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公开(公告)号:DE59306029D1
公开(公告)日:1997-05-07
申请号:DE59306029
申请日:1993-12-08
Applicant: HOECHST AG
Inventor: LANG HANS-JOCHEN DR , ENGLERT HEINRICH DR , WEICHERT ANDREAS DR , KLEEMANN HEINZ-WERNER DR , SCHOLZ WOLFGANG DR , ALBUS UDO DR
IPC: A61K31/165 , A61K31/155 , A61K49/00 , A61P1/04 , A61P9/00 , A61P9/10 , A61P35/00 , A61P43/00 , C07C279/22
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公开(公告)号:DE59305042D1
公开(公告)日:1997-02-20
申请号:DE59305042
申请日:1993-09-14
Applicant: HOECHST AG
Inventor: LANG HANS-JOCHEN DR , WEICHERT ANDREAS DR , KLEEMANN HEINZ-WERNER DR , ENGLERT HEINRICH DR , SCHOLZ WOLFGANG DR , ALBUS UDO DR
IPC: A61K31/00 , A61K31/155 , A61K31/445 , A61P1/16 , A61P9/00 , A61P9/06 , A61P9/08 , A61P9/10 , A61P9/12 , A61P13/02 , A61P15/00 , A61P35/00 , C07C311/16 , C07C311/21 , C07C311/29 , C07C317/24 , C07C317/44 , C07C317/46 , C07C317/48 , C07C323/22 , C07C323/65 , C07D211/14 , C07D211/70 , C07D295/14 , C07D295/155 , A61K31/54 , A61K31/45 , A61K49/00
Abstract: The invention relates to benzoylguanidines of the formula I where R(1) or R(2) is equal to R(3)-S(O)n- or R(4)R(5)N-O2S- and the other substituent R(1) or R(2) is in each case equal to H, OH, F, Cl, Br, I, alkyl, alkoxy, benzyloxy or phenoxy, R(3)-S(O)n or R(4)R(5)N- or 3,4-dehydropiperidine and R(3) is equal to alkyl, cycloalkyl, cyclopentylmethyl, cyclohexylmethyl or phenyl, R(4) and R(5) are equal to alkyl or phenylalkyl or phenyl, and in which R(4) and R(5) together can also be a C4-C7-chain, and in which R(4) and R(5), together with the nitrogen atom to which they are bonded, can denote a dihydroindol, tetrahydroquinoline or tetrahydroisoquinoline system, and where n is equal to zero, 1 or 2 and their pharmaceutically tolerable salts are outstanding antiarrhythmic agents. They are obtained by a process in which compounds of the formula II in which X stands for a leaving group which can be easily nucleophilically substituted, are reacted with guanidine.
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公开(公告)号:ES2089600T3
公开(公告)日:1996-10-01
申请号:ES93101842
申请日:1993-02-05
Applicant: HOECHST AG
Inventor: LANG HANS-JOCHEN DR , MANIA DIETER DR , WEICHERT ANDREAS DR , SCHOLZ WOLFGANG DR , ALBUS UDO DR , ENGLERT HEINRICH DR
IPC: A61K31/155 , A61K31/18 , A61K31/275 , A61P1/16 , A61P3/08 , A61P3/10 , A61P9/00 , A61P9/04 , A61P9/06 , A61P9/08 , A61P9/10 , A61P9/12 , A61P13/02 , A61P15/00 , A61P35/00 , A61P35/04 , C07C217/44 , C07C311/16 , C07C311/37 , C07C311/39 , C07C311/47 , C07C317/42 , C07C317/44 , C07C323/65
Abstract: There are described benzoylguanidines of the formula I where R(1) is equal to R(4)-SOm or R(5)R(6)N-SO2-, where R(4) and R(5) are equal to alk(en)yl, -CnH2n-R(7), and where R(7) is equal to cycloalkyl or phenyl, where R(5) also denotes H, R(6) is equal to H or C1-C4-alkyl, R(2) is hydrogen, halogen, alkyl, -O-(CH2)mCpF2p+1, -X-R(10), where X is equal to O, S, NR(11), R(10) is equal to H, (cyclo)alkyl(methyl), -CnH2n-R(12) where R(12) is equal to phenyl, R(3), inter alia, is defined as R(1), and their pharmaceutically tolerable salts. The compounds I are prepared by reaction of compounds of the formula II in which L represents a leaving group which can be easily substituted nucleophilically, with guanidine. Compounds I are outstandingly suitable as antiarrhythmic medicaments having a cardioprotective component for infarct prophylaxis and infract treatment and for the treatment of angina pectoris, where they also preventively inhibit or strongly decrease the pathophysiological processes during the formation of ischaemically induced damage. They are moreover distinguished by a strong inhibitory action on cell proliferation. They can therefore be used as antiatherosclerotics, agents against diabetic late complications, cancers, fibrotic disorders such as pulmonary fibrosis, fibrosis of the liver or fibrosis of the kidneys. They are effective inhibitors of the cellular sodium/protons antiporter (Na /H exchanger).
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公开(公告)号:CZ9600436A3
公开(公告)日:1996-09-11
申请号:CZ43696
申请日:1996-02-14
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH DR , GERLACH UWE DR , MANIA DIETER DR , GOGELEIN HEINZ DR , KAISER JOACHIM DR
IPC: A61K31/18 , A61K31/64 , A61P9/00 , A61P9/04 , A61P9/06 , A61P9/10 , C07C233/00 , C07C303/40 , C07C311/58 , C07C311/59 , C07C327/40 , C07C335/42 , A61K31/17 , C07C303/36 , C07C311/54
CPC classification number: C07C311/58 , C07C335/42 , Y10S514/821
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公开(公告)号:DE59302959D1
公开(公告)日:1996-07-25
申请号:DE59302959
申请日:1993-02-05
Applicant: HOECHST AG
Inventor: LANG HANS-JOCHEN DR , MANIA DIETER DR , WEICHERT ANDREAS DR , SCHOLZ WOLFGANG DR , ALBUS UDO DR , ENGLERT HEINRICH DR , LANG FLORIAN PROF DR
IPC: A61K31/155 , A61K31/18 , A61K31/275 , A61P1/16 , A61P3/08 , A61P3/10 , A61P9/00 , A61P9/04 , A61P9/06 , A61P9/08 , A61P9/10 , A61P9/12 , A61P13/02 , A61P15/00 , A61P35/00 , A61P35/04 , C07C217/44 , C07C311/16 , C07C311/37 , C07C311/39 , C07C311/47 , C07C317/42 , C07C317/44 , C07C323/65
Abstract: There are described benzoylguanidines of the formula I where R(1) is equal to R(4)-SOm or R(5)R(6)N-SO2-, where R(4) and R(5) are equal to alk(en)yl, -CnH2n-R(7), and where R(7) is equal to cycloalkyl or phenyl, where R(5) also denotes H, R(6) is equal to H or C1-C4-alkyl, R(2) is hydrogen, halogen, alkyl, -O-(CH2)mCpF2p+1, -X-R(10), where X is equal to O, S, NR(11), R(10) is equal to H, (cyclo)alkyl(methyl), -CnH2n-R(12) where R(12) is equal to phenyl, R(3), inter alia, is defined as R(1), and their pharmaceutically tolerable salts. The compounds I are prepared by reaction of compounds of the formula II in which L represents a leaving group which can be easily substituted nucleophilically, with guanidine. Compounds I are outstandingly suitable as antiarrhythmic medicaments having a cardioprotective component for infarct prophylaxis and infract treatment and for the treatment of angina pectoris, where they also preventively inhibit or strongly decrease the pathophysiological processes during the formation of ischaemically induced damage. They are moreover distinguished by a strong inhibitory action on cell proliferation. They can therefore be used as antiatherosclerotics, agents against diabetic late complications, cancers, fibrotic disorders such as pulmonary fibrosis, fibrosis of the liver or fibrosis of the kidneys. They are effective inhibitors of the cellular sodium/protons antiporter (Na /H exchanger).
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公开(公告)号:DK0547523T3
公开(公告)日:1995-09-11
申请号:DK92121155
申请日:1992-12-11
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH DR , MANIA DIETER DR , KIBAT PAUL-GERHARD DR , GEHRING DORIS , PAULUS ERICH DR
IPC: A61K31/35 , A61K9/12 , A61K31/352 , A61K31/353 , A61K31/40 , A61K31/4025 , A61K31/445 , A61P11/00 , A61P11/06 , A61P11/08 , C07D207/12 , C07D311/68 , C07D311/74 , C07D405/04
Abstract: The invention relates to ethanol adducts of the compounds of the formula I I to a process for their preparation and to their use as inhalants in diseases, in particular in asthma.
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公开(公告)号:CZ9204035A3
公开(公告)日:1993-12-15
申请号:CS403592
申请日:1992-12-31
Applicant: HOECHST AG
Inventor: ENGLERT HEINRICH DR , MANIA DIETER DR , WETTLAUFER DAVID DR , KLAUS ERIK DR
IPC: A61K31/44 , A61K31/4402 , A61K31/4406 , A61K31/4409 , A61K31/4418 , A61K31/4425 , A61P9/00 , A61P21/00 , C07D213/64 , C07D213/79 , C07D213/80 , C07D213/81 , C07D213/89 , C07D401/12
CPC classification number: C07D213/80 , C07D213/81 , C07D401/12
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公开(公告)号:CS1092A3
公开(公告)日:1992-07-15
申请号:CS1092
申请日:1992-01-03
Applicant: HOECHST AG
Inventor: WAGNER ADALBERT DR , ENGLERT HEINRICH DR , KLEEMANN HEINZ-WERNER DR , GERHARDS HERMANN DR , SCHOLKENS BERNWARD PROF 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 , C07D231/10 , C07D207/30 , C07D249/04 , C07D249/08 , A61K31/41
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:DE3527409A1
公开(公告)日:1987-02-12
申请号:DE3527409
申请日:1985-07-31
Applicant: HOECHST AG
Inventor: GREGER RAINER PROF DR , ENGLERT HEINRICH DR , LANG HANS-JOCHEN DR , HROPOT MAX DR
IPC: C07D521/00 , A61K31/195 , A61K31/196 , A61K31/33 , A61P3/00 , A61P43/00 , C07C67/00 , C07C227/00 , C07C227/08 , C07C227/16 , C07C227/18 , C07C229/56 , C07D307/52 , C07C101/54 , A61K31/19 , A61K31/34
Abstract: Compounds I where R is equal to hydrogen or alkyl, X is equal to alkylene and Ar is equal to aromatic, show an excellent detumescent action on cerebral oedemas, as well as intestinal action.
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