4,7-benzofurandione derivatives useful as inhibitors of leukotriene
synthesis
    1.
    发明授权
    4,7-benzofurandione derivatives useful as inhibitors of leukotriene synthesis 失效
    可用作白三烯合成抑制剂的4,7-苯并呋喃二酮衍生物

    公开(公告)号:US4778805A

    公开(公告)日:1988-10-18

    申请号:US64152

    申请日:1987-06-18

    摘要: 4,7-Benzofurandione derivatives of Formula I, pharmaceutical compositions, and methods of treatment are disclosed. These compounds are useful as inhibitors of mammalian leukotriene biosynthesis. As such, these compounds are useful therapeutic agents for treating allergic conditions, asthma, cardiovascular disorders, inflammation, psoriasis and allergic conjunctivitis. The compounds are also useful as analgesics and as cytoprotective agents. Also disclosed are novel intermediates useful for the preparation of the 4,7-benzofurandiones of this invention. ##STR1##

    摘要翻译: 公开了式I的4,7-苯并呋喃二酮衍生物,药物组合物和治疗方法。 这些化合物可用作哺乳动物白细胞三烯生物合成的抑制剂。 因此,这些化合物是用于治疗过敏性疾病,哮喘,心血管疾病,炎症,牛皮癣和过敏性结膜炎的有用治疗剂。 该化合物也可用作止痛剂和细胞保护剂。 还公开了可用于制备本发明的4,7-苯并呋喃二酸的新型中间体。

    4,7-benzofurandione derivatives
    2.
    发明授权
    4,7-benzofurandione derivatives 失效
    4,7-苯并呋喃二酮衍生物

    公开(公告)号:US4968821A

    公开(公告)日:1990-11-06

    申请号:US217264

    申请日:1988-07-11

    摘要: 4,7-Benzofurandione derivatives of Formula I, pharmaceutical compositions, and methods of treatment are disclosed. These compounds are useful as inhibitors of mammalian leukotriene biosynthesis. As such, these compounds are useful therapeutic agents for treating allergic conditions, asthma, cardiovascular disorders, inflammation, psoriasis and allergic conjunctivitis. The compounds are also useful as analgesics and as cytoprotective agents. Also disclosed are novel intermediates useful for the preparation of the 4,7-benzofurandiones of this invention. ##STR1##

    摘要翻译: 公开了式I的4,7-苯并呋喃二酮衍生物,药物组合物和治疗方法。 这些化合物可用作哺乳动物白细胞三烯生物合成的抑制剂。 因此,这些化合物是用于治疗过敏性疾病,哮喘,心血管疾病,炎症,牛皮癣和过敏性结膜炎的有用治疗剂。 该化合物也可用作止痛剂和细胞保护剂。 还公开了可用于制备本发明的4,7-苯并呋喃二酸的新型中间体。

    Hydroxyalkylquinoline ether acids as leukotriene antagonists
    5.
    发明授权
    Hydroxyalkylquinoline ether acids as leukotriene antagonists 失效
    羟基烷基喹啉醚酸作为白三烯拮抗剂

    公开(公告)号:US5266568A

    公开(公告)日:1993-11-30

    申请号:US774403

    申请日:1991-10-10

    CPC分类号: C07D215/14 C07D215/18

    摘要: Compounds having the formula I: ##STR1## are leukotriene antagonists and inhibitors of leukotriene biosynthesis. These compounds are useful as anti-asthmatic, anti-allergic, anti-inflammatory, and cytoprotective agents. They are also useful in treating angina, cerebral spasm, glomerular nephritis, hepatitis, endotoxemia, uveitis, and allograft rejection.

    摘要翻译: 具有式I的化合物:I是白三烯拮抗剂和白三烯生物合成的抑制剂。 这些化合物可用作抗哮喘,抗过敏,抗炎和细胞保护剂。 它们也可用于治疗心绞痛,脑痉挛,肾小球肾炎,肝炎,内毒素血症,葡萄膜炎和同种异体移植排斥。

    Quinoline-containing ketoacids as leukotriene antagonists
    7.
    发明授权
    Quinoline-containing ketoacids as leukotriene antagonists 失效
    含喹啉酮酸作为白三烯拮抗剂

    公开(公告)号:US5212180A

    公开(公告)日:1993-05-18

    申请号:US832298

    申请日:1992-02-07

    申请人: Michel L. Belley

    发明人: Michel L. Belley

    IPC分类号: C07D215/18

    CPC分类号: C07D215/18

    摘要: Compounds having the formula I: ##STR1## are antagonists of the actions of leukotrienes. These compounds are useful as anti-asthmatic, anti-allergic, anti-inflammatory, and cytoprotective agents. They are also useful in treating angina, cerebral spasm, glomerular nephritis, hepatitis, endotoxemia, uveitis and allograft rejection.

    摘要翻译: 具有式I的化合物:I是白三烯的作用的拮抗剂。 这些化合物可用作抗哮喘,抗过敏,抗炎和细胞保护剂。 它们也可用于治疗心绞痛,脑痉挛,肾小球肾炎,肝炎,内毒素血症,葡萄膜炎和同种异体移植排斥。