[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

HRP20041060B1 - (imidazol-1-yl-methyl)-pyridazine as nmda receptor blocker - Google Patents

(imidazol-1-yl-methyl)-pyridazine as nmda receptor blocker

Info

Publication number
HRP20041060B1
HRP20041060B1 HRP20041060A HRP20041060B1 HR P20041060 B1 HRP20041060 B1 HR P20041060B1 HR P20041060 A HRP20041060 A HR P20041060A HR P20041060 B1 HRP20041060 B1 HR P20041060B1
Authority
HR
Croatia
Prior art keywords
pyridazine
imidazol
methyl
nmda receptor
receptor blocker
Prior art date
Application number
Other languages
English (en)
Inventor
Bernd Buettelmann
Marie-Paule Heitz Neidhart
Georg Jaeschke
Emmanuel Pinard
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of HRP20041060A2 publication Critical patent/HRP20041060A2/xx
Publication of HRP20041060B1 publication Critical patent/HRP20041060B1/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Psychiatry (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Addiction (AREA)
  • Virology (AREA)
  • Hospice & Palliative Care (AREA)
  • Pain & Pain Management (AREA)
  • Psychology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
HR20041060 2002-05-16 2003-05-16 (imidazol-1-yl-methyl)-pyridazine as nmda receptor blocker HRP20041060B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP02010217 2002-05-16
PCT/EP2003/005151 WO2003097637A1 (fr) 2002-05-16 2003-05-16 (imidazol-1-yl-methyl)-pyridazine en tant qu'antagoniste du recepteur nmda

Publications (2)

Publication Number Publication Date
HRP20041060A2 HRP20041060A2 (en) 2005-06-30
HRP20041060B1 true HRP20041060B1 (en) 2012-11-30

Family

ID=29433072

Family Applications (1)

Application Number Title Priority Date Filing Date
HR20041060 HRP20041060B1 (en) 2002-05-16 2003-05-16 (imidazol-1-yl-methyl)-pyridazine as nmda receptor blocker

Country Status (30)

Country Link
US (1) US7005432B2 (fr)
EP (1) EP1506190B1 (fr)
JP (1) JP4267569B2 (fr)
KR (1) KR100632868B1 (fr)
CN (1) CN1312151C (fr)
AR (1) AR040010A1 (fr)
AT (1) ATE329912T1 (fr)
AU (1) AU2003242542B2 (fr)
BR (1) BR0311177A (fr)
CA (1) CA2485926C (fr)
CL (1) CL2004001251A1 (fr)
CY (1) CY1105159T1 (fr)
DE (1) DE60306152T2 (fr)
DK (1) DK1506190T3 (fr)
ES (1) ES2265581T3 (fr)
HR (1) HRP20041060B1 (fr)
IL (1) IL164922A (fr)
MA (1) MA27117A1 (fr)
ME (1) MEP76708A (fr)
MX (1) MXPA04011253A (fr)
NO (1) NO329605B1 (fr)
NZ (1) NZ536310A (fr)
PL (1) PL211340B1 (fr)
PT (1) PT1506190E (fr)
RS (1) RS51200B (fr)
RU (1) RU2317294C2 (fr)
SI (1) SI1506190T1 (fr)
TN (1) TNSN04224A1 (fr)
WO (1) WO2003097637A1 (fr)
ZA (1) ZA200408789B (fr)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7005432B2 (en) * 2002-05-16 2006-02-28 Hoffman-La Roche Inc. Substituted imidazol-pyridazine derivatives
GB0218876D0 (en) * 2002-08-13 2002-09-25 Merck Sharp & Dohme Therapeutic agents
CN100579579C (zh) * 2002-10-01 2010-01-13 诺华疫苗和诊断公司 抗癌及抗感染性疾病组合物及其使用方法
CN103204996B (zh) 2005-05-03 2015-12-09 默克专利有限公司 有机电致发光器件
US20090054392A1 (en) * 2007-08-20 2009-02-26 Wyeth Naphthylpyrimidine, naphthylpyrazine and naphthylpyridazine analogs and their use as agonists of the wnt-beta-catenin cellular messaging system
JP5315710B2 (ja) * 2008-02-07 2013-10-16 セントラル硝子株式会社 1−ブロモ−3−フルオロ−5−ジフルオロメチルベンゼンの製造方法
DE102008015033A1 (de) 2008-03-17 2009-09-24 Aicuris Gmbh & Co. Kg Substituierte (Pyrazolyl-carbonyl)imidazolidinone und ihre Verwendung
CA2719749A1 (fr) * 2008-03-27 2009-10-01 Evotec Neurosciences Gmbh Procedes pour traiter des troubles utilisant un antagoniste selectif de sous-type nr2b de nmda
SI2393360T1 (sl) 2009-02-05 2016-02-29 Takeda Pharmaceutical Company Limited Piridazinonske spojine
EP2602255B1 (fr) * 2010-08-04 2017-04-26 Takeda Pharmaceutical Company Limited Composé à cycle hétérocyclique fusionné
WO2012019106A2 (fr) * 2010-08-06 2012-02-09 Board Of Regents Of The University Of Nebraska Modulateurs positifs et négatifs des récepteurs nmda
WO2013160728A1 (fr) 2012-04-26 2013-10-31 Alma Mater Studiorum - Universita' Di Bologna Composés à double ciblage pour le traitement de la maladie d'alzheimer
HUE049277T2 (hu) * 2014-08-15 2020-09-28 Janssen Pharmaceuticals Inc Triazolok mint NR2B receptor inhibitorok
DE102015011861B4 (de) 2015-09-10 2018-03-01 Rudolf Schindler Neue cyclische Carboxamide als NMDA NR2B Rezeptor Inhibitoren
HRP20201522T1 (hr) 2015-12-09 2020-12-11 Cadent Therapeutics, Inc. Heteroaromatski nmda receptor modulatori i njihove uporabe
SG11201806750WA (en) 2016-02-10 2018-09-27 Janssen Pharmaceutica Nv Substituted 1,2,3-triazoles as nr2b-selective nmda modulators
MX2018009857A (es) 2016-02-18 2018-11-09 Syngenta Participations Ag Derivados de pirazol pesticidicamente activos.
WO2017158147A1 (fr) 2016-03-18 2017-09-21 Savira Pharmaceuticals Gmbh Dérivés de pyrimidone et leur utilisation pour le traitement, la prévention ou l'atténuation des symptômes d'une maladie virale
WO2017158151A1 (fr) 2016-03-18 2017-09-21 Savira Pharmaceuticals Gmbh Dérivés de pyrimidone et leur utilisation dans le traitement, le soulagement ou la prévention d'une maladie virale
TW201819376A (zh) 2016-10-06 2018-06-01 比利時商健生藥品公司 經取代之1H-咪唑並[4,5-b]吡啶-2(3H)-酮及其作為GLUN2B受體調節劑之用途
WO2018119374A1 (fr) 2016-12-22 2018-06-28 Cadent Therapeutics Modulateurs des récepteurs nmda et utilisations de ceux-ci
US11008302B2 (en) 2018-04-04 2021-05-18 Janssen Pharmaceutica Nv Substituted pyridine and pyrimidines and their use as GluN2B receptor modulators
AR115905A1 (es) 2018-08-03 2021-03-10 Cadent Therapeutics Inc 5-(3-cloro-4-fluorofenil)-7-ciclopropil-3-(2-(3-fluoro-3-metilazetidin-1-il)-2-oxoetil)-3,7-dihidro-4h-pirrolo[2,3-d]pirimidin-4-ona como modulador de los receptores de nmda
JP7667097B2 (ja) 2019-06-14 2025-04-22 ヤンセン ファーマシューティカ エヌ.ベー. 置換ピラゾロ-ピリジンアミド及びglun2b受容体調節因子としてのその使用
MX2021015500A (es) 2019-06-14 2022-02-10 Janssen Pharmaceutica Nv Pirazolo-pirazinas sustituidas y su uso como moduladores del receptor glun2b.
AU2020293642A1 (en) 2019-06-14 2022-01-20 Janssen Pharmaceutica Nv Substituted pyrazolo[4,3-b]pyridines and their use as GluN2B receptor modulators
SG11202112407PA (en) 2019-06-14 2021-12-30 Janssen Pharmaceutica Nv Substituted pyrazolo-pyridine amides and their use as glun2b receptor modulators
JOP20210330A1 (ar) 2019-06-14 2023-01-30 Janssen Pharmaceutica Nv مركبات بيرازولو-بيريدين عطرية غير متجانسة مستبدلة واستخدامها كمعدِّلات لمستقبل الغلوتومات "glun2b"
KR20220020916A (ko) 2019-06-14 2022-02-21 얀센 파마슈티카 엔.브이. GluN2B 수용체 조절제로서의 피리딘 카르바메이트 및 이들의 용도
US11459336B2 (en) 2019-06-14 2022-10-04 Janssen Pharmaceutica Nv Pyrazine carbamates and their use as GluN2B receptor modulators
CN114478210A (zh) * 2022-02-26 2022-05-13 江苏壹药新材料有限公司 一种7-氯萘-2-甲醛的合成方法

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4010797A1 (de) * 1990-04-04 1991-10-10 Hoechst Ag Substituierte azole, verfahren zu deren herstellung, diese enthaltende mittel und deren verwendung
CA2248134A1 (fr) * 1996-03-08 1997-09-12 Anne Bourson Utilisation de derives de 4-phenyl-3,6-dihydro-2h-pyridile comme agents bloquants des sous-types des recepteurs nmda
CA2220649C (fr) * 1996-12-03 2007-02-13 F. Hoffmann-La Roche Ag Derives de 4-hydroxy-piperidine
US6015824A (en) 1998-02-10 2000-01-18 Hoffmann-La Roche Ag Pyrrolidine and piperidine derivatives and treatment of neurodegenerative disorders
TWI254043B (en) * 1999-06-08 2006-05-01 Hoffmann La Roche Ethanesulfonyl-piperidine derivatives having good affinity to N-methyl-D-aspartate (NMDA) receptor
PT1070708E (pt) * 1999-07-21 2004-05-31 Hoffmann La Roche Derivados de triazol
US6339093B1 (en) * 1999-10-08 2002-01-15 Hoffmann-La Roche Inc. Isoquinoline derivatives
ATE274494T1 (de) * 2000-04-20 2004-09-15 Hoffmann La Roche Pyrrolidin und piperidin derivate für die behandlung von neurodegenerativen erkrankungen
US6432985B2 (en) * 2000-04-25 2002-08-13 Hoffmann-La Roche Inc. Neuroprotective substituted piperidine compounds with activity as NMDA NR2B subtype selective antagonists
WO2002028814A2 (fr) 2000-10-06 2002-04-11 Regents Of The University Of California Bloqueur de canal de recepteur nmda a activite neuroprotectrice
CA2381630A1 (fr) 2001-04-23 2002-10-23 Leonard Theodore Meltzer Methode de prevention de la dyskinesie
DE10120159A1 (de) 2001-04-25 2002-10-31 Merck Patent Gmbh NMDA-Antagonisten und NMDA-Agonisten zur Behandlung von Suchterkrankungen
US7005432B2 (en) * 2002-05-16 2006-02-28 Hoffman-La Roche Inc. Substituted imidazol-pyridazine derivatives

Also Published As

Publication number Publication date
HK1080845A1 (en) 2006-05-04
WO2003097637A1 (fr) 2003-11-27
PT1506190E (pt) 2006-11-30
CA2485926A1 (fr) 2003-11-27
RS98504A (en) 2006-12-15
TNSN04224A1 (fr) 2007-03-12
MXPA04011253A (es) 2005-01-25
CA2485926C (fr) 2009-11-24
DE60306152D1 (de) 2006-07-27
ZA200408789B (en) 2005-12-28
NO329605B1 (no) 2010-11-22
RU2317294C2 (ru) 2008-02-20
HRP20041060A2 (en) 2005-06-30
IL164922A (en) 2012-01-31
CY1105159T1 (el) 2009-11-04
US7005432B2 (en) 2006-02-28
AR040010A1 (es) 2005-03-09
ES2265581T3 (es) 2007-02-16
BR0311177A (pt) 2005-03-15
MEP76708A (en) 2011-12-20
RS51200B (sr) 2010-12-31
KR100632868B1 (ko) 2006-10-13
JP4267569B2 (ja) 2009-05-27
JP2005532326A (ja) 2005-10-27
PL211340B1 (pl) 2012-05-31
CN1312151C (zh) 2007-04-25
AU2003242542A1 (en) 2003-12-02
RU2004136979A (ru) 2005-07-10
IL164922A0 (en) 2005-12-18
US20030229096A1 (en) 2003-12-11
EP1506190A1 (fr) 2005-02-16
NO20044666L (no) 2004-12-15
MA27117A1 (fr) 2004-12-20
SI1506190T1 (sl) 2006-10-31
KR20040106558A (ko) 2004-12-17
CL2004001251A1 (es) 2005-04-22
EP1506190B1 (fr) 2006-06-14
ATE329912T1 (de) 2006-07-15
PL374224A1 (en) 2005-10-03
CN1653062A (zh) 2005-08-10
DE60306152T2 (de) 2007-04-26
NZ536310A (en) 2007-08-31
AU2003242542B2 (en) 2008-10-16
DK1506190T3 (da) 2006-10-16

Similar Documents

Publication Publication Date Title
HRP20041060A2 (en) (imidazol-1-yl-methyl)-pyridazine as nmda receptor blocker
PL379420A1 (pl) Pochodne blokerów receptora angiotensyny II
PL376057A1 (en) Diaryl ethers as opioid receptor antagonist
IL198122A0 (en) Triazole derivatives as tachykinin receptor antagonists
AU2002353081A1 (en) Pulsatile release histamine h2 antagonist dosage forms
AU2003257172A1 (en) Cannabinoid receptor ligands
AU2003257032A1 (en) Antibodies against c3a receptor
AP2006003840A0 (en) Indole-2-carboxamidine derivatives as NMDA receptor antagonists
PL1636206T3 (pl) Pochodne imidazolu jako antagoniści receptorów glutaminianu
AU2003248356A1 (en) Beta3-adrenergic receptor agonists
AU2003294449A1 (en) Cannabinoid receptor ligands
AU2003278403A1 (en) 1-alkylpiperazinyl-pyrrolidin-2, 5-dione derivatives as adrenergic receptor antagonist
AU2003302405A8 (en) T-cell receptors
GB0215389D0 (en) Receptor
AU2003281525A1 (en) Serotonin receptor
AU2003240730A1 (en) Morpholinylmethylureas ccr-3 receptor antagonist
GB0321998D0 (en) Receptor
AU2003236673A1 (en) G protein-coupled receptor variants
HK1084298A (en) Receptor
AUPS283002A0 (en) Receptor
AU2002338040A1 (en) Receptor antagonist
GB0329104D0 (en) Receptor
GB0307100D0 (en) Receptor
AU2002951108A0 (en) Receptor specific ligands
AU2002305947A1 (en) Piperidine-piperazine ligand for neurotransmitter receptors

Legal Events

Date Code Title Description
A1OB Publication of a patent application
ARAI Request for the grant of a patent on the basis of the submitted results of a substantive examination of a patent application
B1PR Patent granted
PPPP Transfer of rights

Owner name: EVOTEC INTERNATIONAL GMBH, DE

ODRP Renewal fee for the maintenance of a patent

Payment date: 20140508

Year of fee payment: 12

PBON Lapse due to non-payment of renewal fee

Effective date: 20150516