4-Aminothiazole derivatives
    1.
    发明申请
    4-Aminothiazole derivatives 失效
    4-氨基噻唑衍生物

    公开(公告)号:US20060014958A1

    公开(公告)日:2006-01-19

    申请号:US11170636

    申请日:2005-06-29

    IPC分类号: C07D417/02

    摘要: Novel 4-aminothiazole derivatives are disclosed. These compounds inhibit cyclin-dependent kinases. These compounds and their pharmaceutically acceptable salts and esters have antiproliferative activity and are useful in the treatment or control of cancer, in particular solid tumors. This invention is also directed to pharmaceutical compositions containing such compounds and to methods of treating or controlling cancer, most particularly the treatment or control of breast, lung, colon and prostate tumors. Also disclosed are intermediates useful in the preparation of these novel 4-aminothiazole derivatives.

    摘要翻译: 公开了新的4-氨基噻唑衍生物。 这些化合物抑制细胞周期蛋白依赖性激酶。 这些化合物及其药学上可接受的盐和酯具有抗增殖活性,并且可用于治疗或控制癌症,特别是实体瘤。 本发明还涉及含有这些化合物的药物组合物以及治疗或控制癌症的方法,特别是乳腺癌,肺癌,结肠癌和前列腺肿瘤的治疗或控制。 还公开了可用于制备这些新型4-氨基噻唑衍生物的中间体。

    2,6-Diaminopyridine derivatives
    2.
    发明申请
    2,6-Diaminopyridine derivatives 失效
    2,6-二氨基吡啶衍生物

    公开(公告)号:US20060014708A1

    公开(公告)日:2006-01-19

    申请号:US11165912

    申请日:2005-06-24

    CPC分类号: C07D213/73

    摘要: Novel 2,6-diaminopyridine derivatives of formula wherein R1 and R2 are as defined below, are disclosed. These compounds inhibit cyclin-dependent kinases. These compounds and their pharmaceutically acceptable salts and esters have antiproliferative activity and are useful in the treatment or control of cancer, in particular solid tumors. This invention is also directed to pharmaceutical compositions containing such compounds and to methods of treating or controlling cancer, most particularly the treatment or control of breast, lung, colon and prostate tumors. Also disclosed are intermediates useful in the preparation of these novel 2,6-diaminopyridine derivatives.

    摘要翻译: 公开了下述新的2,6-二氨基吡啶衍生物,其中R 1和R 2定义如下。 这些化合物抑制细胞周期蛋白依赖性激酶。 这些化合物及其药学上可接受的盐和酯具有抗增殖活性,并且可用于治疗或控制癌症,特别是实体瘤。 本发明还涉及含有这些化合物的药物组合物以及治疗或控制癌症的方法,特别是乳腺癌,肺癌,结肠癌和前列腺肿瘤的治疗或控制。 还公开了可用于制备这些新型2,6-二氨基吡啶衍生物的中间体。

    4-Aminopyrimidine-5-thione derivatives
    4.
    发明申请
    4-Aminopyrimidine-5-thione derivatives 失效
    4-氨基嘧啶-5-硫酮衍生物

    公开(公告)号:US20070117821A1

    公开(公告)日:2007-05-24

    申请号:US11581529

    申请日:2006-10-16

    IPC分类号: A61K31/506 C07D403/02

    摘要: Novel 4-aminopyrimidine-5-thione derivatives are disclosed. These compounds inhibit cyclin-dependent kinases, in particular Cdk1, Cdk2 and Cdk4. These compounds and their pharmaceutically acceptable salts have antiproliferative activity and are useful in the treatment or control of cancer, in particular solid tumors. This invention is also directed to pharmaceutical compositions containing such compounds and to methods of treating or controlling cancer, most particularly the treatment or control of breast, lung, colon and prostate tumors.

    摘要翻译: 公开了新的4-氨基嘧啶-5-硫酮衍生物。 这些化合物抑制细胞周期蛋白依赖性激酶,特别是Cdk1,Cdk2和Cdk4。 这些化合物及其药学上可接受的盐具有抗增殖活性,并且可用于治疗或控制癌症,特别是实体瘤。 本发明还涉及含有这些化合物的药物组合物以及治疗或控制癌症的方法,特别是乳腺癌,肺癌,结肠癌和前列腺肿瘤的治疗或控制。

    Diaminothiazoles
    6.
    发明申请
    Diaminothiazoles 失效
    二氨基噻唑

    公开(公告)号:US20050239843A1

    公开(公告)日:2005-10-27

    申请号:US11098563

    申请日:2005-04-04

    CPC分类号: C07D417/12 C07D417/14

    摘要: Novel diaminothiazoles of formula (I): are discussed. These compounds selectively inhibit the activity of Cdk4 and are thus useful in the treatment or control of cancer, in particular, the treatment or control of solid tumors. This invention also provides pharmaceutical compositions containing such compounds and methods of treating or controlling cancer, most particularly, the treatment or control of breast, lung, colon, and prostate tumors.

    摘要翻译: 讨论式(I)的新型二氨基噻唑。 这些化合物选择性地抑制Cdk4的活性,因此可用于治疗或控制癌症,特别是治疗或控制实体瘤。 本发明还提供含有这些化合物的药物组合物和治疗或控制癌症的方法,最特别地,治疗或控制乳腺癌,肺癌,结肠癌和前列腺肿瘤。