Double ester of 16.beta.-ethylestran-17.beta.-ol derivatives
    1.
    发明授权
    Double ester of 16.beta.-ethylestran-17.beta.-ol derivatives 失效
    16β-乙基己烷-17β-醇衍生物的双酯

    公开(公告)号:US4609650A

    公开(公告)日:1986-09-02

    申请号:US594034

    申请日:1984-03-27

    CPC分类号: C07J41/0044 C07J1/0074

    摘要: A novel steroid compound of the formula ##STR1## wherein A is a lower alkylene group; ##STR2## is an acyl group; and is a single bond or a double bond, and methods of producing the compound (I) as follows: ##STR3## and a pharmaceutical composition containing the compound (I). The compound (I) exhibits excellent antiandrogenic activity on oral administration and can be used for the treatment of prostatic hypertrophy.

    摘要翻译: 式(I)的新型类固醇化合物,其中A为低级亚烷基; 是酰基; 并且是单键或双键,以及如下制备化合物(I)的方法:(I)和含有化合物(I)的药物组合物, 。 化合物(I)对口服给药具有优异的抗雄激素活性,可用于治疗前列腺肥大。

    Antimycotic drug composition
    2.
    发明授权
    Antimycotic drug composition 失效
    抗真菌药物组合物

    公开(公告)号:US06583164B1

    公开(公告)日:2003-06-24

    申请号:US09787656

    申请日:2001-03-19

    IPC分类号: A61K3141

    摘要: The composition of the present invention comprises a quaternized nitrogen-containing imidazole-1-yl or 1,2,4-triazole-1-yl compound wherein one of the nitrogen atoms constituting the azole ring is quaternized with a group eliminating in vivo and represented by the formula: wherein R1 represents a hydrocarbon or heterocyclic group which may be substituted, R2 represents a hydrogen atom or a lower alkyl group, and n is 0 or 1, and a saccharide, said compound being capable of being converted into an anti-fungal azole compound upon elimination of said group in vivo. The composition of the present invention is stable and usable particularly as a pharmaceutical preparation for an injection composition.

    摘要翻译: 本发明的组合物包含季铵化的含氮咪唑-1-基或1,2,4-三唑-1-基化合物,其中构成唑环的氮原子之一被一个在体内消除的基团季铵化并代表 其中R 1表示可被取代的烃基或杂环基,R 2表示氢原子或低级烷基,n为0或1,并且所述化合物能够转化为抗 - 真菌唑化合物在体内消除所述组。 本发明的组合物特别是作为注射用组合物的药物制剂是稳定和可用的。