Antimycotic hydroxypropyl-imidazoles
    2.
    发明授权
    Antimycotic hydroxypropyl-imidazoles 失效
    抗真菌羟丙基 - 咪唑

    公开(公告)号:US4246274A

    公开(公告)日:1981-01-20

    申请号:US30799

    申请日:1979-04-17

    CPC分类号: C07D231/12 C07D249/08

    摘要: The invention includes as a series of 2-(substituted-phenyl)-1-aryl-3-(imidazol-1-yl)-propan-2-ols useful as antimicrobial agents. Also included in the invention are methods for the manufacture of the above-identified imidazol-1-yl-propan-2-ols, compositions containing said compounds and the use of said compounds and compositions for antimicrobial use.

    摘要翻译: 本发明包括用作抗微生物剂的一系列2-(取代苯基)-1-芳基-3-(咪唑-1-基) - 丙-2-醇。 本发明还包括制备上述咪唑-1-基 - 丙-2-醇的方法,含有所述化合物的组合物以及所述化合物和组合物用于抗微生物使用的方法。

    N-methyl-imidazole derivatives for treating mycotic infections
    10.
    发明授权
    N-methyl-imidazole derivatives for treating mycotic infections 失效
    用于治疗真菌感染的N-甲基 - 咪唑衍生物

    公开(公告)号:US4062959A

    公开(公告)日:1977-12-13

    申请号:US554009

    申请日:1975-02-28

    摘要: N-methyl-imidazole derivatives of the formula: ##STR1## or a pharmaceutically acceptable non-toxic salt thereof, wherein X is an unsubstituted or substituted 6-membered heteroaromatic moiety having two nitro heteroatoms,Y is an unsubstituted or substituted aliphatic moiety, an unsubstituted or substituted cycloaliphatic moiety, an unsubstituted or substituted aralkyl moiety or an unsubstituted or substituted aryl moiety, andZ is an unsubstituted or substituted aliphatic moiety, an unsubstituted or substituted cycloaliphatic moiety, an unsubstituted or substituted aralkyl moiety, an unsubstituted or substituted aryl moiety, an unsubstituted or substituted pyridyl moiety or an alkoxycarbonyl moiety,Are useful as antimycotic agents.

    摘要翻译: 式(I)的N-甲基 - 咪唑衍生物或其药学上可接受的无毒盐,其中X是具有两个硝基杂原子的未取代或取代的6元杂芳族部分,Y是未取代或取代的脂族 未取代或取代的脂环族部分,未取代或取代的芳烷基部分或未取代或取代的芳基部分,Z为未取代或取代的脂族部分,未取代或取代的脂环族部分,未取代或取代的芳烷基部分,未取代或取代的芳烷基部分, 取代的芳基部分,未取代或取代的吡啶基部分或烷氧基羰基部分,可用作抗生药剂。