发明名称 Tetrazoleacetic acid derivatives having aldose reductase inhibitory activity
摘要 A tetrazoleacetic acid derivative represented by the following general formula (I): <IMAGE> (I) [[in Formula (I),] wherein R1 represents a hydrogen atom or an alkyl group; R2 represents a hydrogen atom, an alkyl group, an aralkyl group, a halogen atom, a haloalkyl group, a hydroxyl group, an alkoxy group, an alkoxyalkyl group, an amino group, an aryl group, an alkyl or aryl thio group, an alkyl or aryl carbonylamino group, an alkyl or aryl sulfonylamino group, an alkyl or aryl aminosulfonyl group, an alkyl or aryl sulfonyl group or an alkyl or aryl sulfinyl group; and X represents -O- or -S-[]] except for [5-(2-thienyl)tetrazol-1-yl] acetic acid, [5-(2-furyl)tetrazol-1-yl) acetic acid, (5-(5-bromo-2-furyl)tetrazol-1-yl)acetic acid, (5-(5-phenylthio-2-furyl)tetrazol-1-yl)acetic acid, (5-(5-phenylsulfonyl-2-furyl)tetrazol-1-yl)acetic acid and ethyl esters thereof, or a salt thereof shows excellent aldose reductase inhibitory activity, has low toxicity to organisms and is quite effective as an essential component of a preventative medicine and/or remedy for diabetic complications.
申请公布号 USRE35321(E) 申请公布日期 1996.08.27
申请号 US19920951720 申请日期 1992.09.25
申请人 WAKAMOTO PHARMACEUTICAL CO., LTD. 发明人 INUKAI, SINJI;AGATA, MITSUZI;UMEZAWA, MANAMI;HORIO, YOSHIHIRO;OOTAKE, YASUHIRO;SAWAKI, SHOHEI;GOTO, MASAYOSHI
分类号 A61K31/41;A61P3/08;A61P3/10;A61P13/02;A61P15/00;A61P25/02;A61P27/02;A61P27/12;C07D257/04;C07D405/04;C07D409/04;(IPC1-7):C07D257/04 主分类号 A61K31/41
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