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公开(公告)号:US5256677A
公开(公告)日:1993-10-26
申请号:US901057
申请日:1992-06-19
Applicant: Hing L. Sham , Daniel W. Norbeck , Dale J. Kempf , Chen Zhao
Inventor: Hing L. Sham , Daniel W. Norbeck , Dale J. Kempf , Chen Zhao
IPC: A61K38/00 , C07C33/46 , C07C43/164 , C07C43/174 , C07C43/205 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/00 , C07C45/29 , C07C45/56 , C07C45/59 , C07C45/62 , C07C45/67 , C07C45/74 , C07C53/134 , C07C69/34 , C07C69/65 , C07C69/732 , C07C211/27 , C07C215/18 , C07C215/20 , C07C215/28 , C07C229/08 , C07C229/26 , C07C229/34 , C07C233/36 , C07C233/40 , C07C235/10 , C07C235/12 , C07C235/34 , C07C235/78 , C07C237/10 , C07C237/20 , C07C237/22 , C07C239/10 , C07C239/18 , C07C239/20 , C07C247/10 , C07C251/40 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/16 , C07C275/24 , C07C311/03 , C07C311/13 , C07C311/18 , C07C317/10 , C07C317/28 , C07C317/44 , C07C323/12 , C07C323/25 , C07C381/00 , C07D207/08 , C07D207/24 , C07D209/42 , C07D211/62 , C07D213/30 , C07D213/40 , C07D213/42 , C07D213/56 , C07D213/70 , C07D213/81 , C07D213/82 , C07D215/16 , C07D217/16 , C07D217/26 , C07D233/84 , C07D239/38 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/36 , C07D277/42 , C07D277/56 , C07D295/088 , C07D295/15 , C07D295/155 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D303/04 , C07D303/22 , C07D303/36 , C07D303/48 , C07D307/42 , C07D317/12 , C07D417/12 , C07D487/04 , C07D521/00 , C07F9/32 , C07F9/53 , C07K5/02 , C07K5/06 , C07K5/078 , A61K31/44
CPC classification number: C07D207/08 , C07C211/27 , C07C215/18 , C07C215/20 , C07C215/28 , C07C229/08 , C07C229/26 , C07C229/34 , C07C233/36 , C07C233/40 , C07C235/10 , C07C235/12 , C07C235/34 , C07C235/78 , C07C237/10 , C07C237/20 , C07C237/22 , C07C239/10 , C07C239/18 , C07C239/20 , C07C247/10 , C07C251/40 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/16 , C07C275/24 , C07C311/03 , C07C311/13 , C07C311/18 , C07C317/10 , C07C317/28 , C07C317/44 , C07C323/12 , C07C323/25 , C07C33/46 , C07C381/00 , C07C43/164 , C07C43/1742 , C07C43/2055 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/004 , C07C45/29 , C07C45/567 , C07C45/59 , C07C45/62 , C07C45/673 , C07C45/74 , C07C53/134 , C07C69/34 , C07C69/65 , C07C69/732 , C07D207/24 , C07D209/42 , C07D211/62 , C07D213/30 , C07D213/40 , C07D213/42 , C07D213/56 , C07D213/70 , C07D213/81 , C07D213/82 , C07D215/16 , C07D217/16 , C07D217/26 , C07D231/12 , C07D233/56 , C07D233/84 , C07D239/38 , C07D249/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/36 , C07D277/42 , C07D277/56 , C07D295/088 , C07D295/15 , C07D295/155 , C07D295/185 , C07D295/205 , C07D295/215 , C07D295/26 , C07D303/04 , C07D303/22 , C07D303/36 , C07D303/48 , C07D307/42 , C07D317/12 , C07D417/12 , C07D487/04 , C07F9/3241 , C07F9/5333 , C07K5/021 , C07K5/06043 , C07K5/06052 , C07K5/06139 , A61K38/00 , C07C2101/14
Abstract: Compounds are disclosed which are retroviral protease inhibitors. Also disclosed are methods of using the compounds and compositions for inhibiting a retroviral protease and for treating an HIV infection.
Abstract translation: 公开了作为逆转录病毒蛋白酶抑制剂的化合物。 还公开了使用化合物和组合物抑制逆转录病毒蛋白酶和治疗HIV感染的方法。
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公开(公告)号:US4857507A
公开(公告)日:1989-08-15
申请号:US946883
申请日:1987-01-09
Applicant: Saul H. Rosenberg , Joseph Dellaria , Anthony K, L. Fung , Dale J. Kempf , Jay R. Luly , Jacob J. Plattner
Inventor: Saul H. Rosenberg , Joseph Dellaria , Anthony K, L. Fung , Dale J. Kempf , Jay R. Luly , Jacob J. Plattner
IPC: 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
CPC classification number: 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 , Y10S530/86
Abstract: The invention relates to renin inhibiting compounds of the formula ##STR1## wherein A is hydrogen; loweralkyl; arylalkyl; OR.sub.10 or SR.sub.10 wherein R.sub.10 is hydrogen, loweralkyl or aminoalkyl; NR.sub.11 R.sub.12 wherein R.sub.11 and R.sub.12 are independently selected from hydrogen, loweralkyl, aminoalkyl, cyanoalkyl and hydroxyalkyl; ##STR2## wherein B is NH, alkylamino, S, O, CH.sub.2 or CHOH and R.sub.13 is loweralkyl, cycloalkyl, aryl, arylalkyl, alkoxy, alkenyloxy, hydroxyalkoxy, dihydroxyalkoxy, arylalkoxy, arylalkoxyalkyl, amino, alkylamino, dialkylamino, (hydroxyalkyl)(alkyl)amino, (dihydroxyalkyl)(alkyl)amino, aminoalkyl, alkoxycarbonylalkyl, carboxyalkyl, N-protected aminoalkyl, alkylaminoalkyl, (N-protected)(alkyl)aminoalkyl, dialkylaminoalkyl, (heterocyclic) alkyl or a substituted or unsubstituted heterocyclic; W is CO or CHOH and U is CH.sub.2 or NR.sub.2 with the proviso that when W is CHOH then U is CH.sub.2 ; R.sub.1 is loweralkyl, cycloaklylmethyl, benzyl, .alpha.,.alpha.-dimethylbenzyl, 4-methoxybenzyl, halobenzyl, (1-naphthyl)methyl, (2-naphthyl)methyl, (4-imidazoyl)-methyl, phenethyl, phenoxy, thiophenoxy or anilino; provided if R.sub.1 is phenoxy, thiophenoxy or anilino, B is CH.sub.2 or CHOH or A is hydrogen, R.sub.3 is loweralkyl, vinylloweralkyl, benzyl or heterocyclic ring substituted methyl, R.sub.5 is loweralkyl, cycloalkylmethyl or benzyl; R.sub.2 and R.sub.4 are independently selected from hydrogen and loweralkyl; R.sub.6 is CHOH or CO; R.sub.7 is CH.sub.2, CF.sub.2 or CF with the proviso that when R.sub.6 is CO, R.sub.7 is CF.sub.2 ; R.sub.8 is CH.sub.2, CHR.sub.14 wherein R.sub.14 is lower-alkyl, cycloalkyl, cycloalkylalkyl, aryl or arylalkyl, or R.sub.7 and R.sub.8 taken together can be ##STR3## with the proviso that when R.sub.7 is CF.sub.2, R.sub.8 is CH.sub.2 ; E is O, S, SO, SO.sub.2, NR.sub.15 wherein R.sub.15 is hydrogen or loweralkyl or NR.sub.16 CO wherein R.sub.16 is hydrogen or loweralkyl; R.sub.9 is loweralkyl, cycloalkyl, cycloalkylalkyl, aryl, arylalkyl or an N-protected group, or E and R.sub.9 taken together can be N.sub.3, with the proviso that when E is NH, R.sub.9 is an N-protecting group; and pharmaceutically acceptable salts thereof.
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公开(公告)号:US4826815A
公开(公告)日:1989-05-02
申请号:US946881
申请日:1987-01-09
Applicant: Jay R. Luly , Joseph Dellaria , Anthony K. L. Fung , Dale J. Kempf , Jacob J. Plattner , Saul H. Rosenberg , Hing L. Sham
Inventor: Jay R. Luly , Joseph Dellaria , Anthony K. L. Fung , Dale J. Kempf , Jacob J. Plattner , Saul H. Rosenberg , Hing L. Sham
IPC: 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 classification number: 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
Abstract: 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.
Abstract translation: 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。
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