12;C07D241/20;C07D295/13;C07D307/14;C07D317/58;C07D333/68;C07D335/06;C07D401/04;C07D401/12;C07D401/14;C07D403/06;C07D403/14;C07D405/06;C07D471/04;C07D491/048;C07D495/04;C07D498/04 主分类号 C07D401/06
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