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公开(公告)号:CZ9203811A3
公开(公告)日:1993-12-15
申请号:CS381192
申请日:1992-12-21
Applicant: HOECHST AG
Inventor: HEITSCH HOLGER DR , HENNING RAINER DR , WAGNER ADALBERT DR , GERHARDS HERMANN DR , BECKER REINHARD DR , SCHOLKENS BERNWARD PROF DR
IPC: A61K31/415 , A61K31/4164 , A61K31/64 , A61P9/10 , A61P9/12 , C07D233/84 , C07D233/86 , C07D233/90
CPC classification number: C07D233/84 , C07D233/90
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公开(公告)号:CZ416291A3
公开(公告)日:1993-09-15
申请号:CS416291
申请日:1991-12-30
Applicant: HOECHST AG
Inventor: TEETZ VOLKER DR , GEIGER ROLF PROF DR , URBACH HANSJORG DR , BECKER REINHARD DR , SCHOLKENS BERNWARD DR
IPC: C07C227/08 , A61K31/40 , A61K31/403 , A61K38/00 , A61P9/12 , C07C227/10 , C07C227/16 , C07C229/28 , C07C229/36 , C07C237/06 , C07D209/52 , C07D451/04 , C07K5/02 , C07K5/06
Abstract: Compounds of the formula I (I) in which the carboxyl group on carbon atom 3 is orientated in the endo-position relative to the bicyclic ring system of cis-configuration, and in which R1 denotes hydrogen, allyl, vinyl or a side-chain of a naturally occurring alpha -aminoacid, which may be protected, R2 denotes hydrogen, alkyl, alkenyl or aralkyl, Y denotes hydrogen or hydroxyl and Z denotes hydrogen, or Y and Z together denote oxygen, and X denotes alkyl, alkenyl or cycloalkyl, or aryl which is optionally mono-, di- or tri-substituted by alkyl, alkoxy, hydroxyl, halogen, nitro, amino, alkylamino, dialkylamino or methylenedioxy, or denotes indol-3-yl, a process for their preparation, agents containing these compounds and their use.
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公开(公告)号:BR9200011A
公开(公告)日:1992-09-08
申请号:BR9200011
申请日:1992-01-03
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , ENGLERT HEINRICH DR , KLEEMANN HEINZ-WERNER DR , GERHARDS HERMANN DR , SCHOELKENS BERNWARD DR , BECKER REINHARD DR , LINZ WOLFGANG DR
IPC: A61K31/40 , A61K31/415 , A61K31/425 , A61K31/435 , A61K31/44 , A61K31/4427 , A61K31/443 , A61K31/4433 , A61K31/445 , A61K31/505 , A61K31/535 , A61K31/54 , A61K31/64 , A61P9/00 , A61P9/08 , A61P9/10 , A61P9/12 , A61P13/02 , A61P15/00 , A61P43/00 , C07D207/34 , C07D207/36 , C07D233/54 , C07D233/66 , C07D233/68 , C07D233/70 , C07D233/84 , C07D233/90 , C07D249/02 , C07D255/02 , C07D257/02 , C07D257/04 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D417/12 , C07D453/02 , C07D521/00 , C07D231/12 , C07D409/14
Abstract: Azole derivative of the general formula (I) in which A, L, O, R , X, Y, Z and q have the meanings given, a process for their preparation, pharmaceutical preparations and the use of the compounds are described. Azole derivatives of the formula I where the symbols have, for example, the following meanings: R = (C2-C10)-alkyl Z = nitrogen X and Y = independently of one another CR L = -CH2- q = zero or 1 A = biphenyl radical which is substituted, for example, by R R = halogen or hydrogen R = SO2-NH-CO-OR and R = phenyl, are highly active antagonists of angiotensin II receptors.
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公开(公告)号:DE3685177D1
公开(公告)日:1992-06-11
申请号:DE3685177
申请日:1986-08-29
Applicant: HOECHST AG
Inventor: BECKER REINHARD DR , GEIGER ROLF PROF DR , HENNING RAINER DR , TEETZ VOLKER DR , URBACH HANSJOERG DR
Abstract: The preparation contains an angiotensin converting enzyme inhibitor and a loop diuretic.
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公开(公告)号:AT75610T
公开(公告)日:1992-05-15
申请号:AT86111973
申请日:1986-08-29
Applicant: HOECHST AG
Inventor: BECKER REINHARD DR , GEIGER ROLF PROF DR , HENNING RAINER DR , TEETZ VOLKER DR , URBACH HANSJOERG DR
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公开(公告)号:CS9104095A3
公开(公告)日:1992-04-15
申请号:CS409591
申请日:1991-12-27
Applicant: HOECHST AG
Inventor: URBACH HANSJORG DR , HENNING RAINER DR , TEETZ VOLKER DR , GEIGER ROLF PROF DR , BECKER REINHARD DR , GAUL HOLGER
IPC: A61K38/55 , A61K31/40 , A61K31/403 , A61K31/404 , A61K38/00 , A61P7/10 , A61P9/08 , A61P9/12 , C07D209/02 , C07D209/08 , C07D209/32 , C07D209/34 , C07D209/42 , C07D209/52 , C07D215/22 , C07D215/227 , C07K1/02 , C07K1/113 , C07K5/02 , C07K5/06
CPC classification number: C07D215/227 , A61K38/00 , C07D209/08 , C07D209/34 , C07D209/42 , C07D209/52 , C07K5/0222
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公开(公告)号:AT74366T
公开(公告)日:1992-04-15
申请号:AT86106515
申请日:1986-05-14
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , BECKER REINHARD DR
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公开(公告)号:AT53203T
公开(公告)日:1990-06-15
申请号:AT84107607
申请日:1984-06-30
Applicant: HOECHST AG
Inventor: URBACH HANSJOERG DR , HENNING RAINER DR , BECKER REINHARD DR
IPC: A61K31/40 , A61K31/403 , A61K31/405 , A61K38/00 , A61K38/55 , A61P9/12 , A61P43/00 , C07D209/52 , C07D221/04 , C07K1/113 , C07K5/02 , C07K5/06 , C07K5/08 , C07K14/81
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公开(公告)号:DE3731085A1
公开(公告)日:1989-04-06
申请号:DE3731085
申请日:1987-09-16
Applicant: HOECHST AG
Inventor: RUEGER WOLFGANG DR , URBACH HANSJOERG DR , BECKER REINHARD DR , HOCK FRANZ DR
IPC: C07D317/34 , A61K38/00 , A61K38/55 , A61P25/28 , A61P29/00 , C07D317/36 , C07D317/40 , C07D405/12 , C07K1/02 , C07K1/113 , C07K5/02 , C07K5/06 , C07K14/81
Abstract: The esters have the formula I … … in which n is 1 or 2, R, R , R and R are hydrogen or a defined radical, R together with R and the atoms carrying them form a heterocyclic ring system.
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公开(公告)号:DE3476067D1
公开(公告)日:1989-02-16
申请号:DE3476067
申请日:1984-01-09
Applicant: HOECHST AG
Inventor: HENNING RAINER DR , URBACH HANSJORG DR , TEETZ VOLKER DR , BECKER REINHARD DR
IPC: A61K38/00 , A61K38/55 , A61P9/12 , A61P43/00 , C07D209/96 , C07D317/28 , C07D317/30 , C07D317/32 , C07D317/72 , C07K1/02 , C07K1/113 , C07K5/02 , C07K5/06 , C07K5/078 , C07K14/81 , A61K37/02
Abstract: The invention relates to new spirocyclic aminoacid derivatives of the formula I (I) in which m denotes 1 or 2, n denotes 0 or 1, R denotes hydrogen, alkyl or aralkyl, R1 denotes hydrogen or alkyl which can be optionally substituted by amino, acylamino or benzoylamino, alkenyl, cycloalkyl, cycloalkenyl, cycloalkylalkyl, aryl or partially hydrogenated aryl, each of which can be substituted by alkyl, alkoxy or halogen, arylalkyl or aroylalkyl, both of which can be substituted as defined above in the aryl radical, an S- or O- and/or N-heterocyclic radical or a side chain of an alpha -aminoacid, R2 denotes hydrogen, alkyl, alkenyl or aralkyl, Y denotes hydrogen or hydroxyl, Z denotes hydrogen, or Y and Z together denote oxygen and X denotes alkyl, alkenyl, cycloalkyl, aryl, which can be monosubstituted, disubstituted or trisubstituted by alkyl, alkoxy, hydroxyl, halogen, nitro, amino, alkylamino, dialkylamino and/or methylenedioxy, or 3-indolyl, processes for their preparation, agents containing them and their use and new spirocyclic aminoacids as intermediates and a process for their preparation.
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