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Thiazepine inhibitors of HIV-1 integrase

机译:硫氮平HIV-1整合酶抑制剂

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.
机译:本发明公开了作为抗整合酶抑制剂的非邻苯二酚化合物,例如噻唑并噻嗪类及其类似物和衍生物。可用作治疗HIV疾病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为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; X-Y为CH2-S,S-CH2,CH2-O,CH2-S(O),S(O)-CH2,CH2-CH2,CH2-CH2-CH2或CH2-CH2-CH2-CH2; R4是H或羟基; R5是H,苯基或烷基胺; W是S或O; R6是H,取代或未取代的烷基或胺; Z为S,O,CH 2,CH 2 CH 2或C = O。

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