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公开(公告)号:DE4036782A1
公开(公告)日:1992-05-21
申请号:DE4036782
申请日:1990-11-17
Applicant: BASF AG
Inventor: LUBISCH WILFRIED DR , PHILIPSBORN GERDA VON DR MED , SCHULT SABINE DR , KIRCHENGAST MICHAEL DR
IPC: A61K31/165 , A61K31/00 , A61K31/16 , A61K31/167 , A61K31/40 , A61K31/445 , A61K31/4453 , A61P9/00 , A61P9/06 , C07C233/29 , C07C235/38 , C07D295/08 , C07D295/088 , C07D295/092
Abstract: Substituted anilides of the formula I I (where R1 is C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, halogen, cyano, nitro, C2-C4-alkenyl, C2-C4-alkynyl; X is methylene, ethylene, vinylene; R2 and R3 are each C1-C4-alkyl, C3-C6-cycloalkyl or together are tetra- or pentamethylene; R4 is C1-C4-alkyl, methoxy; n is 2, 3 or 4), and the physiologically tolerated acid addition salts thereof, the pharmaceutical use thereof, drugs produced therefrom and the use thereof for treating cardiac arrhythmias and/or for lowering the heart rate, are described.
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公开(公告)号:DE59204456D1
公开(公告)日:1996-01-11
申请号:DE59204456
申请日:1992-02-29
Applicant: BASF AG
Inventor: LUBISCH WILFRIED DR , SCHULT SABINE DR , BEHL BERTHOLD DR , KIRCHENGAST MICHAEL DR
IPC: A61K31/445 , A61K31/4427 , A61K31/4465 , A61K31/4468 , A61K31/451 , A61K31/495 , A61K31/496 , A61P9/06 , C07D211/26 , C07D211/56 , C07D211/58 , C07D401/04 , C07D401/06
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公开(公告)号:DE4117904A1
公开(公告)日:1992-12-03
申请号:DE4117904
申请日:1991-05-31
Applicant: BASF AG
Inventor: LUBISCH WILFRIED DR , SCHULT SABINE DR , BEHL BERTHOLD DR , KIRCHENGAST MICHAEL DR
IPC: C07D211/26 , C07D211/56 , C07D211/58 , C07D401/04
Abstract: Substituted N-phenylpiperidines I (* CHEMICAL STRUCTURE *) I (R1=H, NO2, CN, halogen, C1-C4-alkyl, CF3, OCF3, OH, CH2OH, COOH, CHO, NH-CHO, NH2, CO-NH2, 5-tetrazinyl, R4-O-, R4-O-CH2-, R4O-CO-, R4-CO-, R4-NH-CO, R4-CO-NH-, R4-SO2-NH-; R2=H, NO2, halogen, C1-C4-alkyl or R4-O-; (* CHEMICAL STRUCTURE *) (* CHEMICAL STRUCTURE *) (* CHEMICAL STRUCTURE *) (* CHEMICAL STRUCTURE *) (* CHEMICAL STRUCTURE *) R4=C1-C4-alkyl or phenyl which can carry one of the R2 radicals; R5, R6=H or one of the R4 radicals; R7 =one of the R1 radicals; n=0 or 1; m=1 or 2; with the proviso that R3 is (* CHEMICAL STRUCTURE *) only when n is 1, and the optical isomers in the case of optical isomerism, and the physiologically tolerated acid addition salts, are suitable as drugs.
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公开(公告)号:AT130851T
公开(公告)日:1995-12-15
申请号:AT92103514
申请日:1992-02-29
Applicant: BASF AG
Inventor: LUBISCH WILFRIED DR , SCHULT SABINE DR , BEHL BERTHOLD DR , KIRCHENGAST MICHAEL DR
IPC: A61K31/445 , A61K31/4427 , A61K31/4465 , A61K31/4468 , A61K31/451 , A61K31/495 , A61K31/496 , A61P9/06 , C07D211/26 , C07D211/56 , C07D211/58 , C07D401/04 , C07D401/06 , C07D211/00 , C07D215/00
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公开(公告)号:DE59107342D1
公开(公告)日:1996-03-14
申请号:DE59107342
申请日:1991-11-07
Applicant: BASF AG
Inventor: LUBISCH WILFRIED DR , VON PHILIPSBORN GERDA DR , SCHULT SABINE DR , KIRCHENGAST MICHAEL DR
IPC: A61K31/165 , A61K31/00 , A61K31/16 , A61K31/167 , A61K31/40 , A61K31/445 , A61K31/4453 , A61P9/00 , A61P9/06 , C07C233/29 , C07C235/38 , C07D295/08 , C07D295/088 , C07D295/092
Abstract: Substituted anilides of the formula I I (where R1 is C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, halogen, cyano, nitro, C2-C4-alkenyl, C2-C4-alkynyl; X is methylene, ethylene, vinylene; R2 and R3 are each C1-C4-alkyl, C3-C6-cycloalkyl or together are tetra- or pentamethylene; R4 is C1-C4-alkyl, methoxy; n is 2, 3 or 4), and the physiologically tolerated acid addition salts thereof, the pharmaceutical use thereof, drugs produced therefrom and the use thereof for treating cardiac arrhythmias and/or for lowering the heart rate, are described.
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公开(公告)号:AT133668T
公开(公告)日:1996-02-15
申请号:AT91118954
申请日:1991-11-07
Applicant: BASF AG
Inventor: LUBISCH WILFRIED DR , VON PHILIPSBORN GERDA DR , SCHULT SABINE DR , KIRCHENGAST MICHAEL DR
IPC: A61K31/165 , A61K31/00 , A61K31/16 , A61K31/167 , A61K31/40 , A61K31/445 , A61K31/4453 , A61P9/00 , A61P9/06 , C07C233/29 , C07C235/38 , C07D295/08 , C07D295/088 , C07D295/092
Abstract: Substituted anilides of the formula I I (where R1 is C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, halogen, cyano, nitro, C2-C4-alkenyl, C2-C4-alkynyl; X is methylene, ethylene, vinylene; R2 and R3 are each C1-C4-alkyl, C3-C6-cycloalkyl or together are tetra- or pentamethylene; R4 is C1-C4-alkyl, methoxy; n is 2, 3 or 4), and the physiologically tolerated acid addition salts thereof, the pharmaceutical use thereof, drugs produced therefrom and the use thereof for treating cardiac arrhythmias and/or for lowering the heart rate, are described.
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公开(公告)号:DE4114330A1
公开(公告)日:1992-11-05
申请号:DE4114330
申请日:1991-05-02
Applicant: BASF AG
Inventor: KIRCHENGAST MICHAEL DR , RUEBSAMEN KLAUS DR , SCHMIED BERNHARD DR , SEITZ WERNER DR
IPC: A61K31/275 , A61K45/06
Abstract: The description relates to combinations of medicaments of calcium/serotonin antagonists and thromboxane-A2-receptors suitable for treating diseases.
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