Combination medications containing alpha-lipoic acid and related
    4.
    发明授权
    Combination medications containing alpha-lipoic acid and related 失效
    含有α-硫辛酸和相关的组合药物

    公开(公告)号:US5569670A

    公开(公告)日:1996-10-29

    申请号:US404153

    申请日:1995-03-14

    摘要: A pharmaceutical composition containing alpha-lipoic acid, dihydrolipoic acid, metabolites of alpha-lipoic acid (inter alia bisnortetralipoic acid and tetranorlipoic acid), optical isomers R- and S- forms of alpha-lipoic acid in oxidized and reduced form together with a vitamin, especially vitamins A, B1, B2, B6, B12, C and E and their pharmaceutically acceptable salts. The compositions are useful for producing analgesic, anti-inflammatory, antidiabetic, cytoprotective, anti-ulcer, antinecrotic, neuroprotective, detoxifying, anti-ischemic, liver function regulating, anti-allergic, immune-stimulating and antioncogenic effects.

    摘要翻译: 含有α-硫辛酸,二氢硫辛酸,α-硫辛酸(特别是二肉桂酸和四肉桂酸)的代谢物的药物组合物,氧化还原形式的α-硫辛酸的旋光异构体R-和S-形式以及维生素 特别是维生素A,B1,B2,B6,B12,C和E及其药学上可接受的盐。 该组合物可用于产生镇痛,抗炎,抗糖尿病,细胞保护,抗溃疡,抗坏死,神经保护,解毒,抗缺血,肝功能调节,抗过敏,免疫刺激和抗阴离子作用。

    Ethylenediamine and guanidine-derivatives
    5.
    发明授权
    Ethylenediamine and guanidine-derivatives 失效
    乙二胺和胍衍生物

    公开(公告)号:US4738983A

    公开(公告)日:1988-04-19

    申请号:US558984

    申请日:1983-12-07

    CPC分类号: C07D307/52 C07D333/20

    摘要: This invention relates to new compounds corresponding to the general formula: ##STR1## R.sub.1 represents a C.sub.3 -C.sub.10 cycloalkyl group substituted by C.sub.1 -C.sub.6 alkyl radicals, a C.sub.3 -C.sub.19 -cycloalkyl-C.sub.1 -C.sub.4 alkyl group which may be substituted by C.sub.1 -C.sub.6 alkyl radicals, a C.sub.6 -C.sub.8 bicycloalkyl group, a C.sub.6 -C.sub.8 bicycloalkyl-C.sub.1 -C.sub.4 alkyl group, a C.sub.6 -C.sub.10 tricycloalkyl group, a C.sub.6 -C.sub.10 tricycloalkyl-C.sub.1 -C.sub.4 alkyl group, a C.sub.6 -C.sub.9 tetracycloalkyl group or a C.sub.6 -C.sub.9 -tetracycloalkyl-C.sub.1 -C.sub.4 alkyl group,R.sub.2 represents hydrogen, a C.sub.1 -C.sub.6 alkyl group, a phenyl-C.sub.1 -C.sub.4 alkyl group or a C.sub.1 -C.sub.6 alkyl group which is substituted by halogen atoms, nitro groups, hydroxy groups, C.sub.2 -C.sub.6 alkanoyloxy groups, C.sub.1 -C.sub.4 alkoxy groups, C.sub.1 -C.sub.4 alkoxy carbonyl groups or carboxy groups,R.sub.3 represented hydrogen, the 2-[5-(dimethylaminomethyl)-2-furyl-methylthio]-ethyl group, a C.sub.1 -C.sub.18 -alkyl group, a C.sub.3 -C.sub.6 -cycloalkyl group, a C.sub.3 -C.sub.6 -alkenyl group, a C.sub.3 -C.sub.6 -alkinyl group, an amino-C.sub.1 -C.sub.4 -alkyl group, a C.sub.2 -C.sub.6 -alkanoylamino-C.sub.1 -C.sub.4 -alkyl group, a mono-C.sub.1 -C.sub.6 -alkylamino-C.sub.1 -C.sub.4 -alkyl group, a di-C.sub.1 -C.sub.6 -alkylamino-C.sub.1 -C.sub.4 -alkyl group or a C.sub.1 -C.sub.18 -alkyl group, which is substituted by halogen atoms, nitro groups, hydroxy groups, C.sub.2 -C.sub.6 alkanoyloxy groups, C.sub.1 -C.sub.4 alkoxy groups, C.sub.1 -C.sub.4 alkoxycarbonyl groups or carboxy groups,A represents a nitrogen atom or a methine group,B represents a cyano radical or a nitro group, andX represents an oxygen atom or a sulphur atom, and salts thereof.The compounds inhibit the secretion of gastric juice. Moreover, they have an ulcer-inhibiting and stomach-spasmolytic effect.

    摘要翻译: 本发明涉及对应于通式的新化合物:其中R1表示被C1-C6烷基取代的C3-C10环烷基,可被C1取代的C3-C19-环烷基-C1-C4烷基 -C 6烷基,C 6 -C 8双环烷基,C 6 -C 8双环烷基-C 1 -C 4烷基,C 6 -C 10三环烷基,C 6 -C 10三环烷基-C 1 -C 4烷基,C 6 -C 9四环烷基或 C 6 -C 9 - 四环烷基-C 1 -C 4烷基,R 2表示氢,C 1 -C 6烷基,苯基-C 1 -C 4烷基或被卤素原子取代的C 1 -C 6烷基,硝基,羟基 基团,C 2 -C 6烷酰氧基,C 1 -C 4烷氧基,C 1 -C 4烷氧基羰基或羧基,R 3表示氢,2- [5-(二甲基氨基甲基)-2-呋喃基 - 甲硫基] - 乙基, -C 18 - 烷基,C 3 -C 6 - 环烷基,C 3 -C 6 - 烯基,C 3 -C 6 - 炔基,氨基-C 1 -C 4 - 烷基,C 2 -C 6 - 烷酰基氨基-C 1 -C 4 - 烷基,单-C 1 -C 6烷基 烯基-C 1 -C 4 - 烷基,被卤素原子取代的二-C 1 -C 6烷基氨基-C 1 -C 4 - 烷基或C 1 -C 18烷基,硝基,羟基,C 2 -C 6烷酰氧基 基团,C 1 -C 4烷氧基,C 1 -C 4烷氧基羰基或羧基,A表示氮原子或次甲基,B表示氰基或硝基,X表示氧原子或硫原子, 其中。 这些化合物抑制胃液的分泌。 此外,它们具有溃疡抑制和胃解痉作用。