β-lactamyl phenylalanine, cysteine, and serine vasopressin antagonists
    1.
    发明授权
    β-lactamyl phenylalanine, cysteine, and serine vasopressin antagonists 有权
    β-内酰胺基苯丙氨酸,半胱氨酸和丝氨酸加压素拮抗剂

    公开(公告)号:US08426400B2

    公开(公告)日:2013-04-23

    申请号:US13285590

    申请日:2011-10-31

    CPC分类号: C07D413/14 C07D413/04

    摘要: Substituted 2-(azetidin-2-on-1-yl)alkoxyalkylalkanoic acids and 2-(azetidin-2-on-1-yl)arylalkylalkanoic acids, and analogs and derivatives thereof are described. Methods for using the described compounds, and pharmaceutical compositions thereof, to treat disease states responsive to antagonism of one or more vasopressin receptors are also described.

    摘要翻译: 描述了取代的2-(氮杂环丁烷-2-基-1-基)烷氧基烷基链烷酸和2-(氮杂环丁烷-2-基-1-基)芳基烷基链烷酸及其类似物和衍生物。 还描述了使用所述化合物及其药物组合物治疗对一种或多种血管加压素受体的拮抗作用有反应的疾病状态的方法。

    BETA-LACTAMYL PHENYLALANINE, CYSTEINE, AND SERINE VASOPRESSIN ANTAGONISTS
    2.
    发明申请
    BETA-LACTAMYL PHENYLALANINE, CYSTEINE, AND SERINE VASOPRESSIN ANTAGONISTS 有权
    苯丙氨酸苯丙氨酸,CYSTEINE和SERINE VASOPRESSIN ANTAGONISTS

    公开(公告)号:US20120220765A1

    公开(公告)日:2012-08-30

    申请号:US13285590

    申请日:2011-10-31

    IPC分类号: C07D205/085

    CPC分类号: C07D413/14 C07D413/04

    摘要: Substituted 2-(azetidin-2-on-1-yl)alkoxyalkylalkanoic acids and 2-(azetidin-2-on-1-yl)arylalkylalkanoic acids, and analogs and derivatives thereof are described. Methods for using the described compounds, and pharmaceutical compositions thereof, to treat disease states responsive to antagonism of one or more vasopressin receptors are also described.

    摘要翻译: 描述了取代的2-(氮杂环丁烷-2-基-1-基)烷氧基烷基链烷酸和2-(氮杂环丁烷-2-基-1-基)芳基烷基链烷酸及其类似物和衍生物。 还描述了使用所述化合物及其药物组合物治疗对一种或多种血管加压素受体的拮抗作用有反应的疾病状态的方法。

    Beta-lactamyl phenylalanine, cysteine, and serine vasopressin antagonists
    3.
    发明授权
    Beta-lactamyl phenylalanine, cysteine, and serine vasopressin antagonists 有权
    β-内酰胺基苯丙氨酸,半胱氨酸和丝氨酸加压素拮抗剂

    公开(公告)号:US08048874B2

    公开(公告)日:2011-11-01

    申请号:US11996006

    申请日:2006-07-18

    CPC分类号: C07D413/14 C07D413/04

    摘要: Substituted 2-(azetidin-2-on-1-yl)alkoxyalkylalkanoic acids and 2-(azetidin-2-on-1-yl)arylalkylalkanoic acids, and analogs and derivatives thereof are described. Methods for using the described compounds, and pharmaceutical compositions thereof, to treat disease states responsive to antagonism of one or more vasopressin receptors are also described.

    摘要翻译: 描述了取代的2-(氮杂环丁烷-2-基-1-基)烷氧基烷基链烷酸和2-(氮杂环丁烷-2-基-1-基)芳基烷基链烷酸及其类似物和衍生物。 还描述了使用所述化合物及其药物组合物治疗对一种或多种血管加压素受体的拮抗作用有反应的疾病状态的方法。

    Beta-Lactamyl Phenylalanine, Cysteine, and Serine Vasopressin Antagonists
    6.
    发明申请
    Beta-Lactamyl Phenylalanine, Cysteine, and Serine Vasopressin Antagonists 有权
    β-内酰胺基苯丙氨酸,半胱氨酸和丝氨酸加压素拮抗剂

    公开(公告)号:US20080280870A1

    公开(公告)日:2008-11-13

    申请号:US11996006

    申请日:2006-07-18

    CPC分类号: C07D413/14 C07D413/04

    摘要: Substituted 2-(azetidin-2-on-1-yl)alkoxyalkylalkanoic acids and 2-(azetidin-2-on-1-yl)arylalkylalkanoic acids, and analogs and derivatives thereof are described. Methods for using the described compounds, and pharmaceutical compositions thereof, to treat disease states responsive to antagonism of one or more vasopressin receptors are also described.

    摘要翻译: 描述了取代的2-(氮杂环丁烷-2-基-1-基)烷氧基烷基链烷酸和2-(氮杂环丁烷-2-基-1-基)芳基烷基链烷酸及其类似物和衍生物。 还描述了使用所述化合物及其药物组合物治疗对一种或多种血管加压素受体的拮抗作用有反应的疾病状态的方法。

    Antimycobacterial agents
    10.
    发明授权
    Antimycobacterial agents 失效
    抗分枝杆菌药

    公开(公告)号:US06310058B1

    公开(公告)日:2001-10-30

    申请号:US09578973

    申请日:2000-05-25

    IPC分类号: A61K3155

    CPC分类号: C07D403/12 C07D413/12

    摘要: Compounds represented by the formula [1] R1 is H or a substituent; R2 and R3 are C1-C3 alkyl; R4 is siderophore group e.g. CH3—(CH2)n—C(O)—N(OH)—(CH2)m— with n=10-22, m=2-6; X is O, S, or NH; X1 is O or NH; Y is H or alkyl; Z is H or substituted amino, e.g., t-BocNH or CbzNH, and r is 2-4; are useful in the method provided for treating tuberculosis. [1] is prepared by coupling [7], wherein HX1 is HO— or H2N—,  with [4] obtained as the free acid after saponification of the methyl ester.

    摘要翻译: 由式[1] R 1表示的化合物是H或取代基; R2和R3是C1-C3烷基; R4是铁载体基团 CH 3 - (CH 2)n -C(O)-N(OH) - (CH 2)m - ,其中n = 10-22,m = 2-6; X是O,S或NH; X1是O或NH; Y是H或烷基; Z是H或取代的氨基,例如t-BocNH或CbzNH,r是2-4; 可用于治疗结核病的方法。 [1]通过偶联[7]制备,其中HX1是HO-或H2N-,其中[4]在甲酯皂化后作为游离酸获得。