DZ3192A1 - Dérivés de diaryl ether utilises comme inhibiteursdu recaptage de monoamines. - Google Patents
Dérivés de diaryl ether utilises comme inhibiteursdu recaptage de monoamines.Info
- Publication number
- DZ3192A1 DZ3192A1 DZ003192A DZ003192A DZ3192A1 DZ 3192 A1 DZ3192 A1 DZ 3192A1 DZ 003192 A DZ003192 A DZ 003192A DZ 003192 A DZ003192 A DZ 003192A DZ 3192 A1 DZ3192 A1 DZ 3192A1
- Authority
- DZ
- Algeria
- Prior art keywords
- reuptake inhibitors
- ether derivatives
- derivatives used
- monoamine reuptake
- diaryl ether
- Prior art date
Links
- 150000001987 diarylethers Chemical class 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- 230000000407 monoamine reuptake Effects 0.000 title 1
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- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
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- C07D207/27—2-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/22—Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
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- Chemical & Material Sciences (AREA)
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- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
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- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Gynecology & Obstetrics (AREA)
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- Dermatology (AREA)
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- Hospice & Palliative Care (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15927699P | 1999-10-13 | 1999-10-13 | |
| US16776199P | 1999-11-29 | 1999-11-29 | |
| PCT/IB2000/001373 WO2001027068A1 (fr) | 1999-10-13 | 2000-09-27 | Derives de diarylether utilises comme inhibiteurs du recaptage de monoamines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DZ3192A1 true DZ3192A1 (fr) | 2001-04-19 |
Family
ID=26855804
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DZ003192A DZ3192A1 (fr) | 1999-10-13 | 2000-09-27 | Dérivés de diaryl ether utilises comme inhibiteursdu recaptage de monoamines. |
Country Status (43)
Families Citing this family (71)
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| US6448293B1 (en) | 2000-03-31 | 2002-09-10 | Pfizer Inc. | Diphenyl ether compounds useful in therapy |
| US6610747B2 (en) | 2000-08-31 | 2003-08-26 | Pfizer Inc. | Phenoxybenzylamine derivatives as SSRIs |
| US6630504B2 (en) | 2000-08-31 | 2003-10-07 | Pfizer Inc. | Phenoxyphenylheterocyclyl derivatives as SSRIs |
| US6436938B1 (en) * | 2001-01-22 | 2002-08-20 | Pfizer Inc. | Combination treatment for depression |
| GB0109103D0 (en) * | 2001-04-11 | 2001-05-30 | Pfizer Ltd | Novel compounds |
| US20030207857A1 (en) | 2001-04-11 | 2003-11-06 | Adam Mavis D. | Phenyl heterocyclyl ethers |
| US20020165217A1 (en) * | 2001-05-01 | 2002-11-07 | Pfizer Inc. | Combination treatment for anxiety and depression |
| EP1262196A3 (fr) * | 2001-05-23 | 2002-12-18 | Pfizer Products Inc. | Combinaison d'un inhibiteur de la recapture de monoamines et d'un antagoniste opioique pour l'utilisation dans l'alcoolisme et la dépendance alcoolique |
| US20020183306A1 (en) * | 2001-05-30 | 2002-12-05 | Pfizer Inc. | Combination treatment for sleep disorders including sleep apnea |
| BR0213581A (pt) * | 2001-12-11 | 2004-08-24 | Lilly Co Eli | Uso de um inibidor de recaptação de norepinefrina seletivo |
| US7105526B2 (en) | 2002-06-28 | 2006-09-12 | Banyu Pharmaceuticals Co., Ltd. | Benzimidazole derivatives |
| WO2004054560A1 (fr) | 2002-12-13 | 2004-07-01 | Warner-Lambert Company Llc | Ligand alpha-2-delta pour traiter des symptomes des voies urinaires inferieures |
| US7772188B2 (en) | 2003-01-28 | 2010-08-10 | Ironwood Pharmaceuticals, Inc. | Methods and compositions for the treatment of gastrointestinal disorders |
| HRP20080478T3 (hr) | 2003-04-04 | 2009-02-28 | H. Lundbeck A/S | Derivati 4-(2-fenilsulfanil-fenil)-piperidina kaoinhibitori ponovne pohrane serotonina |
| CL2004000726A1 (es) * | 2003-04-04 | 2005-05-20 | Lundbeck & Co As H | Compuestos derivados de 4-[2-(feniloxi sustituido)fenil]piperidina o -1,2,3,6-tetrahidropiridina; composcion farmaceutica que los contiene; y su uso para el tratamiento de trastornos afectivos, tales como la depresion, trastornos de ansiedad, de ansi |
| UA81300C2 (en) * | 2003-04-04 | 2007-12-25 | Lundbeck & Co As H | Derivates of 4-(2-fenilsulfanilfenil)-1,2,3,6-tetrahydropiridin as retarding agents of serotonin recapture |
| PT1635828E (pt) * | 2003-04-04 | 2008-07-01 | Lundbeck & Co As H | Derivados de 4-(2-feniloxifenil) piperidina ou de 1,2,3,6-tetrahidropiridina como inibidores da recaptação da serotonina |
| CL2004000725A1 (es) * | 2003-04-04 | 2005-02-18 | Lundbeck & Co As H | Compuestos derivados de 4-(2-fenilsulfanilfenil)piperidina; composicion farmaceutica; y uso del compuesto para el tratamiento de trastornos afectivos como la depresion, trastornos de ansiedad, trastorno obsesivo compulsivo, trastorno de panico, ataqu |
| GB0309440D0 (en) * | 2003-04-25 | 2003-06-04 | Lilly Co Eli | Quinolone derivatives |
| AU2004274309B2 (en) | 2003-09-22 | 2010-04-08 | Msd K.K. | Novel piperidine derivative |
| RS50589B (sr) * | 2003-12-23 | 2010-05-07 | H. Lundbeck A/S. | 2-(1h-indolilsulfanil)-benzil amin derivati kao ssri |
| US20080125403A1 (en) | 2004-04-02 | 2008-05-29 | Merck & Co., Inc. | Method of Treating Men with Metabolic and Anthropometric Disorders |
| AR052308A1 (es) | 2004-07-16 | 2007-03-14 | Lundbeck & Co As H | Derivados de 2-(1h-indolilsulfanil)-arilamina y una composicion farmaceutica que contiene al compuesto |
| US7737155B2 (en) | 2005-05-17 | 2010-06-15 | Schering Corporation | Nitrogen-containing heterocyclic compounds and methods of use thereof |
| CA2609388C (fr) | 2005-05-30 | 2013-08-06 | Banyu Pharmaceutical Co., Ltd. | Nouveau derive de piperidine |
| US7629473B2 (en) | 2005-06-17 | 2009-12-08 | H. Lundbeck A/S | 2-(1H-indolylsulfanyl)-aryl amine derivatives |
| AR054393A1 (es) | 2005-06-17 | 2007-06-20 | Lundbeck & Co As H | Derivados de benzo(b)furano y benzo(b)tiofeno, composiciones farmaceuticas que los contienen y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por la inhibicion de la reabsorcion de neurotransmisores de amina biogenicos. |
| JPWO2007018248A1 (ja) | 2005-08-10 | 2009-02-19 | 萬有製薬株式会社 | ピリドン化合物 |
| EP1921065B1 (fr) | 2005-08-24 | 2010-10-20 | Banyu Pharmaceutical Co., Ltd. | Dérivé phénylpyridone |
| WO2007029847A1 (fr) | 2005-09-07 | 2007-03-15 | Banyu Pharmaceutical Co., Ltd. | Dérivé de pyridone substitué aromatique bicylique |
| BRPI0616463A2 (pt) | 2005-09-29 | 2011-06-21 | Merck & Co Inc | composto, composição farmacêutica, e, uso de um composto |
| WO2007048027A2 (fr) | 2005-10-21 | 2007-04-26 | Novartis Ag | Combinaison de composes organiques |
| AU2006307046A1 (en) | 2005-10-27 | 2007-05-03 | Msd K.K. | Novel benzoxathiin derivative |
| US8158791B2 (en) | 2005-11-10 | 2012-04-17 | Msd K.K. | Aza-substituted spiro derivatives |
| CA2656089A1 (fr) * | 2006-06-29 | 2008-01-03 | Janssen Pharmaceutica N.V. | Composes de benzylamine substituee |
| JP5489333B2 (ja) | 2006-09-22 | 2014-05-14 | メルク・シャープ・アンド・ドーム・コーポレーション | 脂肪酸合成阻害剤を用いた治療の方法 |
| AU2007301126A1 (en) | 2006-09-28 | 2008-04-03 | Banyu Pharmaceutical Co., Ltd. | Diaryl ketimine derivative |
| CA2673545A1 (fr) | 2006-12-22 | 2008-07-03 | Recordati Ireland Limited | Therapie combinee de troubles du tractus urinaire inferieur a l'aide de ligands de l'.alpha.2.delta. et d'ains |
| CN100413782C (zh) * | 2007-02-13 | 2008-08-27 | 袁茂豪 | 一种高纯超细球形硅微粉的制备方法 |
| CA2682727C (fr) | 2007-04-02 | 2016-03-22 | Banyu Pharmaceutical Co., Ltd. | Derive d'indoledione |
| US8969514B2 (en) | 2007-06-04 | 2015-03-03 | Synergy Pharmaceuticals, Inc. | Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases |
| EP2527360B1 (fr) | 2007-06-04 | 2015-10-28 | Synergy Pharmaceuticals Inc. | Agonistes de guanylase cyclase utiles pour le traitement de troubles gastro-intestinaux, d'inflammation, de cancer et d'autres troubles |
| EP2520561B1 (fr) | 2007-06-08 | 2016-02-10 | MannKind Corporation | Inhibiteurs IRE-1A |
| US20110015181A1 (en) | 2008-03-06 | 2011-01-20 | Makoto Ando | Alkylaminopyridine derivative |
| EP2272841A1 (fr) | 2008-03-28 | 2011-01-12 | Banyu Pharmaceutical Co., Ltd. | Dérivé de diarylméthylamide à activité antagoniste sur un récepteur d'hormone concentrant la mélanine |
| EP2810951B1 (fr) | 2008-06-04 | 2017-03-15 | Synergy Pharmaceuticals Inc. | Agonistes de guanylate cyclase utile dans le traitement de troubles gastro-intestinaux, d'une inflammation, d'un cancer et d'autres troubles |
| AU2009261248A1 (en) | 2008-06-19 | 2009-12-23 | Banyu Pharmaceutical Co., Ltd. | Spirodiamine-diarylketoxime derivative |
| EP3241839B1 (fr) | 2008-07-16 | 2019-09-04 | Bausch Health Ireland Limited | Agonistes de guanylate cyclase utiles pour le traitement de troubles gastro-intestinaux, inflammatoires, cancéreux et autres |
| WO2010013595A1 (fr) | 2008-07-30 | 2010-02-04 | 萬有製薬株式会社 | Dérivé de cycloalkylamine à noyaux fusionnés à (5 chaînons)-(5 chaînons) ou (5 chaînons)–(6 chaînons) |
| WO2010047982A1 (fr) | 2008-10-22 | 2010-04-29 | Merck Sharp & Dohme Corp. | Nouveaux dérivés de benzimidazole cycliques utiles comme agents anti-diabétiques |
| JP5557845B2 (ja) | 2008-10-31 | 2014-07-23 | メルク・シャープ・アンド・ドーム・コーポレーション | 糖尿病用剤として有用な新規環状ベンゾイミダゾール誘導体 |
| WO2010075069A1 (fr) | 2008-12-16 | 2010-07-01 | Schering Corporation | Dérivés de pyranone bicycliques en tant qu'agonistes des récepteurs nicotiniques |
| US20110245209A1 (en) | 2008-12-16 | 2011-10-06 | Schering Corporation | Pyridopyrimidine derivatives and methods of use thereof |
| US8895596B2 (en) | 2010-02-25 | 2014-11-25 | Merck Sharp & Dohme Corp | Cyclic benzimidazole derivatives useful as anti-diabetic agents |
| WO2012004743A1 (fr) | 2010-07-09 | 2012-01-12 | Pfizer Limited | Benzènesulfonamides utiles en tant qu'inhibiteurs des canaux sodiques |
| US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
| BR112013021236B1 (pt) | 2011-02-25 | 2021-05-25 | Merck Sharp & Dohme Corp | composto derivado de benzimidazol, e, composição |
| US9605002B2 (en) | 2012-07-18 | 2017-03-28 | University Of Notre Dame Du Lac | 5,5-heteroaromatic anti-infective compounds |
| US9527875B2 (en) | 2012-08-02 | 2016-12-27 | Merck Sharp & Dohme Corp. | Antidiabetic tricyclic compounds |
| RU2015140066A (ru) | 2013-02-22 | 2017-03-30 | Мерк Шарп И Доум Корп. | Противодиабетические бициклические соединения |
| WO2014139388A1 (fr) | 2013-03-14 | 2014-09-18 | Merck Sharp & Dohme Corp. | Nouveaux dérivés d'indole utiles en tant qu'agents antidiabétiques |
| CA2905438A1 (fr) | 2013-03-15 | 2014-09-25 | Synergy Pharmaceuticals Inc. | Agonistes de la guanylate cyclase et leurs utilisations |
| CA2905435A1 (fr) | 2013-03-15 | 2014-09-25 | Synergy Pharmaceuticals Inc. | Compositions utiles pour le traitement de troubles gastro-intestinaux |
| SI3004138T1 (sl) | 2013-06-05 | 2024-07-31 | Bausch Health Ireland Limited | Ultra čisti agonisti gvanilat ciklaze C, postopek za njihovo pripravo in uporabo |
| CN104341336B (zh) * | 2013-08-02 | 2018-10-16 | 上海科胜药物研发有限公司 | 一种合成阿哌沙班重要中间体的新方法 |
| WO2015051496A1 (fr) | 2013-10-08 | 2015-04-16 | Merck Sharp & Dohme Corp. | Composés tricycliques antidiabétiques |
| KR102431436B1 (ko) | 2014-08-29 | 2022-08-10 | 테스 파마 에스.알.엘. | α-아미노-β-카복시뮤콘산 세미알데히드 데카복실라제의 억제제 |
| AR109950A1 (es) | 2016-10-14 | 2019-02-06 | Tes Pharma S R L | INHIBIDORES DE LA ÁCIDO a-AMINO-b-CARBOXIMUCÓNICO SEMIALDEHÍDO DESCARBOXILASA |
| US11072602B2 (en) | 2016-12-06 | 2021-07-27 | Merck Sharp & Dohme Corp. | Antidiabetic heterocyclic compounds |
| WO2018118670A1 (fr) | 2016-12-20 | 2018-06-28 | Merck Sharp & Dohme Corp. | Composés de spirochromane antidiabétiques |
| AR117122A1 (es) | 2018-11-20 | 2021-07-14 | Tes Pharma S R L | INHIBIDORES DE LA ÁCIDO a-AMINO-b-CARBOXIMUCÓNICO SEMIALDEHÍDO DESCARBOXILASA |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ZA923283B (en) * | 1991-05-29 | 1993-01-27 | Akzo Nv | Phenoxyphenyl derivatives |
| DE4303676A1 (de) * | 1993-02-09 | 1994-08-11 | Bayer Ag | 1-Aryltriazolin(thi)one |
| CZ293595A3 (cs) * | 1995-11-09 | 1999-12-15 | Farmak A. S. | Deriváty N,N-dimethyl-2-(arylthio)benzylaminu, jejich soli, způsoby jejich přípravy a jejich použití v léčivých přípravcích |
| DE19853864A1 (de) * | 1998-07-09 | 2000-01-13 | Bayer Ag | Substituierte Phenyluracile |
| DE19838706A1 (de) * | 1998-08-26 | 2000-03-02 | Bayer Ag | Substituierte 3-Aryl-pyrazole |
| DE19901846A1 (de) * | 1999-01-19 | 2000-07-20 | Bayer Ag | Substituierte Arylheterocyclen |
-
2000
- 2000-09-27 AP APAP/P/2002/002481A patent/AP2002002481A0/en unknown
- 2000-09-27 CN CNB008141592A patent/CN1203047C/zh not_active Expired - Fee Related
- 2000-09-27 DZ DZ003192A patent/DZ3192A1/fr active
- 2000-09-27 SK SK473-2002A patent/SK4732002A3/sk unknown
- 2000-09-27 PT PT00960916T patent/PT1220831E/pt unknown
- 2000-09-27 DE DE60020726T patent/DE60020726T2/de not_active Expired - Fee Related
- 2000-09-27 WO PCT/IB2000/001373 patent/WO2001027068A1/fr not_active Ceased
- 2000-09-27 MX MXPA02003793A patent/MXPA02003793A/es active IP Right Grant
- 2000-09-27 GE GEAP20006411A patent/GEP20043160B/en unknown
- 2000-09-27 TR TR2002/01004T patent/TR200201004T2/xx unknown
- 2000-09-27 PL PL00355289A patent/PL355289A1/xx not_active Application Discontinuation
- 2000-09-27 NZ NZ517696A patent/NZ517696A/xx unknown
- 2000-09-27 CZ CZ20021180A patent/CZ20021180A3/cs unknown
- 2000-09-27 ES ES00960916T patent/ES2240155T3/es not_active Expired - Lifetime
- 2000-09-27 EP EP00960916A patent/EP1220831B1/fr not_active Expired - Lifetime
- 2000-09-27 HK HK02109177.4A patent/HK1047577B/zh not_active IP Right Cessation
- 2000-09-27 CA CA002387517A patent/CA2387517C/fr not_active Expired - Fee Related
- 2000-09-27 IL IL14910500A patent/IL149105A0/xx unknown
- 2000-09-27 HR HR20020324A patent/HRP20020324A2/hr not_active Application Discontinuation
- 2000-09-27 AT AT00960916T patent/ATE297374T1/de not_active IP Right Cessation
- 2000-09-27 YU YU21602A patent/YU21602A/sh unknown
- 2000-09-27 BR BR0014733-8A patent/BR0014733A/pt not_active Application Discontinuation
- 2000-09-27 JP JP2001530089A patent/JP2003511434A/ja active Pending
- 2000-09-27 DK DK00960916T patent/DK1220831T3/da active
- 2000-09-27 EE EEP200200191A patent/EE200200191A/xx unknown
- 2000-09-27 HU HU0203448A patent/HUP0203448A3/hu unknown
- 2000-09-27 EA EA200200291A patent/EA005671B1/ru not_active IP Right Cessation
- 2000-09-27 KR KR10-2002-7004767A patent/KR100524159B1/ko not_active Expired - Fee Related
- 2000-09-27 OA OA1200200106A patent/OA12062A/en unknown
- 2000-09-27 AU AU73070/00A patent/AU769430B2/en not_active Ceased
- 2000-10-06 TW TW094111255A patent/TW200526549A/zh unknown
- 2000-10-10 GT GT200000167A patent/GT200000167A/es unknown
- 2000-10-11 PE PE2000001092A patent/PE20010683A1/es not_active Application Discontinuation
- 2000-10-11 PA PA20008504801A patent/PA8504801A1/es unknown
- 2000-10-12 AR ARP000105371A patent/AR030533A1/es unknown
- 2000-10-12 TN TNTNSN00200A patent/TNSN00200A1/fr unknown
- 2000-10-12 SV SV2000000197A patent/SV2002000197A/es unknown
- 2000-10-12 CO CO00077988A patent/CO5261551A1/es not_active Application Discontinuation
-
2002
- 2002-03-19 IS IS6313A patent/IS6313A/is unknown
- 2002-04-08 NO NO20021659A patent/NO20021659L/no unknown
- 2002-04-08 CR CR6616A patent/CR6616A/es not_active Application Discontinuation
- 2002-04-08 MA MA26589A patent/MA26827A1/fr unknown
- 2002-04-10 BG BG106603A patent/BG106603A/bg unknown
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