ATE509014T1 - Malonyl coa-decarboxylase inhibitoren als stoffwechselmodulatoren - Google Patents

Malonyl coa-decarboxylase inhibitoren als stoffwechselmodulatoren

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Publication number
ATE509014T1
ATE509014T1 AT02713444T AT02713444T ATE509014T1 AT E509014 T1 ATE509014 T1 AT E509014T1 AT 02713444 T AT02713444 T AT 02713444T AT 02713444 T AT02713444 T AT 02713444T AT E509014 T1 ATE509014 T1 AT E509014T1
Authority
AT
Austria
Prior art keywords
malonyl
decarboxylase
malonyl coa
decarboxylase inhibitors
compounds
Prior art date
Application number
AT02713444T
Other languages
English (en)
Inventor
Thomas Arrhenius
Mi Chen
Jie Fei Cheng
Yujin Huang
Alex Nadzan
Richard Penuliar
David Wallace
Lin Zhang
Gary Lopaschuk
Jason Dyck
Original Assignee
Chugai Pharmaceutical Co Ltd
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Filing date
Publication date
Application filed by Chugai Pharmaceutical Co Ltd filed Critical Chugai Pharmaceutical Co Ltd
Application granted granted Critical
Publication of ATE509014T1 publication Critical patent/ATE509014T1/de

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    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
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Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1353662B1 (de) * 2001-01-26 2007-04-18 Chugai Seiyaku Kabushiki Kaisha Verfahren zur behandlung von erkrankungen mit malonyl coa-decarboxylase-inhibitoren
US7709510B2 (en) 2001-02-20 2010-05-04 Chugai Seiyaku Kabushiki Kaisha Azoles as malonyl-CoA decarboxylase inhibitors useful as metabolic modulators
JP4155351B2 (ja) 2001-02-20 2008-09-24 中外製薬株式会社 代謝調節剤として有用なマロニル−ＣｏＡ脱炭酸酵素阻害剤としてのアゾール
AU2003228614A1 (en) * 2002-04-23 2003-11-10 Chugai Seiyaku Kabushiki Kaisha Lxr modulators
GB0302094D0 (en) 2003-01-29 2003-02-26 Pharmagene Lab Ltd EP4 receptor antagonists
JP2006519229A (ja) * 2003-02-13 2006-08-24 アルバート・アインシュタイン・カレッジ・オヴ・メディシン・オヴ・イェシヴァ・ユニヴァーシティ 視床下部内の長鎖脂肪アシルＣｏＡレベルの変調による摂食量およびグルコース産生量の調節
EP2208495B1 (de) 2003-08-01 2011-12-14 Chugai Seiyaku Kabushiki Kaisha Azol-Verbindungen auf Cyanoguanidin-Basis als Malonyl-Coa Decarboxylase-Hemmer
EP1653957B1 (de) 2003-08-01 2008-07-09 Chugai Seiyaku Kabushiki Kaisha Piperidin-verbindungen als malonyl-coa decarboxylase-hemmer
JP4727579B2 (ja) * 2003-08-01 2011-07-20 中外製薬株式会社 マロニル−ＣｏＡデカルボキシラーゼ阻害剤として有用なシアノアミド化合物
DE602004030017D1 (de) 2003-08-01 2010-12-23 Chugai Pharmaceutical Co Ltd Heterocyclische verbindungen als nützliche malonyl-coa decarboxylase-hemmer
GB0324269D0 (en) 2003-10-16 2003-11-19 Pharmagene Lab Ltd EP4 receptor antagonists
CN100509808C (zh) * 2003-12-08 2009-07-08 霍夫曼-拉罗奇有限公司 新型噻唑衍生物
ES2340510T3 (es) * 2004-05-28 2010-06-04 Laboratoires Expanscience Uso de alquil-furanos para la preparacion de un medicamento destinado al tratamiento de la obesidad y para el tratamiento cosmetico del exceeso de peso.
FR2870743B1 (fr) * 2005-03-21 2012-03-09 Expanscience Lab Utilisation d'alkyle furannes pour la preparation d'un medicament destine au traitement de l'obesite et pour le traitement cosmetique de la surcharge ponderale
FR2870742B1 (fr) 2004-05-28 2008-03-14 Expanscience Laboratoires Sa Utilisation d'alkyle furannes pour la preparation d'un medicament destine au traitement du diabete, de l'obesite et pour le traitement cosmetique de la cellulite et de la surcharge ponderale
DE602005027563D1 (de) 2004-05-28 2011-06-01 Expanscience Lab Verwendung von furanalkylen zur kosmetischen behandlung von zellulitis
MX2007000631A (es) 2004-07-16 2007-03-30 Sunesis Pharmaceuticals Inc Tienopirimidinas utiles como inhibidores de aurora cinasa.
WO2006041922A2 (en) * 2004-10-08 2006-04-20 Dara Biosciences, Inc. Agents and methods for administration to the central nervous system
US20070026079A1 (en) * 2005-02-14 2007-02-01 Louis Herlands Intranasal administration of modulators of hypothalamic ATP-sensitive potassium channels
US9808544B2 (en) 2005-08-31 2017-11-07 Ultraviolet Sciences, Inc. Ultraviolet light treatment chamber
US10251396B2 (en) 2014-07-28 2019-04-09 Sumitomo Chemical Company, Limited Amide compound and use of same for noxious arthropod control
TWI664905B (zh) * 2014-07-29 2019-07-11 日商住友化學股份有限公司 含有醯胺化合物之有害節肢動物控制劑
JP6217866B2 (ja) * 2014-10-24 2017-10-25 小野薬品工業株式会社 Ｋｃｎｑ２〜５チャネル活性化剤
TWI773657B (zh) 2015-12-18 2022-08-11 美商亞德利克斯公司 作爲非全身ｔｇｒ５促效劑之經取代之4-苯基吡啶化合物
US12084472B2 (en) 2015-12-18 2024-09-10 Ardelyx, Inc. Substituted 4-phenyl pyridine compounds as non-systemic TGR5 agonists
WO2018236745A1 (en) 2017-06-20 2018-12-27 Carnot, Llc COMPOSITIONS AND METHODS FOR INCREASING THE EFFICACY OF CARDIAC METABOLISM
EP4497474A3 (de) 2018-10-17 2025-04-23 Imbria Pharmaceuticals, Inc. Verfahren zur behandlung von rheumatischen erkrankungen unter verwendung von trimetazidinbasierten verbindungen
EP3976101A4 (de) 2019-05-31 2023-06-21 Imbria Pharmaceuticals, Inc. Verfahren zur behandlung von fibrose unter verwendung von verbindungen zur förderung der glucoseoxidation
US11530184B2 (en) 2020-06-30 2022-12-20 Imbria Pharmaceuticals, Inc. Crystal forms of 2-[4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl]ethyl pyridine-3-carboxylate
US11780811B2 (en) 2020-06-30 2023-10-10 Imbria Pharmaceuticals, Inc. Methods of synthesizing 2-[4-[(2,3,4-trimethoxyphenyl)methyl]piperazin-1-yl]ethyl pyridine-3-carboxylate
US11883396B2 (en) 2021-05-03 2024-01-30 Imbria Pharmaceuticals, Inc. Methods of treating kidney conditions using modified forms of trimetazidine
EP4328046A4 (de) * 2021-05-17 2024-11-13 Sumitomo Rubber Industries, Ltd. Nitriloxidverbindung und polymer mit ionischen funktionen

Family Cites Families (69)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3666769A (en) 1969-10-09 1972-05-30 Du Pont Thermally stable 2-perfluoro-substituted benzothiazoles
JPS57134480A (en) 1980-12-29 1982-08-19 Du Pont Antiinflammatory 4,5-diaryl-alpha- (polyhalomethyl)-2-thiophene methanols
US4381311A (en) 1980-12-29 1983-04-26 E. I. Du Pont De Nemours And Company Antiinflammatory 4,5-diaryl-α-(polyhalomethyl)-2-thiophenemethanols
US4632930A (en) * 1984-11-30 1986-12-30 E. I. Du Pont De Nemours And Company Antihypertensive alkyl-arylimidazole, thiazole and oxazole derivatives
US4783443A (en) 1986-03-03 1988-11-08 The University Of Chicago Amino acyl cephalosporin derivatives
GB8714537D0 (en) 1987-06-22 1987-07-29 Ici Plc Pyrazine derivatives
EP0733366B1 (de) 1988-01-07 1998-04-01 E.I. Du Pont De Nemours And Company Angiotensin II-Rezeptor blockierende Imidazole und Diuretika enthaltende pharmazeutische Zusammensetzungen
US4832930A (en) * 1988-05-02 1989-05-23 Tekatch William M Decomposition of ammonium thiocyanate
EP0479892A1 (de) 1989-06-30 1992-04-15 E.I. Du Pont De Nemours And Company Arylgruppe substituierte imidazole mit zusammengeschmolzenen ringen
HU217958B (hu) 1989-06-30 2000-05-28 E. I. Du Pont De Nemours And Co. Helyettesített imidazolszármazékok, ezeket tartalmazó gyógyszerkészítmények és eljárás előállításukra
US5117097A (en) * 1990-02-27 1992-05-26 Kabushiki Kaisha Tokai Rika Denki Seisakusho Key system for a vehicle
RU1743153C (ru) 1990-06-04 1995-02-27 ВНИИ химических средств защиты растений N-[4-2'-гидроксигексафторизопропил)фенил] -n-этил-n'-фенилмочевина, обладающая рострегулирующим и антидотным действием
DE69123582T2 (de) 1990-06-22 1997-05-15 E.I. Du Pont De Nemours & Co., Wilmington, Del. Behandlung des chronischen nierenversagens mit imidazol-angiotensin-ii-rezeptorantagonisten
US5428033A (en) 1990-10-12 1995-06-27 Merck Frosst Canada, Inc. Saturated hydroxyalkylquinoline acids as leukotriene antagonists
US5470975A (en) 1990-10-16 1995-11-28 E.R. Squibb & Sons, Inc. Dihydropyrimidine derivatives
CA2053148A1 (en) 1990-10-16 1992-04-17 Karnail Atwal Dihydropyrimidine derivatives
US5374615A (en) 1990-10-31 1994-12-20 E. R. Squibb & Sons, Inc. Indole- and benzimidazole-substituted imidazole and benzimidazole derivatives
SU1825496A3 (ru) 1991-04-04 1994-12-30 Всесоюзный научно-исследовательский институт химических средств защиты растений Производные n-[4-(1-гидрокси-1-трифторметил-2,2,2-трифторэтил)фенил]мочевины, обладающие антидотной активностью к 2-хлор-n-[(4-метокси-6-метил-1,3,5-триазин-2-ил)аминокарбонил] бензолсульфамиду в посевах льна
US5190942A (en) 1991-04-22 1993-03-02 E. R. Squibb & Sons, Inc. Benzoxazole and related heterocyclic substituted imidazole and benzimidazole derivatives
US5256695A (en) 1991-07-24 1993-10-26 E. R. Squibb & Sons, Inc. Acyl amidine and acyl guanidine substituted biphenyl derivatives
US5177097A (en) 1991-07-24 1993-01-05 E. R. Squibb & Sons, Inc. Acyl amidine and acyl, guanidine substituted biphenyl derivatives
JPH06510763A (ja) 1991-08-19 1994-12-01 イー・アイ・デュポン・ドゥ・ヌムール・アンド・カンパニー アンジオテンシン２受容体遮断イミダゾリノン誘導体
US5212177A (en) 1991-12-16 1993-05-18 E. R. Squibb & Sons, Inc. Indole and benzimidazole-substituted dihydropyrimidine derivatives
US5350752A (en) 1991-12-16 1994-09-27 E. R. Squibb & Sons, Inc. Dihydropyrimidine derivatives
US5225408A (en) 1991-12-20 1993-07-06 E. R. Squibb & Sons, Inc. Biphenyl oxadiazinone angiotensin II inhibitors
TW297025B (de) 1992-02-14 1997-02-01 Squibb & Sons Inc
US5208235A (en) 1992-03-10 1993-05-04 E. R. Squibb & Sons, Inc. Indole- and benzimidazole-substituted imidazole derivatives
US5208234A (en) 1992-03-10 1993-05-04 E. R. Squibb & Sons, Inc. Substituted imidazole phosphonic and phosphinic acid derivatives
CA2132724A1 (en) 1992-04-10 1993-10-28 Robert Zamboni Thiazole-substituted benzyl alcohols as leukotriene antagonists
US5506227A (en) 1992-04-13 1996-04-09 Merck Frosst Canada, Inc. Pyridine-substituted benzyl alcohols as leukotriene antagonists
US5378704A (en) 1992-04-15 1995-01-03 E. R. Squibb & Sons, Inc. Non-peptidic angiotensin-II-receptor-antagonists
US5534347A (en) 1992-09-04 1996-07-09 Eastman Kodak Company Fusing roll having a fluorocarbon-silicone barrier layer
WO1994010692A1 (en) 1992-10-30 1994-05-11 Lord Corporation Low viscosity magnetorheological materials
GB9226860D0 (en) 1992-12-23 1993-02-17 Leo Pharm Prod Ltd Novel treatment
EP0679157B1 (de) 1993-01-15 1997-11-19 G.D. Searle & Co. 3,4-diarylthiophene und analoga davon, sowie deren verwendung als entzündungshemmende mittel
DE4302681A1 (de) 1993-02-01 1994-08-04 Hoechst Ag Sulfonsäureester, damit hergestellte strahlungsempfindliche Gemische und deren Verwendung
DE4306152A1 (de) 1993-02-27 1994-09-01 Hoechst Ag Positiv arbeitendes strahlungsempfindliches Gemisch und damit hergestelltes Aufzeichnungsmaterial
GB9408577D0 (en) 1994-04-29 1994-06-22 Fujisawa Pharmaceutical Co New compound
US5637599A (en) 1994-06-17 1997-06-10 Corvas International, Inc. Arginine mimic derivatives as enzyme inhibitors
US5932733A (en) 1994-06-17 1999-08-03 Corvas International, Inc. 3-amino-2-oxo-1-piperidineacetic derivatives containing an arginine mimic as enzyme inhibitors
JPH10503176A (ja) 1994-06-17 1998-03-24 コーバス インターナショナル， インコーポレイテッド 酵素インヒビターとしての３−アミノ−２−オキソ−１−ピペリジン酢酸誘導体
US5519143A (en) 1994-09-19 1996-05-21 The Du Pont Merck Pharmaceutical Company Process for the isolation and purification of an imidazole stereoisomer from a mixture of stereoisomers by selective precipitation
US5552437A (en) 1994-10-27 1996-09-03 Merck Frosst Canada, Inc. Bisarylcarbinol derivatives as inhibitors of leukotriene biosynthesis
US5527827A (en) 1994-10-27 1996-06-18 Merck Frosst Canada, Inc. Bisarylcarbinol cinnamic acids as inhibitors of leukotriene biosynthesis
JPH08311036A (ja) 1995-03-14 1996-11-26 Takeda Chem Ind Ltd ピラゾール誘導体、その用途
IL117534A0 (en) 1995-03-24 1996-07-23 Rhone Poulenc Agrochimie Reagent and process which are useful for grafting a substituted difluoromethyl group onto a compound containing at least one electrophilic function
JPH0912585A (ja) 1995-06-30 1997-01-14 Ube Ind Ltd 高配位典型元素錯体
JPH0912795A (ja) 1995-06-30 1997-01-14 Sumitomo Chem Co Ltd 押出成形用エチレン系樹脂組成物及び押出成形体
GB2321244B (en) 1997-01-20 2000-11-22 Pharmacia & Upjohn Spa Vitamin D3 analogues,process for preparing them,and their use as antiproliferative and antitumour agents
DE19716231A1 (de) 1997-04-18 1998-10-22 Studiengesellschaft Kohle Mbh Olefinmetathese in komprimiertem Kohlendioxid
DE19722952A1 (de) 1997-05-31 1998-12-03 Huels Chemische Werke Ag Verwendung von Polymeren zur Inhibierung der Denaturierung von adsorbierten Eiweißstoffen
US5895771A (en) 1997-06-05 1999-04-20 Akzo Nobel Nv Fluorinated alkoxy and/or aryloxy aluminates as cocatalysts for metallocene-catalyzed olefin polymerizations
US5977413A (en) 1997-08-04 1999-11-02 Nippon Kayaku Kabushiki Kaisha Method for producing bis(3-amino-4-hydroxyphenyl) compounds
WO1999012894A1 (en) 1997-09-08 1999-03-18 F. Hoffmann-La Roche Ag 1,3-dihydroxy-20,20-dialkyl-vitamin d3 analogs
JP4275311B2 (ja) 1997-09-11 2009-06-10 コロラド ステート ユニバーシティ リサーチ ファンデーション ポリフルオロアルコキシド配位子を含有する弱配位結合アニオン
EP1071648A2 (de) 1998-03-13 2001-01-31 Merck Frosst Canada & Co. CARBONSÄUREN UND ACYLSULFONAMIDE, SOLCHE VERBINDUNGEN ENTHALTENDE Gemenge UND BEHANDLUNGSVERFAHREN
GB2337701A (en) 1998-05-26 1999-12-01 United Medical And Dental Schools Of Guys St Thomas Hospitals Treatment of ischemia with an angiotensin II antagonist
EP1087951B9 (de) * 1998-06-18 2006-09-13 Bristol-Myers Squibb Company Durch kohlenstoff substituierte aminothiazole als inhibitoren von zyclin-abhägigen kinasen
FR2784114B1 (fr) 1998-09-18 2001-02-02 Thomson Csf Materiaux polymeres absorbant les composes organophosphores. procede de synthese de ces materiaux. capteurs chimiques comprenant ces materiaux
EP1034196B1 (de) 1998-10-05 2005-01-12 Promerus LLC Katalysator und verfahren zur polymerisation von cycloolefinen
CN1208360C (zh) 1998-12-09 2005-06-29 住友电木株式会社 使用10族金属配合物进行降冰片烯型单体的模内加成聚合
EP1140784A2 (de) 1998-12-22 2001-10-10 Neurosearch A/S Ionenkanal modulierende mittel
AU2871900A (en) 1999-02-04 2000-08-25 Millennium Pharmaceuticals, Inc. G-protein coupled heptahelical receptor binding compounds and methods of use thereof
GB9904933D0 (en) 1999-03-04 1999-04-28 Glaxo Group Ltd Compounds
US6316503B1 (en) 1999-03-15 2001-11-13 Tularik Inc. LXR modulators
EP1212065A4 (de) 1999-07-08 2004-02-11 Tularik Inc Zusammenstellungen und methoden zur erhöhung des hdl cholesterolspiegels
EP1353662B1 (de) 2001-01-26 2007-04-18 Chugai Seiyaku Kabushiki Kaisha Verfahren zur behandlung von erkrankungen mit malonyl coa-decarboxylase-inhibitoren
DE60215139T2 (de) 2001-01-26 2007-08-16 Chugai Seiyaku K.K. Malonyl coa-decarboxylase inhibitoren als stoffwechselmodulatoren
JP4539565B2 (ja) 2006-01-13 2010-09-08 株式会社ジェイ・エム・エス 血液浄化回路

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KR100637564B1 (ko) 2006-10-20
ES2362270T3 (es) 2011-06-30
WO2002058698A2 (en) 2002-08-01
US20040082576A1 (en) 2004-04-29
EP1411929A2 (de) 2004-04-28
CA2435067A1 (en) 2002-08-01
CN1537001A (zh) 2004-10-13
CA2435067C (en) 2011-11-15
US7524969B2 (en) 2009-04-28
US20100016259A1 (en) 2010-01-21
JP5113823B2 (ja) 2013-01-09
JP2004527475A (ja) 2004-09-09
CA2735478A1 (en) 2002-08-01
CN101596191B (zh) 2011-06-15
CA2735267A1 (en) 2002-08-01
HK1138521A1 (en) 2010-08-27
US8119819B2 (en) 2012-02-21
WO2002058698A3 (en) 2004-02-12
EP1411929B1 (de) 2011-05-11
AU2002245294B2 (en) 2005-09-22
JP2010065054A (ja) 2010-03-25
CN101596191A (zh) 2009-12-09
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