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87 条记录 (耗时 0.024 秒)

    3-Nitro-5-amide-1,4-dihydropyridines with positive inotropic activity
    41.
    发明授权
    3-Nitro-5-amide-1,4-dihydropyridines with positive inotropic activity 失效
    具有正性肌力活性的3-硝基-5-酰胺-1,4-二氢吡啶

    公开(公告)号：US4540684A

    公开(公告)日：1985-09-10

    申请号：US612093

    申请日：1984-05-18

    申请人： Jurgen Stoltefuss ,  Gerhard Franckowiak ,  Horst Boshagen ,  Siegfried Goldmann ,  Matthias Schramm ,  Gunter Thomas ,  Rainer Gross

    发明人： Jurgen Stoltefuss ,  Gerhard Franckowiak ,  Horst Boshagen ,  Siegfried Goldmann ,  Matthias Schramm ,  Gunter Thomas ,  Rainer Gross

    IPC分类号： A61K31/455 ,  A61P3/08 ,  A61P9/02 ,  A61P9/04 ,  C07D211/90 ,  C07D211/98 ,  A61K31/70 ,  C07D405/12

    CPC分类号： C07D211/90

    摘要： A 1,4-dihydropyridine derivative of the formula ##STR1## in which R and R.sub.1 each independently is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 to C.sub.12 -alkoxy, C.sub.1 -C.sub.4 -halogenoalkoxy, halogen, nitro, trifluoromethyl, ##STR2## X is oxygen or sulphur, R.sub.4 and R.sub.5 each independently is hydrogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.6 -alkoxy, halogen, trifluoromethyl, amino or nitro, andR.sub.2 and R.sub.3 each independently is hydrogen, a C.sub.1 -C.sub.10 -alkyl, C.sub.2 -C.sub.10 -alkenyl or C.sub.3 -C.sub.10 -alkinyl radical which is optionally substituted by halogen, hydroxyl, C.sub.1 -C.sub.4 -alkoxy, amino, mono- and di-C.sub.1 -C.sub.4 -alkylamino, carbo-C.sub.1 -C.sub.6 -alkoxy and/or nitro, a C.sub.3 to C.sub.6 -membered cycloalkyl radical, a phenyl radical which is optionally substituted by C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.6 -alkoxy, halogen, amino and/or nitro, or a phenyl-C.sub.1 -C.sub.3 -alkyl radical, or a carbohydrate radical which is optionally bonded via a C.sub.1 -C.sub.8 -alkyl chain to the amide nitrogen atomor a pharmaceutically acceptable acid addition salt thereof, which improves the contractility of the heart, raises the blood pressure, lowers the blood sugar, reduces the swelling of mucous membranes and affects the salt and fluid balances of a patient.

    摘要翻译： 其中R和R 1各自独立地为氢，C 1 -C 4 - 烷基，C 1 -C 12 - 烷氧基，C 1 -C 4卤代烷氧基，卤素，硝基，三氟甲基， X是氧或硫，R4和R5各自独立地是氢，C1-C4-烷基，C1-C6-烷氧基，卤素，三氟甲基，氨基或硝基，R2和R3各自独立地是氢，C1-C10 - 烷基，C 2 -C 10 - 烯基或C 3 -C 10 - 炔基，其任选被卤素，羟基，C 1 -C 4 - 烷氧基，氨基，单 - 和二-C 1 -C 4 - 烷基氨基，C 1 -C 6 - 和/或硝基，C3至C6元环烷基，任选被C 1 -C 4 - 烷基，C 1 -C 6 - 烷氧基，卤素，氨基和/或硝基取代的苯基，或苯基-C 1 -C 3 - 烷基或通过C1-C8烷基链任选与酰胺氮原子键合的碳水化合物基团或其药学上可接受的酸加成盐，其改善心脏的收缩力，使血压升高 ure，降低血糖，减少粘膜肿胀，影响患者的盐和液体平衡。

    2-heterocyclically substituted dihydropyrimidines
    43.
    发明授权
    2-heterocyclically substituted dihydropyrimidines 失效
    2-杂环取代的二氢嘧啶

    公开(公告)号：US06503913B1

    公开(公告)日：2003-01-07

    申请号：US09673597

    申请日：2000-10-18

    申请人： Siegfried Goldmann ,  Jürgen Stoltefuss ,  Arnold Paessens ,  Erwin Graef ,  Stefan Lottmann

    发明人： Siegfried Goldmann ,  Jürgen Stoltefuss ,  Arnold Paessens ,  Erwin Graef ,  Stefan Lottmann

    IPC分类号： C07D41704

    CPC分类号： C07D413/04 ,  C07D417/04

    摘要： The invention relates to new 2-heterocyclically substituted dihydropyrimidines, medicaments which contain these 2-heterocyclically substituted dihydropyrimidines, and a process for preparation of medicaments. The invention furthermore relates to the use of the 2-heterocyclically substituted dihydropyrimidines for the production of a medicament, in particular for the treatment of acute or chronic viral diseases, in particular for the production of a medicament for the treatment of acute or chronic hepatitis B infections.

    摘要翻译： 本发明涉及新的2-杂环取代的二氢嘧啶，含有这些2-杂环取代的二氢嘧啶的药物和制备药物的方法。 本发明还涉及2-杂环取代的二氢嘧啶在制备药物中的用途，特别是用于治疗急性或慢性病毒性疾病，特别是用于生产用于治疗急性或慢性乙型肝炎的药物 感染。