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UY26372A1 - "imidazo-3-il-aminas bicíclicas procedimiento para su preparación y medicamentos que las contienen " - Google Patents

"imidazo-3-il-aminas bicíclicas procedimiento para su preparación y medicamentos que las contienen "

Info

Publication number
UY26372A1
UY26372A1 UY26372A UY26372A UY26372A1 UY 26372 A1 UY26372 A1 UY 26372A1 UY 26372 A UY26372 A UY 26372A UY 26372 A UY26372 A UY 26372A UY 26372 A1 UY26372 A1 UY 26372A1
Authority
UY
Uruguay
Prior art keywords
preparation
imidazo
bicíclicas
aminas
drugs
Prior art date
Application number
UY26372A
Other languages
English (en)
Inventor
Dr Matthias Gerlach
Dr Corinna Maul
Original Assignee
Gruenenthal Chemie
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
Priority claimed from DE1999148438 external-priority patent/DE19948438B4/de
Priority claimed from DE19948434A external-priority patent/DE19948434A1/de
Application filed by Gruenenthal Chemie filed Critical Gruenenthal Chemie
Publication of UY26372A1 publication Critical patent/UY26372A1/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P23/00—Anaesthetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02—Phosphorus compounds
    • C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
    • C—CHEMISTRY; METALLURGY
    • C40—COMBINATORIAL TECHNOLOGY
    • C40B—COMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES
    • C40B40/00—Libraries per se, e.g. arrays, mixtures

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (AREA)
  • Anesthesiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Imidazo-3-il-aminas bicíclicas de la fórmula generamente aceptables, procedimiento para su preparación y medicamentos que contienen como sustancia activa al menos un imidazo-3- il-amina bicíclica de la fórmula general I en forma de su base o una sal farmacéuticamente aceptable.
UY26372A 1999-10-08 2000-10-05 "imidazo-3-il-aminas bicíclicas procedimiento para su preparación y medicamentos que las contienen " UY26372A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE1999148438 DE19948438B4 (de) 1999-10-08 1999-10-08 Bicyclische Imidazo-3-aminderivate
DE19948434A DE19948434A1 (de) 1999-10-08 1999-10-08 Substanzbibliothek enthaltend bicyclische Imidazo-5-amine und/oder bicyclische Imidazo-3-amine

Publications (1)

Publication Number Publication Date
UY26372A1 true UY26372A1 (es) 2000-12-29

Family

ID=26055218

Family Applications (1)

Application Number Title Priority Date Filing Date
UY26372A UY26372A1 (es) 1999-10-08 2000-10-05 "imidazo-3-il-aminas bicíclicas procedimiento para su preparación y medicamentos que las contienen "

Country Status (26)

Country Link
US (1) US6638933B2 (es)
EP (1) EP1218382B1 (es)
JP (1) JP2003511451A (es)
KR (1) KR100756592B1 (es)
CN (1) CN1257169C (es)
AR (1) AR025962A1 (es)
AT (1) ATE258554T1 (es)
AU (1) AU779197B2 (es)
BR (1) BR0014818A (es)
CA (1) CA2382919C (es)
CO (1) CO5251378A1 (es)
CZ (1) CZ20021210A3 (es)
DE (1) DE50005155D1 (es)
DK (1) DK1218382T3 (es)
ES (1) ES2213611T3 (es)
HK (1) HK1047747B (es)
HU (1) HUP0203052A3 (es)
NO (1) NO322754B1 (es)
NZ (2) NZ518439A (es)
PE (1) PE20010634A1 (es)
PL (1) PL355206A1 (es)
PT (1) PT1218382E (es)
RU (1) RU2264402C2 (es)
SK (1) SK286788B6 (es)
UY (1) UY26372A1 (es)
WO (1) WO2001027111A2 (es)

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US20040077605A1 (en) 2001-06-20 2004-04-22 Salvati Mark E. Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
DE10043845A1 (de) * 2000-09-06 2002-03-14 Gruenenthal Gmbh Verfahren zur Messung der Aktivität der NO-Synthase
EP1854798A3 (en) 2000-09-19 2007-11-28 Bristol-Myers Squibb Company Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
EP1343785A2 (de) * 2000-12-13 2003-09-17 Basf Aktiengesellschaft Verwendung von substituierten imidazoazinen, neue imidazoazine, verfahren zu deren herstellung, sowie sie enthaltende mittel
US20040087548A1 (en) 2001-02-27 2004-05-06 Salvati Mark E. Fused cyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
ES2310622T3 (es) 2001-12-19 2009-01-16 Bristol-Myers Squibb Company Compuestos heterociclicos condensados y analogos de los mismos, moduladores de la funcion de los receptores nucleares de hormonas.
DE102004021716A1 (de) * 2004-04-30 2005-12-01 Grünenthal GmbH Substituierte Imidazo[1,2-a]pyridin-Verbindungen und Arzneimittel enthaltend substituierte Imidazo[1,2-a]pyridin-Verbindungen
ATE424208T1 (de) * 2004-06-09 2009-03-15 Oncalis Ag Proteinkinaseinhibitoren
US7923041B2 (en) * 2005-02-03 2011-04-12 Signum Biosciences, Inc. Compositions and methods for enhancing cognitive function
RU2412943C2 (ru) * 2005-03-23 2011-02-27 Ф. Хоффманн-Ля Рош Аг ПРОИЗВОДНЫЕ АЦЕТИЛЕНИЛ-ПИРАЗОЛО-ПИРИМИДИНА В КАЧЕСТВЕ АНТАГОНИСТОВ mGluR2
WO2006125101A2 (en) * 2005-05-20 2006-11-23 Array Biopharma Inc. Raf inhibitor compounds and methods of use thereof
CA2611391A1 (en) * 2005-06-09 2006-12-14 Oncalis Ag Angiogenesis inhibitors
TW200800213A (en) 2005-09-02 2008-01-01 Abbott Lab Novel imidazo based heterocycles
US7399769B2 (en) * 2005-12-27 2008-07-15 Hoffmann-La Roche Inc. Aryl-isoxazol-4-yl-imidazo[1,5-a]pyridine derivatives
AU2007207053B2 (en) * 2006-01-17 2012-05-24 F. Hoffmann-La Roche Ag Aryl-isoxazol-4-yl-imidazo[1,2-a]pyridine useful for the treatment of Alzheimer's disease via GABA receptors
EP1845098A1 (en) * 2006-03-29 2007-10-17 Ferrer Internacional, S.A. Imidazo[1,2-b]pyridazines, their processes of preparation and their use as GABA receptor ligands
CA2653506A1 (en) * 2006-05-31 2007-12-06 Galapagos Nv. Triazolopyrazine compounds useful for the treatment of degenerative & inflammatory diseases
US20100173930A1 (en) * 2006-08-01 2010-07-08 Alex Muci Certain Chemical Entities, Compositions and Methods
US8227603B2 (en) * 2006-08-01 2012-07-24 Cytokinetics, Inc. Modulating skeletal muscle
US8299248B2 (en) 2006-08-02 2012-10-30 Cytokinetics, Incorporated Certain 1H-imidazo[4,5-b]pyrazin-2(3H)-ones and 1H-imidazo[4,5-b]pyrazin-2-ols and methods for their use
HUE026571T2 (hu) * 2006-08-02 2016-06-28 Cytokinetics Inc Adott kémiai anyagok, készítmények és imidazopiridineket magukba foglaló eljárások
EP1974729A1 (en) * 2007-03-28 2008-10-01 Santhera Pharmaceuticals (Schweiz) AG Substituted imidazopyridine derivates as melanocortin- 4 receptor antagonists
WO2008121333A1 (en) * 2007-03-30 2008-10-09 Cytokinetics, Incorporated Certain chemical entities, compositions and methods
GB0708188D0 (en) * 2007-04-27 2007-06-06 Merck Sharp & Dohme Therapeutic compounds
SI2266990T1 (sl) * 2008-04-15 2013-01-31 Eisai R&D Management Co. Ltd. Spojina 3-fenilpirazolo(5,1-b)tiazola
AU2009268406A1 (en) * 2008-07-10 2010-01-14 Southern Research Institute 5-Quinolinone and Imidazopyridine compounds and use thereof
WO2010032195A1 (en) * 2008-09-16 2010-03-25 Csir Imidazopyridines and imidazopyrimidines as hiv-i reverse transcriptase inhibitors
TWI573874B (zh) 2008-12-05 2017-03-11 武田疫苗股份有限公司 用於誘導病毒生長之組成物、方法及用途
AR078521A1 (es) * 2009-10-08 2011-11-16 Eisai R&D Man Co Ltd Compuesto pirazolotiazol
CN109316480A (zh) 2011-07-13 2019-02-12 赛特凯恩蒂克公司 组合als疗法
KR20150082308A (ko) 2012-11-14 2015-07-15 에프. 호프만-라 로슈 아게 이미다조피리딘 유도체
EP3269716B1 (en) * 2013-03-14 2020-09-16 Galapagos N.V. Novel compounds and pharmaceutical compositions thereof for the treatment of inflammatory disorders
WO2017160922A1 (en) 2016-03-16 2017-09-21 Kalyra Pharmaceuticals, Inc. Analgesic compounds
US11731967B2 (en) 2017-04-28 2023-08-22 Dana-Farber Cancer Institute, Inc. Inhibitors of TRIM33 and methods of use
EP3692052A4 (en) 2017-10-04 2021-03-17 Dana Farber Cancer Institute, Inc. INHIBITION BY SMALL MOLECULES OF THE TRANSCRIPTION FACTOR SALL4 AND ITS USES

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Publication number Priority date Publication date Assignee Title
EP0068378B1 (en) 1981-06-26 1986-03-05 Schering Corporation Novel imidazo(1,2-a)pyridines and pyrazines, processes for their preparation and pharmaceutical compositions containing them
EP0266890A1 (en) * 1986-10-07 1988-05-11 Yamanouchi Pharmaceutical Co. Ltd. Imidazopyridine derivatives, their production, and pharmaceutical compositions containing them
RU2043716C1 (ru) * 1989-06-23 1995-09-20 Такеда Кемикал Индастриз Лтд. Амидное производное и фунгицидный состав на его основе
NZ238863A (en) * 1990-07-19 1993-03-26 Janssen Pharmaceutica Nv Substituted thiazolyl and pyridinyl derivatives
TW274551B (es) * 1991-04-16 1996-04-21 Takeda Pharm Industry Co Ltd
DE4327027A1 (de) * 1993-02-15 1994-08-18 Bayer Ag Imidazoazine
US6020342A (en) * 1995-04-21 2000-02-01 Shinnippon Pharmaceutical, Inc. Fused imidazo[1,2-A]pyridines
US6552037B2 (en) * 2000-06-30 2003-04-22 Neurogen Corporation 2-Substituted imidazo[1,2-A]pyridine derivatives

Also Published As

Publication number Publication date
HK1047747B (zh) 2004-12-03
PL355206A1 (en) 2004-04-05
SK4362002A3 (en) 2002-08-06
US6638933B2 (en) 2003-10-28
CN1391573A (zh) 2003-01-15
HUP0203052A3 (en) 2004-06-28
NZ518390A (en) 2003-10-31
SK286788B6 (sk) 2009-05-07
CZ20021210A3 (cs) 2002-08-14
ATE258554T1 (de) 2004-02-15
NO322754B1 (no) 2006-12-04
CA2382919C (en) 2008-12-09
PT1218382E (pt) 2004-06-30
KR100756592B1 (ko) 2007-09-10
CO5251378A1 (es) 2003-02-28
KR20020038805A (ko) 2002-05-23
AU7777100A (en) 2001-04-23
CN1257169C (zh) 2006-05-24
DE50005155D1 (de) 2004-03-04
NO20021565L (no) 2002-05-27
BR0014818A (pt) 2002-06-18
EP1218382B1 (de) 2004-01-28
CA2382919A1 (en) 2001-04-19
WO2001027111A2 (de) 2001-04-19
AU779197B2 (en) 2005-01-13
US20030018032A1 (en) 2003-01-23
NO20021565D0 (no) 2002-04-03
RU2264402C2 (ru) 2005-11-20
ES2213611T3 (es) 2004-09-01
NZ518439A (en) 2003-10-31
AR025962A1 (es) 2002-12-26
PE20010634A1 (es) 2001-07-07
DK1218382T3 (da) 2004-03-22
WO2001027111A3 (de) 2001-06-14
EP1218382A2 (de) 2002-07-03
HK1047747A1 (zh) 2003-03-07
JP2003511451A (ja) 2003-03-25
HUP0203052A2 (hu) 2003-01-28

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Legal Events

Date Code Title Description
109 Application deemed to be withdrawn

Effective date: 20130111