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公开(公告)号:EP0486948A2
公开(公告)日:1992-05-27
申请号:EP91119464.5
申请日:1991-11-04
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Codacovi, Lynn M. , Norbeck, Daniel W. , Plattner, Jacob J. , Sham, Hing L. , Wittenberger, Steven J. , Zhao, Chen
IPC: C07D213/26 , C07D213/30 , C07D213/40 , C07K5/06 , A61K37/64 , C07D213/56 , C07D211/16 , C07D295/20 , C07D277/30 , C07D277/42 , C07D417/12 , C07D277/40 , C07D401/12 , C07D277/24 , C07D277/28 , C07D235/14 , C07D235/16
CPC classification number: C07D213/30 , A61K38/00 , C07C53/134 , C07C215/18 , C07C215/20 , C07C215/28 , C07C233/40 , C07C237/10 , C07C237/22 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/24 , C07D213/26 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D413/10 , C07D417/12 , C07K5/06026 , C07K5/06078
Abstract: A retroviral protease inhibiting compound of the formula A -X- B is disclosed. Also disclosed are a composition and method for inhibiting a retroviral protease and for treating an HIV infection. Also disclosed are processes and intermediates useful for the preparation of the retroviral protease inhibitors.
Abstract translation: 公开了具有式A -X-B的逆转录病毒蛋白酶抑制化合物。 还公开了抑制逆转录病毒蛋白酶和治疗HIV感染的组合物和方法。 还公开了可用于制备逆转录病毒蛋白酶抑制剂的方法和中间体。
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公开(公告)号:EP0364804A1
公开(公告)日:1990-04-25
申请号:EP89118270.1
申请日:1989-10-03
Applicant: ABBOTT LABORATORIES
Inventor: Fung, Anthony K. L. , Plattner, Jacob J. , Baker, William R. , Armiger, Yoek-Lin , Rosenberg, Saul H. , De, Biswanath , Mantei, Robert A. , Boyd, Steven A. , Kempf, Dale J. , Sham, Hing Leung , Kleinert, Hollis D.
IPC: C07D211/30 , C07D211/44 , C07D295/185 , C07D307/12 , C07D401/12 , C07D405/12 , C07D407/12 , C07D409/12 , C07D411/12 , C07D413/12 , A61K31/445
CPC classification number: C07D233/64 , C07C237/08 , C07C317/28 , C07C323/58 , C07C2601/14 , C07D203/18 , C07D211/44 , C07D211/62 , C07D211/96 , C07D295/185 , C07D401/12 , C07D407/12 , C07D413/12
Abstract: A renin inhibiting compound of the formula:
wherein A is a substituent; R 1 is hydrogen, loweralkyl, substituted loweralkyl or loweralkenyl; X is CH 2 , CHOH, C(O), O, S, S(O), S0 2 , NH, N(O) or -P(O)O-; R 3 is loweralkyl, loweralkenyl or substituted loweralkyl; and T is mimic of the Leu-Val cleavage site of angiotensinogen; or a pharmaceutically acceptable salt, ester or prodrug thereof.Abstract translation: 一种下列化学式的肾素抑制化合物:其中A为取代基的
R1是氢,低级烷基,取代的低级烷基或低级烯基; X是CH 2,CHOH,C(O),O,S,S(O),SO 2,NH,N(O)或-P(O) R3是低级烷基,低级烯基或取代的低级烷基; 并且T是模拟血管紧张素原的Leu-Val切割位点; 或其药学上可接受的盐,酯或前药。 -
公开(公告)号:EP0307837A2
公开(公告)日:1989-03-22
申请号:EP88114867.0
申请日:1988-09-12
Applicant: ABBOTT LABORATORIES
Inventor: Rosenberg, Saul Howard , Sham, Hing Leung , Baker, William R. , Dellaria, Joseph F., Jr. , Kempf, Dale J.
IPC: C07D521/00 , A61K31/33 , C07K5/06 , C07K5/02 , A61K37/64
CPC classification number: C07D213/40 , A61K38/00 , C07C215/10 , C07C215/20 , C07C217/08 , C07C229/36 , C07C233/11 , C07C233/22 , C07C233/40 , C07C233/47 , C07C233/51 , C07C239/20 , C07C265/04 , C07C271/16 , C07C271/20 , C07C271/22 , C07C275/24 , C07C317/28 , C07C317/44 , C07C317/48 , C07C323/56 , C07C323/59 , C07C2601/08 , C07C2601/14 , C07D207/12 , C07D211/76 , C07D231/12 , C07D233/32 , C07D233/56 , C07D249/08 , C07D263/04 , C07D263/06 , C07D263/16 , C07D263/22 , C07D263/28 , C07D277/24 , C07D285/10 , C07D295/13 , C07D295/185 , C07D295/205 , C07D295/215 , C07D309/14 , C07D319/06 , C07D413/06 , C07K5/0227 , C07K5/06078
Abstract: A renin inhibiting compound of the formula:
wherein A is a substituent; W is C=O, CHOH or NR₂ wherein R₂ is hydrogen or loweralkyl; U is C=O, CH₂ or NR₂ wherein R₂ is hydrogen or loweralkyl, with the proviso that when W is CHOH then U is CH₂ and with the proviso that U is C=O or CH₂ when W is NR₂; V is CH, C(OH) or C(halogen) with the proviso that V is CH when U is NR₂; R₁ is loweralkyl, cycloalkylalkyl, benzyl, (alpha, alpha)-dimethylbenzyl, 4-methoxybenzyl, halobenzyl, 4-hydroxybenzyl, (1-naphthyl)methyl, (2-naphthyl)methyl, (unsubstituted heterocyclic)methyl, (substituted heterocyclic)methyl, phenethyl, 1-benzyloxyethyl, phenoxy, thiophenoxy or anilino, provided that B is CH₂ or CHOH or A is hydrogen when R₁ is phenoxy, thiophenoxy or anilino; R₃ is loweralkyl, loweralkenyl, ((alkoxy)alkoxy)alkyl, carboxyalkyl, (thioalkoxy)alkyl, azidoalkyl, aminoalkyl, (alkyl)aminoalkyl, dialkylaminoalkyl, (alkoxy)(alkyl)aminoalkyl, (alkoxy)aminoalkyl, benzyl or heterocyclic ring substituted methyl; R₄ is loweralkyl, cycloalkylmethyl or benzyl; R₅ is OH or NH₂; and Z is a substituent.
Also disclosed are compositions for and a method of treating hypertension, methods of making the renin inhibiting compounds and intermediates useful in making the renin inhibiting compounds.Abstract translation: 一种下列化学式的肾素抑制化合物:其中A为取代基的
W是C = O,CHOH或NR2,其中R2是氢或低级烷基; U是C = O,CH 2或NR 2,其中R 2是氢或低级烷基,条件是当W是CHOH时,则U是CH 2,条件是当W是NR 2时,U是C = O或CH 2; V是CH,C(OH)或C(卤素),条件是当U是NR 2时,V是CH; R 1是低级烷基,环烷基烷基,苄基,(α,α) - 二甲基苄基,4-甲氧基苄基,卤代苄基,4-羟基苄基,(1-萘基)甲基,(2-萘基)甲基,(未取代的杂环)甲基,(取代的杂环) 甲基,苯乙基,1-苄氧基乙基,苯氧基,硫代苯氧基或苯胺基,条件是当R 1为苯氧基,苯硫基或苯胺基时,B为CH 2或CHOH或A为氢; R3是低级烷基,低级烯基,((烷氧基)烷氧基)烷基,羧基烷基,(硫代烷氧基)烷基,叠氮基烷基,氨基烷基,(烷基)氨基烷基,二烷基氨基烷基,(烷氧基)(烷基)氨基烷基,(烷氧基)氨基烷基,苄基或杂环取代 甲基; R4是低级烷基,环烷基甲基或苄基; R5是OH或NH2; Z为取代基。 还公开了治疗高血压的组合物和方法,制备肾素抑制化合物的方法和可用于制备肾素抑制化合物的中间体。 -
14.Processes and intermediates for manufacturing retroviral protease inhibiting compounds 失效
Title translation: Verfahren und Intermediate zur Herstellung von retroviralen Proteasehemmern公开(公告)号:EP1302468A1
公开(公告)日:2003-04-16
申请号:EP02079949.0
申请日:1993-12-16
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Sham, Hing Leung , Zhao, Chen , Sowin, Thomas J. , Reno, Daniel S. , Haight, Anthony R. , Cooper, Arthur J.
IPC: C07D277/24 , C07D277/28 , C07D303/36 , C07D277/34 , C07D277/42 , C07D417/12 , C07D263/32 , C07D413/12 , C07F5/02 , A61K31/426 , A61P31/18
CPC classification number: C07D413/12 , A61K31/425 , A61K31/427 , A61K31/70 , A61K38/00 , A61K45/06 , C07C33/46 , C07C43/164 , C07C43/1742 , C07C43/2055 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/004 , C07C45/29 , C07C45/567 , C07C45/62 , C07C45/673 , 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 , C07D213/26 , C07D213/30 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/34 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D417/12 , C07K5/06026 , C07K5/06078 , A61K31/00 , A61K2300/00 , C07C49/233 , C07C49/255 , C07C49/215 , C07C49/245 , C07C49/235 , C07C49/223
Abstract: A retroviral protease inhibiting compound of formula (A) is disclosed for use in combination with other active pharmaceutical agents for treating a human infected by HIV. Intermediates and processes useful in the manufacture of compounds of formula (A) are also disclosed.
Abstract translation: 公开了用于与用于治疗HIV感染的人的其它活性药剂组合使用的式(A)的逆转录病毒蛋白酶抑制化合物。 还公开了可用于制备式(A)化合物的中间体和方法。
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公开(公告)号:EP1170289A2
公开(公告)日:2002-01-09
申请号:EP01124290.6
申请日:1996-12-06
Applicant: Abbott Laboratories
Inventor: Sham, Hing Leung , Norbeck, Daniel W. , Chen, Xiaoqi , Betebenner, David A. , Kempf, Dale J. , Herrin, Thomas R. , Kumar, Gondi N. , Condon, Stephen L. , Cooper, Arthur J. , Dickman, Daniel A. , Hannick, Steven M. , Kolaczkowski, Lawrence , Oliver, Patricia A. , Plata, Daniel J. , Stengel, Peter J. , Stoner, Eric J. , Tien, Jieh-Heh J. , Liu, Jih-Hua , Patel, Ketan M.
IPC: C07D233/32 , C07D239/10 , C07D239/22 , C07D207/40 , C07D207/26 , C07D263/22 , C07D233/36 , C07D233/42 , C07D253/06 , C07D401/12 , C07D403/12 , C07D405/14 , C07D409/12 , C07D409/14 , C07D417/12 , C07D405/12 , C07C275/28 , A61K31/415
CPC classification number: C07D207/27 , C07D207/404 , C07D207/408 , C07D223/10 , C07D233/32 , C07D233/42 , C07D239/10 , C07D239/22 , C07D241/08 , C07D241/18 , C07D253/06 , C07D263/22 , C07D307/20 , C07D401/12 , C07D401/14 , C07D403/12 , C07D405/12 , C07D405/14 , C07D407/12 , C07D409/12 , C07D409/14 , C07D417/12
Abstract: A compound comprising a substituent of the formula (II) is disclosed as an HIV protease inhibitor. Intermediates for making such compounds and processes for making such intermediates are also disclosed.
Abstract translation: 公开了包含式(II)的取代基的化合物作为HIV蛋白酶抑制剂。 还公开了制造这种化合物的中间体和制备这种中间体的方法。
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16.Processes and intermediates for manufacturing retroviral protease inhibiting compounds 失效
Title translation: 方法和中间体逆转录病毒蛋白酶抑制剂的制备中公开(公告)号:EP1090914A3
公开(公告)日:2001-04-18
申请号:EP00124382.3
申请日:1993-12-16
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Sham, Hing Leung , Zhao, Chen , Sowin, Thomas J. , Reno, Daniel S. , Haight, Anthony R. , Cooper, Arthur J.
IPC: C07D277/24 , C07D277/28 , C07D303/36 , C07D277/34 , C07D277/42 , C07D417/12 , C07D263/32 , C07D413/12 , C07F5/02 , A61K31/426 , A61P31/18
CPC classification number: C07D413/12 , A61K31/425 , A61K31/427 , A61K31/70 , A61K38/00 , A61K45/06 , C07C33/46 , C07C43/164 , C07C43/1742 , C07C43/2055 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/004 , C07C45/29 , C07C45/567 , C07C45/62 , C07C45/673 , 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 , C07D213/26 , C07D213/30 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/34 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D417/12 , C07K5/06026 , C07K5/06078 , A61K31/00 , A61K2300/00 , C07C49/233 , C07C49/255 , C07C49/215 , C07C49/245 , C07C49/235 , C07C49/223
Abstract: A retroviral protease inhibiting compound of formula (A) is disclosed for use in combination with other active pharmaceutical agents for treating a human infected by HIV. Intermediates and processes useful in the manufacture of compounds of formula (A) are also disclosed.
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公开(公告)号:EP0486948B1
公开(公告)日:2000-10-04
申请号:EP91119464.5
申请日:1991-11-04
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Codacovi, Lynn M. , Norbeck, Daniel W. , Plattner, Jacob J. , Sham, Hing L. , Wittenberger, Steven J. , Zhao, Chen
IPC: C07D213/26 , C07D213/30 , C07D213/40 , C07K5/06 , A61K38/55 , C07D213/56 , C07D211/16 , C07D295/20 , C07D277/30 , C07D277/42 , C07D417/12 , C07D277/40 , C07D401/12 , C07D277/24 , C07D277/28 , C07D235/14 , C07D235/16
CPC classification number: C07D213/30 , A61K38/00 , C07C53/134 , C07C215/18 , C07C215/20 , C07C215/28 , C07C233/40 , C07C237/10 , C07C237/22 , C07C271/20 , C07C271/22 , C07C271/34 , C07C275/24 , C07D213/26 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D413/10 , C07D417/12 , C07K5/06026 , C07K5/06078
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公开(公告)号:EP0402646B1
公开(公告)日:1998-07-22
申请号:EP90109319.5
申请日:1990-05-17
Applicant: ABBOTT LABORATORIES
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Erickson, John W. , Codacovi, Lynn M. , Sham, Hing Leung , Plattner, Jacob J.
IPC: C07D213/40 , C07D213/56 , C07D211/44 , C07D215/14 , C07D211/34 , C07D215/18 , C07D295/26 , C07D295/145 , C07D303/04 , C07D303/23 , C07D303/36
CPC classification number: C07D207/08 , A61K38/00 , C07C33/46 , 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 , 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 , C07C2601/14 , 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 , C07D413/12 , C07D417/12 , C07D487/04 , C07F9/3241 , C07F9/5333 , C07K5/021 , C07K5/06043 , C07K5/06052 , C07K5/06139 , Y02P20/55 , C07C49/233 , C07C49/255 , C07C49/215 , C07C49/245 , C07C49/235 , C07C49/223
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公开(公告)号:EP0727419A3
公开(公告)日:1996-10-30
申请号:EP96106301.3
申请日:1993-12-16
Applicant: Abbott Laboratories
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Sham, Hing Leung , Zhao, Chen , Sowin, Thomas J. , Reno, Daniel S. , Haight, Anthony R. , Cooper, Arthur J.
IPC: C07D277/28 , A61K31/425 , C07D277/24 , C07D303/36 , C07D417/12
CPC classification number: C07D413/12 , A61K31/425 , A61K31/427 , A61K31/70 , A61K38/00 , A61K45/06 , C07C33/46 , C07C43/164 , C07C43/1742 , C07C43/2055 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/004 , C07C45/29 , C07C45/567 , C07C45/62 , C07C45/673 , 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 , C07D213/26 , C07D213/30 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/34 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D417/12 , C07K5/06026 , C07K5/06078 , A61K31/00 , A61K2300/00 , C07C49/233 , C07C49/255 , C07C49/215 , C07C49/245 , C07C49/235 , C07C49/223
Abstract: A retroviral protease inhibiting compound of formula (A) is disclosed for use in combination with other active pharmaceutical agents for treating a human infected by HIV. Intermediates and processes useful in the manufacture of compounds of formula (A) are also disclosed.
Abstract translation: 公开了式(A)的逆转录病毒蛋白酶抑制化合物与其他活性药物组合用于治疗HIV感染的人。 也公开了用于制造式(A)化合物的中间体和方法。
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公开(公告)号:EP0727419A2
公开(公告)日:1996-08-21
申请号:EP96106301.3
申请日:1993-12-16
Applicant: Abbott Laboratories
Inventor: Kempf, Dale J. , Norbeck, Daniel W. , Sham, Hing Leung , Zhao, Chen , Sowin, Thomas J. , Reno, Daniel S. , Haight, Anthony R. , Cooper, Arthur J.
IPC: C07D277/28 , A61K31/425 , C07D277/24 , C07D303/36 , C07D417/12
CPC classification number: C07D413/12 , A61K31/425 , A61K31/427 , A61K31/70 , A61K38/00 , A61K45/06 , C07C33/46 , C07C43/164 , C07C43/1742 , C07C43/2055 , C07C43/215 , C07C43/23 , C07C43/30 , C07C43/315 , C07C45/004 , C07C45/29 , C07C45/567 , C07C45/62 , C07C45/673 , 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 , C07D213/26 , C07D213/30 , C07D213/34 , C07D213/40 , C07D213/54 , C07D213/56 , C07D213/61 , C07D213/75 , C07D231/12 , C07D233/56 , C07D233/64 , C07D233/84 , C07D235/14 , C07D235/16 , C07D239/26 , C07D241/12 , C07D249/08 , C07D261/08 , C07D263/32 , C07D277/24 , C07D277/28 , C07D277/30 , C07D277/34 , C07D277/36 , C07D277/40 , C07D277/42 , C07D277/56 , C07D295/13 , C07D295/205 , C07D295/215 , C07D303/36 , C07D307/42 , C07D333/16 , C07D401/12 , C07D417/12 , C07K5/06026 , C07K5/06078 , A61K31/00 , A61K2300/00 , C07C49/233 , C07C49/255 , C07C49/215 , C07C49/245 , C07C49/235 , C07C49/223
Abstract: A retroviral protease inhibiting compound of formula (A) is disclosed for use in combination with other active pharmaceutical agents for treating a human infected by HIV. Intermediates and processes useful in the manufacture of compounds of formula (A) are also disclosed.
Abstract translation: 公开了用于与用于治疗HIV感染的人的其它活性药剂组合使用的式(A)的逆转录病毒蛋白酶抑制化合物。 还公开了可用于制备式(A)化合物的中间体和方法。
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