MX2009006694A - Polimorfos de un antagonista del receptor mglur5. - Google Patents

Polimorfos de un antagonista del receptor mglur5.

Info

Publication number
MX2009006694A
MX2009006694A MX2009006694A MX2009006694A MX2009006694A MX 2009006694 A MX2009006694 A MX 2009006694A MX 2009006694 A MX2009006694 A MX 2009006694A MX 2009006694 A MX2009006694 A MX 2009006694A MX 2009006694 A MX2009006694 A MX 2009006694A
Authority
MX
Mexico
Prior art keywords
mglur5 receptor
treatment
polymorphs
receptor antagonist
receptor
Prior art date
Application number
MX2009006694A
Other languages
English (en)
Inventor
Regina Moog
Thomas P Cleary
Alexander Glomme
Shan-Ming Kuang
Roland Meier
Doreen Miller
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=MX2009006694(A) "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 MX2009006694A publication Critical patent/MX2009006694A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic 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
    • C07D401/02—Heterocyclic 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
    • C07D401/06—Heterocyclic 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • 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
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • 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
    • A61P25/24—Antidepressants
    • 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
    • A61P25/28—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • 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

Abstract

La presente invención se refiere a sales mono-sulfato y hemi-sulfato de la 2-cloro-4-[l-(4-fluor-fenil)-2,5-dimetil-1H-imi dazol-4-iletinil]-piridina, a las formas cristalina y amorfa de las mismas y a su utilización en formulaciones farmacéuticas. Los compuestos presentes son activos contra el receptor mGluR5 para el tratamiento de enfermedades, relacionadas con este receptor, por ejemplo los trastornos neurológicos agudos y/o crónicos, en particular la ansiedad, o para el tratamiento del dolor crónico y agudo, la protección contra la lesión hepática, las insuficiencias inducidos por fármacos o por enfermedades, la incontinencia urinaria, la obesidad, el X frágil o el autismo.
MX2009006694A 2006-12-21 2007-12-11 Polimorfos de un antagonista del receptor mglur5. MX2009006694A (es)

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 (1)

Publication Number Publication Date
MX2009006694A true MX2009006694A (es) 2009-06-30

Family

ID=39186951

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2009006694A MX2009006694A (es) 2006-12-21 2007-12-11 Polimorfos de un antagonista del receptor mglur5.

Country Status (33)

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

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2007336369B2 (en) 2006-12-21 2013-01-17 F. Hoffmann-La Roche Ag Polymorphs of a mGluR5 receptor antagonist
US20120039999A1 (en) * 2010-08-11 2012-02-16 Ashish Chatterji Pharmaceutical compositions of metabotropic glutamate 5 receptor (mglu5) antagonists
KR20140018286A (ko) 2011-03-18 2014-02-12 노파르티스 아게 파킨슨병에서의 도파민 유발 이상운동증에서 사용하기 위한 알파 7 니코틴성 아세틸콜린 수용체 활성화제 및 mGluR5 길항제의 조합물
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
CA2936377A1 (en) 2014-01-10 2015-07-16 Shanghai Birdie Biotech, Inc. Compounds and compositions for treating egfr expressing tumors
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
WO2021245281A1 (en) 2020-06-05 2021-12-09 Noema Pharma Ag Methods of treatment of tuberous sclerosis complex
WO2022023519A1 (en) * 2020-07-30 2022-02-03 Noema Pharma Ag Methods of treatment of trigeminal neuralgia

Family Cites Families (20)

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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
US4508560A (en) * 1981-11-11 1985-04-02 Ciba Geigy Corporation Certain pyridylacetylene compounds, compositions containing same and herbicidal methods of use
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
HU217958B (hu) 1989-06-30 2000-05-28 E. I. Du Pont De Nemours And Co. Helyettesített imidazolszármazékok, ezeket tartalmazó gyógyszerkészítmények és eljárás előállításukra
TW544448B (en) * 1997-07-11 2003-08-01 Novartis Ag Pyridine derivatives
CA2297732C (en) 1997-08-14 2008-04-29 F. Hoffmann-La Roche Ag Heterocyclic vinylethers against neurological disorders
CA2383524C (en) 1999-08-31 2010-09-28 Merck & Co., Inc. Thiazolyl alkynyl compounds and methods of use thereof
US7205297B2 (en) 2000-07-24 2007-04-17 Krenitsky Pharmaceuticals, Inc. Substituted 5-alkynyl pyrimidines having neurotrophic activity
CN1257894C (zh) 2000-12-04 2006-05-31 弗·哈夫曼-拉罗切有限公司 作为谷氨酸受体拮抗剂的苯基乙烯基或苯基乙炔基衍生物
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
EP1756086B1 (en) * 2004-06-01 2008-06-04 F.Hoffmann-La Roche Ag Pyridin-4-yl-ethynyl-imidazoles and pyrazoles as mglu5 receptor antagonists
AU2007336369B2 (en) 2006-12-21 2013-01-17 F. Hoffmann-La Roche Ag Polymorphs of a mGluR5 receptor antagonist

Also Published As

Publication number Publication date
PE20081484A1 (es) 2008-10-18
DK2125779T3 (en) 2016-07-04
JP5405311B2 (ja) 2014-02-05
HUE029324T2 (en) 2017-02-28
ES2577391T3 (es) 2016-07-14
CA2673444A1 (en) 2008-06-26
UA96970C2 (en) 2011-12-26
RS54853B1 (sr) 2016-10-31
BRPI0720954A2 (pt) 2014-03-18
CL2007003695A1 (es) 2008-07-04
WO2008074697A1 (en) 2008-06-26
US20080312288A1 (en) 2008-12-18
PL2125779T3 (pl) 2016-11-30
IL199181A (en) 2016-02-29
NO342451B1 (no) 2018-05-22
NZ577440A (en) 2011-12-22
CO6210731A2 (es) 2010-10-20
US8329912B2 (en) 2012-12-11
ECSP099431A (es) 2009-07-31
CA2673444C (en) 2015-01-20
PT2125779T (pt) 2016-07-19
KR101148580B1 (ko) 2012-05-24
AR064654A1 (es) 2009-04-15
US8063076B2 (en) 2011-11-22
CN101568531A (zh) 2009-10-28
NO20092357L (no) 2009-07-15
MA31008B1 (fr) 2009-12-01
CY1117810T1 (el) 2017-05-17
US20120035222A1 (en) 2012-02-09
SI2125779T1 (sl) 2016-07-29
EP2125779A1 (en) 2009-12-02
JP2010513378A (ja) 2010-04-30
TWI347320B (en) 2011-08-21
AU2007336369B2 (en) 2013-01-17
AU2007336369A1 (en) 2008-06-26
CN101568531B (zh) 2013-11-13
EP2125779B1 (en) 2016-04-27
ZA200904289B (en) 2010-04-28
RU2009123135A (ru) 2011-01-27
TW200833679A (en) 2008-08-16
RU2460728C2 (ru) 2012-09-10
HRP20160950T1 (hr) 2016-10-07
KR20090081026A (ko) 2009-07-27
MY148217A (en) 2013-03-29

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