MX9701630A - Isoxazoles. - Google Patents
Isoxazoles.Info
- Publication number
- MX9701630A MX9701630A MX9701630A MX9701630A MX9701630A MX 9701630 A MX9701630 A MX 9701630A MX 9701630 A MX9701630 A MX 9701630A MX 9701630 A MX9701630 A MX 9701630A MX 9701630 A MX9701630 A MX 9701630A
- Authority
- MX
- Mexico
- Prior art keywords
- alkylthio
- integer
- amino
- diseases
- alkanoylamino
- Prior art date
Links
- 150000002545 isoxazoles Chemical class 0.000 title abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical group C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 102000010909 Monoamine Oxidase Human genes 0.000 abstract 1
- 108010062431 Monoamine oxidase Proteins 0.000 abstract 1
- 208000018737 Parkinson disease Diseases 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000005236 alkanoylamino group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 150000002431 hydrogen Chemical group 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 230000003449 preventive effect Effects 0.000 abstract 1
- 229910052717 sulfur Chemical group 0.000 abstract 1
- 239000011593 sulfur Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/20—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
-
- 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
- A61K31/42—Oxazoles
-
- 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
- A61P25/24—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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Neurosurgery (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Psychology (AREA)
- Pain & Pain Management (AREA)
- Epidemiology (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un derivado de isoxazol representado por la formula general I: que tiene una excelente actividad inhibidora de monoamina oxidasa, y que es util como un remedio o para prevencion de enfermedades nerviosas tales como enfermedad de Parkinson, en donde R1 representa hidrogeno, halogeno, alquilo, alcoxi, hidroxi, alquiltio, amino, alcanoilo, alcanoilamino, alcanooloxi, alcoxicarbonilo, carboxi, (alquiltio)-tiocarbonilo, carbamoilo, nitro o ciano; R2 representa amino; m representa un entero de 1 a 3; representa un entero de 1 a 6; el anillo A representa benceno, naftaleno o un heterociclo aromático; y X representa oxígeno o azufre.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20536394 | 1994-08-30 | ||
| JP15057195 | 1995-06-16 | ||
| PCT/JP1995/001714 WO1996006837A1 (en) | 1994-08-30 | 1995-08-29 | Isoxazoles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX9701630A true MX9701630A (es) | 1997-06-28 |
Family
ID=26480122
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX9701630A MX9701630A (es) | 1994-08-30 | 1995-08-29 | Isoxazoles. |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US5965591A (es) |
| EP (1) | EP0779281B1 (es) |
| KR (1) | KR970705549A (es) |
| CN (1) | CN1098843C (es) |
| AT (1) | ATE253057T1 (es) |
| AU (1) | AU688102B2 (es) |
| CA (1) | CA2198457A1 (es) |
| CZ (1) | CZ290961B6 (es) |
| DE (1) | DE69532039T2 (es) |
| DK (1) | DK0779281T3 (es) |
| ES (1) | ES2208690T3 (es) |
| FI (1) | FI970864A7 (es) |
| HU (1) | HU221138B1 (es) |
| MX (1) | MX9701630A (es) |
| NO (1) | NO308741B1 (es) |
| NZ (1) | NZ291508A (es) |
| PT (1) | PT779281E (es) |
| RU (1) | RU2140414C1 (es) |
| WO (1) | WO1996006837A1 (es) |
Families Citing this family (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2208690T3 (es) * | 1994-08-30 | 2004-06-16 | Sankyo Company Limited | Isoxazol. |
| CZ272598A3 (cs) * | 1996-02-27 | 1999-01-13 | Sankyo Company, Limited | Isoxazolové deriváty |
| US6339099B1 (en) * | 1997-06-20 | 2002-01-15 | Dupont Pharmaceuticals Company | Guanidine mimics as factor Xa inhibitors |
| EP1135023A4 (en) * | 1998-11-12 | 2003-03-05 | Lilly Co Eli | AMINOBENZISOXAZOLE COMPOUNDS AND LIBRARIES THEREOF |
| US6497928B1 (en) | 1999-05-14 | 2002-12-24 | Canon Kabushiki Kaisha | Liquid crystal device, mesomorphic functional material and liquid crystal apparatus |
| DE10000577A1 (de) | 2000-01-10 | 2001-07-26 | Fumapharm Ag Muri | Verwendung von Fumarsäurederivaten zur Behandlung mitochondrialer Krankheiten |
| US6638981B2 (en) | 2001-08-17 | 2003-10-28 | Epicept Corporation | Topical compositions and methods for treating pain |
| US6660736B2 (en) * | 2002-03-27 | 2003-12-09 | Hoffmann-La Roche Inc. | Phthalimido derivatives and a process for their preparation |
| MY134480A (en) * | 2002-09-20 | 2007-12-31 | Hoffmann La Roche | 4-pyrrolidino-phenyl-benzyl ether derivatives |
| CN101798291A (zh) * | 2003-12-29 | 2010-08-11 | 塞普拉科公司 | 苯并[d]异噁唑-3-醇DAAO抑制剂 |
| CZ2006427A3 (cs) * | 2003-12-29 | 2006-11-15 | Sepracor Inc. | Pyrrolové a pyrazolové inhibitory DAAO |
| EP1746991A2 (en) * | 2004-03-16 | 2007-01-31 | Janssen Pharmaceutica N.V. | Daao inhibiting benzisoxazoles for treating mental disorders |
| EP1776337A2 (en) * | 2004-08-02 | 2007-04-25 | F. Hoffmann-Roche AG | Benzyloxy derivatives as maob inhibitors |
| DE102005018389A1 (de) * | 2005-04-20 | 2006-10-26 | Sanofi-Aventis Deutschland Gmbh | Azolderivate als Inhibitoren von Lipasen und Phospholipasen |
| US20080293726A1 (en) | 2005-07-06 | 2008-11-27 | Sepracor Inc. | Combinations of Eszopiclone and Trans 4-(3,4-Dichlorophenyl)-1,2,3,4-Tetrahydro-N-Methyl-1-Napthalenamine or Trans 4-(3,4-Dichlorophenyl)-1,2,3,4-Tetrahydro-1-Napthalenamine, and Methods of Treatment of Menopause and Mood, Anxiety, and Cognitive Disorders |
| ATE529430T1 (de) * | 2005-07-28 | 2011-11-15 | Vertex Pharma | Caspase-hemmer-propharmaka |
| CN101426372A (zh) * | 2006-01-06 | 2009-05-06 | 塞普拉柯公司 | 基于四氢萘酮的单胺再摄取抑制剂 |
| BRPI0706365A2 (pt) * | 2006-01-06 | 2011-03-22 | Sepracor Inc | Cicloalquilaminas como inibidores da recaptação de monoamina |
| RU2434002C2 (ru) * | 2006-02-21 | 2011-11-20 | Тояма Кемикал Ко., Лтд. | Способ получения сложного эфира 3-[5-[4-(циклопентилокси)-2-гидроксибензоил]-2-[(3-оксо-2-замещенный-2, 3-дигидро-1, 2-бензизоксазол-6-ил)метокси]фенил]пропионовой кислоты и промежуточного продукта для данного способа |
| CN103588659A (zh) | 2006-03-31 | 2014-02-19 | 赛诺维信制药公司 | 手性酰胺和胺的制备 |
| US7579370B2 (en) * | 2006-06-30 | 2009-08-25 | Sepracor Inc. | Fused heterocycles |
| US7884124B2 (en) * | 2006-06-30 | 2011-02-08 | Sepracor Inc. | Fluoro-substituted inhibitors of D-amino acid oxidase |
| US20080082066A1 (en) * | 2006-10-02 | 2008-04-03 | Weyerhaeuser Co. | Crosslinked carboxyalkyl cellulose fibers having non-permanent and temporary crosslinks |
| EP2079694B1 (en) | 2006-12-28 | 2017-03-01 | Rigel Pharmaceuticals, Inc. | N-substituted-heterocycloalkyloxybenzamide compounds and methods of use |
| BRPI0806604A2 (pt) * | 2007-01-18 | 2011-09-06 | Sepracor Inc | inibidores de d-aminoácido oxidase |
| US7902252B2 (en) * | 2007-01-18 | 2011-03-08 | Sepracor, Inc. | Inhibitors of D-amino acid oxidase |
| BRPI0811639A2 (pt) | 2007-05-31 | 2014-09-30 | Sepracor Inc | Cicloaquilaminas fenil substituídas como inibidores da recaptação de monoamina |
| EP2254420A4 (en) | 2008-02-20 | 2012-02-15 | Targia Pharmaceuticals | CNS PHARMACEUTICALS AND METHOD FOR THEIR USE |
| WO2010017418A1 (en) * | 2008-08-07 | 2010-02-11 | Sepracor Inc. | Prodrugs of fused heterocyclic inhibitors of d-amino acid oxidase |
| US20110034434A1 (en) * | 2009-08-07 | 2011-02-10 | Sepracor Inc. | Prodrugs of fused heterocyclic inhibitors of d-amino acid oxidase |
| CN102834009A (zh) | 2010-02-11 | 2012-12-19 | 范德比尔特大学 | 苯异唑和氮杂苯并异恶唑用于治疗神经学上的功能失调的mglur4变构增效剂、组合物和方法 |
| ES2586213T3 (es) | 2011-10-31 | 2016-10-13 | Xenon Pharmaceuticals Inc. | Compuestos de bencenosulfonamida y su uso como agentes terapéuticos |
| EP2773641B1 (en) | 2011-10-31 | 2017-09-27 | Xenon Pharmaceuticals Inc. | Biaryl ether sulfonamides and their use as therapeutic agents |
| HK1209100A1 (en) | 2012-05-22 | 2016-03-24 | 基因泰克有限公司 | N-substituted benzamides and their use in the treatment of pain |
| RU2015103913A (ru) | 2012-07-06 | 2016-08-27 | Дженентек, Инк. | N-замещенные бензамиды и способы их применение |
| JP6096370B2 (ja) | 2013-03-14 | 2017-03-15 | ジェネンテック, インコーポレイテッド | 置換トリアゾロピリジンとその使用方法 |
| JP6227112B2 (ja) * | 2013-03-15 | 2017-11-08 | ジェネンテック, インコーポレイテッド | 置換ベンゾオキサゾールとその使用方法 |
| CN105492430B (zh) * | 2013-03-15 | 2017-10-10 | 基因泰克公司 | 取代的苯并噁唑及其使用方法 |
| CA2931732A1 (en) | 2013-11-27 | 2015-06-04 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
| US10005724B2 (en) | 2014-07-07 | 2018-06-26 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| EP3297989A1 (en) | 2015-05-22 | 2018-03-28 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
| WO2017035271A1 (en) | 2015-08-27 | 2017-03-02 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| US10899732B2 (en) | 2015-11-25 | 2021-01-26 | Genentech, Inc. | Substituted benzamides useful as sodium channel blockers |
| EP3854782A1 (en) | 2016-03-30 | 2021-07-28 | Genentech, Inc. | Substituted benzamides and methods of use thereof |
| CN105801510A (zh) * | 2016-04-08 | 2016-07-27 | 李勇 | 一种治疗抑郁症的药物组合物 |
| WO2018072602A1 (en) | 2016-10-17 | 2018-04-26 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| JP2020511511A (ja) | 2017-03-24 | 2020-04-16 | ジェネンテック, インコーポレイテッド | ナトリウムチャネル阻害剤としての4−ピペリジン−n−(ピリミジン−4−イル)クロマン−7−スルホンアミド誘導体 |
| US11028075B2 (en) | 2018-02-26 | 2021-06-08 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| US10947251B2 (en) | 2018-03-30 | 2021-03-16 | Genentech, Inc. | Therapeutic compounds and methods of use thereof |
| TW202003490A (zh) | 2018-05-22 | 2020-01-16 | 瑞士商赫孚孟拉羅股份公司 | 治療性化合物及其使用方法 |
| CN114349690B (zh) * | 2022-02-15 | 2023-04-25 | 甘肃皓天医药科技有限责任公司 | 一种多拉韦林中间体合成方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1265824A (es) * | 1968-03-28 | 1972-03-08 | ||
| SU539522A3 (ru) * | 1970-02-05 | 1976-12-15 | Мерк Энд Ко. Инк. (Фирма) | Способ получени гидразин- -фенилпропионовой кислоты |
| US3812187A (en) * | 1970-02-05 | 1974-05-21 | Merck & Co Inc | Hydrazides |
| JPS476302Y1 (es) * | 1970-06-08 | 1972-03-04 | ||
| US5321037A (en) * | 1986-12-26 | 1994-06-14 | Sankyo Company, Limited | Isoxazole derivatives for use as cerebro-active drugs and central muscle relaxants |
| IE62276B1 (en) * | 1988-03-30 | 1995-01-25 | Sankyo Co | "New isoxazole derivatives for use as cerebro-active drugs and central muscle relaxants" |
| US5116839A (en) * | 1989-06-26 | 1992-05-26 | Sankyo Company, Limited | Use of isoxazolin-3-one derivatives as antidepressants |
| US5352688A (en) * | 1991-02-14 | 1994-10-04 | The Mount Sinai School Of Medicine Of The City University Of New York | Methods for the treatment of bradyphrenia in parkinson's disease |
| US5750542A (en) * | 1993-09-28 | 1998-05-12 | Pfizer | Benzisoxazole and benzisothizole derivatives as cholinesterase inhibitors |
| JPH0588630A (ja) * | 1991-09-30 | 1993-04-09 | Toshiba Lighting & Technol Corp | 表示装置 |
| US5578627A (en) * | 1992-10-25 | 1996-11-26 | Toyama Chemical Co., Ltd. | 1,2-benzoisoxazole derivative or its salt and brain-protecting agent comprising the same |
| US5494908A (en) * | 1992-11-23 | 1996-02-27 | Hoechst-Roussel Pharmaceutical Incorporated | Substituted 3-(aminoalkylamino)-1,2-benzisoxazoles and related compounds |
| ES2208690T3 (es) * | 1994-08-30 | 2004-06-16 | Sankyo Company Limited | Isoxazol. |
| CA2190708A1 (en) * | 1995-12-08 | 1997-06-09 | Johannes Aebi | Aminoalkyl substituted benzo-heterocyclic compounds |
| JP5229734B2 (ja) * | 2008-11-26 | 2013-07-03 | 住化エンビロサイエンス株式会社 | 木材保存組成物 |
-
1995
- 1995-08-29 ES ES95929249T patent/ES2208690T3/es not_active Expired - Lifetime
- 1995-08-29 DK DK95929249T patent/DK0779281T3/da active
- 1995-08-29 MX MX9701630A patent/MX9701630A/es unknown
- 1995-08-29 CZ CZ1997598A patent/CZ290961B6/cs not_active IP Right Cessation
- 1995-08-29 KR KR1019970701279A patent/KR970705549A/ko not_active Abandoned
- 1995-08-29 HU HU9701740A patent/HU221138B1/hu not_active IP Right Cessation
- 1995-08-29 WO PCT/JP1995/001714 patent/WO1996006837A1/ja not_active Ceased
- 1995-08-29 AU AU32660/95A patent/AU688102B2/en not_active Ceased
- 1995-08-29 CA CA002198457A patent/CA2198457A1/en not_active Abandoned
- 1995-08-29 PT PT95929249T patent/PT779281E/pt unknown
- 1995-08-29 RU RU97103132/04A patent/RU2140414C1/ru not_active IP Right Cessation
- 1995-08-29 CN CN95195758A patent/CN1098843C/zh not_active Expired - Fee Related
- 1995-08-29 AT AT95929249T patent/ATE253057T1/de not_active IP Right Cessation
- 1995-08-29 EP EP95929249A patent/EP0779281B1/en not_active Expired - Lifetime
- 1995-08-29 DE DE69532039T patent/DE69532039T2/de not_active Expired - Fee Related
- 1995-08-29 NZ NZ291508A patent/NZ291508A/xx unknown
-
1997
- 1997-02-26 US US08/806,854 patent/US5965591A/en not_active Expired - Fee Related
- 1997-02-27 NO NO970892A patent/NO308741B1/no unknown
- 1997-02-28 FI FI970864A patent/FI970864A7/fi not_active IP Right Cessation
-
1999
- 1999-02-03 US US09/243,885 patent/US6096771A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN1098843C (zh) | 2003-01-15 |
| WO1996006837A1 (en) | 1996-03-07 |
| FI970864A7 (fi) | 1997-04-24 |
| EP0779281A4 (en) | 2000-07-26 |
| RU2140414C1 (ru) | 1999-10-27 |
| AU3266095A (en) | 1996-03-22 |
| ES2208690T3 (es) | 2004-06-16 |
| AU688102B2 (en) | 1998-03-05 |
| US6096771A (en) | 2000-08-01 |
| CZ59897A3 (en) | 1997-07-16 |
| US5965591A (en) | 1999-10-12 |
| NO970892D0 (no) | 1997-02-27 |
| CN1162957A (zh) | 1997-10-22 |
| PT779281E (pt) | 2004-02-27 |
| KR970705549A (ko) | 1997-10-09 |
| EP0779281B1 (en) | 2003-10-29 |
| NO308741B1 (no) | 2000-10-23 |
| HU221138B1 (en) | 2002-08-28 |
| DE69532039D1 (de) | 2003-12-04 |
| DK0779281T3 (da) | 2004-03-08 |
| EP0779281A1 (en) | 1997-06-18 |
| HK1018878A1 (en) | 2000-01-07 |
| NO970892L (no) | 1997-04-29 |
| NZ291508A (en) | 1999-07-29 |
| FI970864A0 (fi) | 1997-02-28 |
| ATE253057T1 (de) | 2003-11-15 |
| CZ290961B6 (cs) | 2002-11-13 |
| DE69532039T2 (de) | 2004-07-08 |
| HUT77225A (hu) | 1998-03-02 |
| CA2198457A1 (en) | 1996-03-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX9701630A (es) | Isoxazoles. | |
| BRPI0314344B8 (pt) | composto 2,3-diidro-6-nitroimidazo[2,1-b]oxazol, composição farmacêutica compreendendo o mesmo e método para produzir um composto | |
| MX9800415A (es) | Compuestos quimicos. | |
| NZ330973A (en) | Azolobenzazepine derivatives as neurologically active agents | |
| TW370450B (en) | Substituted 1H-3-aryl-pyrrolidine-2,4-dione derivatives | |
| AU1282495A (en) | Anthranilic acid derivative | |
| AU5462796A (en) | Benzimidazole derivatives, their preparation and their therapeutic use | |
| MY109382A (en) | New herbicides. | |
| AU4120699A (en) | Piperidine and pyrrolidine derivatives comprising a nitric oxide donor for treating stress | |
| NO952129L (no) | Oksalylamino-benzofuran- og benzotienyl-derivater | |
| BR9307387A (pt) | Agentes terapêuticos | |
| WO2005070919A8 (en) | N-type calcium channel blockers | |
| EP0885891A4 (en) | ISOXAZOLE DERIVATIVES | |
| TW200616969A (en) | Imidazole compound | |
| EP1238973A4 (en) | NEW SUBSTITUTED TRICYCLIC COMPOUNDS | |
| IE890464L (en) | New 1,4-Benzoxazine and 1,4-Benzothiazine Derivatives and process for their preparation | |
| TW355124B (en) | Substituted pyrazolylpyrazole derivatives and their use as herbicides | |
| WO2003074046A1 (en) | Antidepressant | |
| ZA822792B (en) | Amide derivatives | |
| WO2001000185A3 (en) | 1,4-denzothiazepines to treat obesity related disorders | |
| CA2440186A1 (en) | Medicinal composition containing 1,3-thiazine derivative | |
| AU1505300A (en) | Piperazinone derivatives | |
| TW267094B (es) | ||
| YU69399A (sh) | Postupak dobijanja obogaćenih enantiomera n-derivata laktama | |
| ES8506662A1 (es) | Procedimiento para la preparacion de derivados de naftaleniltiazol |