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    Renin inhibiting compounds
    1.
    发明授权
    Renin inhibiting compounds 失效
    肾素抑制化合物

    公开(公告)号：US4826815A

    公开(公告)日：1989-05-02

    申请号：US946881

    申请日：1987-01-09

    申请人： Jay R. Luly ,  Joseph Dellaria ,  Anthony K. L. Fung ,  Dale J. Kempf ,  Jacob J. Plattner ,  Saul H. Rosenberg ,  Hing L. Sham

    发明人： Jay R. Luly ,  Joseph Dellaria ,  Anthony K. L. Fung ,  Dale J. Kempf ,  Jacob J. Plattner ,  Saul H. Rosenberg ,  Hing L. Sham

    IPC分类号： A61K38/00 ,  C07D207/12 ,  C07D231/12 ,  C07D233/54 ,  C07D263/20 ,  C07D295/185 ,  C07D317/28 ,  C07D319/06 ,  C07D339/06 ,  C07D339/08 ,  C07D405/06 ,  C07D409/06 ,  C07K5/02 ,  C07K5/065 ,  A61K37/02 ,  C07K5/08

    CPC分类号： C07D231/12 ,  C07D207/12 ,  C07D233/64 ,  C07D263/20 ,  C07D295/185 ,  C07D317/28 ,  C07D319/06 ,  C07D339/06 ,  C07D339/08 ,  C07D405/06 ,  C07D409/06 ,  C07K5/02 ,  C07K5/0227 ,  C07K5/06078 ,  A61K38/00 ,  Y02P20/55 ,  Y10S530/80 ,  Y10S530/86

    摘要： The invention relates to renin inhibiting compounds of the formula ##STR1## wherein A is hydrogen; loweralkyl; arylalkyl; Or.sub.10 wherein R.sub.10 is hydrogen or loweralkyl; NR.sub.11 R.sub.12 wherein R.sub.11 and R.sub.12 are independently selected from hydrogen and loweralkyl; or R.sub.13 --CO--B wherein B is NH, O, CH.sub.2, HNCH.sub.2 and R.sub.13 is loweralkyl, alkoxy, arylalkoxy, arylalkoxyalkyl, amino, alkylamino, dialkylamino, aminoalkyl, N-protected aminoalkyl, hydroxylated dialkylamino, (heterocyclic)alkyl or a substituted or unsubstituted heterocyclic, carboxyalkyl, or lower alkyl carboxyalkyl esters; W is N or CH: U,V may be the following combinations H,OH; OH,H; H,H; or when taken together as O represents a carbonyl with the provisos that if U,V.dbd.H,OH, then W=CH, and if U,V.dbd.O then W.dbd.N; R.sub.1 , R.sub.3 and R.sub.5 are loweralkyl or hydrophilic, lipophilic or aromatic amino acid side chains and may be the same or different; R.sub.2, R.sub.4, R.sub.7, R.sub.8 and R.sub.9 are hydrogen or loweralkyl and may be the same or different; X is NH, O, S, SO, SO.sub.2, or CH.sub.2 ; and R.sub.6 is loweralkyl cycloalkyl, cycloalkylalkyl, aryl, arylalkyl or an N-protecting group, with the proviso that R.sub.6 may be an N-protecting group when X is NH.

    摘要翻译： 本发明涉及下式的肾素抑制化合物：其中A是氢; 低级烷基 芳烷基 其中R 10是氢或低级烷基; NR11R12其中R11和R12独立地选自氢和低级烷基; 或R13-CO-B，其中B是NH，O，CH2，HNCH2和R13是低级烷基，烷氧基，芳基烷氧基，芳基烷氧基烷基，氨基，烷基氨基，二烷基氨基，氨基烷基，N-保护的氨基烷基，羟基化二烷基氨基，（杂环）烷基或取代 或未取代的杂环，羧基烷基或低级烷基羧烷基酯; W是N或CH：U，V可以是以下组合：H，OH; OH，H; H，H; 或者当O代表羰基时，条件是如果U，V = H，OH，则W = CH，并且如果U，V = O，则W = N; R 1，R 3和R 5是低级烷基或亲水性，亲油性或芳族氨基酸侧链，可以相同或不同; R2，R4，R7，R8和R9是氢或低级烷基，可以相同或不同; X是NH，O，S，SO，SO 2或CH 2; 并且R 6是低级烷基环烷基，环烷基烷基，芳基，芳烷基或N-保护基，条件是当X是NH时，R6可以是N-保护基。