AR057218A1 - Compuestos de oxazolidinona y su uso como pontenciadores del receptor metabotropico de glutamato - Google Patents
Compuestos de oxazolidinona y su uso como pontenciadores del receptor metabotropico de glutamatoInfo
- Publication number
- AR057218A1 AR057218A1 ARP060105350A ARP060105350A AR057218A1 AR 057218 A1 AR057218 A1 AR 057218A1 AR P060105350 A ARP060105350 A AR P060105350A AR P060105350 A ARP060105350 A AR P060105350A AR 057218 A1 AR057218 A1 AR 057218A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkylene
- alkyl
- nr4r5
- heterocycloalkyl
- cycloalkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/08—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing alicyclic rings
-
- 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
- A61P21/00—Drugs for disorders of the muscular or neuromuscular 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
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
- A61P25/10—Antiepileptics; Anticonvulsants for petit-mal
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
- A61P25/12—Antiepileptics; Anticonvulsants for grand-mal
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D263/18—Oxygen atoms
- C07D263/20—Oxygen atoms attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Urology & Nephrology (AREA)
- Psychology (AREA)
- Anesthesiology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Hospice & Palliative Care (AREA)
- Rheumatology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Composiciones farmacéuticas que contienen los compuestos, y uso de los mismos en trastornos neurologicos y psiquiátricos. Reivindicacion 1: Un compuesto caracterizado porque responde a la formula (1) donde: R1 se selecciona del grupo que consiste en H, hidroxilo, F, Cl, Br, I, nitro, CN, alquilo, alquilhalo, O-alquilo, O-alquilhalo, alquenilo, O-alquenilo, alquinilo, O-alquinilo, cicloalquilo, alquilen-ciclo-alquilo, O-cicloalquilo, O-alquilen-cicloalquilo, heterocicloalquilo, alquilen- heterocicloalquilo, O-heterocicloalquilo, O-alquilen-heterocicloalquilo, arilo, alquilenarilo, O-arilo, O-alquilenarilo, heteroarilo, alquilenheteroarilo, O-heteroarilo, O-alquilenheteroarilo, (CO)cicloalquilo, (CO)heterocicloalquilo, (CO)arilo, (CO)heteroarilo, alquilenOR4, O-alquilenOR4, (CO)R7, O(CO)R7, alquilenO(CO)R7, alquilen(CO)R7, O-alquilen(CO)R7, CO2R7, alquilenCO2R7, O-alquilenCO2R7, alquilenciano, O-alquilenciano, NR4R5, alquilenNR4R5, O-alquilenNR4R5, (CO)NR4R5, alquilen(CO)NR4R5, O-(CO)NR4R5, O-alquilen(CO)NR4R5, NR4(CO)R3, alquilenNR4(CO)R3, O-alquilenNR4(CO)R5, NR4(CO)NR4R5, alquilenNR4(CO)NR4R5, SR4, alquilenSR4, O-alquilenSR4, (SO)R3, alquilen(SO)R3, O-alquilen(SO)R3, SO2R3, alquilenSO2R3, O- alquilenSO2R3, (SO)2NR4R5, alquilen(SO)2NR4R5, O-alquilen(SO)2NR4R5, NR4(SO)2R5, alquilenNR4(SO)2R5, O-alquilenNR4(SO)2R5, NR4(SO)2NR4R5, alquilenNR4(SO)2NR4R5, O-alquilenNR4(SO)2NR4R5, NR4OR5, NR4(CO)OR7, alquilNR4(CO)OR7, O-alquilNR4(CO)OR7, y cualquier porcion cíclica está opcionalmente sustituida con uno o más sustituyentes R6 seleccionados independientemente; R2 se selecciona del grupo que consiste en H, hidroxilo, F, Cl, Br, I, CN, alquilo, alquilhalo, O-alquilo, O-alquilhalo, cicloalquilo, alquilen-cicloalquilo, O-cicloalquilo, O-alquilen-cicloalquilo, heterocicloalquilo, alquilen-heterocicloalquilo, O-heterocicloalquilo, O-alquilen-heterocicloalquilo, arilo, alquilenarilo, O-arilo, O-alquilenarilo, heteroarilo, alquilenheteroarilo, O-heteroarilo, O-alquilenheteroarilo, alquilenOR4, O-alquilenOR4, (CO)R7, alquilen(CO)R7, alquilenNR4R5, O-alquilenNR4R5, (CO)NR4R5, alquilen(CO)NR4R5, O-alquilen(CO)NR4R5, alquilenNR4(CO)R3, y cualquier porcion cíclica está opcionalmente sustituida con uno o más sustituyentes R6 seleccionados independientemente; R3, en cada caso, se selecciona del grupo que consiste en H y alquilo; R4 y R5 se seleccionan independientemente del grupo que consiste en H, alquilo, alquilhalo, alquenilo, alquinilo, cicloalquilo, alquilencicloalquilo, heterocicloalquilo, alquilenheterocicloalquilo, arilo, alquilenarilo, heteroarilo, y alquilenheteroarilo, NR7R8, alquilenNR7R8, OR7, alquilenOR7, y cualquier porcion cíclica está opcionalmente sustituida con un sustituyente seleccionado del grupo que consiste en alquilo, halo, haloalquil, O-alquilo, O-haloalquilo, arilo, alquilenarilo, heteroarilo y alquilenheteroarilo; R6, en cada caso, se selecciona del grupo que consiste en H, hidroxilo, F, Cl, Br, I, nitro, CN, oxo, alquilo, alquilhalo, O-alquilo, O-alquilhalo, alquenilo, O-alquenilo, alquinilo, O-alquinilo, cicloalquilo, alquilen-cicloalquilo, O-cicloalquilo, O-alquil-cicloalquilo, heterocicloalquilo, alquilen- heterocicloalquilo, O-heterocicloalquilo, O-alquilen-heterocicloalquilo, arilo, alquilenarilo, O-arilo, O-alquilenarilo, heteroarilo, alquilenheteroarilo, O-heteroarilo, O-alquilenheteroarilo, (CO)cicloalquilo, (CO)heterocicloalquilo, (CO)arilo, (CO)heteroarilo, alquilenOR4, O-alquilenOR4, (CO)R3, O(CO)R3, alquilenO(CO)R3, alquilen(CO)R3, O-alquilen(CO)R3, CO2R4, alquilenCO2R3, O-alquilenCO2R3, alquilenciano, O-alquilenciano, NR4R5, alquilenNR4R5, O-alquilenNR4R5, (CO)NR4R5, alquilen(CO)NR4R5, O-(CO)NR4R5, O-alquilen(CO)NR4R5, NR4(CO)R3, alquilenNR4(CO)R3, O-alquilenNR4(CO)R3, NR4(CO)NR4R13, SR4, alquilenSR5, O-alquilenSR4, (SO)R3, alquilen(SO)R3, O-alquilen(SO)R3, SO2R3, alquilenSO2R3, O-alquilenSO2R3, (SO2)NR4R5, alquilen(SO2)NR4R5, O-alquilen(SO2)NR7R8, NR7(SO2)R8, alquilenNR7(SO2)R8, O-alquilenNR4(SO2)R5, NR4(CO)OR5, alquilNR4(CO)OR5, O-alquilNR4(CO)OR5, SO3R4, y cualquier porcion cíclica está opcionalmente sustituida con un sustituyente seleccionado del grupo que consiste en halo, alquilo, O-alquilo haloalquilo, O-haloalquilo y NR4R5; R7 y R8 se seleccionan independientemente del grupo que consiste en H y alquilo; Y se selecciona del grupo que consiste en alquileno, alquenileno y alquinileno, donde cualquier átomo de H de Y puede estar sustituido independientemente con uno o más sustituyentes seleccionados del grupo que consiste en hidroxilo, F, Cl, Br, I alquilo, alquilhalo y O-alquilo; y m y n se seleccionan independientemente del grupo que consiste en 0, 1, 2, 3 y 4; con la condicion de que el compuesto no se selecciona del grupo que consiste en: 3-bencil-5-fenil-2-oxazolidinona; 3-(alfa-metil-(4-metilbencil))-5-fenil-2-oxazolidinona; 3-((2-tienil)metil)-5-fenil-2-oxazolidinona; 5- (3,4-dimetoxifenil)-3-bencil-2-oxazolidinona; 5-(3,4-dimetoxifenil)-3-(2-(3,4-dimetoxifeniletil))-2-oxazolidinona; 4[2-[5-(3-clorofenil)-2-oxazolidin-3-il]propil]fenoxi etanoato de metilo; ácido 4[2-[5-(3-clorofenil)-2-oxazolidin-3-il]propil]fenoxi etanoico, 3-[1-(4-metilfenil)etil]-5-fenil-2-oxazolidinona; 5-(3-clorofenil)-3-(2-(3,4-dihidroxifenil)-1-metiletil)-2-oxazolidinona y 5-(3-clorofenil)-3-[(3,4-dimetoxifenil)-butan-2-il]-2-oxazolidinona.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US75034705P | 2005-12-15 | 2005-12-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR057218A1 true AR057218A1 (es) | 2007-11-21 |
Family
ID=38030087
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP060105350A AR057218A1 (es) | 2005-12-15 | 2006-12-04 | Compuestos de oxazolidinona y su uso como pontenciadores del receptor metabotropico de glutamato |
Country Status (8)
| Country | Link |
|---|---|
| US (2) | US20090012089A1 (es) |
| EP (1) | EP1994016A2 (es) |
| JP (1) | JP2009519929A (es) |
| CN (1) | CN101426773A (es) |
| AR (1) | AR057218A1 (es) |
| TW (1) | TW200732313A (es) |
| UY (1) | UY29988A1 (es) |
| WO (1) | WO2007078523A2 (es) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI417095B (zh) | 2006-03-15 | 2013-12-01 | Janssen Pharmaceuticals Inc | 1,4-二取代之3-氰基-吡啶酮衍生物及其作為mGluR2-受體之正向異位性調節劑之用途 |
| TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
| TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
| JP4827986B2 (ja) | 2007-06-08 | 2011-11-30 | マンカインド コーポレ−ション | IRE−1αインヒビター |
| WO2009004430A1 (en) * | 2007-06-29 | 2009-01-08 | Pfizer Inc. | N-benzyl oxazolidinones and related heterocycleic compounds as potentiators of glutamate receptors |
| NZ584148A (en) | 2007-09-14 | 2011-05-27 | Ortho Mcneil Janssen Pharm | 1,3-disubstituted-4-phenyl-1 h-pyridin-2-ones |
| MY152078A (en) | 2007-09-14 | 2014-08-15 | Ortho Mcneil Janssen Pharm | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h,1'h-[1,4']bipyridinyl-2'-ones |
| WO2009094265A1 (en) * | 2008-01-24 | 2009-07-30 | Merck & Co., Inc. | 3,5-substituted-1,3-oxazolidin-2-one derivatives |
| US20090325964A1 (en) * | 2008-05-23 | 2009-12-31 | Wyeth | Piperazine Metabotropic Glutamate Receptor 5 (MGLUR5) Negative Allosteric Modulators For Anxiety/Depression |
| AU2009289784B2 (en) | 2008-09-02 | 2012-03-22 | Addex Pharma S.A. | 3-azabicyclo[3.1.0]hexyl derivatives as modulators of metabotropic glutamate receptors |
| ES2466341T3 (es) | 2008-10-16 | 2014-06-10 | Janssen Pharmaceuticals, Inc. | Derivados de indol y benzomorfolina como moduladores de receptores de glutamato metabotrópicos |
| WO2010060589A1 (en) | 2008-11-28 | 2010-06-03 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors |
| MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| AU2010246609B2 (en) | 2009-05-12 | 2013-09-05 | Addex Pharma S.A. | 1,2,4-triazolo [4,3-a] pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders |
| NZ596053A (en) | 2009-05-12 | 2013-05-31 | Janssen Pharmaceuticals Inc | 1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| GB201002563D0 (en) * | 2010-02-15 | 2010-03-31 | Cambridge Entpr Ltd | Compounds |
| AU2011303597A1 (en) | 2010-09-17 | 2013-04-11 | Purdue Pharma L.P. | Pyridine compounds and the uses thereof |
| EP2661435B1 (en) | 2010-11-08 | 2015-08-19 | Janssen Pharmaceuticals, Inc. | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
| EP2643320B1 (en) | 2010-11-08 | 2015-03-04 | Janssen Pharmaceuticals, Inc. | 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS |
| CN103298810B (zh) | 2010-11-08 | 2016-03-16 | 杨森制药公司 | 1,2,4-三唑并[4,3-a]吡啶衍生物及其作为MGLUR2受体的正变构调节剂的用途 |
| KR20130119964A (ko) * | 2010-12-22 | 2013-11-01 | 퍼듀 퍼머 엘피 | 나트륨 채널 차단제로서의 치환된 피리딘 |
| JO3368B1 (ar) | 2013-06-04 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 6، 7- ثاني هيدرو بيرازولو [5،1-a] بيرازين- 4 (5 يد)- اون واستخدامها بصفة منظمات تفارغية سلبية لمستقبلات ميجلور 2 |
| JO3367B1 (ar) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2 |
| DK3096790T3 (da) | 2014-01-21 | 2019-10-07 | Janssen Pharmaceutica Nv | Kombinationer omfattende positive allosteriske modulatorer eller orthosteriske agonister af metabotrop glutamaterg subtype 2-receptor og anvendelse af disse |
| KR20220038826A (ko) | 2014-01-21 | 2022-03-29 | 얀센 파마슈티카 엔.브이. | 대사 조절형 글루탐산 작동성 수용체 제2아형의 양성 알로스테릭 조절제 또는 오르토스테릭 작동제를 포함하는 조합 및 그 용도 |
| JP2021050161A (ja) | 2019-09-25 | 2021-04-01 | 武田薬品工業株式会社 | 複素環化合物及びその用途 |
| JP2021080177A (ja) * | 2019-11-14 | 2021-05-27 | 武田薬品工業株式会社 | 複素環化合物及びその用途 |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4186126A (en) * | 1978-04-11 | 1980-01-29 | Messick John J | Sulfonate antioxidants for synthetic and natural rubber |
| DD153682A1 (de) * | 1978-10-19 | 1982-01-27 | Horst Bercher | Verfahren zur herstellung neuer alkanolamine |
| DE3438839A1 (de) | 1984-10-19 | 1986-04-24 | Schering AG, 1000 Berlin und 4709 Bergkamen | Pharmazeutische praeparate |
| HU203330B (en) | 1987-06-10 | 1991-07-29 | Pfizer | Process for producing oxazolidin-2-one derivatives and hypoglychemic pharmaceutical compositions containing them |
| JP2782105B2 (ja) * | 1990-02-14 | 1998-07-30 | 曙ブレーキ工業株式会社 | ノンアスベストス摩擦材 |
| US5106867A (en) | 1990-05-04 | 1992-04-21 | American Cyanamid Company | Method of increasing lean meat in edible animals |
| US5061727A (en) | 1990-05-04 | 1991-10-29 | American Cyanamid Company | Substituted 5-(2-((2-aryl-2-hydroxyethyl)amino)propyl)-1,3-benzodioxoles |
| US5688785A (en) * | 1991-07-23 | 1997-11-18 | Schering Corporation | Substituted azetidinone compounds useful as hypocholesterolemic agents |
| US5574030A (en) * | 1992-07-14 | 1996-11-12 | Nippon Chemiphar Co., Ltd. | N-aminoalkyl-substituted nitrogen-containing five membered heterocyclic compounds |
| EP0579169B1 (en) | 1992-07-14 | 1998-09-02 | Nippon Chemiphar Co., Ltd. | Alkylenediamine derivatives |
| TW280812B (es) * | 1993-07-02 | 1996-07-11 | Bayer Ag | |
| US5482971A (en) * | 1993-10-01 | 1996-01-09 | American Cyanamid Company | Beta3 -adrenergic agents and their use in pharmaceutical compositions |
| US5420291A (en) * | 1993-12-09 | 1995-05-30 | American Cyanamid Company | Process improvement in the synthesis of [R-(R*,R*)1-5-(3-chlorophenyl)-3-[2-]-2-oxazolidinone |
| DE69404269T2 (de) | 1993-12-09 | 1997-10-30 | American Cyanamid Co | Verbesserung bei der Herstellung [R-(R*, R*)]-5-(3-chlorophenyl)-3-(2-(3,4-dihydroxyphenyl)-1-methylethyl-2-Oxazolidinone |
| US5776983A (en) | 1993-12-21 | 1998-07-07 | Bristol-Myers Squibb Company | Catecholamine surrogates useful as β3 agonists |
| CA2188269A1 (en) | 1994-04-21 | 1995-11-02 | Helmut Wachtel | Pde iv inhibitors for treating multiple sclerosis |
| US5461163A (en) * | 1994-06-06 | 1995-10-24 | American Cyanamid Company | Synthesis and purification of [R-(R*,R*)]-5-[2-[5-(3-chloro-phenyl)-2-oxo-3-oxazolidinyl]-propyl]-1,-3-benzodiozole-2,2-dicarboxylic acid dimethyl ester |
| US5491134A (en) * | 1994-09-16 | 1996-02-13 | Bristol-Myers Squibb Company | Sulfonic, phosphonic or phosphiniic acid β3 agonist derivatives |
| AU706159B2 (en) * | 1995-02-10 | 1999-06-10 | Schering Aktiengesellschaft | Pharmaceutical preparations for TNF inhibition |
| IT1274571B (it) * | 1995-05-25 | 1997-07-17 | Fabbrica Italiana Sintetici Spa | Procedimento per la preparazione di ¬r-(r*,r*)|-5-(3-clorofenil)-3- ¬2-(3,4-dimetossifenil)-1-metil-etil|-ossazolidin-2-one |
| JPH09268171A (ja) * | 1996-04-03 | 1997-10-14 | Sumika Fine Chem Kk | 光学活性オキサゾリジノン誘導体の製造方法 |
| JPH1036359A (ja) | 1996-07-22 | 1998-02-10 | Sumitomo Chem Co Ltd | 5−(3−クロロフェニル)−3−〔2−(3,4−ジメトキシフェニル)−1−メチルエチル〕−2−オキサゾリジノンの製造方法 |
| US5965607A (en) * | 1996-12-30 | 1999-10-12 | American Home Products Corporation | Substituted Benzo[1,4]dioxines as antiobesity agents |
| CA2271885A1 (en) | 1996-12-30 | 1998-07-09 | American Home Products Corporation | Substituted benzo[1,4]dioxanes as antiobesity agents |
| JPH1135534A (ja) | 1997-07-17 | 1999-02-09 | Sawai Seiyaku Kk | フェノキシ酢酸誘導体 |
| WO1999059586A1 (en) * | 1998-05-19 | 1999-11-25 | Regents Of The University Of California | Thiazolidine and oxazolidine derivatives for the treatment of acute myocardial infarction and inhibition of cardiomyocyte apoptosis |
| AUPP796798A0 (en) * | 1998-12-30 | 1999-01-28 | Fujisawa Pharmaceutical Co., Ltd. | New compound |
| WO2001072723A1 (en) * | 2000-03-28 | 2001-10-04 | Nippon Soda Co.,Ltd. | Oxa(thia)zolidine derivative and anti-inflammatory drug |
| EP1236723A1 (en) * | 2001-03-01 | 2002-09-04 | Pfizer Products Inc. | Sulfamide derivatives useful as beta3 agonists and pharmaceutical uses thereof |
| EP1389185A2 (en) * | 2001-05-24 | 2004-02-18 | Fujisawa Pharmaceutical Co., Ltd. | Aminoalcohol derivatives |
| JP2004534772A (ja) * | 2001-05-24 | 2004-11-18 | 藤沢薬品工業株式会社 | アミノアルコール誘導体 |
| WO2003031414A1 (en) | 2001-10-03 | 2003-04-17 | Nippon Soda Co.,Ltd. | Novel heterocyclic compound and anti-inflammatory agent |
| MXPA05006657A (es) | 2002-12-23 | 2005-08-16 | Hoffmann La Roche | Oxazoles como potenciadores de los receptores de glutamato metabotropicos 1 (mglu1). |
| TWI301760B (en) * | 2004-02-27 | 2008-10-11 | Merz Pharma Gmbh & Co Kgaa | Tetrahydroquinolinones and their use as antagonists of metabotropic glutamate receptors |
| DOP2005000123A (es) * | 2004-07-02 | 2011-07-15 | Merck Sharp & Dohme | Inhibidores de cetp |
| KR100890886B1 (ko) * | 2005-02-24 | 2009-03-31 | 니혼노야쿠가부시키가이샤 | 신규 할로알킬설폰아닐리드 유도체, 제초제 및 이의 이용방법 |
-
2006
- 2006-12-04 AR ARP060105350A patent/AR057218A1/es unknown
- 2006-12-04 TW TW095144949A patent/TW200732313A/zh unknown
- 2006-12-05 UY UY29988A patent/UY29988A1/es not_active Application Discontinuation
- 2006-12-06 EP EP06838983A patent/EP1994016A2/en not_active Withdrawn
- 2006-12-06 WO PCT/US2006/046344 patent/WO2007078523A2/en not_active Ceased
- 2006-12-06 US US12/095,906 patent/US20090012089A1/en not_active Abandoned
- 2006-12-06 CN CNA200680051938XA patent/CN101426773A/zh active Pending
- 2006-12-06 US US11/634,250 patent/US7816354B2/en not_active Expired - Fee Related
- 2006-12-06 JP JP2008545641A patent/JP2009519929A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| WO2007078523A3 (en) | 2007-11-15 |
| TW200732313A (en) | 2007-09-01 |
| JP2009519929A (ja) | 2009-05-21 |
| US20070275966A1 (en) | 2007-11-29 |
| WO2007078523A2 (en) | 2007-07-12 |
| UY29988A1 (es) | 2007-07-31 |
| US20090012089A1 (en) | 2009-01-08 |
| CN101426773A (zh) | 2009-05-06 |
| EP1994016A2 (en) | 2008-11-26 |
| US7816354B2 (en) | 2010-10-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR057218A1 (es) | Compuestos de oxazolidinona y su uso como pontenciadores del receptor metabotropico de glutamato | |
| AR035523A1 (es) | Uso de compuestos de aminoacetonitrilo para combatir animales daninos endoparasitarios en animales utiles y domesticos de sangre caliente | |
| PE20120229A1 (es) | Compuestos heterociclicos como inhibidores de proteasa aspartica | |
| AR079224A1 (es) | Compuestos insecticidas basados en derivados de isoxazolina | |
| ECSP077178A (es) | Agentes herbicidas | |
| PE20060417A1 (es) | Indazoles como moduladores de lxrs | |
| AR068074A1 (es) | Compuestos de piperazina con accion herbicida. proceso de preparacion | |
| AR059516A1 (es) | Derivados de isoxazolina, procesos de obtencion y composiciones herbicidas | |
| ES2530431T3 (es) | Compuestos heterocíclicos como moduladores positivos del receptor de glutamato metabotrópico 2 (receptor mGlu2) | |
| PE20090276A1 (es) | Compuestos derivados de imidazoquinolina como moduladores de tlr7 | |
| AR059895A1 (es) | Derivados biciclicos de acidos carboxilicos que resultan de utilidad para tratar trastornos metabolicos | |
| AR067663A1 (es) | Derivados heterociclicos de etiloxi amidas, composiciones que los comprenden y usos de los mismos en agricultura u horticultura, como agentes antifungicos. | |
| PE20120656A1 (es) | 2-acetamido-5-aril-1, 2, 4-triazolonas sustituidas y su uso | |
| PE20120657A1 (es) | Compuesto para el tratamiento de trastornos metabolicos | |
| AR074696A1 (es) | Derivados heterociclicos de isoxazol para su uso como reguladores del crecimiento de plantas. | |
| AR068075A1 (es) | Compuestos de piperazina con accion herbicida. proceso de preparacion | |
| AR064355A1 (es) | Herbicidas derivados de isoxazol | |
| ATE513546T1 (de) | Imidazolidin-derivate, ihre verwendungen, ihre zubereitung und diese enthaltende zusammensetzungen | |
| AR073136A1 (es) | Compuestos de pirrol | |
| PE20091444A1 (es) | Derivados de isoxazolo-pirazina | |
| AR059184A1 (es) | Derivados de sulfonamidas, su preparacion y su aplicacion en tarapeutica | |
| CO6140056A2 (es) | Compuestos amino -5-4(difluorometoxi)fenil sustituido-5-fenilimidazolona como inhibidores de beta -secretasa | |
| AR073487A1 (es) | Diaminopirimidinas 4- alquil sustituidas | |
| CO5631434A2 (es) | Derivados de piridina-carboxamida y su uso como plaguicidas | |
| PE20091490A1 (es) | Derivados sustituidos de indol |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |