BRPI0418082A - antagonista de receptor de adenosina a2a, agente para tratar e/ou prevenir doenças, composto, composição farmacêutica, e, método para tratar e/ou prevenir doenças associadas com receptor de adenosina a2a - Google Patents
antagonista de receptor de adenosina a2a, agente para tratar e/ou prevenir doenças, composto, composição farmacêutica, e, método para tratar e/ou prevenir doenças associadas com receptor de adenosina a2aInfo
- Publication number
- BRPI0418082A BRPI0418082A BRPI0418082-8A BRPI0418082A BRPI0418082A BR PI0418082 A BRPI0418082 A BR PI0418082A BR PI0418082 A BRPI0418082 A BR PI0418082A BR PI0418082 A BRPI0418082 A BR PI0418082A
- Authority
- BR
- Brazil
- Prior art keywords
- substituted
- adenosine
- unsubstituted
- treating
- preventing diseases
- Prior art date
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- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/425—Thiazoles
- A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
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- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- A61K31/445—Non condensed piperidines, e.g. piperocaine
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- Plural Heterocyclic Compounds (AREA)
Abstract
"ANTAGONISTA DE RECEPTOR DE ADENOSINA A~ 2A~, AGENTE PARA TRATAR E/OU PREVENIR DOENçAS, COMPOSTO, COMPOSIçãO FARMACêUTICA, E, MéTODO PARA TRATAR E/OU PREVENIR DOENçAS ASSOCIADAS COM RECEPTOR DE ADENOSINA A~ 2A~". Um antagonista de receptor de adenosina A~ 2A~ que contém como o ingrediente ativo, um derivado de tiazol representado por uma fórmula geral (1), ou um sal farmacologicamente aceitável do derivado, (em que n é um número inteiro de 0 a 3; R¬ 1¬ é cicloalquila substituído ou não substituído, arila substituído ou não substituído, um grupo heterocíclico alicíclico substituído ou não substituído, ou um grupo heterocíclico aromático substituído ou não substituído; R¬ 2¬ é halogênio, alquila inferior substituído ou não substituído, arila substituído ou não substituído, um grupo heterocíclico alicíclico substituído ou não substituído, um grupo heterocíclico aromático substituído ou não substituído, -COR¬ 8¬, ou análogos; R¬ 3¬ e R¬ 4¬ pode ser igual ou diferente, e cada um representa um átomo de hidrogênio, alquila inferior substituído ou não substituído, aralquila substituído ou não substituído, COR¬ 12¬, etc)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP2003432777 | 2003-12-26 | ||
JP2003-432777 | 2003-12-26 | ||
PCT/JP2004/019778 WO2005063743A1 (ja) | 2003-12-26 | 2004-12-24 | チアゾール誘導体 |
Publications (3)
Publication Number | Publication Date |
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BRPI0418082A true BRPI0418082A (pt) | 2007-04-17 |
BRPI0418082B1 BRPI0418082B1 (pt) | 2019-09-24 |
BRPI0418082B8 BRPI0418082B8 (pt) | 2021-05-25 |
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ID=34736491
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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BRPI0418082A BRPI0418082B8 (pt) | 2003-12-26 | 2004-12-24 | derivados de tiazol úteis como antagonistas de receptor de adenosina a2a |
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US (4) | US7718808B2 (pt) |
EP (2) | EP3002283B1 (pt) |
JP (1) | JP4638355B2 (pt) |
KR (1) | KR101168625B1 (pt) |
CN (1) | CN1902196B (pt) |
AU (1) | AU2004309279B2 (pt) |
BR (1) | BRPI0418082B8 (pt) |
CA (1) | CA2551611C (pt) |
CY (2) | CY1117132T1 (pt) |
DK (2) | DK3002283T3 (pt) |
EA (1) | EA013249B1 (pt) |
ES (2) | ES2555308T3 (pt) |
HK (1) | HK1091837A1 (pt) |
HU (1) | HUE025659T2 (pt) |
LT (1) | LT3002283T (pt) |
NO (1) | NO338017B1 (pt) |
PL (2) | PL3002283T3 (pt) |
PT (2) | PT1700856E (pt) |
SI (2) | SI1700856T1 (pt) |
TW (1) | TWI349550B (pt) |
WO (1) | WO2005063743A1 (pt) |
ZA (1) | ZA200606027B (pt) |
Families Citing this family (37)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200524887A (en) * | 2003-10-27 | 2005-08-01 | Lundbeck & Co As H | N-thiazol-2-yl-benzamide derivatives |
EP1794157B1 (en) | 2004-09-22 | 2014-02-26 | H. Lundbeck A/S | 2-acylaminothiazole derivatives |
WO2006105237A2 (en) * | 2005-03-29 | 2006-10-05 | The University Of Maryland, Baltimore | Inhibitors for extracellular signal-regulated kinase docking domains and uses therefor |
US7674912B2 (en) * | 2005-04-25 | 2010-03-09 | H. Lundbeck A/S | Pro-drugs of N-thiazol-2-yl-benzamide derivatives |
EP1894930A4 (en) * | 2005-06-23 | 2010-06-23 | Kyowa Hakko Kirin Co Ltd | THIAZOLE DERIVATIVE |
JP5121453B2 (ja) * | 2005-08-02 | 2013-01-16 | 協和発酵キリン株式会社 | 睡眠障害の治療および/または予防剤 |
WO2007022415A2 (en) * | 2005-08-18 | 2007-02-22 | Pharmacopeia, Inc. | Substituted 2-aminothiazoles for treating neurodegenerative diseases |
US8455658B2 (en) | 2006-01-25 | 2013-06-04 | Synta Pharmaceuticals Corp. | Thiazole and thiadiazole compounds for inflammation and immune-related uses |
AU2007290359B2 (en) | 2006-09-01 | 2012-09-20 | Vertex Pharmaceuticals Incorporated | 5- (2-furyl)-1, 3-thiazole derivatives useful as inhibitors of phosphatidylinositol 3-kinase |
GB0701426D0 (en) * | 2007-01-25 | 2007-03-07 | Univ Sheffield | Compounds and their use |
BRPI0814672A2 (pt) * | 2007-07-23 | 2014-09-30 | Synosia Therapeutics | Método de tratamento de um paciente, e de distúrbio de estresse pós-traumático, e, métodos para melhorar a resiliência em um paciente e para diagnosticar distúrbio de estresse pós-traumático em um paciente. |
TWI473614B (zh) | 2008-05-29 | 2015-02-21 | Kyowa Hakko Kirin Co Ltd | Anti-analgesic inhibitors |
CA2731573C (en) * | 2008-07-23 | 2018-09-18 | Kyowa Hakko Kirin Co., Ltd. | Selective adenosine a2a receptor antagonists useful in the treatment and prevention of migraine |
CN101747327B (zh) * | 2008-12-02 | 2013-03-27 | 中国人民解放军军事医学科学院毒物药物研究所 | 芳酰胺基噻唑类衍生物及其制备方法和用途 |
EP2198710A1 (de) | 2008-12-19 | 2010-06-23 | Bayer CropScience AG | Verwendung von 5-Pyridin-4yl-(1,3)Thiazole zur Bekämpfung phytopathogener Pilze |
US8426590B2 (en) * | 2009-03-23 | 2013-04-23 | Cipla Limited | Process for the preparation of doxazosin and salts thereof |
TWI548411B (zh) * | 2009-04-28 | 2016-09-11 | Kyowa Hakko Kirin Co Ltd | Exercise disorder treatment |
UA113383C2 (xx) * | 2009-09-02 | 2017-01-25 | Терапевтичний агент для лікування тривожних розладів | |
UA110097C2 (uk) * | 2009-09-02 | 2015-11-25 | Терапевтичний агент для лікування розладів настрою | |
US9095596B2 (en) | 2009-10-15 | 2015-08-04 | Southern Research Institute | Treatment of neurodegenerative diseases, causation of memory enhancement, and assay for screening compounds for such |
US9079891B2 (en) | 2010-08-27 | 2015-07-14 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
WO2012027965A1 (en) * | 2010-09-01 | 2012-03-08 | Glaxo Group Limited | Novel compounds |
ES2580961T3 (es) * | 2011-02-24 | 2016-08-30 | Nerviano Medical Sciences S.R.L. | Derivados Tiazolilfenil-bencenosulfonamido como Inhibidores de Cinasa |
CA2873097A1 (en) * | 2012-05-11 | 2013-11-14 | Todd M. Hansen | Pyridazine and pyridine derivatives as nampt inhibitors |
RU2534617C2 (ru) * | 2012-09-21 | 2014-11-27 | Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Оренбургский государственный университет" | Регулятор коллективного поведения ("чувство кворума") у бактерий |
US9512116B2 (en) | 2012-10-12 | 2016-12-06 | Calcimedica, Inc. | Compounds that modulate intracellular calcium |
EP2878339A1 (en) * | 2013-12-02 | 2015-06-03 | Siena Biotech S.p.A. | SIP3 antagonists |
MA41090A (fr) * | 2014-12-03 | 2017-10-10 | H Lundbeck As | Antagoniste de a2a faiblement dosé pour le traitement du tdah et de la maladie de parkinson |
JOP20200093A1 (ar) | 2015-01-09 | 2017-06-16 | Kyowa Kirin Co Ltd | طريقة لإنتاج مشتق ثيازول |
ES2578363B1 (es) * | 2015-01-22 | 2017-01-31 | Palobiofarma, S.L. | Moduladores de los receptores A3 de adenosina |
JO3544B1 (ar) * | 2015-03-19 | 2020-07-05 | Kyowa Kirin Co Ltd | عامل علاجي للاختلال الوظيفي في الفص الجبهي |
WO2016160938A1 (en) * | 2015-04-02 | 2016-10-06 | Abbvie Inc. | N-(1,3-thiazol-2-yl)pyrimidine-5-carboxamides as trpv3 modulators |
ES2676535B1 (es) * | 2017-01-20 | 2019-04-29 | Palobiofarma Sl | Moduladores de los receptores a3 de adenosina |
CN109293652B (zh) * | 2017-07-24 | 2021-10-22 | 四川科伦博泰生物医药股份有限公司 | 一种取代的噻唑衍生物及其用途 |
WO2019072143A1 (zh) * | 2017-10-11 | 2019-04-18 | 上海迪诺医药科技有限公司 | 4-氨基吡啶衍生物、其药物组合物、制备方法及应用 |
GB202011996D0 (en) * | 2020-07-31 | 2020-09-16 | Adorx Therapeutics Ltd | Antagonist compounds |
GB2615307A (en) * | 2022-01-28 | 2023-08-09 | Adorx Therapeutics Ltd | Antagonist compounds |
Family Cites Families (86)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1183061B (it) * | 1984-07-31 | 1987-10-05 | Zambon Spa | Composti dotati di attivita'antiallergica |
US4666138A (en) * | 1985-09-06 | 1987-05-19 | Dearman Timothy Charles | External reforming pipe clamp |
EP0372125A1 (en) * | 1988-11-08 | 1990-06-13 | Akzo N.V. | Oxazole and thiazole derivatives |
IE68593B1 (en) | 1989-12-06 | 1996-06-26 | Sanofi Sa | Heterocyclic substituted acylaminothiazoles their preparation and pharmaceutical compositions containing them |
US5166203A (en) | 1990-08-30 | 1992-11-24 | Kanebo, Ltd. | Quinolinecarboxylic acid derivatives, antibacterial agent containing the same |
FR2677356B1 (fr) | 1991-06-05 | 1995-03-17 | Sanofi Sa | Derives heterocycliques d'acylamino-2 thiazoles-5 substitues, leur preparation et compositions pharmaceutiques en contenant. |
GB9204958D0 (en) | 1992-03-06 | 1992-04-22 | Fujisawa Pharmaceutical Co | Thiazole derivatives |
AU3884893A (en) | 1992-04-10 | 1993-11-18 | Merck Frosst Canada Inc. | Thiazole-substituted benzyl alcohols as leukotriene antagonists |
FR2692893B1 (fr) * | 1992-06-24 | 1994-09-02 | Sanofi Elf | Dérivés alkylamino ramifiés du thiazole, leurs procédés de préparation et les compositions pharmaceutiques qui les contiennent. |
US5856347A (en) | 1994-11-29 | 1999-01-05 | Hisamitsu Pharmaceutical Co., Inc. | Antibacterial preparation or bactericide comprising 2-aminothiazole derivative and/or salt thereof |
WO1997003058A1 (fr) | 1995-07-07 | 1997-01-30 | Taisho Pharmaceutical Co., Ltd. | Derives de 4-alkylthiazoline |
JPH1087490A (ja) | 1996-09-10 | 1998-04-07 | Sagami Chem Res Center | インターロイキン6生産抑制剤、骨吸収抑制剤、抗骨粗鬆症剤、及びチアゾール化合物 |
HRP980334A2 (en) | 1997-06-19 | 1999-04-30 | Mimi Lifen Quan | INHIBITORS OF FACTOR Xa WITH A NEUTRAL P1 SPECIFICITY GROUP |
JPH11193281A (ja) | 1997-10-27 | 1999-07-21 | Takeda Chem Ind Ltd | アデノシンa3受容体拮抗剤およびチアゾール化合物 |
JPH11209284A (ja) | 1998-01-27 | 1999-08-03 | Sagami Chem Res Center | 骨形成促進剤 |
AU4506399A (en) | 1998-06-05 | 1999-12-30 | Novartis Ag | Aryl pyridinyl thiazoles |
EP1112275B9 (en) | 1998-09-09 | 2004-03-10 | Metabasis Therapeutics, Inc. | Novel heteroaromatic inhibitors of fructose 1,6-bisphosphatase |
US6756360B1 (en) | 1998-12-24 | 2004-06-29 | Metabasis Therapeutics, Inc. | Combination of FBPase inhibitors and insulin sensitizers for the treatment of diabetes |
PT1143955E (pt) * | 1998-12-24 | 2005-11-30 | Metabasis Therapeutics Inc | Combinacao de inibidores de fbpase e sensibilizadores de insulina para o tratamento de diabete |
US6414011B1 (en) | 1999-03-26 | 2002-07-02 | Euro-Celtique S.A. | Aryl substituted pyrazoles, and pyrroles, and the use thereof |
JP3333774B2 (ja) | 1999-04-23 | 2002-10-15 | 武田薬品工業株式会社 | 5−ピリジル−1,3−アゾール化合物、その製造法及び用途 |
JP2000302680A (ja) | 1999-04-23 | 2000-10-31 | Takeda Chem Ind Ltd | 脳保護剤 |
ES2275500T3 (es) * | 1999-04-23 | 2007-06-16 | Takeda Pharmaceutical Company Limited | Compuestos de 5-piridil-1,3-azol, procedimiento para su produccion y uso de los mismos. |
WO2001010865A1 (fr) * | 1999-08-06 | 2001-02-15 | Takeda Chemical Industries, Ltd. | INHIBITEURS DE p38MAP KINASE |
JP2001114690A (ja) * | 1999-08-06 | 2001-04-24 | Takeda Chem Ind Ltd | p38MAPキナーゼ阻害剤 |
AR035016A1 (es) | 1999-08-25 | 2004-04-14 | Takeda Chemical Industries Ltd | Composicion de azol promotor de produccion/secrecion de neurotrofina, compuesto prodroga del mismo, composicion farmaceutica que lo comprende y uso del mismo para preparar esta ultima. |
KR100875335B1 (ko) | 1999-12-22 | 2008-12-22 | 메타베이시스 테라퓨틱스, 인크. | 신규 비스아미데이트 포스포네이트 프로드러그 |
MXPA02007099A (es) | 2000-01-19 | 2004-08-23 | Alteon Inc | Compuestos de tiazola, imidazola y oxazola y tratamientos de desordenes asociados con la maduracion de la proteina. |
TWI284639B (en) | 2000-01-24 | 2007-08-01 | Shionogi & Co | A compound having thrombopoietin receptor agonistic effect |
JP2002302488A (ja) * | 2000-03-30 | 2002-10-18 | Takeda Chem Ind Ltd | 置換1,3−チアゾール化合物、その製造法および用途 |
EP1268474A2 (en) * | 2000-03-30 | 2003-01-02 | Takeda Chemical Industries, Ltd. | Substituted 1,3-thiazole compounds, their production and use |
US7563774B2 (en) | 2000-06-29 | 2009-07-21 | Metabasis Therapeutics, Inc. | Combination of FBPase inhibitors and antidiabetic agents useful for the treatment of diabetes |
EP1372660A2 (en) | 2000-07-06 | 2004-01-02 | Metabasis Therapeutics, Inc. | A combination of fbpase inhibitors and antidiabetic agents useful for the treatment of diabetes |
JP2002053566A (ja) | 2000-08-11 | 2002-02-19 | Japan Tobacco Inc | チアゾール化合物及びその医薬用途 |
WO2002030358A2 (en) | 2000-10-11 | 2002-04-18 | Tularik Inc. | Modulation of ccr4 function |
JP2004513935A (ja) | 2000-11-17 | 2004-05-13 | ノボ ノルディスク アクティーゼルスカブ | グルカゴンアンタゴニスト/逆アゴニスト |
GB0028383D0 (en) | 2000-11-21 | 2001-01-03 | Novartis Ag | Organic compounds |
CA2436739A1 (en) * | 2000-12-26 | 2002-07-04 | Takeda Chemical Industries, Ltd. | Combination agent |
JP2002302458A (ja) * | 2000-12-26 | 2002-10-18 | Takeda Chem Ind Ltd | 併用薬 |
US20040097555A1 (en) * | 2000-12-26 | 2004-05-20 | Shinegori Ohkawa | Concomitant drugs |
JPWO2002051836A1 (ja) | 2000-12-27 | 2004-04-22 | 協和醗酵工業株式会社 | ジペプチジルペプチダーゼ−iv阻害剤 |
WO2002053156A1 (en) | 2000-12-29 | 2002-07-11 | Alteon, Inc. | Method for treating glaucoma ii b |
EP1353676A4 (en) | 2000-12-29 | 2006-05-31 | Alteon Inc | METHOD FOR THE TREATMENT OF FIBROUS OR OTHER INDICATIONS |
EP1361220A4 (en) | 2001-01-26 | 2005-09-07 | Shionogi & Co | CYCLIC COMPOUNDS WITH THROMBOPOIETIN RECEPTAGONISM |
EP1394154A4 (en) * | 2001-03-23 | 2005-05-18 | Takeda Pharmaceutical | HETEROCYCLIC DERIVATIVE WITH FIVE MEMBERS OF ALKANOIC ACID |
WO2002079204A1 (fr) * | 2001-03-28 | 2002-10-10 | Kyowa Hakko Kogyo Co., Ltd. | Derive 8-thiazolyl[1,2,4]triazolo[1,5-c]pyrimidine |
GB2375517A (en) | 2001-05-17 | 2002-11-20 | Reckitt Benckiser | A water-soluble injection moulded container |
US7144903B2 (en) | 2001-05-23 | 2006-12-05 | Amgen Inc. | CCR4 antagonists |
WO2002094798A1 (fr) | 2001-05-23 | 2002-11-28 | Nippon Soda Co.,Ltd. | Preparation de composes thiazole |
WO2002100433A1 (en) * | 2001-06-11 | 2002-12-19 | Takeda Chemical Industries, Ltd. | Medicinal compositions |
WO2003000257A1 (fr) | 2001-06-26 | 2003-01-03 | Takeda Chemical Industries, Ltd. | Promoteur de production/secretion de la superfamille des tgf-$g(b) |
ATE381542T1 (de) | 2001-08-13 | 2008-01-15 | Phenex Pharmaceuticals Ag | Nr1h4-kern-rezeptor-bindende verbindungen |
EP1423113A4 (en) | 2001-08-13 | 2007-04-18 | Phenex Pharmaceuticals Ag | NR1H4 NUCLEAR RECEPTOR BINDING COMPOUNDS |
TWI330183B (pt) | 2001-10-22 | 2010-09-11 | Eisai R&D Man Co Ltd | |
WO2003037451A1 (en) * | 2001-11-01 | 2003-05-08 | Samuel Stone | Golfing aid |
WO2003039529A1 (en) | 2001-11-07 | 2003-05-15 | 4Sc A.G. | Selective antibacterial agents |
JP2005510508A (ja) * | 2001-11-08 | 2005-04-21 | 藤沢薬品工業株式会社 | アデノシンアンタゴニストとしてのチアゾールピリダジノン類 |
US6620811B2 (en) | 2001-11-19 | 2003-09-16 | Hoffmann-La Roche Inc. | Isonicotin- and nicotinamide derivatives of benzothiazoles |
ES2416304T3 (es) | 2002-01-18 | 2013-07-31 | Astellas Pharma Inc. | Derivado de 2-acilaminotiazol o sal del mismo |
CA2474322A1 (en) | 2002-01-25 | 2003-07-31 | Kylix Pharmaceuticals B.V. | 4(hetero-) aryl substituted (thia-/oxa-/pyra) zoles for inhibition of tie-2 |
US20030158199A1 (en) | 2002-01-25 | 2003-08-21 | Kylix, B.V. | Novel compounds for inhibition of Tie-2 |
US7183276B2 (en) | 2002-02-28 | 2007-02-27 | Takeda Pharmaceutical Company Limited | Azole compounds |
US7338969B2 (en) | 2002-03-08 | 2008-03-04 | Quonova, Llc | Modulation of pathogenicity |
US7335779B2 (en) | 2002-03-08 | 2008-02-26 | Quonova, Llc | Modulation of pathogenicity |
US7462635B2 (en) | 2002-03-14 | 2008-12-09 | Takeda Pharmaceutical Company Limited | Thiazole and oxazole VDAC regulator |
US20030236287A1 (en) * | 2002-05-03 | 2003-12-25 | Piotrowski David W. | Positive allosteric modulators of the nicotinic acetylcholine receptor |
JP2003335680A (ja) | 2002-05-21 | 2003-11-25 | Otsuka Pharmaceut Factory Inc | Acat−1阻害剤 |
AU2003242124A1 (en) | 2002-06-11 | 2003-12-22 | Institute Of Medicinal Molecular Design, Inc. | Medicament for treatment of neurodegenerative diseases |
JP4881559B2 (ja) | 2002-06-27 | 2012-02-22 | ノボ・ノルデイスク・エー/エス | 治療薬としてのアリールカルボニル誘導体 |
FR2842523A1 (fr) | 2002-07-17 | 2004-01-23 | Sanofi Synthelabo | Derives d'acylaminothiazole, leur preparation et leur application en therapeutique |
EP1539722A1 (en) | 2002-08-07 | 2005-06-15 | F. Hoffmann-La Roche Ag | Thiazole derivatives |
EP1558607B1 (en) | 2002-10-30 | 2010-05-05 | Vertex Pharmaceuticals Incorporated | Compositions useful as inhibitors of rock and other protein kinases |
US20040235925A1 (en) * | 2002-12-17 | 2004-11-25 | Pharmacia Corporation | Method for the treatment, prevention, or inhibition of a CNS disorder and/or pain and inflammation using a combination of duloxetine, venlafaxine or atomoxetine and a cyclooxygenase-2 selective inhibitor and compositions thereof |
CA2514363A1 (en) | 2003-02-12 | 2004-08-26 | Transtech Pharma, Inc. | Substituted azole derivatives as therapeutic agents |
EP1615698B1 (en) * | 2003-04-11 | 2010-09-29 | High Point Pharmaceuticals, LLC | New amide derivatives and pharmaceutical use thereof |
US20040248937A1 (en) * | 2003-04-14 | 2004-12-09 | The Institute For Pharmaceutical Discovery Llc | Substituted phenylalkanoic acids for the treatment of diabetes |
JP2006525366A (ja) * | 2003-04-30 | 2006-11-09 | ジ インスチチュート フォー ファーマシューティカル ディスカバリー、エルエルシー | 複素環式カルボン酸置換基 |
GB0313914D0 (en) * | 2003-06-16 | 2003-07-23 | Smithkline Beecham Corp | Compounds |
EP1664006A2 (en) | 2003-09-06 | 2006-06-07 | Vertex Pharmaceuticals Incorporated | Modulators of atp-binding cassette transporters |
US20060015494A1 (en) | 2003-11-26 | 2006-01-19 | Keating Brett M | Use of image similarity in selecting a representative visual image for a group of visual images |
EP1794157B1 (en) * | 2004-09-22 | 2014-02-26 | H. Lundbeck A/S | 2-acylaminothiazole derivatives |
JP5121453B2 (ja) * | 2005-08-02 | 2013-01-16 | 協和発酵キリン株式会社 | 睡眠障害の治療および/または予防剤 |
CA2731573C (en) * | 2008-07-23 | 2018-09-18 | Kyowa Hakko Kirin Co., Ltd. | Selective adenosine a2a receptor antagonists useful in the treatment and prevention of migraine |
TWI548411B (zh) * | 2009-04-28 | 2016-09-11 | Kyowa Hakko Kirin Co Ltd | Exercise disorder treatment |
UA110097C2 (uk) * | 2009-09-02 | 2015-11-25 | Терапевтичний агент для лікування розладів настрою | |
UA113383C2 (xx) * | 2009-09-02 | 2017-01-25 | Терапевтичний агент для лікування тривожних розладів |
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- 2004-12-24 HU HUE04808128A patent/HUE025659T2/en unknown
- 2004-12-24 PT PT151923810T patent/PT3002283T/pt unknown
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2006
- 2006-07-20 ZA ZA2006/06027A patent/ZA200606027B/en unknown
- 2006-07-26 NO NO20063446A patent/NO338017B1/no not_active IP Right Cessation
- 2006-12-08 HK HK06113527.9A patent/HK1091837A1/xx not_active IP Right Cessation
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2010
- 2010-04-26 US US12/766,986 patent/US7880013B2/en active Active
- 2010-12-06 US US12/960,937 patent/US8420827B2/en active Active
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2013
- 2013-03-14 US US13/826,654 patent/US8889718B2/en active Active
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2016
- 2016-01-15 CY CY20161100040T patent/CY1117132T1/el unknown
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2017
- 2017-08-30 CY CY20171100913T patent/CY1119261T1/el unknown
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