EP0533837A4 - Inhibition of 5-lipoxygenase and cyclooxygenase pathway mediated diseases - Google Patents

Inhibition of 5-lipoxygenase and cyclooxygenase pathway mediated diseases

Info

Publication number
EP0533837A4
EP0533837A4 EP19910912750 EP91912750A EP0533837A4 EP 0533837 A4 EP0533837 A4 EP 0533837A4 EP 19910912750 EP19910912750 EP 19910912750 EP 91912750 A EP91912750 A EP 91912750A EP 0533837 A4 EP0533837 A4 EP 0533837A4
Authority
EP
European Patent Office
Prior art keywords
lipoxygenase
inhibition
mediated diseases
pathway mediated
cyclooxygenase pathway
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP19910912750
Other versions
EP0533837A1 (en
Inventor
Jerry Leroy Adams
Paul Elliot Bender
Timothy Francis Gallagher
John Richard Heys
Carl Perchonock
Anthony John Villani
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SmithKline Beecham Corp
Original Assignee
SmithKline Beecham Corp
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 SmithKline Beecham Corp filed Critical SmithKline Beecham Corp
Publication of EP0533837A1 publication Critical patent/EP0533837A1/en
Publication of EP0533837A4 publication Critical patent/EP0533837A4/en
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
EP19910912750 1990-06-12 1991-06-07 Inhibition of 5-lipoxygenase and cyclooxygenase pathway mediated diseases Withdrawn EP0533837A4 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US53719590A 1990-06-12 1990-06-12
US537195 1990-06-12
PCT/US1991/004022 WO1991019497A1 (en) 1990-06-12 1991-06-07 Inhibition of 5-lipoxygenase and cyclooxygenase pathway mediated diseases

Publications (2)

Publication Number Publication Date
EP0533837A1 EP0533837A1 (en) 1993-03-31
EP0533837A4 true EP0533837A4 (en) 1994-11-17

Family

ID=24141624

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19910912750 Withdrawn EP0533837A4 (en) 1990-06-12 1991-06-07 Inhibition of 5-lipoxygenase and cyclooxygenase pathway mediated diseases

Country Status (10)

Country Link
EP (1) EP0533837A4 (en)
JP (1) JPH05508153A (en)
KR (1) KR930700104A (en)
AU (1) AU8205991A (en)
CA (1) CA2084290A1 (en)
IE (1) IE911977A1 (en)
NZ (1) NZ238485A (en)
PT (1) PT97960A (en)
WO (1) WO1991019497A1 (en)
ZA (1) ZA914491B (en)

Families Citing this family (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0679396A1 (en) * 1994-03-02 1995-11-02 Pfizer Inc. Use of 3-substituted-2-oxidole-1-carboxamides for the manufacture of a medicament in the treatment and prevention of ischemia induced myocardial injury and cytokine mediated myocardial injury
US5552422A (en) * 1995-01-11 1996-09-03 Merck Frosst Canada, Inc. Aryl substituted 5,5 fused aromatic nitrogen compounds as anti-inflammatory agents
AU6111796A (en) * 1995-06-12 1997-01-09 G.D. Searle & Co. Compositions comprising a cyclooxygenase-2 inhibitor and a 5 -lipoxygenase inhibitor
US7301021B2 (en) 1997-07-02 2007-11-27 Smithkline Beecham Corporation Substituted imidazole compounds
ATE317845T1 (en) 1997-09-05 2006-03-15 Glaxo Group Ltd PHARMACEUTICAL COMPOSITION CONTAINING 2,3-DIARYL-PYRAZOLO(1,5-B)PYRIDAZINE DERIVATIVES
EP1037639A4 (en) 1997-12-19 2002-04-17 Smithkline Beecham Corp Compounds of heteroaryl substituted imidazole, their pharmaceutical compositions and uses
US6858617B2 (en) 1998-05-26 2005-02-22 Smithkline Beecham Corporation Substituted imidazole compounds
CA2341370A1 (en) 1998-08-20 2000-03-02 Smithkline Beecham Corporation Novel substituted triazole compounds
KR20010075673A (en) 1998-11-03 2001-08-09 그레이엄 브레레톤, 레슬리 에드워즈 Pyrazolopyridine Derivatives as Selective COX-2 Inhibitors
AU1909200A (en) 1998-11-04 2000-05-22 Smithkline Beecham Corporation Pyridin-4-yl or pyrimidin-4-yl substituted pyrazines
AU2661400A (en) 1999-02-27 2000-09-21 Glaxo Group Limited Pyrazolopyridines
HUP0200207A3 (en) * 1999-11-10 2004-07-28 Ortho Mcneil Pharm Inc Substituted 2-aryl-3-(hetroaryl)-imidazo [1,2-a] pyrimidines, and related pharmaceutical compositions and methods for their preparation
DE60023025T2 (en) 1999-11-23 2006-07-13 Smithkline Beecham Corp. 3,4-DIHYDRO- (1H) CHINAZOLIN-2-ON COMPOUNDS AS CSBP / P39 KINASE INHIBITORS
ATE281439T1 (en) 1999-11-23 2004-11-15 Smithkline Beecham Corp 3,4-DIHYDRO-(1H)CHINAZOLINE-2-ONE COMPOUNDS AS CSBP/P38 KINASE INHIBITORS
US6759410B1 (en) 1999-11-23 2004-07-06 Smithline Beecham Corporation 3,4-dihydro-(1H)-quinazolin-2-ones and their use as CSBP/p38 kinase inhibitors
ES2241675T3 (en) 1999-11-23 2005-11-01 Smithkline Beecham Corporation 3,4-DIHIDRO- (1H) QUINAZOLIN-2-ONA COMPOUNDS AS CSPB / P38 QUINASA INHIBITORS.
GB9930358D0 (en) 1999-12-22 2000-02-09 Glaxo Group Ltd Process for the preparation of chemical compounds
US7235551B2 (en) 2000-03-02 2007-06-26 Smithkline Beecham Corporation 1,5-disubstituted-3,4-dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one compounds and their use in treating csbp/p38 kinase mediated diseases
PE20020506A1 (en) 2000-08-22 2002-07-09 Glaxo Group Ltd PIRAZOLE DERIVATIVES FUSED AS PROTEIN KINASE INHIBITORS
EP1341788B1 (en) 2000-12-15 2005-08-10 Glaxo Group Limited Pyrazolopyridines
ES2243579T3 (en) 2000-12-15 2005-12-01 Glaxo Group Ltd DERIVATIVES OF PIRAZOLOPIRIDENO.
JP2004529119A (en) 2001-03-08 2004-09-24 スミスクライン ビーチャム コーポレーション Pyrazolopyridine derivative
US6596731B2 (en) 2001-03-27 2003-07-22 Hoffmann-La Roche Inc. Substituted imidazo[1,2-A] pyridine derivatives
US7034030B2 (en) 2001-03-30 2006-04-25 Smithkline Beecham Corporation Pyralopyridines, process for their preparation and use as therapeutic compounds
ATE332301T1 (en) 2001-04-10 2006-07-15 Smithkline Beecham Corp ANTIVIRAL PYRAZOLOPYRIDINE COMPOUNDS
ATE296826T1 (en) 2001-04-27 2005-06-15 Smithkline Beecham Corp PYRAZOLO(1,5)PYRIDINE DERIVATIVES
US6756498B2 (en) 2001-04-27 2004-06-29 Smithkline Beecham Corporation Process for the preparation of chemical compounds
CZ20033518A3 (en) 2001-06-21 2004-05-12 Smithklineábeechamácorporation Imidazo(1,2-a)pyridine derivatives for the prophylaxis and treatment of herpes viral infections
JP2005508955A (en) 2001-10-05 2005-04-07 スミスクライン ビーチャム コーポレーション Imidazo-pyridine derivatives for use in the treatment of herpesvirus infections
ES2292839T3 (en) 2001-12-11 2008-03-16 Smithkline Beecham Corporation DERIVATIVES OF PIRAZOLO-PIRIDINA AS AGENTS AGAINST HERPES.
AU2003275266A1 (en) 2002-10-03 2004-05-04 Smithkline Beecham Corporation Therapeutic compounds based on pyrazolopyridine derivatives
EP1928237A4 (en) 2005-09-02 2011-03-09 Abbott Lab Novel imidazo based heterocycles
EP2170337A4 (en) 2007-06-28 2013-12-18 Abbvie Inc Novel triazolopyridazines
ES2651296T3 (en) 2009-10-30 2018-01-25 Janssen Pharmaceutica, N.V. Imidazo [1,2-b] pyridacin derivatives and their use as PDE10 inhibitors
CA2782601C (en) 2009-12-18 2015-07-21 Mitsubishi Tanabe Pharma Corporation Novel antiplatelet agent
AR080754A1 (en) 2010-03-09 2012-05-09 Janssen Pharmaceutica Nv IMIDAZO DERIVATIVES (1,2-A) PIRAZINA AND ITS USE AS PDE10 INHIBITORS
CN103649079B (en) 2010-12-22 2016-11-16 Abbvie公司 Hepatitis c inhibitor and application thereof
MX344600B (en) 2011-06-27 2016-12-20 Janssen Pharmaceutica Nv 1-ARYL-4-METHYL-[1,2,4]TRIAZOLO[4,3-a]QUINOXALINE DERIVATIVES.
EP2863909B1 (en) 2012-06-26 2020-11-04 Janssen Pharmaceutica N.V. Combinations comprising 4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline compounds as pde 2 inhibitors and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders
AU2013289284B2 (en) 2012-07-09 2017-03-30 Janssen Pharmaceutica Nv Inhibitors of phosphodiesterase 10 enzyme

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0231622A2 (en) * 1985-12-12 1987-08-12 Smithkline Beecham Corporation Inhibition of the 5-lipoxygenase pathway
EP0364204A1 (en) * 1988-10-11 1990-04-18 Smithkline Beecham Corporation Pyrrolo[1,2-a]imidazole and imidazo[1,2-a]pyridine derivatives and their use as 5-lipoxygenase pathway inhibitors
EP0411754A2 (en) * 1989-06-13 1991-02-06 Smithkline Beecham Corporation Medicament for the inhibition of interleukin-1 or tumor necrosis factor production by monocytes and/or macrophages

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0231622A2 (en) * 1985-12-12 1987-08-12 Smithkline Beecham Corporation Inhibition of the 5-lipoxygenase pathway
EP0364204A1 (en) * 1988-10-11 1990-04-18 Smithkline Beecham Corporation Pyrrolo[1,2-a]imidazole and imidazo[1,2-a]pyridine derivatives and their use as 5-lipoxygenase pathway inhibitors
EP0411754A2 (en) * 1989-06-13 1991-02-06 Smithkline Beecham Corporation Medicament for the inhibition of interleukin-1 or tumor necrosis factor production by monocytes and/or macrophages

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO9119497A1 *

Also Published As

Publication number Publication date
NZ238485A (en) 1994-03-25
AU8205991A (en) 1992-01-07
CA2084290A1 (en) 1991-12-13
WO1991019497A1 (en) 1991-12-26
ZA914491B (en) 1992-12-30
EP0533837A1 (en) 1993-03-31
JPH05508153A (en) 1993-11-18
IE911977A1 (en) 1991-12-18
PT97960A (en) 1992-03-31
KR930700104A (en) 1993-03-13

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Effective date: 19941219