CL2012002225A1 - Metodo para el tratamiento de una disfuncion de neurotransmision y otros estados asociados con la actividad de mglur4en que comprende el uso de compuestos heterociclicos derivados de pirazol condensado con otro heterociclo; compuestos; composiciones que los comprenden y el uso en el tratamiento de una disfuncion neurologica. - Google Patents
Metodo para el tratamiento de una disfuncion de neurotransmision y otros estados asociados con la actividad de mglur4en que comprende el uso de compuestos heterociclicos derivados de pirazol condensado con otro heterociclo; compuestos; composiciones que los comprenden y el uso en el tratamiento de una disfuncion neurologica.Info
- Publication number
- CL2012002225A1 CL2012002225A1 CL2012002225A CL2012002225A CL2012002225A1 CL 2012002225 A1 CL2012002225 A1 CL 2012002225A1 CL 2012002225 A CL2012002225 A CL 2012002225A CL 2012002225 A CL2012002225 A CL 2012002225A CL 2012002225 A1 CL2012002225 A1 CL 2012002225A1
- Authority
- CL
- Chile
- Prior art keywords
- treatment
- dysfunction
- mglur4en
- compositions
- activity
- Prior art date
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Classifications
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- 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
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- 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
- A61K31/415—1,2-Diazoles
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- A—HUMAN NECESSITIES
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- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
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- A—HUMAN NECESSITIES
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- 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
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
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- A—HUMAN NECESSITIES
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- 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
- A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- 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
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- A—HUMAN NECESSITIES
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- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- 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
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- C07D487/04—Ortho-condensed systems
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- 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
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US30348110P | 2010-02-11 | 2010-02-11 | |
US201161430521P | 2011-01-06 | 2011-01-06 |
Publications (1)
Publication Number | Publication Date |
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CL2012002225A1 true CL2012002225A1 (es) | 2014-03-07 |
Family
ID=44368167
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CL2012002225A CL2012002225A1 (es) | 2010-02-11 | 2012-08-10 | Metodo para el tratamiento de una disfuncion de neurotransmision y otros estados asociados con la actividad de mglur4en que comprende el uso de compuestos heterociclicos derivados de pirazol condensado con otro heterociclo; compuestos; composiciones que los comprenden y el uso en el tratamiento de una disfuncion neurologica. |
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US (2) | US9163015B2 (es) |
EP (1) | EP2533639A4 (es) |
JP (1) | JP5883399B2 (es) |
KR (1) | KR20130029368A (es) |
CN (1) | CN102892288B (es) |
AU (1) | AU2011215638B2 (es) |
BR (1) | BR112012020273A8 (es) |
CA (1) | CA2789427A1 (es) |
CL (1) | CL2012002225A1 (es) |
EA (1) | EA201290774A1 (es) |
IL (1) | IL221390A0 (es) |
MX (1) | MX2012009378A (es) |
SG (1) | SG183263A1 (es) |
TN (1) | TN2012000400A1 (es) |
WO (1) | WO2011100607A1 (es) |
ZA (1) | ZA201206416B (es) |
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CA2751176A1 (en) | 2009-01-28 | 2010-08-05 | Vanderbilt University | Substituted 1,1,3,3-tetraoxidobenzo[d][1,3,2]dithiazoles as mglur4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
US8759377B2 (en) | 2009-11-23 | 2014-06-24 | Vanderbilt University | Substituted dioxopiperidines and dioxopyrrolidines as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
WO2011100607A1 (en) * | 2010-02-11 | 2011-08-18 | Vanderbilt University | Pyrazolopyridine, pyrazolopyrazine, pyrazolopyrimidine, pyrazolothiophene and pyrazolothiazole compounds as mglur4 allosteric potentiators, compounds, and methods of treating neurological dysfunction |
EP2755976B1 (en) | 2011-09-15 | 2018-07-18 | Novartis AG | 6-substituted 3-(quinolin-6-ylthio)-[1,2,4]triazolo[4,3-a]pyridines as c-met tyrosine kinase inhibitors |
WO2013060029A1 (en) * | 2011-10-28 | 2013-05-02 | Merck Sharp & Dohme Corp | Allosteric modulators of metabotropic glutamate receptors |
JP6058023B2 (ja) | 2011-12-15 | 2017-01-11 | ファイザー・リミテッドPfizer Limited | スルホンアミド誘導体 |
BR112014031899A8 (pt) * | 2012-06-20 | 2017-10-24 | Univ Vanderbilt | composto, composição farmacêutica, e, método para tratamento de um distúrbio |
CN104955826B (zh) * | 2013-02-04 | 2019-05-31 | 默克专利股份公司 | 可用于治疗神经学疾病和病症的螺-喹唑酮衍生物 |
JP6355719B2 (ja) * | 2013-05-10 | 2018-07-11 | ジエンス ハンセン ファーマセウティカル カンパニー リミテッド | [1,2,4]トリアゾール[4,3−a]ピリジン誘導体、その製造方法またはその医薬応用 |
KR102365952B1 (ko) | 2013-10-14 | 2022-02-22 | 에자이 알앤드디 매니지먼트 가부시키가이샤 | 선택적으로 치환된 퀴놀린 화합물 |
PL3057964T3 (pl) | 2013-10-14 | 2020-05-18 | Eisai R&D Management Co., Ltd. | Selektywnie podstawione związki chinolinowe |
CN107074843A (zh) | 2014-04-25 | 2017-08-18 | 辉瑞公司 | 杂芳族化合物及其作为多巴胺d1配体的用途 |
US9980945B2 (en) | 2015-01-13 | 2018-05-29 | Vanderbilt University | Benzoisoxazole-substituted compounds as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
WO2016115272A1 (en) | 2015-01-13 | 2016-07-21 | Vanderbilt University | Benzothiazole and benzisothiazole-substituted compounds as mglur4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
WO2016123629A1 (en) * | 2015-01-30 | 2016-08-04 | Vanderbilt University | Indazole and azaindazole substituted compounds as mglur4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
US10227343B2 (en) | 2015-01-30 | 2019-03-12 | Vanderbilt University | Isoquiniline and napthalene-substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
WO2016172547A1 (en) * | 2015-04-24 | 2016-10-27 | Vanderbilt University | Substituted imidazopyridine and triazolopyridine analogs as positive allosteric modulators of muscarinic acetylcholine receptor m1 |
US9987242B2 (en) | 2015-05-05 | 2018-06-05 | Northwestern University | Treatment of Levodopa-induced Dyskinesias |
US10710997B2 (en) | 2016-09-01 | 2020-07-14 | Vanderbilt University | Isoquinoline amide and isoquinoline amide-substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
US10294222B2 (en) | 2016-09-01 | 2019-05-21 | Vanderbilt University | Benzomorpholine and benzomorpholine-substituted compounds as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
WO2018080918A1 (en) * | 2016-10-26 | 2018-05-03 | Janssen Pharmaceutica Nv | 3-aryl-2h-pyrazolo[4,3-b]pyridine compounds and their use as ampa receptor modulators |
JP7098167B2 (ja) * | 2016-11-07 | 2022-07-11 | ヴァンダービルト ユニヴァーシティ | ムスカリン性アセチルコリンレセプターm4のポジティブアロステリック調節因子 |
WO2018089544A1 (en) | 2016-11-08 | 2018-05-17 | Vanderbilt University | Isoquinoline amine compounds as mglur4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
US10968227B2 (en) | 2016-11-08 | 2021-04-06 | Vanderbilt University | Isoquinoline ether compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction |
WO2019006157A1 (en) | 2017-06-28 | 2019-01-03 | Vanderbilt University | QUINOLINE PYRIDINE COMPOUNDS AS MGLUR4 ALLOSTERIC POTENTIALIZERS, COMPOSITIONS, AND METHODS FOR TREATING NEUROLOGICAL DYSFUNCTIONS |
JP7253832B2 (ja) * | 2017-08-16 | 2023-04-07 | ヴァンダービルト ユニバーシティー | mGLuR4アロステリック増強剤としてのインダゾール化合物、組成物、および神経機能不全を治療する方法 |
JP2022511236A (ja) | 2018-07-26 | 2022-01-31 | ドメイン・セラピューティクス | 置換キナゾリノン誘導体、及びmGluR4のポジティブアロステリック調節剤としてのその使用 |
CN111620874B (zh) * | 2019-02-28 | 2022-11-15 | 汇瀚医疗科技有限公司 | 取代5,6-双杂环氨基化合物作为wnt信号通路抑制剂及其治疗应用 |
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GB1247493A (en) | 1967-11-24 | 1971-09-22 | Kodak Ltd | Photographic colour processes |
JP4922539B2 (ja) | 2000-09-15 | 2012-04-25 | バーテックス ファーマシューティカルズ インコーポレイテッド | プロテインキナーゼインヒビターとして有用なピラゾール化合物 |
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US20080194557A1 (en) | 2007-01-18 | 2008-08-14 | Joseph Barbosa | Methods and compositions for the treatment of pain, inflammation and cancer |
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WO2011100607A1 (en) * | 2010-02-11 | 2011-08-18 | Vanderbilt University | Pyrazolopyridine, pyrazolopyrazine, pyrazolopyrimidine, pyrazolothiophene and pyrazolothiazole compounds as mglur4 allosteric potentiators, compounds, and methods of treating neurological dysfunction |
-
2011
- 2011-02-11 WO PCT/US2011/024618 patent/WO2011100607A1/en active Application Filing
- 2011-02-11 JP JP2012553051A patent/JP5883399B2/ja not_active Expired - Fee Related
- 2011-02-11 EP EP20110742910 patent/EP2533639A4/en not_active Withdrawn
- 2011-02-11 BR BR112012020273A patent/BR112012020273A8/pt not_active IP Right Cessation
- 2011-02-11 KR KR20127023699A patent/KR20130029368A/ko not_active Application Discontinuation
- 2011-02-11 CA CA 2789427 patent/CA2789427A1/en not_active Abandoned
- 2011-02-11 AU AU2011215638A patent/AU2011215638B2/en not_active Ceased
- 2011-02-11 US US13/578,812 patent/US9163015B2/en active Active
- 2011-02-11 MX MX2012009378A patent/MX2012009378A/es not_active Application Discontinuation
- 2011-02-11 SG SG2012059325A patent/SG183263A1/en unknown
- 2011-02-11 CN CN201180017221.4A patent/CN102892288B/zh not_active Expired - Fee Related
- 2011-02-11 EA EA201290774A patent/EA201290774A1/ru unknown
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2012
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- 2012-08-09 TN TNP2012000400A patent/TN2012000400A1/en unknown
- 2012-08-10 CL CL2012002225A patent/CL2012002225A1/es unknown
- 2012-08-13 US US13/584,735 patent/US9108963B2/en active Active
- 2012-08-27 ZA ZA2012/06416A patent/ZA201206416B/en unknown
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MX2012009378A (es) | 2012-09-12 |
JP2013519684A (ja) | 2013-05-30 |
AU2011215638A1 (en) | 2012-09-20 |
JP5883399B2 (ja) | 2016-03-15 |
EP2533639A1 (en) | 2012-12-19 |
US20130065895A1 (en) | 2013-03-14 |
CA2789427A1 (en) | 2011-08-18 |
BR112012020273A2 (pt) | 2017-08-29 |
US9108963B2 (en) | 2015-08-18 |
SG183263A1 (en) | 2012-09-27 |
EA201290774A1 (ru) | 2013-03-29 |
US9163015B2 (en) | 2015-10-20 |
CN102892288A (zh) | 2013-01-23 |
WO2011100607A1 (en) | 2011-08-18 |
US20130096110A1 (en) | 2013-04-18 |
BR112012020273A8 (pt) | 2017-12-26 |
EP2533639A4 (en) | 2013-08-21 |
IL221390A0 (en) | 2012-10-31 |
ZA201206416B (en) | 2013-10-30 |
CN102892288B (zh) | 2016-02-24 |
AU2011215638B2 (en) | 2016-04-28 |
KR20130029368A (ko) | 2013-03-22 |
TN2012000400A1 (en) | 2014-01-30 |
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