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公开(公告)号:EP1263716B1
公开(公告)日:2008-01-02
申请号:EP01914865.9
申请日:2001-03-07
IPC分类号: C07C311/19 , C07C311/29 , C07C311/18 , C07C311/10 , C07C311/42 , C07C311/13 , C07C311/46 , C07C271/22 , A61K31/325 , A61K31/395
CPC分类号: C07D215/36 , C07C271/22 , C07C311/10 , C07C311/13 , C07C311/19 , C07C311/29 , C07C311/42 , C07C323/60 , C07C2601/02 , C07C2602/42 , C07C2603/18 , C07D209/18 , C07D209/42 , C07D215/48 , C07D311/84 , C07D317/60
摘要: The present invention relates to a class of amino acid derivatives with HIV aspartyl protease inhibitory properties.
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2.
公开(公告)号:EP1377542B1
公开(公告)日:2007-08-01
申请号:EP02704504.6
申请日:2002-02-12
发明人: STRANIX, Brent, Richard , SAUVE, Gilles , BOUZIDE, Abderrahim , COTE, Alexandre , BERUBE, Gervais , SOUCY, Patrick , ZHAO, Yongsen , YELLE, Jocelyn
IPC分类号: C07C311/19 , C07D209/16 , C07C311/46 , C07D333/34 , C07D333/60 , C07C311/42 , C07D295/215 , C07C327/48 , C07D409/12 , A61K31/198 , A61K31/405 , A61K31/381 , A61K31/5375 , A61P31/18
CPC分类号: C07D295/185 , A61K38/00 , C07C311/19 , C07C311/42 , C07C311/46 , C07C323/60 , C07C327/44 , C07C327/48 , C07C2601/08 , C07D209/16 , C07D333/34 , C07D333/60 , C07K5/0215
摘要: A compound selected from the group consisting of a compound of formula I or formula II: (I) (II) wherein n is 3 or 4 wherein Cx is selected from the group consisting of -COOM, COOR6, -CHO, -CH2OR7, -CH2OCOR8, -CONHR9 and -CONR10R11, wherein M is an alkali metal or alkaline earth metal, wherein R2 is selected from the group consisting of a benzenesulfonyl group of formula III, or formula IV : (III) (IV) and when the compound of formula (I) and (II) comprises an amino group pharmaceutically acceptable ammonium salts thereof, wherein R1, R2, Cx, n, R3, R4, R5, Y are as defined in the specification.
摘要翻译: 本申请是指选自式I化合物的化合物,其中化合物1至10分别定义如下。该化合物可用于治疗HIV和HTLV感染。
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