PH31466A - Imidazole derivatives with a biphenylsulfonyl-ureaor biphenyl-sulfonylurethane side chain, process for their preparation and their use. - Google Patents

Imidazole derivatives with a biphenylsulfonyl-ureaor biphenyl-sulfonylurethane side chain, process for their preparation and their use.

Info

Publication number
PH31466A
PH31466A PH45819A PH45819A PH31466A PH 31466 A PH31466 A PH 31466A PH 45819 A PH45819 A PH 45819A PH 45819 A PH45819 A PH 45819A PH 31466 A PH31466 A PH 31466A
Authority
PH
Philippines
Prior art keywords
ureaor
sulfonylurethane
biphenylsulfonyl
biphenyl
preparation
Prior art date
Application number
PH45819A
Other languages
English (en)
Inventor
Heitsch Holger
Gerhards Hermann
Scholkens Bernward
Henning Rainer
Wagner Adalbert
Becker Reinhard
Original Assignee
Hoechst Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoechst Ag filed Critical Hoechst Ag
Publication of PH31466A publication Critical patent/PH31466A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/84—Sulfur atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Cephalosporin Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
PH45819A 1992-03-07 1993-03-05 Imidazole derivatives with a biphenylsulfonyl-ureaor biphenyl-sulfonylurethane side chain, process for their preparation and their use. PH31466A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4207241 1992-03-07

Publications (1)

Publication Number Publication Date
PH31466A true PH31466A (en) 1998-11-03

Family

ID=6453463

Family Applications (1)

Application Number Title Priority Date Filing Date
PH45819A PH31466A (en) 1992-03-07 1993-03-05 Imidazole derivatives with a biphenylsulfonyl-ureaor biphenyl-sulfonylurethane side chain, process for their preparation and their use.

Country Status (25)

Country Link
US (1) US5604251A (fr)
EP (1) EP0560177B1 (fr)
JP (1) JP3542813B2 (fr)
KR (1) KR930019637A (fr)
CN (1) CN1036341C (fr)
AT (1) ATE230732T1 (fr)
AU (1) AU663565B2 (fr)
BR (1) BR9300761A (fr)
CA (1) CA2091135A1 (fr)
CZ (1) CZ281983B6 (fr)
DE (1) DE59310323D1 (fr)
DK (1) DK0560177T3 (fr)
ES (1) ES2187501T3 (fr)
FI (1) FI930970A7 (fr)
HU (1) HUT64041A (fr)
IL (1) IL104971A0 (fr)
MA (1) MA22814A1 (fr)
NO (1) NO303632B1 (fr)
NZ (1) NZ247059A (fr)
PH (1) PH31466A (fr)
PL (1) PL173023B1 (fr)
RU (1) RU2116300C1 (fr)
SK (1) SK279109B6 (fr)
TW (1) TW215434B (fr)
ZA (1) ZA931585B (fr)

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DE4010797A1 (de) * 1990-04-04 1991-10-10 Hoechst Ag Substituierte azole, verfahren zu deren herstellung, diese enthaltende mittel und deren verwendung
US5514696A (en) * 1992-05-06 1996-05-07 Bristol-Myers Squibb Co. Phenyl sulfonamide endothelin antagonists
CA2111662C (fr) * 1992-12-17 2004-11-23 Hiroaki Yanagisawa Derives de biphenyles, leur preparation et leur utilisation pour le traitement de l'hypertension et des maladies cardiaques
FR2716883B1 (fr) * 1994-03-04 1996-04-26 Roussel Uclaf Nouveaux dérivés tétrasubstitués de l'imidazole, leur préparation, nouveaux intermédiaires obtenus, leur application à titre de médicaments, compositions pharmaceutiques les renfermant.
FR2716882B1 (fr) * 1994-03-04 1996-04-05 Roussel Uclaf Utilisation de dérivés de l'imidazole au traitement d'affections impliquant les récepteurs AT1 et AT2 de l'Angiotensine, certains de ces produits, leur préparation, compositions pharmaceutiques.
US5612359A (en) * 1994-08-26 1997-03-18 Bristol-Myers Squibb Company Substituted biphenyl isoxazole sulfonamides
US5760038A (en) * 1995-02-06 1998-06-02 Bristol-Myers Squibb Company Substituted biphenyl sulfonamide endothelin antagonists
US5780473A (en) * 1995-02-06 1998-07-14 Bristol-Myers Squibb Company Substituted biphenyl sulfonamide endothelin antagonists
US5846990A (en) * 1995-07-24 1998-12-08 Bristol-Myers Squibb Co. Substituted biphenyl isoxazole sulfonamides
JPH09124620A (ja) 1995-10-11 1997-05-13 Bristol Myers Squibb Co 置換ビフェニルスルホンアミドエンドセリン拮抗剤
US5856507A (en) * 1997-01-21 1999-01-05 Bristol-Myers Squibb Co. Methods for the preparation of biphenyl isoxazole sulfonamides
BR9708151A (pt) 1996-02-20 1999-07-27 Bristol Myers Squibb Co Processo para a preparaç o de bifenil isoxazol sulfonamidas
US5939446A (en) * 1996-04-09 1999-08-17 Bristol-Myers Squibb Co. Heteroaryl substituted phenyl isoxazole sulfonamide endothelin antagonists
DE69734832T2 (de) * 1996-12-13 2006-08-31 Zymogenetics, Inc., Seattle Zusammensetzungen und verfahren zum stimulieren von knochenwachstum
EP0855392A3 (fr) 1997-01-22 2000-01-05 Hoechst Aktiengesellschaft Hétérocycles à cinq chaínons contenant des substituants biphénylylsulphoniques, leur procédé de préparation, leur utilisation comme médicament ou agent diagnostique ainsi que médicament les contenant
TW536540B (en) * 1997-01-30 2003-06-11 Bristol Myers Squibb Co Endothelin antagonists: N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide and N-(4,5-dimethyl-3-isoxazolyl)-2'-[(3,3-dimethyl-2-oxo-1-pyrrolidinyl)methyl]-4'-(2-oxazolyl)[1,1'-biphe
AU6187898A (en) * 1997-01-30 1998-08-25 Bristol-Myers Squibb Company Method for preventing or treating low renin hypertension by administering an endothelin antagonist
AU748334B2 (en) 1997-10-16 2002-05-30 Board Of Regents, The University Of Texas System Models and treatments for cardiac hypertrophy in relation with NF-AT3 function
DE19802969A1 (de) 1998-01-27 1999-07-29 Hoechst Marion Roussel De Gmbh Verfahren zur Herstellung von S-Alkyl(Aryl)-substituierten Imidazol-Derivaten
DE19820064A1 (de) * 1998-05-06 1999-11-11 Hoechst Marion Roussel De Gmbh Substituierte Sulfonylcyanamide, Verfahren zu ihrer Herstellung und ihre Verwendung als Medikament
DE19832429A1 (de) * 1998-07-18 2000-01-20 Hoechst Marion Roussel De Gmbh Imidazolderivate mit Biphenylsulfonylsubstitution, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament
DE19832428A1 (de) * 1998-07-18 2000-01-20 Hoechst Marion Roussel De Gmbh Imidazolderivate mit Biphenylsulfonylsubstitution, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament
EP1165472A4 (fr) 1999-03-19 2002-11-20 Bristol Myers Squibb Co Procedes pour la preparation de diphenylisoxazolesulfonamides
US20040106647A1 (en) * 2002-06-28 2004-06-03 Schneider Michael D. Modulators of Cdk9 as a therapeutic target in cardiac hypertrophy
WO2004002226A1 (fr) * 2002-06-28 2004-01-08 Baylor College Of Medicine Modulateurs de cdk9 utilises comme cible therapeutique dans l'hypertrophie cardiaque
EP1631268A2 (fr) * 2003-05-21 2006-03-08 Board Of Regents The University Of Texas System Inhibition de la proteine kinase c-mu (pkd) dans le traitement de l'hypertrophie cardiaque et de l'insuffisance cardiaque
US8309562B2 (en) * 2003-07-03 2012-11-13 Myrexis, Inc. Compounds and therapeutical use thereof
CN1984660B (zh) 2003-07-03 2010-12-15 美瑞德生物工程公司 作为天冬氨酸特异性半胱氨酸蛋白酶活化剂和细胞程序死亡诱导剂的4-芳基氨基-喹唑啉
DE602004016547D1 (de) * 2003-11-03 2008-10-23 Myogen Inc 1,4-dihydropyridinverbindungen, pharmazeutische verbindungen, und verfahren zur behandlung von herzkreislauferkrankungen
EP1685108B1 (fr) * 2003-11-03 2008-07-23 Myogen, Inc. Composes1,4-dihydropyridine, compositions pharmaceutiques et methodes de traitement des maladies cardiovasculaires
EP1699436A2 (fr) * 2003-12-12 2006-09-13 Myogen, Inc. Preparations a base d'enoximone et leur utilisation pour traiter l'hypertrophie cardiaque et l'insuffisance cardiaque
WO2005092332A1 (fr) * 2004-03-22 2005-10-06 Myogen, Inc. Sulfoxyde de (s)-enoximone et son utilisation dans le traitement de maladies mediees par pde-iii
US20060030611A1 (en) * 2004-03-22 2006-02-09 Myogen, Inc. Enoximone sulfoxide enantiomers and their use in the treatment of PDE-III mediated diseases
CA2572179A1 (fr) * 2004-06-23 2006-01-19 Myogen, Inc. Formulations d'enoximone et utilisation dans le traitement de maladies a mediation par pde-iii
EP1833482A4 (fr) 2005-01-03 2011-02-16 Myriad Genetics Inc Composés bicycliques azotés et utilisation thérapeutique associée
US8258145B2 (en) * 2005-01-03 2012-09-04 Myrexis, Inc. Method of treating brain cancer
WO2007014029A2 (fr) * 2005-07-22 2007-02-01 The Regents Of The University Of Colorado, A Body Corporate Yin yang 1 utilise comme traitement pour une hypertrophie cardiaque et pour une insuffisance cardiaque
CA2634158A1 (fr) * 2005-12-20 2007-06-28 Gilead Colorado, Inc. Utilisation de composes de 4,7-dihydrothieno¬2,3-b|pyridine dans le traitement de maladies cardiovasculaires
ES2397439T3 (es) 2006-08-01 2013-03-07 Board Of Regents Of The University Of Texas System Identificación de un microARN que activa la expresión de la cadena pesada beta de la miosina
US8440636B2 (en) 2007-07-31 2013-05-14 The Board Of Regents, The University Of Texas System Micro-RNA family that modulates fibrosis and uses thereof
EP2265291B1 (fr) 2008-03-17 2016-10-19 The Board of Regents of The University of Texas System Identification des micro-arn dans l'entretien et la régénération de synapses neuromusculaires
US9539427B2 (en) 2010-11-08 2017-01-10 The Johns Hopkins University Methods for improving heart function
GB2605148A (en) * 2021-03-23 2022-09-28 Vicore Pharma Ab New compounds

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JPS5671074A (en) * 1979-11-12 1981-06-13 Takeda Chem Ind Ltd 1,2-disubstituted-4-halogenoimidazole-5-acetic acid derivative
US4355044A (en) * 1980-12-19 1982-10-19 Bernardo Heller D-Phenylalanine treatment
US5138069A (en) * 1986-07-11 1992-08-11 E. I. Du Pont De Nemours And Company Angiotensin II receptor blocking imidazoles
CA1334092C (fr) * 1986-07-11 1995-01-24 David John Carini Imidazoles bloquant les recepteurs de l'angiotensine ii
SU1518949A1 (ru) * 1987-04-09 1995-04-30 Всесоюзный научно-исследовательский институт химии и технологии лекарственных средств Способ получения инъекционного раствора 5-этокси-2-этилтиобензимидазола
CA1338238C (fr) * 1988-01-07 1996-04-09 David John Carini Imidazoles bloquant les recepteurs de l'angiotensine ii et combinaisons de ces imidazoles avec des diuretiques et des anti-inflammatoires non steroidiens
US5015651A (en) * 1988-01-07 1991-05-14 E. I. Du Pont De Nemours And Company Treatment of hypertension with 1,2,4-angiotensin II antagonists
US5064825A (en) * 1989-06-01 1991-11-12 Merck & Co., Inc. Angiotensin ii antagonists
DE4010797A1 (de) * 1990-04-04 1991-10-10 Hoechst Ag Substituierte azole, verfahren zu deren herstellung, diese enthaltende mittel und deren verwendung
NZ238688A (en) * 1990-06-28 1992-05-26 Smithkline Beecham Corp Substituted histidines: pharmaceutical compositions, preparation and uses thereof
US5135197A (en) * 1990-08-30 1992-08-04 Qualtec Data Products, Inc. Equipment security method and apparatus
US5126342A (en) * 1990-10-01 1992-06-30 Merck & Co., Inc. Imidazole angiotensin ii antagonists incorporating acidic functional groups
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Also Published As

Publication number Publication date
CZ381192A3 (en) 1993-12-15
NO930817L (no) 1993-09-08
DK0560177T3 (da) 2003-04-14
BR9300761A (pt) 1993-09-14
DE59310323D1 (de) 2003-02-13
KR930019637A (ko) 1993-10-18
SK381192A3 (en) 1998-06-03
NO930817D0 (no) 1993-03-05
ES2187501T3 (es) 2003-06-16
PL173023B1 (pl) 1998-01-30
CA2091135A1 (fr) 1993-09-08
JP3542813B2 (ja) 2004-07-14
RU2116300C1 (ru) 1998-07-27
HUT64041A (en) 1993-11-29
AU663565B2 (en) 1995-10-12
SK279109B6 (sk) 1998-06-03
HU9300618D0 (en) 1993-05-28
ZA931585B (en) 1993-09-27
PL297955A1 (en) 1993-09-20
NZ247059A (en) 1995-03-28
AU3401193A (en) 1993-09-09
ATE230732T1 (de) 2003-01-15
FI930970A0 (fi) 1993-03-04
TW215434B (fr) 1993-11-01
MA22814A1 (fr) 1993-10-01
US5604251A (en) 1997-02-18
CN1036341C (zh) 1997-11-05
EP0560177A1 (fr) 1993-09-15
NO303632B1 (no) 1998-08-10
EP0560177B1 (fr) 2003-01-08
FI930970A7 (fi) 1993-09-08
JPH069572A (ja) 1994-01-18
CZ281983B6 (cs) 1997-04-16
IL104971A0 (en) 1993-07-08
CN1076192A (zh) 1993-09-15

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