发明名称 Imidazolderivate, starke und selektive Angiotensin-II-Rezeptor-Antagonisten
摘要 <p>A compound of the formula : <CHEM> wherein R<1> is hydrogen, halogen, nitro, lower alkyl, lower alkoxy, amino or acylamino, R<2>, R<3> and R<4> are each hydrogen, halogen, nitro, cyano, lower alkyl, lower alkenyl, lower alkylthio, more or di or trihalo(lower)alkyl, oxo(lower)alkyl, hydroxy(lower)alkyl or optionally esterified carboxy; or R<2> and R<3> are linked together to form l,3-butadienylene, R<5> is hydrogen or imino-protective group, A is lower alkylene, Q is CH or N, X is N or CH, Y is NH, O or S, and <CHEM> is condensed or uncondensed imidazolyl which may have suitable substituent(s), and pharmaceutically acceptable salt thereof; processes for their preparation and pharmaceutical compositions comprising them.</p>
申请公布号 DE69118082(D1) 申请公布日期 1996.04.25
申请号 DE1991618082 申请日期 1991.09.14
申请人 FUJISAWA PHARMACEUTICAL CO., LTD., OSAKA, JP 发明人 OKU, TERUO, TSUKUBA-SHI, IBARAKI 305, JP;SETOI, HIROYUKI, TSUKUBA-SHI, IBARAKI 305, JP;KAYAKIRI, HIROSHI, TSUKUBA-SHI, IBARAKI 305, JP;SATOH, SHIGEKI, TSUKUBA-SHI, IBARAKI 305, JP;INOUE, TAKAYUKI, TSUKUBA-SHI, IBARAKI 305, JP;SAITOH, YUKI, TSUKUBA-SHI, IBARAKI 305, JP;KURODA, AKIO, TSUKUBA-SHI, IBARAKI 305, JP;TANAKA, HIROKAZU, TSUCHIURA-SHI, IBARAKI 300, JP
分类号 A61K31/415;A61K31/435;A61K31/52;A61P9/00;A61P9/12;A61P43/00;C07D403/14;C07D413/14;C07D417/14;C07D471/04;C07D473/00;C07D487/04;C07D495/04;(IPC1-7):C07D401/14;C07D403/04;A61K31/44;C07D409/14;C07D407/14 主分类号 A61K31/415
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