Phenyl and benzoyl substituted imidazo-fused heterocyclic calcium
channel blockers
    33.
    发明授权
    Phenyl and benzoyl substituted imidazo-fused heterocyclic calcium channel blockers 失效
    苯基和苯甲酰基取代的咪唑稠合杂环钙通道阻断剂

    公开(公告)号:US4880824A

    公开(公告)日:1989-11-14

    申请号:US99417

    申请日:1987-09-21

    摘要: Heterocyclic compounds of formulae (I) and (II): ##STR1## where R.sup.1 and R.sup.2 are alkyl, R.sup.3 is H or alkyl, m is 2-5 and Het is a hetercycle such as thiazole, benzothiazole, substituted benzothiazole, pyrazine, triazine, thiadiazole, substituted thiadiazole, pyrimidine or substituted pyrimidine. The compounds are calcium channel blockers useful in the treatment of cardiovascular conditions such as hypertension or angina.

    摘要翻译: (I)和(II)的杂环化合物:其中R 1和R 2是烷基,R 3是H或烷基,m是2-5,Het是杂环如噻唑 苯并噻唑,取代的苯并噻唑,吡嗪,三嗪,噻二唑,取代的噻二唑,嘧啶或取代的嘧啶。 这些化合物是可用于治疗心血管疾病如高血压或心绞痛的钙通道阻滞剂。

    SUBSTITUTED BENZIMIDAZOLE-, BENZTRIAZOLE-, AND BENZIMIDAZOLONE-O-GLUCOSIDES
    37.
    发明申请
    SUBSTITUTED BENZIMIDAZOLE-, BENZTRIAZOLE-, AND BENZIMIDAZOLONE-O-GLUCOSIDES 有权
    取代的苯并咪唑,苯并唑和 - 苯并咪唑酮-O-葡萄糖苷

    公开(公告)号:US20100004188A1

    公开(公告)日:2010-01-07

    申请号:US12557629

    申请日:2009-09-11

    申请人: Maud Urbanski

    发明人: Maud Urbanski

    CPC分类号: C07H15/26

    摘要: This invention relates to to substituted benzimidazole-O-glucosides, benztriazole-O-glucosides, and benzimidazolone-O-glucosides, compositions containing them, and methods of using them, for example, for the treatment or prophylaxis of diabetes and Syndrome X.

    摘要翻译: 本发明涉及取代的苯并咪唑-O-葡糖苷,苯并三唑-O-葡糖苷和苯并咪唑酮-O-葡萄糖苷,含有它们的组合物,以及使用它们的方法,例如用于治疗或预防糖尿病和综合征X.