WO1997015555A3 - Imidazolderivate und deren verwendung als stickstoffmonoxid-synthase-inhibitoren - Google Patents

Imidazolderivate und deren verwendung als stickstoffmonoxid-synthase-inhibitoren Download PDF

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Publication number
WO1997015555A3
WO1997015555A3 PCT/DE1996/002079 DE9602079W WO9715555A3 WO 1997015555 A3 WO1997015555 A3 WO 1997015555A3 DE 9602079 W DE9602079 W DE 9602079W WO 9715555 A3 WO9715555 A3 WO 9715555A3
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WO
WIPO (PCT)
Prior art keywords
nitrogen monoxide
imidazole derivatives
synthase inhibitors
monoxide synthase
inhibitors
Prior art date
Application number
PCT/DE1996/002079
Other languages
English (en)
French (fr)
Other versions
WO1997015555A2 (de
Inventor
Peter Hoelscher
Hartmut Rehwinkel
Gerardine Burton
Gary Phillips
John Parkinson
Original Assignee
Schering Ag
Peter Hoelscher
Hartmut Rehwinkel
Gerardine Burton
Gary Phillips
John Parkinson
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 Schering Ag, Peter Hoelscher, Hartmut Rehwinkel, Gerardine Burton, Gary Phillips, John Parkinson filed Critical Schering Ag
Priority to EP96944573A priority Critical patent/EP0857171A2/de
Priority to AU13009/97A priority patent/AU1300997A/en
Priority to JP9516208A priority patent/JPH11515008A/ja
Publication of WO1997015555A2 publication Critical patent/WO1997015555A2/de
Publication of WO1997015555A3 publication Critical patent/WO1997015555A3/de

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic 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
    • C07D233/56Heterocyclic 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 only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic 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
    • C07D233/66Heterocyclic 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
    • C07D233/68Halogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Die Erfindung betrifft die Verbindungen der Formel (I), deren Herstellung und Verwendung in Arzneimitteln.
PCT/DE1996/002079 1995-10-25 1996-10-24 Imidazolderivate und deren verwendung als stickstoffmonoxid-synthase-inhibitoren WO1997015555A2 (de)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP96944573A EP0857171A2 (de) 1995-10-25 1996-10-24 Imidazolderivate und deren verwendung als stickstoffmonoxid-synthase-inhibitoren
AU13009/97A AU1300997A (en) 1995-10-25 1996-10-24 Imidazole derivatives and the use thereof as nitrogen monoxide synthase inhibitors
JP9516208A JPH11515008A (ja) 1995-10-25 1996-10-24 イミダゾール誘導体及びその一酸化窒素合成酵素阻害剤としての使用

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19541146.3 1995-10-25
DE19541146A DE19541146A1 (de) 1995-10-25 1995-10-25 Imidazolderivate und deren Verwendung als Stickstoffmonoxid-Synthase-Inhibitoren

Publications (2)

Publication Number Publication Date
WO1997015555A2 WO1997015555A2 (de) 1997-05-01
WO1997015555A3 true WO1997015555A3 (de) 1997-07-10

Family

ID=7776625

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/DE1996/002079 WO1997015555A2 (de) 1995-10-25 1996-10-24 Imidazolderivate und deren verwendung als stickstoffmonoxid-synthase-inhibitoren

Country Status (7)

Country Link
EP (1) EP0857171A2 (de)
JP (1) JPH11515008A (de)
AU (1) AU1300997A (de)
CA (1) CA2235621A1 (de)
DE (1) DE19541146A1 (de)
WO (1) WO1997015555A2 (de)
ZA (1) ZA969019B (de)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
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DE19627310A1 (de) * 1996-06-27 1998-01-02 Schering Ag Imidazolderivate als Stickstoffmonoxid-Synthase-Inhibitoren
DE69715769T2 (de) * 1996-11-04 2003-05-28 Bayer Cropscience S.A., Lyon 1-Polyarylpyrazole als Pestizide
EP1186296B1 (de) * 1999-05-25 2007-04-18 Mitsubishi Pharma Corporation PROMOTOREN FüR DIE EXPRESSION DES MYELIN ASSOZIIERTEN GLYCOPROTEINS (MAG)
AUPQ142599A0 (en) * 1999-07-05 1999-07-29 Fujisawa Pharmaceutical Co., Ltd. New amide compounds
US6525051B2 (en) * 2000-03-27 2003-02-25 Schering Aktiengesellschaft N-heterocyclic derivatives as NOS inhibitors
AU2001264223A1 (en) * 2000-06-28 2002-01-08 Ssp Co., Ltd. Imidazole derivatives or salts thereof and drugs containing the derivatives or the salts
EP1178038A1 (de) * 2000-08-04 2002-02-06 Aventis Cropscience S.A. Fungizide Phenylamidin Derivative
NZ528450A (en) 2001-05-11 2006-02-24 Biovitrum Ab Novel, arylsulfonamide compounds for the treatment of obesity, type II diabetes and CNS-disorders
US7718650B2 (en) 2001-05-11 2010-05-18 Biovitrum Ab Aryl sulfonamide compounds for treating obesity
PL375375A1 (en) * 2002-08-02 2005-11-28 Pharmacia Corporation Methods for treatment and prevention of gastrointestinal conditions
US7449481B2 (en) * 2004-04-13 2008-11-11 Cephalon, Inc. Thio-substituted biaryl-methanesulfinyl derivatives
US20070123572A1 (en) * 2005-11-28 2007-05-31 Kalypsys, Inc. Novel method of preparation of 5-chloro-3-imidazol-1-yl-[1,2,4]thiadiazole and (3-imidazol-1-yl-[1,2,4]thiadiazol-5yl)-dialkyl-amines
JP2008521908A (ja) * 2004-12-01 2008-06-26 カリプシス・インコーポレーテッド 誘導型一酸化窒素シンターゼ阻害剤
EP1741708A1 (de) * 2005-06-28 2007-01-10 Sanofi-Aventis Deutschland GmbH Heteroaryl substituierte Amide mit ungesättigtem oder zyklischem Linker, und deren Verwendung als Pharmaka
WO2007039580A1 (en) * 2005-10-05 2007-04-12 Nycomed Gmbh Imidazolyl-substituted benzophenone compounds
WO2007039578A1 (en) * 2005-10-05 2007-04-12 Nycomed Gmbh Imidazolyl-substituted azabenzophenone compounds
EP2674417A3 (de) * 2007-11-21 2014-04-09 Decode Genetics EHF Biaryl-PDE4-Inhibitoren zur Behandlung von Entzündungen
AU2010234526B2 (en) 2009-04-06 2016-07-21 Agios Pharmaceuticals, Inc. Pyruvate kinase M2 modulators, therapeutic compositions and related methods of use
NZ597379A (en) 2009-06-29 2014-04-30 Agios Pharmaceuticals Inc Therapeutic compounds and compositions
DK2448581T3 (en) 2009-06-29 2017-03-13 Agios Pharmaceuticals Inc Therapeutic compositions and methods for their applications
WO2012083246A1 (en) 2010-12-17 2012-06-21 Agios Pharmaceuticals, Inc. Novel n- (4- (azetidine - 1 - carbonyl) phenyl) - (hetero - ) arylsulfonamide derivatives as pyruvate kinase m2 (pmk2) modulators
CA2822432C (en) 2010-12-21 2019-09-24 Agios Pharmaceuticals, Inc. Bicyclic pkm2 activators
TWI549947B (zh) 2010-12-29 2016-09-21 阿吉歐斯製藥公司 治療化合物及組成物
US9181231B2 (en) 2011-05-03 2015-11-10 Agios Pharmaceuticals, Inc Pyruvate kinase activators for use for increasing lifetime of the red blood cells and treating anemia
CN108451955B (zh) 2011-05-03 2022-02-01 安吉奥斯医药品有限公司 用于治疗的丙酮酸激酶活化剂
WO2014139144A1 (en) 2013-03-15 2014-09-18 Agios Pharmaceuticals, Inc. Therapeutic compounds and compositions
US9206211B2 (en) 2013-04-17 2015-12-08 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
CN105439946B (zh) * 2014-08-13 2018-02-02 益方生物科技(上海)有限公司 羧酸化合物及其制备方法和用途
PL3307271T3 (pl) 2015-06-11 2024-02-05 Agios Pharmaceuticals, Inc. Sposoby stosowania aktywatorów kinazy pirogronianowej
TWI780281B (zh) * 2017-12-14 2022-10-11 丹麥商Nmd藥品公司 用於治療神經肌肉病症的化合物

Citations (5)

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Publication number Priority date Publication date Assignee Title
US3541109A (en) * 1968-06-25 1970-11-17 Du Pont 1-substituted imidazoles useful in acth reserve assay
FR2267101A1 (de) * 1974-04-11 1975-11-07 Schering Ag
EP0270091A1 (de) * 1986-12-02 1988-06-08 Tanabe Seiyaku Co., Ltd. Imidazol-Derivate, Verfahren zu ihrer Herstellung, pharmazeutische Zubereitungen, welche diese enthalten, Verwendung dieser zur Herstellung therapeutisch wirksamer Arzneimittel und Zwischenprodukte, welche beim Herstellungsverfahren entstehen
EP0385850A2 (de) * 1989-03-03 1990-09-05 Laboratoires Upsa Benzimidazol- und Azabenzimidazol-Derivate, Verfahren zu deren Herstellung, Synthese-Zwischenprodukte, diese enthaltende pharmazeutische Zusammensetzungen, verwendbar bei der Behandlung von Herzgefässerkrankungen und duodenalem Ulcus
DE3942475A1 (de) * 1989-12-22 1991-06-27 Basf Ag Substituierte salicylsaeurealkylester und verfahren zu ihrer herstellung

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3541109A (en) * 1968-06-25 1970-11-17 Du Pont 1-substituted imidazoles useful in acth reserve assay
FR2267101A1 (de) * 1974-04-11 1975-11-07 Schering Ag
EP0270091A1 (de) * 1986-12-02 1988-06-08 Tanabe Seiyaku Co., Ltd. Imidazol-Derivate, Verfahren zu ihrer Herstellung, pharmazeutische Zubereitungen, welche diese enthalten, Verwendung dieser zur Herstellung therapeutisch wirksamer Arzneimittel und Zwischenprodukte, welche beim Herstellungsverfahren entstehen
EP0385850A2 (de) * 1989-03-03 1990-09-05 Laboratoires Upsa Benzimidazol- und Azabenzimidazol-Derivate, Verfahren zu deren Herstellung, Synthese-Zwischenprodukte, diese enthaltende pharmazeutische Zusammensetzungen, verwendbar bei der Behandlung von Herzgefässerkrankungen und duodenalem Ulcus
DE3942475A1 (de) * 1989-12-22 1991-06-27 Basf Ag Substituierte salicylsaeurealkylester und verfahren zu ihrer herstellung

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BRITISH JOURNAL OF PHARMACOLOGY, vol. 119, no. 2, 1996, pages 423 - 31 *
C. ESCOLASTICO ET. AL.: "Imidazole and Benzimidazole Addition to Quinones. Formation of meso and d,l Isomers and Crystal Structure of the d,l Isomer of 2,3-Bis(benzimidazol-1'-yl)- 1,4-Dihydroxybenzene.", TETRAHEDRON, vol. 50, no. 43, 1994, OXFORD, GB, pages 12489 - 12510, XP000652111 *
CHEMICAL ABSTRACTS, vol. 125, no. 21, 18 November 1996, Columbus, Ohio, US; abstract no. 265016r, R. L. HANDY ET. AL.: "Inhibition of nitric oxide synthase by 1-(2-trifluoromethylphenyl) imidazole." page 38; column 1; XP002029806 *
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Also Published As

Publication number Publication date
EP0857171A2 (de) 1998-08-12
AU1300997A (en) 1997-05-15
DE19541146A1 (de) 1997-04-30
JPH11515008A (ja) 1999-12-21
CA2235621A1 (en) 1997-05-01
ZA969019B (en) 1997-05-29
WO1997015555A2 (de) 1997-05-01

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