Azacycloalkane Derivatives as Inhibitors of Stearoyl-Coenzyme a Delta-9 Desaturase
    1.
    发明申请
    Azacycloalkane Derivatives as Inhibitors of Stearoyl-Coenzyme a Delta-9 Desaturase 审中-公开
    氮杂环烷烃衍生物作为硬脂酰辅酶A-9去饱和酶的抑制剂

    公开(公告)号:US20090318476A1

    公开(公告)日:2009-12-24

    申请号:US12309782

    申请日:2007-08-09

    摘要: Azacycloalkane derivatives of structural formula I are selective inhibitors of stearoyl-coenzyme A delta-9 desaturase (SCD1) relative to other known stearoyl-coenzyme A desaturases. The compounds of the present invention are useful for the prevention and treatment of conditions related to abnormal lipid synthesis and metabolism, including cardiovascular disease, such as atherosclerosis; obesity; diabetes; neurological disease; metabolic syndrome; insulin resistance; and liver steatosis. Formula (I).

    摘要翻译: 结构式I的Azacycalkalkane衍生物是相对于其它已知的硬脂酰辅酶A去饱和酶的硬脂酰辅酶A delta-9去饱和酶(SCD1)的选择性抑制剂。 本发明的化合物可用于预防和治疗与脂质合成和代谢异常有关的病症,包括心血管疾病,如动脉粥样硬化; 肥胖; 糖尿病; 神经系统疾病; 代谢综合征; 胰岛素抵抗; 和肝脂肪变性。 式(I)。