EA201391700A1 - АГОНИСТЫ РЕЦЕПТОРА mGlu2 - Google Patents
АГОНИСТЫ РЕЦЕПТОРА mGlu2Info
- Publication number
- EA201391700A1 EA201391700A1 EA201391700A EA201391700A EA201391700A1 EA 201391700 A1 EA201391700 A1 EA 201391700A1 EA 201391700 A EA201391700 A EA 201391700A EA 201391700 A EA201391700 A EA 201391700A EA 201391700 A1 EA201391700 A1 EA 201391700A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- agonis
- mglu2
- receptor
- schizophrenia
- treatment
- Prior art date
Links
- 101001071429 Homo sapiens Metabotropic glutamate receptor 2 Proteins 0.000 title abstract 2
- 102100036837 Metabotropic glutamate receptor 2 Human genes 0.000 title abstract 2
- 241001514645 Agonis Species 0.000 title 1
- 208000020925 Bipolar disease Diseases 0.000 abstract 1
- 208000011688 Generalised anxiety disease Diseases 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 208000029364 generalized anxiety disease Diseases 0.000 abstract 1
- 201000000980 schizophrenia Diseases 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/14—Nitrogen 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
- A61K31/41—Heterocyclic 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
- A61K31/4196—1,2,4-Triazoles
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/04—1,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Neurology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
В настоящем изобретении предложены новые агонисты mGlu2, подходящие для применения для лечения биполярного расстройства, шизофрении и генерализованного тревожного расстройства.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11382208 | 2011-06-17 | ||
US201161522791P | 2011-08-12 | 2011-08-12 | |
PCT/US2012/041229 WO2012173850A1 (en) | 2011-06-17 | 2012-06-07 | Bicyclo (3.1.0) hexane- 2, 6 -dicarboxylic acid derivatives as mglu2 receptor agonist |
Publications (2)
Publication Number | Publication Date |
---|---|
EA201391700A1 true EA201391700A1 (ru) | 2014-04-30 |
EA023553B1 EA023553B1 (ru) | 2016-06-30 |
Family
ID=47357416
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201391700A EA023553B1 (ru) | 2011-06-17 | 2012-06-07 | Агонисты рецептора mglu2 |
Country Status (20)
Country | Link |
---|---|
US (1) | US9296710B2 (ru) |
EP (1) | EP2721012B1 (ru) |
JP (1) | JP5945592B2 (ru) |
KR (1) | KR101598679B1 (ru) |
CN (1) | CN103596933B (ru) |
AU (1) | AU2012271024B2 (ru) |
BR (1) | BR112013031928B1 (ru) |
CA (1) | CA2836485C (ru) |
CY (1) | CY1117682T1 (ru) |
DK (1) | DK2721012T3 (ru) |
EA (1) | EA023553B1 (ru) |
ES (1) | ES2587204T3 (ru) |
HR (1) | HRP20160676T1 (ru) |
HU (1) | HUE030171T2 (ru) |
MX (1) | MX2013014802A (ru) |
PL (1) | PL2721012T3 (ru) |
PT (1) | PT2721012T (ru) |
RS (1) | RS54888B1 (ru) |
SI (1) | SI2721012T1 (ru) |
WO (1) | WO2012173850A1 (ru) |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993006127A1 (en) | 1991-09-17 | 1993-04-01 | Warner-Lambert Company | Novel amino acid prodrug renin inhibitors |
US5576323A (en) | 1993-12-03 | 1996-11-19 | Eli Lilly And Company | Excitatory amino acid receptor antagonists |
US5849525A (en) | 1994-03-09 | 1998-12-15 | Brigham And Women's Hospital, Inc. | Compositions corresponding to a proton-coupled peptide transporter and methods of making and using same |
BR9611511A (pt) | 1995-11-16 | 1999-05-04 | Lilly Co Eli | Derivados de aminoácidos excitatórios |
GB9605429D0 (en) * | 1995-11-16 | 1996-05-15 | Lilly Co Eli | Excitatory amino acid receptor antagonists |
US5688826A (en) | 1995-11-16 | 1997-11-18 | Eli Lilly And Company | Excitatory amino acid derivatives |
US5952294A (en) | 1996-07-31 | 1999-09-14 | University Of Pittsburgh Of The Commonwealth System Of Higher Education | Peptidyl prodrugs and methods of making and using the same |
ZA983930B (en) | 1997-05-14 | 1999-11-08 | Lilly Co Eli | Excitatory amino acid receptor modulators. |
ES2191412T3 (es) | 1998-01-28 | 2003-09-01 | Taisho Pharmaceutical Co Ltd | Derivados de aminoacidos que contienen fluor. |
PT1110943E (pt) | 1998-08-31 | 2004-08-31 | Taisho Pharmaceutical Co Ltd | Derivados 6-fluorobiciclo¬3.1.0|hexano |
US6716452B1 (en) | 2000-08-22 | 2004-04-06 | New River Pharmaceuticals Inc. | Active agent delivery systems and methods for protecting and administering active agents |
WO2002000605A1 (fr) | 2000-06-28 | 2002-01-03 | Taisho Pharmaceutical Co., Ltd. | Nouveaux derives d'acide dicarboxylique |
WO2002055485A1 (en) | 2001-01-11 | 2002-07-18 | Eli Lilly And Company | Prodrugs of excitatory amino acids |
CN1267407C (zh) | 2001-01-11 | 2006-08-02 | 伊莱利利公司 | 兴奋性氨基酸前体药物 |
WO2002068380A1 (en) * | 2001-02-22 | 2002-09-06 | Eli Lilly And Company | Synthetic excitatory amino acids |
JP2005505506A (ja) | 2001-06-12 | 2005-02-24 | イーラン ファーマスーティカルズ、インコーポレイテッド | アルツハイマー病の治療に有用な大環状分子 |
DK1459765T3 (da) | 2001-12-27 | 2008-10-06 | Taisho Pharmaceutical Co Ltd | 6-fluorbicyclo 3.1.0 hexan-derivater |
CA2478227A1 (en) | 2002-04-03 | 2003-10-16 | Eli Lilly And Company | Therapy for psychoses combining an atypical antipsychotic and an mglu2/3 receptor agonist |
US20050192273A1 (en) | 2002-04-03 | 2005-09-01 | Johnson Bryan G. | Therapy for psychoses combining an atypical antipsychotic and an mglu2/3 receptor agonist |
MXPA04012518A (es) | 2002-06-11 | 2005-02-17 | Lilly Co Eli | Profarmacos de aminoacidos excitadores. |
CN100482680C (zh) * | 2002-06-11 | 2009-04-29 | 伊莱利利公司 | 兴奋性氨基酸前药 |
ES2355144T3 (es) * | 2003-06-26 | 2011-03-23 | Taisho Pharmaceutical Co., Ltd. | Derivado de éster 2-aminobiciclo 3.1.0 hexano-2,6-dicarboxílico. |
WO2005000790A1 (ja) * | 2003-06-26 | 2005-01-06 | Taisho Pharmaceutical Co., Ltd. | 2-アミノビシクロ[3.1.0]ヘキサン-2,6-ジカルボン酸誘導体 |
RS55469B1 (sr) * | 2009-11-18 | 2017-04-28 | Suven Life Sciences Ltd | Biciklična jedinjenja kao ligandi alfa4beta2 nikotinskih acetilholinskih receptora |
JO2978B1 (en) * | 2009-12-21 | 2016-03-15 | ايلي ليلي اند كومباني | MGLU2 aids |
-
2012
- 2012-06-07 JP JP2014515878A patent/JP5945592B2/ja active Active
- 2012-06-07 BR BR112013031928-3A patent/BR112013031928B1/pt active IP Right Grant
- 2012-06-07 CN CN201280029080.2A patent/CN103596933B/zh active Active
- 2012-06-07 EP EP12729769.5A patent/EP2721012B1/en active Active
- 2012-06-07 RS RS20160491A patent/RS54888B1/sr unknown
- 2012-06-07 DK DK12729769.5T patent/DK2721012T3/en active
- 2012-06-07 EA EA201391700A patent/EA023553B1/ru not_active IP Right Cessation
- 2012-06-07 WO PCT/US2012/041229 patent/WO2012173850A1/en active Application Filing
- 2012-06-07 PL PL12729769T patent/PL2721012T3/pl unknown
- 2012-06-07 HU HUE12729769A patent/HUE030171T2/en unknown
- 2012-06-07 AU AU2012271024A patent/AU2012271024B2/en active Active
- 2012-06-07 MX MX2013014802A patent/MX2013014802A/es active IP Right Grant
- 2012-06-07 CA CA2836485A patent/CA2836485C/en active Active
- 2012-06-07 KR KR1020137033028A patent/KR101598679B1/ko active Active
- 2012-06-07 US US14/123,768 patent/US9296710B2/en active Active
- 2012-06-07 PT PT127297695T patent/PT2721012T/pt unknown
- 2012-06-07 ES ES12729769.5T patent/ES2587204T3/es active Active
- 2012-06-07 SI SI201230569A patent/SI2721012T1/sl unknown
- 2012-06-07 HR HRP20160676TT patent/HRP20160676T1/hr unknown
-
2016
- 2016-06-24 CY CY20161100570T patent/CY1117682T1/el unknown
Also Published As
Publication number | Publication date |
---|---|
DK2721012T3 (en) | 2016-08-15 |
KR101598679B1 (ko) | 2016-02-29 |
PT2721012T (pt) | 2016-07-27 |
MX2013014802A (es) | 2014-01-24 |
EA023553B1 (ru) | 2016-06-30 |
WO2012173850A1 (en) | 2012-12-20 |
BR112013031928B1 (pt) | 2022-05-24 |
KR20140009568A (ko) | 2014-01-22 |
CN103596933B (zh) | 2016-03-23 |
RS54888B1 (sr) | 2016-10-31 |
CA2836485C (en) | 2016-12-13 |
JP2014517035A (ja) | 2014-07-17 |
HUE030171T2 (en) | 2017-05-29 |
SI2721012T1 (sl) | 2016-08-31 |
PL2721012T3 (pl) | 2017-05-31 |
ES2587204T3 (es) | 2016-10-21 |
EP2721012A1 (en) | 2014-04-23 |
CY1117682T1 (el) | 2017-05-17 |
US9296710B2 (en) | 2016-03-29 |
AU2012271024B2 (en) | 2015-07-09 |
BR112013031928A2 (pt) | 2016-12-13 |
JP5945592B2 (ja) | 2016-07-05 |
CN103596933A (zh) | 2014-02-19 |
AU2012271024A1 (en) | 2013-11-21 |
CA2836485A1 (en) | 2012-12-20 |
US20140113944A1 (en) | 2014-04-24 |
EP2721012B1 (en) | 2016-05-25 |
HRP20160676T1 (hr) | 2016-07-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MX2019014654A (es) | Agonistas de fgfr1 y sus metodos de uso. | |
EA201270619A1 (ru) | Применение бетанехола для лечения ксеростомии | |
MX2021000007A (es) | Formulaciones de enzalutamida. | |
UY34352A (es) | 3-pirimidin-4-il-oxazolidin-2-onas como inhibidores de la idh mutante | |
UY34472A (es) | Derivados modificados de 4-fenil-piridina | |
EA201201357A1 (ru) | Антитела к cd40 | |
EA201491617A1 (ru) | Соединения для лечения спинальной мышечной атрофии | |
CY1117214T1 (el) | Συνθεση για ελεγχομενη διεγερση των ωοθηκων | |
EA201400178A1 (ru) | Лечение рака молочной железы | |
EA201490559A1 (ru) | Композиция для лечения свища | |
EA201490778A1 (ru) | АНТИТЕЛА ПРОТИВ HtrA1 И СПОСОБЫ ПРИМЕНЕНИЯ | |
EA201491303A1 (ru) | Конденсированные тетра- или пентациклические дигидродиазепинокарбазолоны в качестве ингибиторов parps | |
ECSP12011989A (es) | Agonistas de mglu2 | |
EA201491610A1 (ru) | Модуляторы x рецепторов печени | |
ECSP14002542A (es) | Nuevos 2hindazoles como antagonistas del receptor ep2 | |
EA201691831A1 (ru) | Гетероароматические соединения и их применение в качестве допаминовых d1 лигандов | |
EA201590503A1 (ru) | Альфа-1-микроглобулин для применения в лечении заболеваний, связанных с митохондриями | |
UY34543A (es) | Derivados de sulfonilaminopirrolidinona, su preparación y aplicación terapéutica. | |
CO7160067A2 (es) | Formulaciones de agonistas del receptor de somatostatina | |
EA201691788A1 (ru) | Гетероароматические соединения и их применение в качестве допаминовых d1 лигандов | |
EA201270315A1 (ru) | Новые формы полициклического соединения | |
EA201590615A1 (ru) | Стимулирующие лактацию композиции на основе фосфатидилсерина | |
EA201491522A1 (ru) | Способы лечения нарушения походки и/или равновесия у пациентов с рассеянным склерозом с использованием аминопиридина | |
EA201391700A1 (ru) | АГОНИСТЫ РЕЦЕПТОРА mGlu2 | |
UY34535A (es) | Nuevo uso terapéutico de antagonistas del receptor p75. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG TJ TM |