Azacycloalkane derivatives as inhibitors of stearoyl-coenzyme a delta-9 desaturase
申请人:Lachance Nicolas
公开号:US20080132542A1
公开(公告)日:2008-06-05
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.
结构式I的氮代环烷衍生物是选择性抑制剂,相对于其他已知的硬脂酰辅酶A delta-9去饱和酶(SCD1)。本发明的化合物可用于预防和治疗与异常脂质合成和代谢相关的疾病,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。