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ES2075672T3 - Amidinocompuestos, su fabricacion y uso como medicamento. - Google Patents

Amidinocompuestos, su fabricacion y uso como medicamento.

Info

Publication number
ES2075672T3
ES2075672T3 ES92810423T ES92810423T ES2075672T3 ES 2075672 T3 ES2075672 T3 ES 2075672T3 ES 92810423 T ES92810423 T ES 92810423T ES 92810423 T ES92810423 T ES 92810423T ES 2075672 T3 ES2075672 T3 ES 2075672T3
Authority
ES
Spain
Prior art keywords
radical
aliphatic
hydrocarbon radical
esterified
halogen
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.)
Expired - Lifetime
Application number
ES92810423T
Other languages
English (en)
Inventor
Michael M Morrissey
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.)
Novartis AG
Original Assignee
Ciba Geigy 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 Ciba Geigy AG filed Critical Ciba Geigy AG
Application granted granted Critical
Publication of ES2075672T3 publication Critical patent/ES2075672T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C251/00Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C251/02Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups
    • C07C251/04Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C251/10Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton
    • C07C251/16Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/62Compounds containing any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylcarbamates
    • C07C271/64Y being a hydrogen or a carbon atom, e.g. benzoylcarbamates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C257/00Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
    • C07C257/10Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
    • C07C257/18Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/50Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • C07C311/51Y being a hydrogen or a carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/12Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14The ring being saturated

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Pulmonology (AREA)
  • Pain & Pain Management (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Vascular Medicine (AREA)
  • Immunology (AREA)
  • Urology & Nephrology (AREA)
  • Rheumatology (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Diaphragms For Electromechanical Transducers (AREA)

Abstract

LA INVENCION SE REFIERE A COMPUESTOS DE LA FORMULA Y A LAS SALES DE LOS MISMOS FARMACEUTICAMENTE ACEPTABLES, EN DONDE: R1 ES AMINO QUE ESTA MONO O DISUBSTITUIDO POR UN SUSTITUYENTE SELECCIONADO ENTRE UN RADICAL DE HIDROCARBONO ALIFATICO, UN RADICAL DE HIDROCARBONO ARALIFATICO, UN RADICAL AROMATICO, Y UN RADICAL DE HIDROCARBONO CICLOALIFATICO O ES AMINO QUE ESTA SUSTITUIDO POR UN RADICAL DE HIDROCARBONO ALIFATICO DIVALENTE; R2 ES HIDROGENO, HALOGENO, TRIFLUOROMETIL, UN RADICAL DE HIDROCARBONO ALIFATICO, O ES HIDROXIDO QUE ESTA ESTERIFICADO POR UN ALCOHOL ALIFATICO, ARALIFATICO O AROMATICO O QUE ESTA ESTERIFICADO POR UN ACIDO CARBOXILICO ALIFATICO O ARALIFATICO; R3 ES HIDROGENO O UN RADICAL ACIL QUE SE DERIVA DE UN ACIDO CARBONICO ORGANICO, DE UN ACIDO CARBOXILICO ORGANICO, DE UN ACIDO SULFONICO O DE UN ACIDO CARBAMICO; X1 Y X3, INDEPENDIENTEMENTE UNA DE LA OTRA, SON OXIGENO (-O-) O AZUFRE (-S-); Y X2 ES UN RADICAL DE HIDROCARBONO ALIFATICO DIVALENTE QUE PUEDE ESTAR INTERRUMPIDO POR UN RADICAL AROMATICO; EN DONDE LOS ANILLOS DE FENIL DE LA FORMULA (I) PUEDEN ESTAR ADEMAS SUSTITUIDOS, INDEPENDIENTEMENTE UNOS DE LOS OTROS, POR UNO O MAS SUSTITUYENTES SELECCIONADOS ENTRE HALOGENO, TRIFLUOROMETIL, UN RADICAL DE HIDROCARBONO ALIFATICO, HIDROXIDO O HIDROXIDO QUE ESTE ESTERIFICADO POR UN ALCOHOL ALIFATICO O QUE ESTE ESTERIFICADO POR UN ACIDO CARBOXILICO ALIFATICO O ARALIFATICO; EN DONDE EL ARIL DE LAS DEFINICIONES ANTERIORES PUEDE ESTAR ADEMAS SUSTITUIDOS, INDEPENDIENTEMENTE UNOS DE LOS OTROS, POR UNO O MAS SUSTITUYENTES SELECCIONADOS ENTRE HALOGENO, TRIFLUOROMETIL, UN RADICAL DE HIDROCARBONO ALIFATICO, HIDROXIDO, E HIDROXIDO QUE ESTE ESTERIFICADO POR UN ALCOHOL ALIFATICO O QUE ESTE ESTERIFICADO POR UN ACIDO CARBOXILICO ALIFATICO O ARALIFATICO; EN DONDE EL RADICAL DE HIDROCARBONO CICLOALIFATICO PUEDE ESTAR SUSTITUIDO POR UN RADICAL ALIFATICO. LOS COMPUESTOS SON UTILES COMO ANTAGONISTAS RECEPTORES SELECTIVOS DEL LTB-4 PARA EL TRATAMIENTO DE CONDICIONES O SINDROMES EN MAMIFEROS QUE SEANSENSIBLES AL ANTAGONISMO LTB-4.
ES92810423T 1991-06-11 1992-06-02 Amidinocompuestos, su fabricacion y uso como medicamento. Expired - Lifetime ES2075672T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US71410891A 1991-06-11 1991-06-11

Publications (1)

Publication Number Publication Date
ES2075672T3 true ES2075672T3 (es) 1995-10-01

Family

ID=24868773

Family Applications (1)

Application Number Title Priority Date Filing Date
ES92810423T Expired - Lifetime ES2075672T3 (es) 1991-06-11 1992-06-02 Amidinocompuestos, su fabricacion y uso como medicamento.

Country Status (21)

Country Link
EP (1) EP0518819B1 (es)
JP (1) JP3370998B2 (es)
KR (1) KR100249068B1 (es)
AT (1) ATE125791T1 (es)
AU (1) AU653603B2 (es)
CA (1) CA2070795A1 (es)
CZ (1) CZ279630B6 (es)
DE (1) DE69203797T2 (es)
DK (1) DK0518819T3 (es)
ES (1) ES2075672T3 (es)
FI (1) FI922643A7 (es)
GR (1) GR3017028T3 (es)
HU (1) HU220226B (es)
IE (1) IE67513B1 (es)
IL (1) IL102105A (es)
MX (1) MX9202749A (es)
NO (1) NO178259C (es)
NZ (1) NZ243079A (es)
PH (1) PH30829A (es)
TW (1) TW201298B (es)
ZA (1) ZA924220B (es)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5451700A (en) * 1991-06-11 1995-09-19 Ciba-Geigy Corporation Amidino compounds, their manufacture and methods of treatment
US5488160A (en) * 1991-06-11 1996-01-30 Ciba-Geigy Corporation Amidino compounds, their manufacture and method of treatment
EP0625138B1 (de) * 1992-02-05 1999-06-02 BOEHRINGER INGELHEIM INTERNATIONAL GmbH Neue amidinderivate, ihre herstellung und verwendung als arzneimittel mit ltb4-antagonistischer wirkung
DE4219158A1 (de) * 1992-06-11 1993-12-16 Thomae Gmbh Dr K Biphenylderivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
JP2736952B2 (ja) * 1992-09-18 1998-04-08 小野薬品工業株式会社 アミジノフェノール誘導体およびその誘導体を有効成分として含有する薬剤
DE4234295A1 (de) * 1992-10-12 1994-04-14 Thomae Gmbh Dr K Carbonsäurederivate, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
DE4309285A1 (de) * 1993-03-23 1994-09-29 Boehringer Ingelheim Kg Heterocyclen enthaltende Amidinderivate, ihre Herstellung und Verwendung
DK0724435T3 (da) * 1993-10-21 2002-11-25 Searle & Co Amidinoderivater, der er nyttige som nitrogenoxid-synthase-inhibitorer
CA2134192A1 (en) * 1993-11-12 1995-05-13 Michael L. Denney 5, 6-bicyclic glycoprotein iib/iiia antagonists
DE4424713A1 (de) * 1994-07-13 1996-01-18 Boehringer Ingelheim Kg Substituierte Benzamidine, ihre Herstellung und Verwendung als Arnzneistoffe
ES2132535T3 (es) 1994-09-20 1999-08-16 Ono Pharmaceutical Co Derivados de amidinofenol como inhibidores de proteasa.
CA2265996A1 (en) * 1996-09-26 1998-04-02 Roger Aki Fujimoto Aryl-substituted acrylamides with leukotriene b4 (ltb-4) receptor antagonist activity
GB9928511D0 (en) * 1999-12-03 2000-02-02 Secr Defence Brit Orally administrable pharmaceutical product and method of fabrication therefor
WO2005027886A2 (en) * 2003-09-17 2005-03-31 Decode Genetics Ehf. Methods of preventing or treating recurrence of myocardial infarction
US7851486B2 (en) 2002-10-17 2010-12-14 Decode Genetics Ehf. Susceptibility gene for myocardial infarction, stroke, and PAOD; methods of treatment
US7507531B2 (en) 2002-10-17 2009-03-24 Decode Genetics Chf. Use of 5-lipoxygenase activating protein (FLAP) gene to assess susceptibility for myocardial infarction
US8158362B2 (en) 2005-03-30 2012-04-17 Decode Genetics Ehf. Methods of diagnosing susceptibility to myocardial infarction and screening for an LTA4H haplotype
PL1877379T3 (pl) * 2005-04-13 2013-06-28 Astex Therapeutics Ltd Pochodne hydroksybenzamidu i ich wykorzystanie, jako inhibitorów hsp90
WO2017095722A1 (en) 2015-11-30 2017-06-08 Merck Sharp & Dohme Corp. Aryl acylsulfonamides as blt1 antagonists
WO2017095725A1 (en) 2015-11-30 2017-06-08 Merck Sharp & Dohme Corp. Aryl sulfonamides as blt1 antagonists
WO2017095724A1 (en) 2015-11-30 2017-06-08 Merck Sharp & Dohme Corp. Aryl sulfonamides as blt1 antagonists
EP3383389B1 (en) 2015-11-30 2021-04-28 Merck Sharp & Dohme Corp. Aryl acylsulfonamides as blt1 antagonists

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1243322A (en) * 1984-01-23 1988-10-18 Joshua Rokach Antagonists of slow reacting substances of anaphylaxis
US4808604A (en) * 1985-10-03 1989-02-28 Ciba-Geigy Corporation N-(substituted phenyl) tetrazol-5-yl carboxamides and anti-allergic use thereof
AU626033B2 (en) * 1988-10-25 1992-07-23 Government Of The United States Of America, As Represented By The Secretary Of The Army, The Methods for the treatment and prophylaxis of pneumocystis carinii pneumonia and other diseases and compounds and formulations for use in said methods
EP0518818A3 (en) * 1991-06-11 1993-04-28 Ciba-Geigy Ag Arylethers, their manufacture and use as medicament

Also Published As

Publication number Publication date
NO178259C (no) 1996-02-21
JP3370998B2 (ja) 2003-01-27
PH30829A (en) 1997-10-17
EP0518819A3 (en) 1993-04-21
HU220226B (hu) 2001-11-28
NO922274L (no) 1992-12-14
DK0518819T3 (da) 1995-09-25
EP0518819B1 (en) 1995-08-02
KR930000470A (ko) 1993-01-15
KR100249068B1 (ko) 2000-03-15
DE69203797D1 (de) 1995-09-07
TW201298B (es) 1993-03-01
MX9202749A (es) 1992-12-01
CZ279630B6 (cs) 1995-05-17
NO922274D0 (no) 1992-06-10
IL102105A (en) 1996-10-31
ATE125791T1 (de) 1995-08-15
AU1807392A (en) 1992-12-17
EP0518819A2 (en) 1992-12-16
NZ243079A (en) 1994-11-25
FI922643A7 (fi) 1992-12-12
GR3017028T3 (en) 1995-11-30
AU653603B2 (en) 1994-10-06
HUT62264A (en) 1993-04-28
CA2070795A1 (en) 1992-12-12
DE69203797T2 (de) 1996-02-08
IE921878A1 (en) 1992-12-16
HU9201938D0 (en) 1992-08-28
FI922643A0 (fi) 1992-06-08
ZA924220B (en) 1993-02-24
IL102105A0 (en) 1993-01-14
IE67513B1 (en) 1996-04-03
CZ178092A3 (en) 1993-01-13
NO178259B (no) 1995-11-13
JPH05239009A (ja) 1993-09-17

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