ES2184876T3 - Derivados de imidazol sustituidos en 1h-4(5). - Google Patents

Derivados de imidazol sustituidos en 1h-4(5).

Info

Publication number
ES2184876T3
ES2184876T3 ES96921378T ES96921378T ES2184876T3 ES 2184876 T3 ES2184876 T3 ES 2184876T3 ES 96921378 T ES96921378 T ES 96921378T ES 96921378 T ES96921378 T ES 96921378T ES 2184876 T3 ES2184876 T3 ES 2184876T3
Authority
ES
Spain
Prior art keywords
formula
present
lower alkyl
disorders
compounds
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
ES96921378T
Other languages
English (en)
Inventor
James G Phillips
Amin Mohammed Khan
Clark E Tedford
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.)
Gliatech Inc
Original Assignee
Gliatech Inc
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 Gliatech Inc filed Critical Gliatech Inc
Application granted granted Critical
Publication of ES2184876T3 publication Critical patent/ES2184876T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C07D233/64Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/41641,3-Diazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic 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
    • A61K31/42Oxazoles
    • A61K31/422Oxazoles not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Obesity (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Luminescent Compositions (AREA)
  • Liquid Crystal Substances (AREA)

Abstract

LA PRESENTE INVENCION ESTA DIRIGIDA A DERIVADOS DE IMIDAZOL 1H (B); O (C) EN LAS CUALES R SUB,1} ES ALQUILO INFERIOR O ALCOXI INFERIOR; R SUB,2}, R SUB,3}, R SUB,4}, R SUB,5}, R SUB,7} Y R SUB,8} SON CADA UNO INDEPENDIENTEMENTE HIDROGENO O ALQUILO INFERIOR; R SUB,6} ES HIDROGENO, ALQUILO INFERIOR O ALCOXI INFERIOR, Y R SUB,5} Y R SUB,6} PUEDEN TOMARSE CONJUNTAMENTE PARA FORMAR UN ANILLO DE 4, 5 O 6 ESLABONES. LOS COMPUESTOS DE FORMULA (I) PRESENTAN ACTIVIDAD AGONISTA DEL RECEPTOR DE HISTAMINA H SUB,3}. TAMBIEN SE CONTEMPLA QUE LAS SALES FARMACEUTICAMENTE ACEPTABLES Y LOS ESTEREOISOMEROS INDIVIDUALES DE LOS COMPUESTOS DE FORMULA (I) ANTERIOR, ASI COMO LAS MEZCLAS DE LOS MISMOS, SE ENCUENTRAN DENTRO DEL ALCANCE DE LA PRESENTE INVENCION. LA PRESENTE INVENCION TAMBIEN DESCRIBE COMPOSICIONES FARMACEUTICAS QUE INCLUYEN UN VEHICULO FARMACEUTICAMENTE ACEPTABLE JUNTO CON UNA CANTIDAD EFICAZ DE UN COMPUESTO DE FORMULA (I). LA PRESENTE INVENCION TAMBIEN DESCRIBE UN PROCEDIMIENTO PARA TRATAR TRASTORNOSEN LOS CUALES LA ACTIVACION DE LOS RECEPTORES H SUB,3} DE HISTAMINA PUEDE PRESENTAR IMPORTANCIA TERAPEUTICA, TALES COMO ALERGIA, INFLAMACION, ENFERMEDAD CARDIO (ES DECIR, HIPER ASCULAR, MIGRAÑA), TRASTORNOS GASTROINTESTINALES (SECRECION DE ACIDOS, MOTILIDAD) Y TRASTORNOS DE SNC QUE IMPLICAN TRASTORNOS PSIQUIATRICOS (ES DECIR, QUE INCLUYEN ANSIEDAD, TRASTORNOS MANIACO/DEPRESIVO, ESQUIZOFRENIA, TRASTORNOS OBSESIVO OS, ETC.).
ES96921378T 1995-06-07 1996-06-06 Derivados de imidazol sustituidos en 1h-4(5). Expired - Lifetime ES2184876T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US47992595A 1995-06-07 1995-06-07

Publications (1)

Publication Number Publication Date
ES2184876T3 true ES2184876T3 (es) 2003-04-16

Family

ID=23905996

Family Applications (1)

Application Number Title Priority Date Filing Date
ES96921378T Expired - Lifetime ES2184876T3 (es) 1995-06-07 1996-06-06 Derivados de imidazol sustituidos en 1h-4(5).

Country Status (11)

Country Link
EP (1) EP0841923B1 (es)
JP (1) JPH11507631A (es)
AT (1) ATE224193T1 (es)
AU (1) AU713166B2 (es)
CA (1) CA2222652A1 (es)
DE (1) DE69623784T2 (es)
DK (1) DK0841923T3 (es)
ES (1) ES2184876T3 (es)
NZ (1) NZ311318A (es)
PT (1) PT841923E (es)
WO (1) WO1996040126A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6133291A (en) * 1998-10-16 2000-10-17 Schering Corporation N-(imidazolylalkyl)substituted cyclic amines as histamine-H3 agonists or antagonists
AU3033100A (en) * 1999-01-18 2000-08-01 Boehringer Ingelheim International Gmbh Substituted imidazoles, their preparation and use
US6908926B1 (en) 1999-04-16 2005-06-21 Novo Nordisk A/S Substituted imidazoles, their preparation and use
US6610721B2 (en) 2000-03-17 2003-08-26 Novo Nordisk A/S Imidazo heterocyclic compounds
US6437147B1 (en) 2000-03-17 2002-08-20 Novo Nordisk Imidazole compounds
WO2002013821A1 (en) 2000-08-17 2002-02-21 Gliatech, Inc. Novel alicyclic imidazoles as h3 agents
CN1960977B (zh) * 2004-05-31 2010-07-21 万有制药株式会社 喹唑啉衍生物
EP1707203A1 (en) 2005-04-01 2006-10-04 Bioprojet Treatment of parkinson's disease obstructive sleep apnea, dementia with lewy bodies, vascular dementia with non-imidazole alkylamines histamine H3- receptor ligands
EP1717233A1 (en) 2005-04-29 2006-11-02 Bioprojet Histamine H3-receptor ligands and their therapeutic application
EP1717235A3 (en) 2005-04-29 2007-02-28 Bioprojet Phenoxypropylpiperidines and -pyrrolidines and their use as histamine H3-receptor ligands
WO2013151982A1 (en) 2012-04-03 2013-10-10 Arena Pharmaceuticals, Inc. Methods and compounds useful in treating pruritus, and methods for identifying such compounds
EP2740474A1 (en) 2012-12-05 2014-06-11 Instituto Europeo di Oncologia S.r.l. Cyclopropylamine derivatives useful as inhibitors of histone demethylases kdm1a

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2586562B1 (fr) * 1985-09-02 1989-03-10 Inst Nat Sante Rech Med Composition pharmaceutique contenant de l'a-methylhistamine
WO1993012093A1 (en) * 1991-12-18 1993-06-24 Schering Corporation Imidazolyl-alkyl-piperazine and -diazepine derivatives as histamine h3 agonists/antagonists

Also Published As

Publication number Publication date
EP0841923B1 (en) 2002-09-18
EP0841923A4 (en) 1999-04-28
CA2222652A1 (en) 1996-12-19
DE69623784T2 (de) 2003-05-15
AU713166B2 (en) 1999-11-25
JPH11507631A (ja) 1999-07-06
ATE224193T1 (de) 2002-10-15
EP0841923A1 (en) 1998-05-20
AU6248296A (en) 1996-12-30
DK0841923T3 (da) 2003-01-27
DE69623784D1 (de) 2002-10-24
PT841923E (pt) 2003-01-31
WO1996040126A1 (en) 1996-12-19
NZ311318A (en) 2000-08-25

Similar Documents

Publication Publication Date Title
ES2184876T3 (es) Derivados de imidazol sustituidos en 1h-4(5).
MX9709211A (es) Derivados de 2-(1h-4(5)-imidazoil) ciclopropilo.
PE20021005A1 (es) Quinazolinas como inhibidores de mmp-13
RU2004109812A (ru) Ингибиторы цистеинпротеазы 2-циано-4-аминопиримидинового строения с ингибирующим действием на катепсин к для лечения воспалительных и других заболеваний
ATE466860T1 (de) Cgrp-rezeptorantagonisten
DE69118082D1 (de) Imidazolderivate, starke und selektive Angiotensin-II-Rezeptor-Antagonisten
PE20020917A1 (es) Derivados de imidazol como bloqueadores del receptor n-metil-d-aspartato
PE20011035A1 (es) Ureas ciclicas sustituidas como antagonistas de los receptores de neuroquinina
ES2111650T3 (es) Derivados aciclicos de etilenodiamina como antagonistas de receptores de la sustancia p.
DE602005027230D1 (de) Cgrp-rezeptorantagonisten
PE20060770A1 (es) Derivados de n-[(4,5-difenil-3-alquil-2-tienil)metil]amina como antagonistas de los receptores cannabinoides cb1
CO6150176A2 (es) Derivados de bencimidazol utiles en el tratamiento de los trastornos relacionados con el receptor vaniloide trpv1
MXPA02011418A (es) 1-aminoalquil-lactamas sustituidas y su uso como antagonistas del receptor muscarinico.
EA200200731A1 (ru) Производные фенилпиперазинила
EA200501122A1 (ru) Замещенные алкиламидопиперидины
ATE316078T1 (de) 1,3,5-triazine-2,4,6-trione, herstellung und anwendungen als antagonisten der gonadotropin- freisetzenden hormonrezeptoren
PL340711A1 (en) Derivatives of 5-(2-imidazolinamino)-benzimidazole, their production and application of them as antagonists of alpha-adrenergic receptors of improved metabolic stability
UY25864A1 (es) Derivados de acetamida antagonistas de receptor de nk1
PE20090967A1 (es) Derivados de imidazolidina 2,4-diona como moduladores del receptor npy y2
PE20050475A1 (es) Antagonistas de la hormona concentradora de melanina
BRPI0510564A (pt) compostos e tautÈmeros, estereoisÈmeros, e sais farmacologicamente aceitáveis dos mesmos, composições farmacêuticas, método para preparar composições farmacêuticas, e, uso de um composto
RU2002121777A (ru) Новые производные имидазола
PE80099A1 (es) Compuesto de amonio cuaternario
RU2005102586A (ru) 2,5-замещенные производные пиримидина в качестве антагонистов ix рецептора ccr-3
DE60224509D1 (de) Imidazolderivate verwendbar als histamin h3 rezeptorliganden