JP2009526793A5 - - Google Patents

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Publication number
JP2009526793A5
JP2009526793A5 JP2008554653A JP2008554653A JP2009526793A5 JP 2009526793 A5 JP2009526793 A5 JP 2009526793A5 JP 2008554653 A JP2008554653 A JP 2008554653A JP 2008554653 A JP2008554653 A JP 2008554653A JP 2009526793 A5 JP2009526793 A5 JP 2009526793A5
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JP
Japan
Prior art keywords
alkyl
alkoxy
independently
hydroxy
membered
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Granted
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JP2008554653A
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English (en)
Japanese (ja)
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JP5175228B2 (ja
JP2009526793A (ja
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Priority claimed from PCT/EP2007/001212 external-priority patent/WO2007093364A1/en
Publication of JP2009526793A publication Critical patent/JP2009526793A/ja
Publication of JP2009526793A5 publication Critical patent/JP2009526793A5/ja
Application granted granted Critical
Publication of JP5175228B2 publication Critical patent/JP5175228B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2008554653A 2006-02-15 2007-02-13 新規なアザシクリル置換アリールジヒドロイソキノリノン、それらの製造方法及び薬剤としてそれらの使用 Expired - Fee Related JP5175228B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE102006007045 2006-02-15
DE102006007045.3 2006-02-15
PCT/EP2007/001212 WO2007093364A1 (en) 2006-02-15 2007-02-13 Azacyclyl-substituted aryldihydroisoquinolinones, process for their preparation and their use as medicaments

Publications (3)

Publication Number Publication Date
JP2009526793A JP2009526793A (ja) 2009-07-23
JP2009526793A5 true JP2009526793A5 (https=) 2010-04-08
JP5175228B2 JP5175228B2 (ja) 2013-04-03

Family

ID=38191074

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008554653A Expired - Fee Related JP5175228B2 (ja) 2006-02-15 2007-02-13 新規なアザシクリル置換アリールジヒドロイソキノリノン、それらの製造方法及び薬剤としてそれらの使用

Country Status (21)

Country Link
US (1) US8822495B2 (https=)
EP (1) EP1987020B1 (https=)
JP (1) JP5175228B2 (https=)
KR (1) KR20080095877A (https=)
CN (1) CN101384583A (https=)
AR (1) AR059458A1 (https=)
AU (1) AU2007214709A1 (https=)
BR (1) BRPI0707872A2 (https=)
CA (1) CA2636873A1 (https=)
CR (1) CR10160A (https=)
EC (1) ECSP088680A (https=)
IL (1) IL193340A0 (https=)
MA (1) MA30221B1 (https=)
NI (1) NI200800217A (https=)
NZ (1) NZ570503A (https=)
RU (1) RU2008136898A (https=)
TN (1) TNSN08326A1 (https=)
TW (1) TW200800908A (https=)
UY (1) UY30166A1 (https=)
WO (1) WO2007093364A1 (https=)
ZA (1) ZA200805939B (https=)

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WO2006066174A1 (en) 2004-12-17 2006-06-22 Eli Lilly And Company Thiazolopyridinone derivates as mch receptor antagonists
US7728031B2 (en) * 2006-02-24 2010-06-01 Abbott Laboratories Octahydro-pyrrolo[3,4-b]pyrrole derivatives
MX2008015486A (es) * 2006-06-08 2009-01-12 Lilly Co Eli Nuevos receptores antagonistas de la hormona concentrador de melanina (mch).
EA015127B1 (ru) * 2006-06-08 2011-06-30 Эли Лилли Энд Компани Антагонисты мсн-рецепторов
US9623021B2 (en) 2007-01-22 2017-04-18 Gtx, Inc. Nuclear receptor binding agents
EA026578B1 (ru) 2007-01-22 2017-04-28 ДЖиТиЭкс, ИНК. Вещества, связывающие ядерные рецепторы
US9604931B2 (en) 2007-01-22 2017-03-28 Gtx, Inc. Nuclear receptor binding agents
US8853392B2 (en) 2007-06-03 2014-10-07 Vanderbilt University Benzamide mGluR5 positive allosteric modulators and methods of making and using same
CN101809021B (zh) 2007-09-11 2013-04-24 雅培制药有限公司 八氢-吡咯并[3,4-b]吡咯n-氧化物
AR068745A1 (es) * 2007-10-08 2009-12-02 Panacea Biotec Ltd Una composicion en forma de dosificacion farmaceutica oral de unidad de alta dosis de micofenolato sodico, metodo para utilizar dicha composicion y sus usos
EP2205558B1 (en) * 2007-10-17 2012-07-25 Sanofi Substituted n-phenyl-pyrrolidinylmethylpyrrolidine amides and therapeutic use thereof as histamine h3 receptor modulators
ES2372332T3 (es) * 2007-10-17 2012-01-18 Sanofi N-fenil-bipirrolidina carboxamidas sustituidas y su uso terapéutico.
US8034806B2 (en) 2007-11-02 2011-10-11 Vanderbilt University Bicyclic mGluR5 positive allosteric modulators and methods of making and using same
UY31968A (es) 2008-07-09 2010-01-29 Sanofi Aventis Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos
JP2012503595A (ja) 2008-07-28 2012-02-09 シダンスク ユニバーシティ 代謝病の治療用の化合物
AR074466A1 (es) * 2008-12-05 2011-01-19 Sanofi Aventis Piperidina espiro pirrolidinona y piperidinona sustituidas y su uso terapeutico en enfermedades mediadas por la modulacion de los receptores h3.
WO2010147234A1 (en) * 2009-06-18 2010-12-23 Banyu Pharmaceutical Co.,Ltd. Diarylamide-spirodiamine derivative
KR101116234B1 (ko) 2009-10-29 2014-03-06 (주)퓨쳐켐 (3-플루오로-2-히드록시)프로필 작용기가 도입된 아릴 유도체 또는 이의 약학적으로 허용가능한 염, 이의 제조방법 및 이를 유효성분으로 함유하는 퇴행성 뇌질환의 진단 또는 치료용 약학적 조성물
AR081498A1 (es) * 2010-05-11 2012-09-19 Sanofi Aventis Derivados de n-alquil -y n-acil-tetrahidroisoquinolina sustituidos, preparacion y su uso terapeutico de los mismos
TW201206444A (en) 2010-05-11 2012-02-16 Sanofi Aventis Substituted N-heteroaryl tetrahydro-isoquinoline derivatives, preparation and therapeutic use thereof
EP2569280B1 (en) 2010-05-11 2015-02-25 Sanofi Substituted phenyl cycloalkyl pyrrolidine (piperidine) spirolactams and amides, preparation and therapeutic use thereof
WO2011143148A1 (en) * 2010-05-11 2011-11-17 Sanofi Substituted n-heteroaryl spirolactam bipyrrolidines, preparation and therapeutic use thereof
EP2569297A1 (en) 2010-05-11 2013-03-20 Sanofi Substituted n-heterocycloalkyl bipyrrolidinylphenyl amide derivatives, preparation and therapeutic use thereof
EP2569294B1 (en) 2010-05-11 2015-03-11 Sanofi Substituted n-heteroaryl bipyrrolidine carboxamides, preparation and therapeutic use thereof
WO2011163355A1 (en) * 2010-06-24 2011-12-29 Takeda Pharmaceutical Company Limited Fused heterocyclic compounds as phosphodiesterases (pdes) inhibitors
US9134238B2 (en) * 2010-12-01 2015-09-15 Nalco Company Method for determination of system parameters for reducing crude unit corrosion
TWI570122B (zh) * 2011-06-22 2017-02-11 武田藥品工業股份有限公司 稠合雜環化合物之結晶
CN103086894B (zh) * 2013-02-25 2014-10-01 武汉迪可表面技术有限公司 一种电镀添加剂3-甲基-3-氨基丁炔的合成方法
HUE040366T2 (hu) 2013-08-08 2019-03-28 Galapagos Nv CFTR modulátor tieno[2,3-c]piránok
EP3762379A1 (en) 2018-03-07 2021-01-13 Bayer Aktiengesellschaft Identification and use of erk5 inhibitors
SG11202103011YA (en) * 2018-10-11 2021-04-29 Basf As Aromatic compounds and pharmaceutical uses thereof

Family Cites Families (9)

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Publication number Priority date Publication date Assignee Title
US4329353A (en) * 1980-10-22 1982-05-11 Janssen Pharmaceutica, N.V. 1-(4-Aryl-cyclohexyl)piperidine derivatives, method of use thereof and pharmaceutical compositions thereof
ES2152938T3 (es) * 1992-09-28 2001-02-16 Hoechst Ag 1(2h)-isoquinolinas sustituidas antiarritmicas y cardioprotectoras, procedimiento para su produccion, medicamento que las contiene y su uso para la produccion de un medicamento para combatir fallos cardiacos.
GB0124627D0 (en) * 2001-10-15 2001-12-05 Smithkline Beecham Plc Novel compounds
AU2002352878B2 (en) * 2001-11-27 2007-11-22 Merck Sharp & Dohme Corp. 2-Aminoquinoline compounds
DE10238865A1 (de) * 2002-08-24 2004-03-11 Boehringer Ingelheim International Gmbh Neue Carbonsäureamid-Verbindungen mit MCH-antagonistischer Wirkung, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
AU2003287880A1 (en) * 2002-12-11 2004-06-30 7Tm Pharma A/S Cyclic quinoline compounds for use in mch receptor related disorders
US20060194871A1 (en) * 2003-04-11 2006-08-31 Barvian Kevin K Heterocyclic mchr1 antagoists
JP2007509158A (ja) * 2003-10-23 2007-04-12 グラクソ グループ リミテッド 肥満、糖尿病、うつ病及び不安を治療するためのmchr1アンタゴニストとしての3−(4−アミノフェニル)チエノピリミド−4−オン誘導体
WO2005103039A1 (en) * 2004-04-15 2005-11-03 Neurocrine Biosciences, Inc. 2- (3-aminopyrrolidin-1-yl) pyridines as melanin-concentrating hormone receptor an tagonists

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