Use of benzylphosphonic acid derivatives for the treatment of diseases
caused by viruses
    7.
    发明授权
    Use of benzylphosphonic acid derivatives for the treatment of diseases caused by viruses 失效
    用于治疗病毒引起的疾病的苯并恶唑酸衍生物的应用

    公开(公告)号:US5242908A

    公开(公告)日:1993-09-07

    申请号:US648622

    申请日:1991-02-01

    摘要: The use of a compound of the formula I ##STR1## in which V is an alkyl group, fluorine, chlorine, bromine, or iodine, n is an integer from 1 to 5, W is an alkyl, alkenyl, alkynyl or alkoxy group, cyanide, nitro, carboxyl, hydrogen or a cycloalkyl, aryl, aralkyl or carboalkoxy group, R.sup.1 and R.sup.2 are an alkyl, alkenyl, alkynyl, cycloalkyl or halogenoalkyl group, sodium, potassium, calcium, magnesium, aluminum, lithium, ammonium, triethylammonium or hydrogen, R.sup.1 and R.sup.2 together form a cyclic diester, R.sup.3 and R.sup.4 are an alkyl, alkenyl, alkynyl, carboalkoxy, cycloalkyl or alkoxy group, hydrogen, fluorine, chlorine, bromine or iodine and X, Y and Z are oxygen or sulfur, for the treatment of diseases caused by DNA viruses or RNA viruses is described.

    摘要翻译: 使用其中V为烷基,氟,氯,溴或碘的式I化合物I,其为1至5的整数,W为烷基,烯基,炔基或烷氧基 ,氰基,硝基,羧基,氢或环烷基,芳基,芳烷基或烷氧基,R1和R2是烷基,烯基,炔基,环烷基或卤代烷基,钠,钾,钙,镁,铝,锂,铵, 或氢,R1和R2一起形成环状二酯,R3和R4是烷基,烯基,炔基,烷氧羰基,环烷基或烷氧基,氢,氟,氯,溴或碘,X,Y和Z是氧或硫, 描述了用于治疗由DNA病毒或RNA病毒引起的疾病。

    Guanidine and amidine derivatives as factor Xa inhibitors
    8.
    发明授权
    Guanidine and amidine derivatives as factor Xa inhibitors 失效
    胍和脒衍生物作为因子Xa抑制剂

    公开(公告)号:US07435747B2

    公开(公告)日:2008-10-14

    申请号:US10886312

    申请日:2004-07-07

    IPC分类号: A61K31/445 C07D211/26

    摘要: The present invention relates to compounds of the formula I, in which R0; Q; X; Q′, D, R10 and V have the meanings indicated in the claims. The compounds of the formula I are valuable pharmacologically active compounds. They exhibit a strong antithrombotic effect and are suitable, for example, for the therapy and prophylaxis of cardiovascular disorders like thromboembolic diseases or restenoses. They are reversible inhibitors of the blood clotting enzymes factor Xa (FXa) and/or factor VIIa (FVIIa), and can in general be applied in conditions in which an undesired activity of factor Xa and/or factor VIIa is present or for the cure or prevention of which an inhibition of factor Xa and/or factor VIIa is intended. The invention furthermore relates to processes for the preparation of compounds of the formula I, their use, in particular as active ingredients in pharmaceuticals, and pharmaceutical preparations comprising them.

    摘要翻译: 本发明涉及式I化合物,其中R 0是 Q; X; Q',D,R 10和V具有权利要求中所示的含义。 式I的化合物是有价值的药理活性化合物。 它们具有强烈的抗血栓形成作用,并且适用于例如治疗和预防心血管疾病如血栓栓塞性疾病或再狭窄。 它们是血液凝固酶因子Xa(FXa)和/或因子VIIa(FVIIa)的可逆抑制剂,并且通常可用于存在因子Xa和/或因子VIIa的不期望活性或用于治愈 或预防因子Xa和/或因子VIIa的抑制。 本发明还涉及式I化合物的制备方法,其用途,特别是作为药物中的活性成分,以及包含它们的药物制剂。