Angiotensin II receptor antagonists
    41.
    发明授权
    Angiotensin II receptor antagonists 有权
    血管紧张素II受体拮抗剂

    公开(公告)号:US07880014B2

    公开(公告)日:2011-02-01

    申请号:US12000247

    申请日:2007-12-11

    IPC分类号: C07D257/00 C07D403/00

    CPC分类号: C07D403/10

    摘要: A compound having the structure wherein R is an angiotensin receptor antagonist active group, Y is -Y1-Y2-Y3-Y4-Y5-; Y1 is C(R1R2); R1 is selected from the group consisting of hydrogen and C1-4 alkyl; R2 is selected from the group consisting of hydrogen, C1-4 alkyl, and —OC(O)C1-4 alkyl; Y2 is O or CH2; Y3 is C(O) or CH2; Y4 is O or CH2; Y5 is —(CH2)1-2—(X)0-1—(CH2)0-1— or is absent; X is —O— or —CR3R4—; and R3 and R4 are independently selected from the group consisting of hydrogen and C1-C4 alkyl; or a pharmaceutically acceptable salt or hydrate thereof, which is useful for treating hypertension.

    摘要翻译: 具有结构的化合物,其中R是血管紧张素受体拮抗剂活性基团,Y是-Y1-Y2-Y3-Y4-Y5-; Y1是C(R1R2); R 1选自氢和C 1-4烷基; R 2选自氢,C 1-4烷基和-OC(O)C 1-4烷基; Y2是O或CH2; Y 3是C(O)或CH 2; Y4是O或CH2; Y 5是 - (CH 2)1-2 - (X)0-1 - (CH 2)0-1-或不存在; X是-O-或-CR 3 R 4 - ; 并且R 3和R 4独立地选自氢和C 1 -C 4烷基; 或其药学上可接受的盐或水合物,其可用于治疗高血压。

    ANGIOTENSIN II RECEPTOR ANTAGONISTS
    44.
    发明申请
    ANGIOTENSIN II RECEPTOR ANTAGONISTS 审中-公开
    ANGIOTENSIN II受体拮抗剂

    公开(公告)号:US20100152259A1

    公开(公告)日:2010-06-17

    申请号:US12516482

    申请日:2007-12-11

    CPC分类号: C07D403/10

    摘要: A compound having the structure (Formula I), wherein R an angiotensin receptor antagonist active group, Y is Y1—Y2—Y3—Y4—Y5. Y1 is C(R1R2); R1 is selected from the group consisting of hydrogen and C1-4 alkyl; R2 is selected from the group consisting of hydrogen, C1-4 alkyl, and -0C(0)C1-4 alkyl; Y2 is O or CH2; Y3 is C(O) or CH2; Y4 is O or CH2; Y5 is —(CH2)1-2—(X)0-1—CH2)0-1— or is absent; X is —O— or —CR3R4—; and R3 and R4 are independently selected from the group consisting of hydrogen and C1-C4 alkyl; or a pharmaceutically acceptable salt or hydrate thereof, which is useful for treating hypertension.

    摘要翻译: 具有结构(式I)的化合物,其中R为血管紧张素受体拮抗剂活性基团,Y为Y1-Y2-Y3-Y4-Y5。 Y1是C(R1R2); R 1选自氢和C 1-4烷基; R 2选自氢,C 1-4烷基和-C(O)C 1-4烷基; Y2是O或CH2; Y 3是C(O)或CH 2; Y4是O或CH2; Y 5是 - (CH 2)1-2 - (X)0-1-CH 2)0-1-或不存在; X是-O-或-CR 3 R 4 - ; 并且R 3和R 4独立地选自氢和C 1 -C 4烷基; 或其药学上可接受的盐或水合物,其可用于治疗高血压。

    Acylated Spiropiperidine Derivatives as Melanocortin-4 Receptor Modulators
    46.
    发明申请
    Acylated Spiropiperidine Derivatives as Melanocortin-4 Receptor Modulators 有权
    酰基化Spiropiperidine衍生物作为黑皮质素-4受体调节剂

    公开(公告)号:US20090170863A1

    公开(公告)日:2009-07-02

    申请号:US11992262

    申请日:2006-09-25

    CPC分类号: C07D471/10

    摘要: Certain novel N-acylated spiropiperidine derivatives are ligands of the human melanocortin receptor(s) and, in particular, are selective ligands of the human melanocortin-4 receptor (MC-4R). They are therefore useful for the treatment, control, or prevention of diseases and disorders responsive to the modulation of MC-4R, such as obesity, diabetes, nicotine addiction, alcoholism, sexual dysfunction, including erectile dysfunction and female sexual dysfunction.

    摘要翻译: 某些新型N-酰化螺哌啶衍生物是人类黑皮质素受体的配体,特别是人黑素皮质素-4受体(MC-4R)的选择性配体。 因此,它们可用于治疗,控制或预防对调节MC-4R的疾病和病症,例如肥胖,糖尿病,尼古丁成瘾,酒精中毒,性功能障碍,包括勃起功能障碍和女性性功能障碍。