Pyrrolo [2,1-b][1,3]benzothiazepines with atypical antipsychotic activity
    2.
    发明授权
    Pyrrolo [2,1-b][1,3]benzothiazepines with atypical antipsychotic activity 失效
    具有非典型抗精神病活性的吡咯并[2,1-b] [1,3]苯并硫氮杂

    公开(公告)号:US06391870B2

    公开(公告)日:2002-05-21

    申请号:US09769740

    申请日:2001-01-26

    IPC分类号: C07D51300

    CPC分类号: C07D513/04

    摘要: Polycondensated heterocycles with a pyrrole[2,1-b][1,3]benzothiazepine structure of the following formula (I) where the groups are defined as in the description are disclosed. As compared to known antipsychotic agents, these compounds present substantial activity associated with a simultaneous reduction in unwanted extrapyramidal symptoms. These compounds can be formulated in pharmaceutical compositions for the treatment of psychoses such as, for example, schizophrenia.

    摘要翻译: 公开了具有如描述中定义的基团的下式(I)的吡咯[2,1-b] [1,3]苯并硫氮杂结构的缩聚杂环。 与已知的抗精神病药相比,这些化合物具有与同时减少不需要的锥体外系症状相关的显着活性。 这些化合物可以配制在用于治疗精神病例如精神分裂症的药物组合物中。

    Thiazepine inhibitors of HIV-1 integrase
    4.
    发明授权
    Thiazepine inhibitors of HIV-1 integrase 失效
    HIV-1整合酶的噻吗嗪抑制剂

    公开(公告)号:US07015212B1

    公开(公告)日:2006-03-21

    申请号:US10009210

    申请日:2000-05-10

    CPC分类号: C07D513/04

    摘要: The present invention discloses non-catechol compounds, such as thiazolothiazepines, and analogs and derivatives thereof, which are anti-integrase inhibitors. The compounds, which are useful as treatments for HIV disease, include compounds (I), (II), (III), or pharmaceutically acceptable salts thereof wherein A is thiazole, benzene, naphthalene, pyridine, pyrimidine, pyrazine, or quinoline; R is one or more of H, halogen, lower alkyl, lower alkoxy, NO2, lower ester or carboxylic acid; X—Y is CH2—S, S—CH2, CH2—O, CH2—S(O). S(O)—CH2, CH2—CH2, CH2—CH2—CH2, or CH2—CH2—CH2—CH2; R4 is H or hydroxy; R5 is H, phenyl, or alkylamine; W is S or O; and R6 is H, substituted or unsubstituted alkyl or amine; and Z is S, O, CH2, CH2CH2, or C═O.

    摘要翻译: 本发明公开了非邻苯二酚化合物,如噻唑并噻嗪类及其类似物及其衍生物,它们是抗整联酶抑制剂。 可用作HIV疾病治疗的化合物包括化合物(I),(II),(III)或其药学上可接受的盐,其中A是噻唑,苯,萘,吡啶,嘧啶,吡嗪或喹啉; R是H,卤素,低级烷基,低级烷氧基,NO 2,低级酯或羧酸中的一种或多种。 XY是CH 2 -S,S-CH 2,CH 2 -O,CH 2 -S( O)。 S(O)-CH 2 CH 2,CH 2 -CH 2,CH 2 -CH 2 CH 2 CH 2或CH 2 -CH 2 -CH 2 CH 2 CH 2, 2 R 4是H或羟基; R 5是H,苯基或烷基胺; W是S或O; R 6是H,取代或未取代的烷基或胺; Z是S,O,CH 2,CH 2 CH 2,或C-O。