Antiproliferative 1,2,3-thiadiazole compounds
    61.
    发明授权
    Antiproliferative 1,2,3-thiadiazole compounds 有权
    抗增殖性1,2,3-噻二唑化合物

    公开(公告)号:US07288556B2

    公开(公告)日:2007-10-30

    申请号:US11218969

    申请日:2005-09-02

    IPC分类号: C07D285/06 A61K31/41

    CPC分类号: A61K31/433 C07D285/06

    摘要: This invention is directed to methods of using compounds having the structure: and including stereoisomers, solvates, and pharmaceutically acceptable salts thereof, wherein each of R1, R2, R3 and R4 is independently selected from hydrogen, R5, R6, and R7; R5 is selected from alkyl, heteroalkyl, aryl and heteroaryl; R6 is selected from (R5)n-alkylene, (R5)n-heteroalkylene, (R5)n-arylene and (R5)n-heteroarylene; R7 is selected from (R6)n-alkylene, (R6)n-heteroalkylene, (R6)n-arylene, and (R6)n-heteroarylene; and n is selected from 0, 1, 2, 3, 4 and 5, where R1 and R2 may together form a heterocyclic structure including the nitrogen to which they are both attached, and R3 and R4 may together form a heterocyclic structure including the nitrogen to which they are both attached; and each of L1 and L2 is independently selected from -A1-A2-A3- where each of A1, A2, and A3 is independently selected from a direct bond, alkylene, heteroalkylene, arylene and heteroarylene. These compounds are useful in treating hyperproliferative disorders and inducing apoptosis.

    摘要翻译: 本发明涉及使用具有以下结构的化合物的方法:其包括立体异构体,溶剂化物和药学上可接受的盐,其中R 1,R 2,R 2, SO 3和R 4独立地选自氢,R 5,R 6和R 7, / SUP>; R 5选自烷基,杂烷基,芳基和杂芳基; R 6选自(R 5)N 1 - 亚烷基,(R 5) 亚磺酰基,(R 5) - 亚芳基和(R 5)5 - 亚杂芳基。 R 7选自(R 6)N - 亚烷基,(R 6) 亚磺酰基,(R 6) - 亚芳基和(R 6) - 亚 - 亚芳基 ; 并且n选自0,1,2,3,4和5,其中R 1和R 2可以一起形成杂环结构,包括它们是氮的杂环结构 两个连接的R 3和R 4可以一起形成包括它们都连接的氮的杂环结构; 并且L 1和L 2各自独立地选自-A1-A2-A3-,其中A1,A2和A3各自独立地选自直接键, 亚烷基,杂亚烷基,亚芳基和亚杂芳基。 这些化合物可用于治疗过度增殖性疾病和诱导凋亡。

    Pyrazole derivative as SCD1 inhibitors for the treatment of diabetes
    66.
    发明授权
    Pyrazole derivative as SCD1 inhibitors for the treatment of diabetes 失效
    吡唑衍生物作为治疗糖尿病的SCD1抑制剂

    公开(公告)号:US08314138B2

    公开(公告)日:2012-11-20

    申请号:US12438654

    申请日:2007-08-22

    IPC分类号: A61K31/415

    CPC分类号: C07D417/04 C07D417/14

    摘要: The present invention provides heterocyclic derivatives of formula I that modulate the activity of stearoyl-CoA desaturase. Methods of using such derivatives to modulate the activity of stearoyl-CoA desaturase and pharmaceutical compositions comprising such derivatives are also encompassed. wherein Q is

    摘要翻译: 本发明提供调节硬脂酰辅酶A去饱和酶活性的式I的杂环衍生物。 还包括使用这些衍生物调节硬脂酰辅酶A去饱和酶活性的方法和包含这些衍生物的药物组合物。 其中Q是