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公开(公告)号:CA2089442C
公开(公告)日:2005-08-23
申请号:CA2089442
申请日:1993-02-12
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH , MANIA DIETER , LANG HANS-JOCHEN , SCHOLZ WOLFGANG , LINZ WOLFGANG , ALBUS UDO
IPC: A61K31/155 , A61K31/165 , A61K31/445 , A61P1/16 , A61P3/08 , A61P3/10 , A61P9/00 , A61P9/04 , A61P9/06 , A61P9/08 , A61P9/10 , A61P9/12 , A61P13/02 , A61P15/00 , A61P35/00 , C07C279/22 , C07D213/65 , C07D295/14 , C07D295/155 , C07D401/12 , A61K31/40
Abstract: Amino-substituted benzoylguanidines, process for their preparation, their use as a medicament and medicament containing them Benzoylguanidines of the formula I are described in which R(1) or R(2) is an amino group -NR(3)R(4), where R(3) and R(4) are H or (cyclo)alkyl or R(3) is phenyl-(CH2)P- where p = 0, 1, 2, 3 or 4, or phenyl, or R(3) and R(4) can also together be a methylene chain, and in which the other substituent R(1) or R(2) in each case is H, F, C1, alkyl, alkoxy, CF3, C m F2m+1-CH2-, benzyl or phenoxy, and their pharmaceutically tolerable salts. The compounds according to the invention have very good antiarrhythmic properties, as occur, for example, in the case of oxygen deficiency symptoms. The compounds are used as antiarrhythmic pharmaceuticals having a cardioprotective component for infarct prophylaxis and infarct treatment as well as for the treatment of angina pectoris, where they also preventively inhibit or greatly decrease the pathophysiological processes in the formation of ischemically induced damage, in particular in the production of ischemically induced cardiac arrhythmias.
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公开(公告)号:PL179268B1
公开(公告)日:2000-08-31
申请号:PL32617094
申请日:1994-02-22
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH , MANIA DIETER , HARTUNG JENS , GOEGELEIN HEINZ , KAISER JOACHIM , LINZ WOLFGANG , WETTLAUFER DAVID
IPC: A61K31/64 , A61P9/00 , A61K31/18 , A61P9/04 , A61P9/10 , C07C303/40 , C07C311/46 , C07C311/58 , C07C323/67 , C07C335/42 , A61K31/17
Abstract: There are described benzenesulphonylureas and -thioureas of the formula I where R(1) is H, (fluoro)methyl, R(2) is H, Hal, (fluoro)(mercapto) alkyl(oxy), E is O, S; Y is -[CR(3)2]n- where R(3) = H or alkyl and n = 1 - 4, X is H, Hal, alkyl, Z is Hal, NO2, alkyl(oxy). The compounds (I) are used for the treatment of cardiac arrhythmias and for the prevention of sudden heart death due to arrhythmias and can therefore be used as antiarrhythmics. They are particularly suitable for those cases in which arrhythmias are the result of constriction of a coronary vessel, such as in angina pectoris or in acute cardiac infarct.
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公开(公告)号:BR9705660A
公开(公告)日:1999-11-23
申请号:BR9705660
申请日:1997-11-13
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN , GERLACH UWE , MANIA DIETER , LINZ WOLFGANG , GOEGELEIN HEINZ , KLAUS ERIK
IPC: B05C17/02 , C07D311/70 , A61K31/64 , C07D405/12
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公开(公告)号:PL330412A1
公开(公告)日:1999-05-10
申请号:PL33041297
申请日:1997-05-20
Applicant: HOECHST AG
Inventor: LANG HANS JOHEN , JANSEN HANS-WILLI , SCHWARK JAN-ROBERT , KLEEMANN HEINZ-WERNER , JUNG OLIVER , SCHAEFER HANS-LUDWIG , LINZ WOLFGANG , KRAMER WERNER , SCHOELKENS BERNWARD , FALK EUGEN
IPC: A61K31/155 , A61K31/00 , A61K31/166 , A61K31/22 , A61K31/255 , A61K31/365 , A61K31/41 , A61K31/455 , A61K45/00 , A61K45/06 , A61P3/00 , A61P3/06 , A61P9/00 , A61P9/10 , A61P43/00
Abstract: The active substances identified as inhibitors of the cellular Na /H exchanger (NHE) are used to prepare a medicament for normalizing serum lipids. They are used in the preparation of a medicament which reduces lipid levels in the blood and can be administered for treating diseases caused by lipid levels which are too high, and for alleviating the endothelial dysfunctional syndrome and for treating diseases caused thereby.
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公开(公告)号:AU4515497A
公开(公告)日:1998-05-21
申请号:AU4515497
申请日:1997-11-13
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN , GERLACH UWE , MANIA DIETER , LINZ WOLFGANG , GOEGELEIN HEINZ , KLAUS ERIK
IPC: C07D311/04 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/355 , A61K31/40 , A61K31/4025 , A61P9/00 , A61P9/06 , C07D207/26 , C07D209/34 , C07D211/76 , C07D217/24 , C07D227/02 , C07D311/16 , C07D311/18 , C07D311/42 , C07D311/58 , C07D311/70 , C07D405/12 , C07D401/12 , C07D403/12
Abstract: 3-Amido-chromanylsulphonyl-urea or -thiourea derivatives of formula (I), in all stereoisomer (or mixture) forms, and their salts are new. R1 = H, alkyl, alkoxy, alkoxyalkoxy, alkylthio, F, Cl, Br, I or CF3; R2 = H, Me or Et; R3 = H or alkyl; Z = O or S; A = phenyl (optionally substituted by 1-3 halo, Me, Et, OMe or OEt), lactam residue of formula (i), 1-oxo-1,2,3,4-tetrahydroisoquinolin-2-yl, 1-oxo-perhydroisoquinolin-2-yl, 1-oxo-2,3-isoindolin-2-yl or 1-oxo-perhydroisoindolin-2-yl; B = 3-6C alkylene or 3-6C alkenylene (both optionally substituted by 1-3 alkyl); all alkyl moieties have 1-4C.
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公开(公告)号:NO975214L
公开(公告)日:1998-05-15
申请号:NO975214
申请日:1997-11-13
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN , GERLACH UWE , MANIA DIETER , LINZ WOLFGANG , GAEGELEIN HEINZ , KLAUS ERIK
IPC: C07D311/04 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/355 , A61K31/40 , A61K31/4025 , A61P9/00 , A61P9/06 , C07D207/26 , C07D209/34 , C07D211/76 , C07D217/24 , C07D227/02 , C07D311/16 , C07D311/18 , C07D311/42 , C07D311/58 , C07D311/70 , C07D405/12 , C07D311/20
Abstract: 3-Amido-chromanylsulphonyl-urea or -thiourea derivatives of formula (I), in all stereoisomer (or mixture) forms, and their salts are new. R1 = H, alkyl, alkoxy, alkoxyalkoxy, alkylthio, F, Cl, Br, I or CF3; R2 = H, Me or Et; R3 = H or alkyl; Z = O or S; A = phenyl (optionally substituted by 1-3 halo, Me, Et, OMe or OEt), lactam residue of formula (i), 1-oxo-1,2,3,4-tetrahydroisoquinolin-2-yl, 1-oxo-perhydroisoquinolin-2-yl, 1-oxo-2,3-isoindolin-2-yl or 1-oxo-perhydroisoindolin-2-yl; B = 3-6C alkylene or 3-6C alkenylene (both optionally substituted by 1-3 alkyl); all alkyl moieties have 1-4C.
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公开(公告)号:ZA9704828B
公开(公告)日:1997-12-03
申请号:ZA9704828
申请日:1997-06-02
Applicant: HOECHST AG
Inventor: LANG HANS JOCHEN , JANSEN HANS-WILLI , SCHWARK JAN-ROBERT , KLEEMANN HEINZ-WERNER , JUNG OLIVER , SCHAEFER HANS-LUDWIG , LINZ WOLFGANG , KRAMER WERNER , SCHOELKENS BERNWARD , FALK EUGEN
IPC: A61K31/155 , A61K31/00 , A61K31/166 , A61K31/22 , A61K31/255 , A61K31/365 , A61K31/41 , A61K31/455 , A61K45/00 , A61K45/06 , A61P3/00 , A61P3/06 , A61P9/00 , A61P9/10 , A61P43/00 , A61K
CPC classification number: A61K31/166 , A61K31/00 , A61K31/155 , A61K31/22 , A61K31/365 , A61K31/165 , A61K2300/00
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公开(公告)号:MX9606397A
公开(公告)日:1997-10-31
申请号:MX9606397
申请日:1996-12-13
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN , GERLACH UWE , MANIA DIETER , LINZ WOLFGANG , GOGELEIN HEINZ , KLAUS ERIK , CRAUSE PETER
IPC: A61K31/35 , A61K31/352 , C07D311/58 , A61K31/353 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/4412 , A61K31/443 , A61K31/445 , A61P9/00 , A61P9/06 , A61P9/10 , C07D311/64 , C07D311/70 , C07D405/12 , C07D311/02 , A61K31/335
Abstract: Las cromanilsufonil(tio)ureas de formula I, son valiosos medicamentos para el tratamiento de trastornos del ritmo cardíaco y para prevenir la muerte cardíaca subita causada por arritmias. Pueden utilizarse como agentes antiarrítmicos, y son apropiadas para prevenir la muerte cardíaca subita, para el tratamiento de la insuficiencia cardíaca, y también del fracaso cardíaco en actuaciones de choque.
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公开(公告)号:PL317397A1
公开(公告)日:1997-06-23
申请号:PL31739796
申请日:1996-12-09
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN , GERLACH UWE , MANIA DIETER , LINZ WOLFGANG , GOEGELEIN HEINZ , KLAUS ERIK , CRAUSE PETER
IPC: A61K31/35 , A61K31/352 , A61K31/353 , C07D311/58 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/4412 , A61K31/443 , A61K31/445 , A61P9/00 , A61P9/06 , A61P9/10 , C07D311/64 , C07D311/70 , C07D405/12 , A61K31/64
Abstract: N-(4-Amidoalkyl-chroman-5-yl-sulphonyl)-urea or -thiourea derivatives of formula (I) and their salts are new. R1 = H, alkyl, alkoxy, F, Cl, Br, I, CF3, NH2, mono- or dialkylamino or alkylthio; R2a = H, Me or Et; R2b, R2d = H, Me or Et; or phenyl or benzyl (both optionally ring-substituted by 1-3 of halogen, Me, Et, OMe and OEt); R2c,R2e = H, Me or Et; R3 = H, alkyl, cycloalkyl, cycloalkylmethyl or CF3; n = 1 or 2; Z = O or S; A = phenyl (optionally substituted by 1-3 of halogen, Me, OMe, Et or OEt), a lactam residue of formula (a), 1-oxo-1,2,3,4-tetrahydroisoquinolin-2-yl, 1-oxo-per-hydro-isoquinolin-2-yl, 1-oxo-1,2-dihydro-iso-indol-2-yl or 1-oxo-per-hydro-iso-indol-2-yl; B = 3-6C alkylene or 3-6C alkenylene (both optionally substituted by 1-3 alkyl); unless specified otherwise alkyl moieties have 1-4C and cycloalkyl moieties 3-6C.
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公开(公告)号:ZA9610461B
公开(公告)日:1997-06-17
申请号:ZA9610461
申请日:1996-12-12
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH CHRISTIAN , GERLACH UWE , MANIA DIETER , LINZ WOLFGANG , GOEGELEIN HEINZ , KLAUS ERIK , CRAUSE PETER
IPC: A61K31/35 , A61K31/352 , C07D311/58 , A61K31/353 , A61K31/40 , A61K31/4015 , A61K31/4025 , A61K31/4412 , A61K31/443 , A61K31/445 , A61P9/00 , A61P9/06 , A61P9/10 , C07D311/64 , C07D311/70 , C07D405/12 , C07D , A61K
Abstract: N-(4-Amidoalkyl-chroman-5-yl-sulphonyl)-urea or -thiourea derivatives of formula (I) and their salts are new. R1 = H, alkyl, alkoxy, F, Cl, Br, I, CF3, NH2, mono- or dialkylamino or alkylthio; R2a = H, Me or Et; R2b, R2d = H, Me or Et; or phenyl or benzyl (both optionally ring-substituted by 1-3 of halogen, Me, Et, OMe and OEt); R2c,R2e = H, Me or Et; R3 = H, alkyl, cycloalkyl, cycloalkylmethyl or CF3; n = 1 or 2; Z = O or S; A = phenyl (optionally substituted by 1-3 of halogen, Me, OMe, Et or OEt), a lactam residue of formula (a), 1-oxo-1,2,3,4-tetrahydroisoquinolin-2-yl, 1-oxo-per-hydro-isoquinolin-2-yl, 1-oxo-1,2-dihydro-iso-indol-2-yl or 1-oxo-per-hydro-iso-indol-2-yl; B = 3-6C alkylene or 3-6C alkenylene (both optionally substituted by 1-3 alkyl); unless specified otherwise alkyl moieties have 1-4C and cycloalkyl moieties 3-6C.
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