NO20092357L - Polymorfe former av en mGluR5 reseptorantagonist - Google Patents

Polymorfe former av en mGluR5 reseptorantagonist

Info

Publication number
NO20092357L
NO20092357L NO20092357A NO20092357A NO20092357L NO 20092357 L NO20092357 L NO 20092357L NO 20092357 A NO20092357 A NO 20092357A NO 20092357 A NO20092357 A NO 20092357A NO 20092357 L NO20092357 L NO 20092357L
Authority
NO
Norway
Prior art keywords
mglur5 receptor
receptor antagonist
polymorphic forms
treatment
receptor
Prior art date
Application number
NO20092357A
Other languages
English (en)
Other versions
NO342451B1 (no
Inventor
Shan-Ming Kuang
Thomas P Cleary
Alexander Glomme
Olaf Grassmann
Roland Meier
Doreen Miller
Regina Moog
Franziska E Rohrer
Jason Yang
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39186951&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO20092357(L) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of NO20092357L publication Critical patent/NO20092357L/no
Publication of NO342451B1 publication Critical patent/NO342451B1/no

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
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • 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
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • 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
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Urology & Nephrology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Epidemiology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Hospice & Palliative Care (AREA)
  • Child & Adolescent Psychology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Foreliggende oppfinnelse angår mono-sulfat- og hemi-sulfatsalter av 2-klor-4-[1-(4-fluorfenyl)-2,5-dimetyl-1H-imidazol-4-yletynyl]pyridin, krystallinske og amorfe former derav, og anvendelse av dem i farmasøytiske formuleringer. De foreliggende forbindelser er aktive på mGluR5-reseptoren for behandling av sykdommer relatert til denne reseptoren, så som akutte og/eller kroniske nevrologiske lidelser, spesielt angst, eller for behandling av kronisk og akutt smerte, beskyttelse mot leverskade, svikt, enten den er medikament- eller sykdomsbevirket, urininkontinens, fedme, fragilt X-syndrom eller autisme. 270 25
NO20092357A 2006-12-21 2009-06-19 Krystallinsk form av mono-sulfatsaltet av 2-klor-4-[1-(4-fluorfenyl)-2,5-dimetyl-1H-imidazol-4-yletynyl]pyridin fremgangsmåte for fremstilling, farmasøytisk preparat samt anvendelse for behandling av sykdom NO342451B1 (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US87639806P 2006-12-21 2006-12-21
PCT/EP2007/063721 WO2008074697A1 (en) 2006-12-21 2007-12-11 Polymorphs of a mglur5 receptor antagonist

Publications (2)

Publication Number Publication Date
NO20092357L true NO20092357L (no) 2009-07-15
NO342451B1 NO342451B1 (no) 2018-05-22

Family

ID=39186951

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20092357A NO342451B1 (no) 2006-12-21 2009-06-19 Krystallinsk form av mono-sulfatsaltet av 2-klor-4-[1-(4-fluorfenyl)-2,5-dimetyl-1H-imidazol-4-yletynyl]pyridin fremgangsmåte for fremstilling, farmasøytisk preparat samt anvendelse for behandling av sykdom

Country Status (33)

Country Link
US (2) US8063076B2 (no)
EP (1) EP2125779B1 (no)
JP (1) JP5405311B2 (no)
KR (1) KR101148580B1 (no)
CN (1) CN101568531B (no)
AR (1) AR064654A1 (no)
AU (1) AU2007336369B2 (no)
BR (1) BRPI0720954A2 (no)
CA (1) CA2673444C (no)
CL (1) CL2007003695A1 (no)
CO (1) CO6210731A2 (no)
CY (1) CY1117810T1 (no)
DK (1) DK2125779T3 (no)
EC (1) ECSP099431A (no)
ES (1) ES2577391T3 (no)
HR (1) HRP20160950T1 (no)
HU (1) HUE029324T2 (no)
IL (1) IL199181A (no)
MA (1) MA31008B1 (no)
MX (1) MX2009006694A (no)
MY (1) MY148217A (no)
NO (1) NO342451B1 (no)
NZ (1) NZ577440A (no)
PE (1) PE20081484A1 (no)
PL (1) PL2125779T3 (no)
PT (1) PT2125779T (no)
RS (1) RS54853B1 (no)
RU (1) RU2460728C2 (no)
SI (1) SI2125779T1 (no)
TW (1) TWI347320B (no)
UA (1) UA96970C2 (no)
WO (1) WO2008074697A1 (no)
ZA (1) ZA200904289B (no)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101568531B (zh) 2006-12-21 2013-11-13 弗·哈夫曼-拉罗切有限公司 Mglur5受体拮抗剂的多晶型物
US20120039999A1 (en) * 2010-08-11 2012-02-16 Ashish Chatterji Pharmaceutical compositions of metabotropic glutamate 5 receptor (mglu5) antagonists
CA2830458A1 (en) 2011-03-18 2012-09-27 Novartis Ag Combinations of alpha 7 nicotinic acetylcholine receptor activators and mglur5 antagonists for use in dopamine induced dyskinesia in parkinson's disease
EP2837631A1 (en) * 2013-08-14 2015-02-18 Merck & Cie New stable salt of 5,10-methylene-(6R)-tetrahydrofolic acid
GB201317022D0 (en) * 2013-09-25 2013-11-06 Addex Pharmaceuticals Sa Polymorphs
JP2017503803A (ja) 2014-01-10 2017-02-02 シャンハイ バーディー バイオテック インコーポレイテッド Egfr発現腫瘍を処置するための化合物及び組成物
CN106943597A (zh) 2016-01-07 2017-07-14 博笛生物科技(北京)有限公司 用于治疗肿瘤的抗-egfr组合
CN108794467A (zh) 2017-04-27 2018-11-13 博笛生物科技有限公司 2-氨基-喹啉衍生物
CA3180794A1 (en) * 2020-06-05 2021-12-09 George GARIBALDI Methods of treatment of tuberous sclerosis complex
IL300124A (en) * 2020-07-30 2023-03-01 Noema Pharma Ag Methods for treating nerve pain related to the trigeminal nerve

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3303199A (en) * 1963-07-15 1967-02-07 Geigy Chem Corp Certain imidazolone derivatives and process for making same
US3341548A (en) * 1964-04-29 1967-09-12 Hoffmann La Roche Nitroimidazoles and their preparation
DE2035905A1 (de) 1970-07-20 1972-02-03 Chemische Fabrik Stockhausen & Cie.,4150Krefeld Imidazolverbindungen und deren Herstellungsverfahren
CA1174673A (en) 1981-02-27 1984-09-18 Walter Hunkeler Imidazodiazepines
EP0079312A3 (de) * 1981-11-11 1984-04-25 Ciba-Geigy Ag Heterocyclische Acetylenverbindungen
US4711962A (en) * 1984-10-18 1987-12-08 Stauffer Chemical Company Process for selective preparation of ratios of isomers formed on N-substitution of asymmetric imidazoles
ES2084702T3 (es) 1989-06-30 1996-05-16 Du Pont Imidazoles sustituidos utiles como inhibidores de la angiotensina ii.
TW544448B (en) * 1997-07-11 2003-08-01 Novartis Ag Pyridine derivatives
YU6100A (sh) 1997-08-14 2002-10-18 F.Hoffmann-La Roche Ag. Heterociklični viniletri protiv neuroloških poremećaja
JP4815083B2 (ja) 1999-08-31 2011-11-16 メルク・シャープ・エンド・ドーム・コーポレイション 複素環化合物およびそれの使用方法
JP5154728B2 (ja) 2000-07-24 2013-02-27 クレニツキー・ファーマシューティカルズ,インコーポレイテッド 神経栄養活性を有する置換5−アルキニルピリミジン
BR0115871A (pt) 2000-12-04 2003-10-28 Hoffmann La Roche Derivados de feniletenila ou feniletinila como antagonistas de receptores de glutamato
US6627646B2 (en) * 2001-07-17 2003-09-30 Sepracor Inc. Norastemizole polymorphs
CA2470612A1 (en) * 2001-12-19 2003-07-03 Merck & Co., Inc. Heteroaryl substituted imidazole modulators of metabotropic glutamate receptor-5
TWI292318B (en) 2003-03-10 2008-01-11 Hoffmann La Roche Imidazol-4-yl-ethynyl-pyridine derivatives
UA80888C2 (en) * 2003-06-05 2007-11-12 Hoffmann La Roche Imidazole derivatives as glutmate receptor antagonists
US7091222B2 (en) 2003-07-03 2006-08-15 Hoffmann-La Roche Inc. Imidazole derivatives
US7452909B2 (en) 2003-09-04 2008-11-18 Hoffman-La Roche Inc. Imidazole derivatives
RS50603B (sr) * 2004-06-01 2010-05-07 F. Hoffmann-La Roche Ag. Piridin-4-il-etinil-imidazoli i pirazoli kao antagonisti mglu5 receptora
CN101568531B (zh) 2006-12-21 2013-11-13 弗·哈夫曼-拉罗切有限公司 Mglur5受体拮抗剂的多晶型物

Also Published As

Publication number Publication date
AR064654A1 (es) 2009-04-15
UA96970C2 (en) 2011-12-26
CL2007003695A1 (es) 2008-07-04
ECSP099431A (es) 2009-07-31
WO2008074697A1 (en) 2008-06-26
CA2673444C (en) 2015-01-20
JP5405311B2 (ja) 2014-02-05
NZ577440A (en) 2011-12-22
CA2673444A1 (en) 2008-06-26
PE20081484A1 (es) 2008-10-18
KR20090081026A (ko) 2009-07-27
TW200833679A (en) 2008-08-16
IL199181A (en) 2016-02-29
CN101568531B (zh) 2013-11-13
DK2125779T3 (en) 2016-07-04
US20120035222A1 (en) 2012-02-09
EP2125779A1 (en) 2009-12-02
CN101568531A (zh) 2009-10-28
RS54853B1 (sr) 2016-10-31
PT2125779T (pt) 2016-07-19
SI2125779T1 (sl) 2016-07-29
KR101148580B1 (ko) 2012-05-24
AU2007336369A1 (en) 2008-06-26
CY1117810T1 (el) 2017-05-17
US8063076B2 (en) 2011-11-22
ZA200904289B (en) 2010-04-28
AU2007336369B2 (en) 2013-01-17
RU2460728C2 (ru) 2012-09-10
US20080312288A1 (en) 2008-12-18
BRPI0720954A2 (pt) 2014-03-18
MY148217A (en) 2013-03-29
JP2010513378A (ja) 2010-04-30
CO6210731A2 (es) 2010-10-20
RU2009123135A (ru) 2011-01-27
HUE029324T2 (en) 2017-02-28
US8329912B2 (en) 2012-12-11
EP2125779B1 (en) 2016-04-27
NO342451B1 (no) 2018-05-22
ES2577391T3 (es) 2016-07-14
PL2125779T3 (pl) 2016-11-30
HRP20160950T1 (hr) 2016-10-07
MX2009006694A (es) 2009-06-30
TWI347320B (en) 2011-08-21
MA31008B1 (fr) 2009-12-01

Similar Documents

Publication Publication Date Title
NO20092357L (no) Polymorfe former av en mGluR5 reseptorantagonist
NO20063620L (no) Arylanilinderivater som beta2 adrenergiske receptoragonister
WO2006110816A3 (en) 1h-benzimidazole-4-carboxamides substituted with a quaternary carbon at the 2-position are potent parp inhibitors
NO20084363L (no) 2-Substituerte 4-benzylftalazinonderivater som histamin H1- og H3-antagonister
EP2178870A4 (en) INDOLE AND INDAZOLE COMPOUNDS AS INHIBITORS OF CELL NECROSIS
WO2008094992A3 (en) 2-aminopyridine derivatives useful as kinase inhibitors
ATE520668T1 (de) Sigmarezeptor-inhibitoren
NO20091590L (no) Heterocykliske amidforbindelser anvendbare som kinaseinhibitorer
NO20092612L (no) Forbindelser og metode for kinasemodulering og indikasjoner for dette
NO20084496L (no) Pyridyl- og pyrimidinylsubstituerte pyrrol-, tiofen- og furanderivater som kinaseinhibitorer
BRPI0812504B8 (pt) composto para profilaxia ou tratamento de doença ou condição associada a receptor de canabinoides em sujeito mamífero
NO20073932L (no) Fuserte bicykliske karboksamidderivater for anvendelse som CXCR2 inhibitorer i behandlingen av inflammasjon
NO20071246L (no) Kinazolinonderivater og deres anvendelse som B-RAF-inhibitorer.
NO20063925L (no) Indazolderivater som inhibitorer av hormonsensitiv lipase
WO2009035997A3 (en) Benzo-fused heterocycles
NO20083923L (no) Pyrazolkinoloner er potente parp-inhibitorer
WO2007059230A3 (en) Substituted 1h-benzimidazole-4-carboxamides are potent parp inhibitors
NO20083058L (no) Cykloheksylsulfonamidderivater med H3 reseptor aktivitet
NO20091741L (no) Pyrazolinforbindelser som mineralkortikoidreceptorantagonister
WO2009036996A3 (en) Small molecule bradykinin b1 receptor antagonists
WO2007087283A3 (en) Thiophene-carboxamides useful as inhibitors of protein kinases
WO2008012338A3 (en) Pharmaceutical formulations comprising azelastine and a corticosteroid for the treatment of inflammatory or allergic conditions
WO2007120760A3 (en) Thiophene-carboxamides useful as inhibitors of protein kinases
NO20076357L (no) Azabicykliske heterocykler som cannabinoid reseptor modulatorer
CL2007002427A1 (es) Compuestos derivados heterociclicos, inhibidores de metaloproteinasa de matriz; proceso de preparacion; composicion farmaceutica, util para el tratamiento o profilaxis de enfermedades inflamatorias o desordenes autoinmunes.