EA200971044A1 - Арил- и гетероарилзамещенные тетрагидробензо-1,4-диазепины и их применение для блокирования обратного захвата норэпинефрина, допамина и серотонина - Google Patents
Арил- и гетероарилзамещенные тетрагидробензо-1,4-диазепины и их применение для блокирования обратного захвата норэпинефрина, допамина и серотонинаInfo
- Publication number
- EA200971044A1 EA200971044A1 EA200971044A EA200971044A EA200971044A1 EA 200971044 A1 EA200971044 A1 EA 200971044A1 EA 200971044 A EA200971044 A EA 200971044A EA 200971044 A EA200971044 A EA 200971044A EA 200971044 A1 EA200971044 A1 EA 200971044A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- aryl
- heteroaryl
- diazepines
- serotonin
- dopamine
- Prior art date
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
- C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D223/16—Benzazepines; Hydrogenated benzazepines
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- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- 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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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Addiction (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Reproductive Health (AREA)
- Endocrinology (AREA)
- Obesity (AREA)
- Diabetes (AREA)
- Psychology (AREA)
- Hematology (AREA)
- Urology & Nephrology (AREA)
- Physical Education & Sports Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Nutrition Science (AREA)
- Gynecology & Obstetrics (AREA)
- Anesthesiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Child & Adolescent Psychology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Арил- и гетероарилзамещенные производные тетрагидробензо-1,4-диазепиновые соединения настоящего изобретения представлены формулой I(A-D), имеющей следующую структуру:где заместители Х и R-Rимеют указанные в описании значения.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US91718907P | 2007-05-10 | 2007-05-10 | |
PCT/US2008/063039 WO2008141081A1 (en) | 2007-05-10 | 2008-05-08 | Aryl- and heteroaryl-substituted tetrahydrobenzo-1,4-diazepines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
Publications (3)
Publication Number | Publication Date |
---|---|
EA200971044A1 true EA200971044A1 (ru) | 2010-06-30 |
EA017249B1 EA017249B1 (ru) | 2012-11-30 |
EA017249B8 EA017249B8 (ru) | 2013-01-30 |
Family
ID=40002593
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA200971044A EA017249B8 (ru) | 2007-05-10 | 2008-05-08 | Арил- и гетероарилзамещенные тетрагидробензо-1,4-диазепины и их применение для блокирования обратного захвата норэпинефрина, допамина и серотонина |
Country Status (14)
Country | Link |
---|---|
US (1) | US9096546B2 (ru) |
EP (1) | EP2146722A4 (ru) |
JP (1) | JP2010526825A (ru) |
KR (1) | KR20100017766A (ru) |
CN (1) | CN101686983A (ru) |
AU (1) | AU2008251557B2 (ru) |
BR (1) | BRPI0811204A8 (ru) |
CA (1) | CA2685860A1 (ru) |
CO (1) | CO6251238A2 (ru) |
EA (1) | EA017249B8 (ru) |
IL (1) | IL201922A0 (ru) |
MX (1) | MX2009011923A (ru) |
NZ (1) | NZ580801A (ru) |
WO (1) | WO2008141081A1 (ru) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2573271C (en) | 2004-07-15 | 2015-10-06 | Amr Technology, Inc. | Aryl-and heteroaryl-substituted tetrahydroisoquinolines and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
JP2011116663A (ja) * | 2008-05-30 | 2011-06-16 | Otsuka Pharmaceut Co Ltd | ベンゾジアゼピン化合物 |
WO2010132437A1 (en) | 2009-05-12 | 2010-11-18 | Albany Molecular Research, Inc. | Aryl, heteroaryl, and heterocycle substituted tetrahydroisoquinolines and use thereof |
KR20120023072A (ko) | 2009-05-12 | 2012-03-12 | 브리스톨-마이어스 스큅 컴퍼니 | (S)-7-(〔1,2,4〕트리아졸〔1,5-a〕피리딘-6-일)-4-(3,4-디클로로페닐)-1,2,3,4-테트라하이드로이소퀴놀린의 결정형 및 이의 용도 |
US9045468B2 (en) | 2010-08-17 | 2015-06-02 | Albany Molecular Research, Inc. | 2,5-methano- and 2,5-ethano-tetrahydrobenzazepine derivatives and use thereof to block reuptake of norepinephrine, dopamine, and serotonin |
KR20160080799A (ko) | 2014-12-30 | 2016-07-08 | 한국해양과학기술원 | 금 촉매를 이용한 α-피론 유도체 전합성 방법 및 이에 의해 합성되어 인간 암세포주에 세포독성을 가지는 α-피론 유도체 |
CR20170513A (es) * | 2015-05-04 | 2018-02-13 | Astrazeneca Ab | Derivados de pirazol útiles como inhibidores de proteína activadora de 5-li-poxigenasa (flap). |
CN105461635B (zh) * | 2015-11-18 | 2018-06-08 | 乳源瑶族自治县大众药品贸易有限公司 | 苯基哌嗪衍生物及其使用方法和用途 |
EA202092490A1 (ru) | 2018-04-18 | 2020-12-23 | Констеллейшен Фармасьютикалс, Инк. | Модуляторы метилмодифицирующих ферментов, композиции и их применения |
US11919912B2 (en) | 2018-05-21 | 2024-03-05 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
Family Cites Families (124)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3144439A (en) | 1964-08-11 | Process for production of benzo- | ||
GB1052144A (ru) | 1964-02-11 | |||
US3517061A (en) | 1965-10-23 | 1970-06-23 | American Home Prod | 5h-1,4-benzodiazepin-5-ones |
US3457258A (en) | 1965-10-23 | 1969-07-22 | American Home Prod | 5h-1,4-benzodiazepin-5-ones and-5-thiones |
US3384635A (en) | 1966-09-28 | 1968-05-21 | Sterling Drug Inc | 1, 4-benzodiazepine derivatives |
US3415814A (en) | 1966-09-28 | 1968-12-10 | Sterling Drug Inc | 4-(cyclopropylmethyl)-3h-1,4-benzodiazepine-2,5(1h,4h)-dione |
US3523939A (en) | 1967-07-03 | 1970-08-11 | Hoffmann La Roche | 5-(2,6-disubstituted phenyl)-1,4-benzodiazepines and methods for their preparation |
AT280290B (de) | 1967-11-24 | 1970-04-10 | Boehringer Sohn Ingelheim | Verfahren zur Herstellung von neuen 1-Phenyl-4-alkyl-3H-1,4-benzodiazepin-2,5-[1H,4H]-dionen |
DE2165310A1 (de) | 1971-12-29 | 1973-07-12 | Boehringer Sohn Ingelheim | Neue 1-aryl-3,4-dihydro-(2h,5h)-1,4benzodiazepin-5-one und verfahren zu ihrer herstellung |
US3985731A (en) | 1974-07-01 | 1976-10-12 | E. R. Squibb & Sons, Inc. | 2H-2-benzazepin-1,3-diones |
US4820834A (en) | 1984-06-26 | 1989-04-11 | Merck & Co., Inc. | Benzodiazepine analogs |
US4666913A (en) | 1985-11-22 | 1987-05-19 | William H. Rorer, Inc. | Hydroxy and aminothiazolyl-benzodiazinone compounds, cardiotonic compositions including the same, and their uses |
US4975439A (en) | 1987-09-25 | 1990-12-04 | Janssen Pharmaceutical N.V. | Novel substituted N-(1-alkyl-3-hydroxy-4-piperidinyl)benzamides |
US4933445A (en) | 1988-11-29 | 1990-06-12 | Rorer Pharmaceutical Corporation | Heteroazabenzobicyclic carboxamide 5-HT3 antagonists |
JP2777159B2 (ja) | 1988-12-22 | 1998-07-16 | エーザイ株式会社 | 環状アミン誘導体を含有する医薬 |
US4957915A (en) | 1989-02-27 | 1990-09-18 | Biomeasure, Inc. | Benzodiazepine analogs |
EP0411751A1 (en) | 1989-06-06 | 1991-02-06 | Beecham Group p.l.c. | Renin inhibitory peptides |
EP0727215A3 (en) | 1989-08-04 | 1996-11-06 | Merck Sharp & Dohme | Central cholecystokinin antagonists for the treatment of psychiatric diseases |
US5175159A (en) | 1989-10-05 | 1992-12-29 | Merck & Co., Inc. | 3-substituted-1,4-benzodiazepines as oxytocin antagonists |
US5258510A (en) | 1989-10-20 | 1993-11-02 | Otsuka Pharma Co Ltd | Benzoheterocyclic compounds |
US5206238A (en) | 1990-11-13 | 1993-04-27 | Merck & Co., Inc. | Cholecystokinin antagonists |
CA2066104C (en) | 1991-04-19 | 2003-05-27 | Hidenori Ogawa | Benzazepine derivatives as vasopressin antagonists |
GB9117852D0 (en) | 1991-08-19 | 1991-10-09 | Merck Sharp & Dohme | Therapeutic agents |
US5153191A (en) | 1991-08-20 | 1992-10-06 | Warner-Lambert Company | Cholecystokinin antagonists useful for treating depression |
US5593988A (en) | 1991-10-11 | 1997-01-14 | Yoshitomi Pharmaceutical Industries, Ltd. | Therapeutic agent for osteoporosis and diazepine compound |
US5681833A (en) | 1992-03-24 | 1997-10-28 | Merck, Sharp & Dohme Ltd. | Benzodiazepine derivatives |
TW249201B (ru) | 1992-07-02 | 1995-06-11 | Otsuka Pharma Co Ltd | |
JPH0616643A (ja) | 1992-07-03 | 1994-01-25 | Yamanouchi Pharmaceut Co Ltd | ビフェニル誘導体 |
EP0652871B1 (en) | 1992-07-29 | 2001-10-17 | MERCK SHARP & DOHME LTD. | Benzodiazepine derivatives |
AU657431B2 (en) | 1992-08-20 | 1995-03-09 | Otsuka Pharmaceutical Co., Ltd. | Benzoheterocyclic compounds as oxytocin and vasopressin antagonists |
AU678503B2 (en) | 1993-09-24 | 1997-05-29 | Takeda Chemical Industries Ltd. | Condensed heterocyclic compounds and their use as squalene synthetase inhibitors |
ES2199251T3 (es) | 1994-06-15 | 2004-02-16 | Otsuka Pharmaceutical Company, Limited | Derivados benzoheterociclicos utilizables como moduladores de vasopresina o de oxitocina. |
US6008214A (en) | 1994-08-22 | 1999-12-28 | Smithkline Beecham Corporation | Bicyclic compounds |
IT1271007B (it) | 1994-09-13 | 1997-05-26 | Zambon Spa | Derivati del 2-ammino-1,2,3,4-tetraidronaftalene attivi sul sistema cardiovascolare |
TW401301B (en) | 1994-10-07 | 2000-08-11 | Takeda Chemical Industries Ltd | Antihypertriglyceridemic composition |
US5770438A (en) | 1994-11-01 | 1998-06-23 | Takeda Chemical Industries, Ltd. | Process for enantioselective hydrolysis of α-(2-amino)-phenyl-benzenemethanol ester type compounds using bacillus, pseudomonas or streptomyces |
US5618792A (en) | 1994-11-21 | 1997-04-08 | Cortech, Inc. | Substituted heterocyclic compounds useful as inhibitors of (serine proteases) human neutrophil elastase |
GB9508637D0 (en) | 1995-04-28 | 1995-06-14 | Fujisawa Pharmaceutical Co | New use |
DE19516483A1 (de) | 1995-05-05 | 1996-11-07 | Merck Patent Gmbh | Adhäsionsrezeptor-Antagonisten |
JPH0987260A (ja) | 1995-09-27 | 1997-03-31 | Takeda Chem Ind Ltd | 縮合環化合物とその用途 |
DE69622677T2 (de) | 1995-12-08 | 2003-03-20 | Takeda Chemical Industries Ltd | Hemmer der Prolaktinsynthese |
JPH09221476A (ja) | 1995-12-15 | 1997-08-26 | Otsuka Pharmaceut Co Ltd | 医薬組成物 |
AU1463997A (en) | 1995-12-22 | 1997-07-17 | Acea Pharmaceuticals, Inc. | Subtype-selective nmda receptor ligands and the use thereof |
CZ203698A3 (cs) | 1995-12-29 | 1999-05-12 | Smithkline Beecham Corporation | Antagonista vitronektinového receptoru, farmaceutický přípravek s jeho obsahem, způsob a použití |
US6011029A (en) | 1996-02-26 | 2000-01-04 | Bristol-Myers Squibb Company | Inhibitors of farnesyl protein transferase |
US5852010A (en) | 1996-04-03 | 1998-12-22 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
CA2250203A1 (en) | 1996-04-03 | 1997-10-09 | Merck & Co., Inc. | Inhibitors of farnesyl-protein transferase |
CA2250908C (en) | 1996-04-30 | 2012-03-13 | Takeda Chemical Industries, Ltd. | Combined use of gnrh agonist and antagonist |
KR20010012072A (ko) | 1997-04-21 | 2001-02-15 | 다케다 야쿠힌 고교 가부시키가이샤 | 4,1-벤족사제핀 및 이의 동족체, 및 소마토스타틴아고니스트로서의 이들의 용도 |
US6333321B1 (en) | 1997-08-11 | 2001-12-25 | Cor Therapeutics, Inc. | Selective factor Xa inhibitors |
US20020022636A1 (en) | 1997-09-03 | 2002-02-21 | Jia-He Li | Oxo-substituted compounds, process of making, and compositions and methods for inhibiting parp activity |
WO1999015524A1 (en) | 1997-09-23 | 1999-04-01 | Fujisawa Pharmaceutical Co., Ltd. | Thiazole derivatives |
JP2001519387A (ja) | 1997-09-29 | 2001-10-23 | ブリストル−マイヤーズ スクイブ カンパニー | ファルネシルたんぱく転移酵素のインヒビター |
US6458783B1 (en) | 1997-09-29 | 2002-10-01 | Bristol-Myers Squibb Company | Non-imidazole benzodiazepine inhibitors of farnesyl protein transferase |
US6100254A (en) | 1997-10-10 | 2000-08-08 | Board Of Regents, The University Of Texas System | Inhibitors of protein tyrosine kinases |
US6943159B1 (en) | 1998-02-18 | 2005-09-13 | Neurosearch A/S | Compounds and their use as positive AMPA receptor modulators |
JP2002509923A (ja) | 1998-03-31 | 2002-04-02 | ワーナー−ランバート・カンパニー | Xa因子およびトロンビンのようなセリンプロテアーゼ阻害剤としてのキノキサリノン |
DE19827640A1 (de) | 1998-06-20 | 1999-12-23 | Bayer Ag | 7-Alkyl- und Cycloalkyl-substituierte Imidazotriazinone |
CA2335102A1 (en) | 1998-09-01 | 2000-03-09 | Innogenetics N.V. | Benzodiazepines and benzothiazepines derivatives and hbsag peptides binding to annexins, their compositions and use |
CN1636011A (zh) | 1998-12-24 | 2005-07-06 | 杜邦药品公司 | 作为Aβ蛋白产生抑制剂的琥珀酰氨基苯并二氮杂䓬 |
DE60007960T2 (de) | 1999-04-30 | 2004-10-21 | Univ Michigan Ann Arbor | Therapeutische Anwendungen von pro-apoptotischen Benzodiazepinen |
WO2001002358A2 (en) | 1999-07-06 | 2001-01-11 | Vertex Pharmaceuticals Incorporated | Cyclized amide derivatives for treating or preventing neuronal damage |
BR0013200A (pt) | 1999-07-16 | 2002-05-07 | Bristol Myers Squibb Pharma Co | Compostos derivados de heterobiciclos contendo nitrogênio, composições farmacêuticas, método de tratamento ou prevenção de uma disfunção tromboembólica e uso dos compostos |
US6955873B1 (en) | 2000-08-04 | 2005-10-18 | Kenneth Blum | Diagnosis and treatment system for reward deficiency syndrome (RDS) and related behaviors |
JP2003506440A (ja) | 1999-08-05 | 2003-02-18 | プレサイエント ニューロファーマ インコーポレイテッド | 中枢神経系に関連する疾患の処置のための1,4−ジアゼピン誘導体 |
US6503902B2 (en) | 1999-09-13 | 2003-01-07 | Bristol-Myers Squibb Pharma Company | Hydroxyalkanoylaminolactams and related structures as inhibitors of a β protein production |
CN1399634A (zh) | 1999-09-13 | 2003-02-26 | 布里斯托尔-迈尔斯斯奎布药品公司 | 用作Aβ蛋白生成抑制剂的羟基链烷醇氨基内酰胺和相关结构 |
DE10028575A1 (de) | 2000-06-14 | 2002-03-14 | Basf Ag | Integrinliganden |
AU7997700A (en) | 1999-10-08 | 2001-04-23 | Du Pont Pharmaceuticals Company | Amino lactam sulfonamides as inhibitors of abeta protein production |
ATE315036T1 (de) | 1999-11-30 | 2006-02-15 | Pfizer Prod Inc | 2,4-diaminopyrimidinderivate als immunosuppressiva |
EP1244457B1 (en) | 1999-12-29 | 2004-10-27 | Glaxo Group Limited | Use of modulators of annexin for the manufacture of a medicament for the treatment and/or prevention of arthritis and arthritic diseases |
GB0000079D0 (en) | 2000-01-05 | 2000-02-23 | Ferring Bv | Novel antidiuretic agents |
KR20020067937A (ko) | 2000-01-26 | 2002-08-24 | 오노 야꾸힝 고교 가부시키가이샤 | 벤젠 축합 헤테로환 유도체 및 그 유도체를 유효성분으로서 함유하는 약제 |
AU2882801A (en) | 2000-01-28 | 2001-08-07 | Kaken Pharmaceutical Co., Ltd. | Azepine derivatives |
ES2275670T3 (es) | 2000-03-03 | 2007-06-16 | EISAI R&D MANAGEMENT CO., LTD. | Metodos novedosos utilizando inhibidores de colinesterasa. |
IL151576A0 (en) | 2000-04-03 | 2003-04-10 | Bristol Myers Squibb Pharma Co | Cyclic lactams as inhibitors of a-beta protein production |
CN1434803A (zh) | 2000-04-03 | 2003-08-06 | 布里斯托尔-迈尔斯斯奎布药品公司 | 作为Aβ蛋白质产生抑制剂的环内酰胺 |
AU2001257006A1 (en) | 2000-04-11 | 2001-10-23 | Du Pont Pharmaceuticals Company | Substituted lactams as inhibitors of abeta protein production |
US20020032262A1 (en) | 2000-04-24 | 2002-03-14 | Jinfang Zhang | 2-aminoarylmethylamine solid support templated for preparation of highly functionalized heterocycle compounds |
GB0012671D0 (en) | 2000-05-24 | 2000-07-19 | Merck Sharp & Dohme | Therapeutic agents |
JO2352B1 (en) | 2000-06-22 | 2006-12-12 | جانسين فارماسيوتيكا ان. في | Compounds for the treatment of non-adaptation of the bottom of the uterus |
GB0015601D0 (en) | 2000-06-26 | 2000-08-16 | Ferring Bv | Novel antidiuretic agents |
HUP0303074A3 (en) | 2000-09-27 | 2007-08-28 | Ajinomoto Kk | Benzodiazepine derivatives and pharmaceutical compositions them |
CA2428669A1 (en) | 2000-11-09 | 2002-05-16 | Takeda Chemical Industries, Ltd. | High-density lipoprotein-cholesterol level elevating agent |
CA2432825A1 (en) | 2000-12-15 | 2002-06-20 | Emory University | Nonpeptide agonists and antagonists of vasopressin receptors |
WO2002051232A2 (en) | 2000-12-27 | 2002-07-04 | Actelion Pharmaceuticals Ltd. | Novel benzazepines and related heterocyclic derivatives |
AU2002257114A1 (en) | 2001-04-06 | 2002-10-21 | Schering Corporation | Treatment of malaria with farsenyl protein transferase inhibitors |
WO2002088087A1 (fr) | 2001-04-26 | 2002-11-07 | Takeda Chemical Industries, Ltd. | Nouveaux derives heterocycliques |
EP1392644A1 (en) | 2001-05-31 | 2004-03-03 | Bristol-Myers Squibb Company | Cinnamide derivatives as kcnq potassium channel modulators |
IL159105A0 (en) | 2001-06-07 | 2004-05-12 | Neuro3D | Cyclic nucleotide phosphodiesterase inhibitors, preparation and uses thereof |
GB0115515D0 (en) | 2001-06-25 | 2001-08-15 | Ferring Bv | Oxytocin agonisys |
CA2451163A1 (en) | 2001-06-28 | 2003-01-09 | Takeda Chemical Industries, Ltd. | Agent for preventing or treating organ functional disorders and order dysfunction |
MXPA04001252A (es) | 2001-08-09 | 2004-05-27 | Actelion Pharmaceuticals Ltd | Nuevos heterociclos benzo-fusionados como antagonistas de endotelina. |
WO2003024456A1 (en) | 2001-09-20 | 2003-03-27 | Eisai Co., Ltd. | Methods for treating and preventing migraines |
US20030134846A1 (en) | 2001-10-09 | 2003-07-17 | Schering Corporation | Treatment of trypanosoma brucei with farnesyl protein transferase inhibitors |
WO2003032914A2 (en) | 2001-10-17 | 2003-04-24 | Eisai Co., Ltd. | Methods for treating substance abuse with cholinesterase inhibitors |
EP1443937B1 (en) | 2001-11-13 | 2008-06-18 | Ortho-McNeil Pharmaceuticals, Inc. | Substituted 1,4-benzodiazepines and uses thereof for the treatment of cancer |
AU2003228796A1 (en) | 2002-05-01 | 2003-11-17 | Eisai Co., Ltd. | Cholinesterase inhibitors to prevent injuries caused by chemicals |
AU2003235504A1 (en) | 2002-05-13 | 2003-11-11 | 3-Dimensional Pharmaceuticals, Inc. | Method for cytoprotection through mdm2 and hdm2 inhibition |
AU2003298514A1 (en) | 2002-05-17 | 2004-05-04 | Eisai Co., Ltd. | Methods and compositions using cholinesterase inhibitors |
WO2003106628A2 (en) | 2002-06-17 | 2003-12-24 | Bristol-Myers Squibb Company | Benzodiazepine inhibitors of mitochondial f1f0 atp hydrolase and methods of inhibiting f1f0 atp hydrolase |
UA79293C2 (en) | 2002-07-03 | 2007-06-11 | Univ Wayne State | 4-(7'-halo-2-quino (xa-) linyloxy)phenoxy propionic acid derivatives as antineoplastic agents |
US7001901B2 (en) | 2002-08-27 | 2006-02-21 | Bristol-Myers Squibb Company | Tetrazolylpropionamides as inhibitors of Aβ protein production |
US7074783B2 (en) | 2002-10-10 | 2006-07-11 | Elan Pharmaceuticals, Inc. | Sulfonylbenzodiazepinone acetamides as bradykinin antagonists |
WO2004067008A1 (ja) | 2003-01-28 | 2004-08-12 | Takeda Pharmaceutical Company Limited | 受容体作動薬 |
US20070129348A1 (en) | 2003-04-18 | 2007-06-07 | Fumio Itoh | Receptor antagonist |
GB0312365D0 (en) | 2003-05-30 | 2003-07-02 | Univ Aston | Novel 3-substituted-1, 4-benzodiazepines |
CN1812982B (zh) | 2003-06-26 | 2010-10-27 | 默沙东公司 | 苯并二氮杂*cgrp受体拮抗剂 |
AU2004263080B2 (en) | 2003-06-26 | 2008-12-18 | Merck Sharp & Dohme Corp. | Benzodiazepine CGRP receptor antagonists |
US20070099938A1 (en) * | 2003-10-24 | 2007-05-03 | Ono Pharmaceutical Co., Ltd. | Antistress drug and medical use thereof |
US20080312189A1 (en) | 2004-03-05 | 2008-12-18 | Eisai Co., Ltd. | Cadasil Treatment with Cholinesterase Inhibitors |
US20050272722A1 (en) | 2004-03-18 | 2005-12-08 | The Brigham And Women's Hospital, Inc. | Methods for the treatment of synucleinopathies |
US7323455B2 (en) | 2004-03-24 | 2008-01-29 | Wyeth | 7-aryl 1,5-dihydro-4,1-benzoxazepin-2(3H)-one derivatives and their use as progesterone receptor modulators |
US20050272723A1 (en) | 2004-04-27 | 2005-12-08 | The Regents Of The University Of Michigan | Methods and compositions for treating diseases and conditions associated with mitochondrial function |
MXPA06014798A (es) | 2004-06-17 | 2007-06-22 | Wyeth Corp | Antagonistas del receptor de hormona para liberar gonadotropina. |
WO2006004201A1 (ja) | 2004-07-01 | 2006-01-12 | Eisai R & D Management Co., Ltd. | 神経再生促進剤 |
US20060135507A1 (en) | 2004-08-13 | 2006-06-22 | Osamu Yokoyama | Therapeutic agent for overactive bladder involved in aging |
EP1627876A1 (en) | 2004-08-20 | 2006-02-22 | Ferring B.V. | Heterocyclic condensed compounds useful as antidiuretic agents |
EP1632494A1 (en) | 2004-08-24 | 2006-03-08 | Ferring B.V. | Vasopressin v1a antagonists |
US20060052369A1 (en) | 2004-09-07 | 2006-03-09 | The Regents Of The University Of Michigan | Compositions and methods relating to novel compounds and targets thereof |
AU2005286733B2 (en) * | 2004-09-23 | 2009-11-05 | Alexander Michalow | Methods for regulating neurotransmitter systems by inducing counteradaptations |
EP1809296A4 (en) | 2004-10-28 | 2009-03-11 | Janssen Pharmaceutica Nv | NEW [1,4] -BENZODIAZEPINES AS VASOPRESSIN V2 RECEPTOR ANTAGONISTS |
JP5258561B2 (ja) * | 2005-07-15 | 2013-08-07 | アルバニー モレキュラー リサーチ, インコーポレイテッド | アリール置換およびヘテロアリール置換テトラヒドロベンズアゼピンならびにノルエピネフリン、ドーパミンおよびセロトニンの再取り込みを遮断するためのその使用 |
JP2011116663A (ja) | 2008-05-30 | 2011-06-16 | Otsuka Pharmaceut Co Ltd | ベンゾジアゼピン化合物 |
-
2008
- 2008-05-08 WO PCT/US2008/063039 patent/WO2008141081A1/en active Application Filing
- 2008-05-08 US US12/598,882 patent/US9096546B2/en not_active Expired - Fee Related
- 2008-05-08 NZ NZ580801A patent/NZ580801A/xx not_active IP Right Cessation
- 2008-05-08 CA CA002685860A patent/CA2685860A1/en not_active Abandoned
- 2008-05-08 EA EA200971044A patent/EA017249B8/ru not_active IP Right Cessation
- 2008-05-08 KR KR1020097025843A patent/KR20100017766A/ko not_active Application Discontinuation
- 2008-05-08 JP JP2010507653A patent/JP2010526825A/ja active Pending
- 2008-05-08 MX MX2009011923A patent/MX2009011923A/es not_active Application Discontinuation
- 2008-05-08 EP EP08780604A patent/EP2146722A4/en not_active Withdrawn
- 2008-05-08 CN CN200880024332A patent/CN101686983A/zh active Pending
- 2008-05-08 AU AU2008251557A patent/AU2008251557B2/en not_active Ceased
- 2008-05-08 BR BRPI0811204A patent/BRPI0811204A8/pt not_active IP Right Cessation
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AU2008251557B2 (en) | 2012-12-06 |
US20100137287A1 (en) | 2010-06-03 |
NZ580801A (en) | 2012-09-28 |
EA017249B1 (ru) | 2012-11-30 |
BRPI0811204A8 (pt) | 2015-09-22 |
EA017249B8 (ru) | 2013-01-30 |
KR20100017766A (ko) | 2010-02-16 |
EP2146722A1 (en) | 2010-01-27 |
CA2685860A1 (en) | 2008-11-20 |
CN101686983A (zh) | 2010-03-31 |
US9096546B2 (en) | 2015-08-04 |
BRPI0811204A2 (pt) | 2014-10-29 |
IL201922A0 (en) | 2010-06-16 |
JP2010526825A (ja) | 2010-08-05 |
MX2009011923A (es) | 2009-11-18 |
EP2146722A4 (en) | 2011-08-03 |
WO2008141081A1 (en) | 2008-11-20 |
AU2008251557A1 (en) | 2008-11-20 |
CO6251238A2 (es) | 2011-02-21 |
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