JP2005508313A5 - - Google Patents

Download PDF

Info

Publication number
JP2005508313A5
JP2005508313A5 JP2003523241A JP2003523241A JP2005508313A5 JP 2005508313 A5 JP2005508313 A5 JP 2005508313A5 JP 2003523241 A JP2003523241 A JP 2003523241A JP 2003523241 A JP2003523241 A JP 2003523241A JP 2005508313 A5 JP2005508313 A5 JP 2005508313A5
Authority
JP
Japan
Prior art keywords
alkyl
phenyl
carboxamide
dihydro
naphthyridin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2003523241A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005508313A (ja
JP4157035B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/CA2002/001324 external-priority patent/WO2003018579A1/en
Publication of JP2005508313A publication Critical patent/JP2005508313A/ja
Publication of JP2005508313A5 publication Critical patent/JP2005508313A5/ja
Application granted granted Critical
Publication of JP4157035B2 publication Critical patent/JP4157035B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2003523241A 2001-08-29 2002-08-27 アルキン−アリールホスホジエステラーゼ−4阻害薬 Expired - Fee Related JP4157035B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US31609301P 2001-08-29 2001-08-29
PCT/CA2002/001324 WO2003018579A1 (en) 2001-08-29 2002-08-27 Alkyne-aryl phosphodiesterase-4 inhibitors

Publications (3)

Publication Number Publication Date
JP2005508313A JP2005508313A (ja) 2005-03-31
JP2005508313A5 true JP2005508313A5 (enExample) 2005-12-22
JP4157035B2 JP4157035B2 (ja) 2008-09-24

Family

ID=23227432

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003523241A Expired - Fee Related JP4157035B2 (ja) 2001-08-29 2002-08-27 アルキン−アリールホスホジエステラーゼ−4阻害薬

Country Status (28)

Country Link
US (2) US6743802B2 (enExample)
EP (2) EP2305677A1 (enExample)
JP (1) JP4157035B2 (enExample)
KR (1) KR100928849B1 (enExample)
CN (1) CN100338061C (enExample)
AR (1) AR036365A1 (enExample)
AU (1) AU2002322940B2 (enExample)
BR (1) BR0212042A (enExample)
CA (1) CA2456817C (enExample)
DO (1) DOP2002000456A (enExample)
EA (1) EA006800B1 (enExample)
EC (1) ECSP044992A (enExample)
GE (1) GEP20063805B (enExample)
HK (1) HK1080073B (enExample)
HR (1) HRP20040151A2 (enExample)
HU (1) HUP0401729A3 (enExample)
IL (1) IL160213A0 (enExample)
IS (1) IS7138A (enExample)
JO (1) JO2311B1 (enExample)
MX (1) MXPA04001889A (enExample)
NO (1) NO330521B1 (enExample)
NZ (1) NZ530931A (enExample)
PE (1) PE20030416A1 (enExample)
PL (1) PL367716A1 (enExample)
RS (1) RS17004A (enExample)
UA (1) UA75957C2 (enExample)
WO (1) WO2003018579A1 (enExample)
ZA (1) ZA200400952B (enExample)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO2311B1 (en) * 2001-08-29 2005-09-12 ميرك فروست كندا ليمتد Alkyl inhibitors Ariel phosphodiesterase-4
DE10250708A1 (de) * 2002-10-31 2004-05-19 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel
US7452911B2 (en) 2002-10-31 2008-11-18 Boehringer Ingelheim Pharma Gmbh & Co. Kg Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds
US7351719B2 (en) 2002-10-31 2008-04-01 Boehringer Ingelheim Pharma Gmbh & Co. Kg Amide compounds having MCH-antagonistic activity and medicaments comprising these compounds
EP1562588A4 (en) * 2002-11-15 2007-10-31 Merck & Co Inc USE OF PDE4 INHIBITORS AS ADDITIONAL TREATMENT IN PSYCHIATRICAL DISEASES
AR042194A1 (es) * 2002-11-22 2005-06-15 Merck & Co Inc Metodo para preparar inhibidores de fosfodiesterasa - 4
AU2003286024A1 (en) * 2002-11-22 2004-06-18 Daniel Dube Use of phosphodiesterase-4 inhibitors as enhancers of cognition
GB0307863D0 (en) * 2003-04-04 2003-05-14 Merck Sharp & Dohme Therapeutic treatment
GB0322722D0 (en) * 2003-09-27 2003-10-29 Glaxo Group Ltd Compounds
GB0322726D0 (en) * 2003-09-27 2003-10-29 Glaxo Group Ltd Compounds
US7592373B2 (en) 2003-12-23 2009-09-22 Boehringer Ingelheim International Gmbh Amide compounds with MCH antagonistic activity and medicaments comprising these compounds
DE102004017934A1 (de) 2004-04-14 2005-11-03 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel
US7524862B2 (en) 2004-04-14 2009-04-28 Boehringer Ingelheim International Gmbh Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds
DE102004017930A1 (de) * 2004-04-14 2005-11-03 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Alkin-Verbindungen mit MCH-antagonistischer Wirkung und diese Verbindungen enthaltende Arzneimittel
EP1742628A4 (en) * 2004-04-26 2009-06-03 Merck Frosst Canada Ltd ALTERNATIVE FORMS OF PHOSPHODIESTERASE-4-HEMMER N-CYCLOPROPYL-1- (3-1 / 4 (1-OXIDOPYRIDIN-3-YL) ETHYNYL-PHENYL) -4-OXO-1,4-DIYHDRO-1,8-NAPHTHYRIDINE- 3-carboxyamide
JP4264388B2 (ja) * 2004-07-01 2009-05-13 富士通株式会社 半導体チップの接合方法および接合装置
WO2006004191A1 (en) * 2004-07-05 2006-01-12 Astellas Pharma Inc. Pyrrolopyridazine derivatives which inhibit pde iv and tnf alfa
US7687490B2 (en) * 2005-04-12 2010-03-30 Meiji Seika Kaisha, Ltd. 2-thioethenyl substituted carbapenem derivatives
JP2006016407A (ja) * 2005-06-15 2006-01-19 Yamaha Motor Co Ltd ホスホジエステラーゼ阻害剤
EP2275096A3 (en) 2005-08-26 2011-07-13 Braincells, Inc. Neurogenesis via modulation of the muscarinic receptors
EP2258357A3 (en) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
AU2006297037A1 (en) * 2005-09-28 2007-04-05 Merck Frosst Canada Ltd Aerosol powder formulation comprising sieved lactose
WO2007047978A2 (en) 2005-10-21 2007-04-26 Braincells, Inc. Modulation of neurogenesis by pde inhibition
EP2314289A1 (en) 2005-10-31 2011-04-27 Braincells, Inc. Gaba receptor mediated modulation of neurogenesis
BRPI0619785A2 (pt) 2005-12-13 2011-10-18 Wyeth Corp composto, composição e método para o tratamento de um transtorno proliferativo e método de prepraração
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
EP2021000A2 (en) 2006-05-09 2009-02-11 Braincells, Inc. Neurogenesis by modulating angiotensin
US7678808B2 (en) 2006-05-09 2010-03-16 Braincells, Inc. 5 HT receptor mediated neurogenesis
WO2008030651A1 (en) 2006-09-08 2008-03-13 Braincells, Inc. Combinations containing a 4-acylaminopyridine derivative
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
CA2676715A1 (en) 2007-02-12 2008-08-21 Merck & Co., Inc. Piperazine derivatives for treatment of ad and related conditions
CA2682730A1 (en) * 2007-04-11 2008-10-23 Alcon Research, Ltd. Use of an inhibitor of tnf.alpha. plus an antihistamine to treat allergic rhinitis and allergic conjunctivitis
US20090182035A1 (en) * 2007-04-11 2009-07-16 Alcon Research, Ltd. Use of a combination of olopatadine and cilomilast to treat non-infectious rhinitis and allergic conjunctivitis
CA2707360A1 (en) 2007-06-20 2008-12-24 Merck Sharp & Dohme Corp. Diphenyl substituted alkanes
MX2010004529A (es) * 2007-10-25 2010-05-10 Merck Frosst Canada Ltd Composiciones de inhalacion que comprenden acido montelukast y un inhibidor de fosfodiesterasa-4 o un corticoesteroide inhalado.
WO2009128057A2 (en) 2008-04-18 2009-10-22 UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN et al Psycho-pharmaceuticals
US20100216805A1 (en) 2009-02-25 2010-08-26 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
US20110082145A1 (en) * 2009-10-01 2011-04-07 Alcon Research, Ltd. Olopatadine compositions and uses thereof
FR2952934B1 (fr) * 2009-11-23 2012-06-22 Sanofi Aventis Derives de pyridino-pyridinones, leur preparation et leur application en therapeutique
CN107260736A (zh) 2010-02-12 2017-10-20 株式会社AskAt 用于治疗痴呆的5‑ht4受体激动剂
EP2680842A4 (en) * 2011-03-02 2014-10-29 Bionomics Ltd METHOD FOR THE TREATMENT OF A DISEASE OR A SENSE OF THE CENTRAL NERVOUS SYSTEM
CN103183675A (zh) * 2011-12-27 2013-07-03 山东轩竹医药科技有限公司 磷酸二酯酶-4抑制剂
CN102643268B (zh) * 2011-12-30 2014-05-21 沈阳药科大学 喹啉类及噌啉类化合物及其应用
WO2013106547A1 (en) 2012-01-10 2013-07-18 President And Fellows Of Harvard College Beta-cell replication promoting compounds and methods of their use
CN103214478B (zh) * 2012-01-19 2015-07-15 山东轩竹医药科技有限公司 吡啶并氧代哒嗪衍生物
MD20150071A2 (ro) 2013-02-19 2016-02-29 Pfizer Inc. Compuşi azabenzimidazolici ca inhibitori ai PDE4 izoenzimelor pentru tratamentul tulburărilor SNC şi altor afecţiuni
WO2016012896A1 (en) 2014-07-24 2016-01-28 Pfizer Inc. Pyrazolopyrimidine compounds
EA031201B1 (ru) 2014-08-06 2018-11-30 Пфайзер Инк. Соединения имидазопиридазина
CA3124670A1 (en) 2018-12-28 2020-07-02 Regeneron Pharmaceuticals, Inc. Treatment of respiratory disorders with arachidonate 15-lipoxygenase (alox15) inhibitors

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9212673D0 (en) 1992-06-15 1992-07-29 Celltech Ltd Chemical compounds
GB9212693D0 (en) 1992-06-15 1992-07-29 Celltech Ltd Chemical compounds
DK0577024T3 (enExample) 1992-07-01 1997-02-24 Hoechst Ag
GB9222253D0 (en) 1992-10-23 1992-12-09 Celltech Ltd Chemical compounds
US5622977A (en) 1992-12-23 1997-04-22 Celltech Therapeutics Limited Tri-substituted (aryl or heteroaryl) derivatives and pharmaceutical compositions containing the same
GB9226830D0 (en) 1992-12-23 1993-02-17 Celltech Ltd Chemical compounds
DE4306152A1 (de) 1993-02-27 1994-09-01 Hoechst Ag Positiv arbeitendes strahlungsempfindliches Gemisch und damit hergestelltes Aufzeichnungsmaterial
GB9304920D0 (en) 1993-03-10 1993-04-28 Celltech Ltd Chemical compounds
GB9304919D0 (en) 1993-03-10 1993-04-28 Celltech Ltd Chemical compounds
US5455252A (en) 1993-03-31 1995-10-03 Syntex (U.S.A.) Inc. Optionally substituted 6,8-quinolines
DE4318756A1 (de) 1993-06-05 1994-12-08 Hoechst Ag Substituierte Benzoylguanidine, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament
EP0738268B1 (en) 1993-12-22 2004-03-03 Celltech R&D Limited Trisubstituted phenyl derivatives, processes for their preparation and their use as phosphodiesterase (type iv) inhibitors
GB9326699D0 (en) 1993-12-22 1994-03-02 Celltech Ltd Chemical compounds
GB9326173D0 (en) 1993-12-22 1994-02-23 Celltech Ltd Chemical compounds and process
US5786354A (en) 1994-06-21 1998-07-28 Celltech Therapeutics, Limited Tri-substituted phenyl derivatives and processes for their preparation
US6245774B1 (en) 1994-06-21 2001-06-12 Celltech Therapeutics Limited Tri-substituted phenyl or pyridine derivatives
GB9412571D0 (en) 1994-06-22 1994-08-10 Celltech Ltd Chemical compounds
GB9412573D0 (en) 1994-06-22 1994-08-10 Celltech Ltd Chemical compounds
GB9412672D0 (en) 1994-06-23 1994-08-10 Celltech Ltd Chemical compounds
EP0765867A1 (de) 1995-09-27 1997-04-02 Hoechst Aktiengesellschaft Substituierte Benzoylguanidine, Verfahren zu ihrer Herstellung, ihre Verwendung als Antiarrhytmika oder Diagnostikum sowie sie enthaltendes Medikament
GB9526243D0 (en) 1995-12-21 1996-02-21 Celltech Therapeutics Ltd Chemical compounds
GB9526245D0 (en) 1995-12-21 1996-02-21 Celltech Therapeutics Ltd Chemical compounds
GB9526246D0 (en) 1995-12-21 1996-02-21 Celltech Therapeutics Ltd Chemical compounds
DE19622370A1 (de) 1996-06-04 1997-12-11 Hoechst Ag Ortho-substituierte Benzoylguanidine, Verfahren zu ihrer Herstellung, ihre Verwendung als Medikament oder Diagnostikum sowie sie enthaltendes Medikament
GB9625184D0 (en) 1996-12-04 1997-01-22 Celltech Therapeutics Ltd Chemical compounds
EP0944582B1 (de) 1996-12-11 2003-07-02 Abbott GmbH & Co. KG Ketobenzamide als calpain-inhibitoren
HUP0001054A3 (en) * 1997-08-06 2001-01-29 Daiichi Asubio Pharma Co Ltd 1-aryl-1,8-naphthyridin-4-one derivative as type iv phosphodiesterase inhibitor
WO1999009504A1 (en) 1997-08-20 1999-02-25 First Data Corporation Interactive tax payment system
CA2285352A1 (en) * 1998-01-29 1999-08-05 Suntory Limited 1-cycloalkyl-1,8-naphthyridin-4-one derivatives with phosphodiesterase iv inhibitory activity
EA200100124A1 (ru) * 1998-08-11 2001-10-22 Пфайзер Продактс Инк. Замещенные 1,8-нафтиридин-4(1h)-оны в качестве ингибиторов фосфодиэстеразы 4
JO2311B1 (en) * 2001-08-29 2005-09-12 ميرك فروست كندا ليمتد Alkyl inhibitors Ariel phosphodiesterase-4
IS7839A (is) * 2002-11-22 2004-05-23 Merck Frosst Canada Ltd. 4-oxó-1-(3-setið fenýl-1,4-díhýdró-1,8-naftýridín-3-karboxamíð fosfódíesterasa-4 hindrar

Similar Documents

Publication Publication Date Title
CA2456817A1 (en) Alkyne-aryl-naphthyridin-4 (1h)-one derivatives as type iv phosphodiesterase inhibitor
AU722472B2 (en) Quinoline carboxamides as TNF inhibitors and as PDE-IV inhibitors
US6784192B2 (en) Piperidine compound and pharmaceutical composition thereof
US9108963B2 (en) Pyrazolopyridine, pyrazolopyrazine, pyrazolopyrimidine, pyrazolothiophene and pyrazolothiazole compounds as MGLUR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction
AU732863B2 (en) Indole derivatives having combined 5HT1A, 5HT1B and 5HT1D receptor antagonist activity
TWI579284B (zh) 咪唑并吡咯啶酮化合物
RU2345070C2 (ru) Производные аминоиндазолов в качестве лекарственных средств, способ их получения и содержащие их фармацевтические композиции
AU2012352555B2 (en) Metalloenzyme inhibitor compounds
JP2006502112A5 (enExample)
JP2007500177A5 (enExample)
CN110156785B (zh) 吲唑类化合物及其制备方法和应用
CA2464981A1 (en) Quinoline compound
JP2012510989A5 (enExample)
JP2005528325A5 (enExample)
WO2004026841A1 (ja) 新規6−置換ウラシル誘導体及びアレルギー性疾患の治療剤
CA2447765A1 (en) 1-biaryl-1,8-napthyridin-4-one phosphodiesterase-4 inhibitors
US11319322B2 (en) Substituted aryl ether compound, preparation method thereof, pharmaceutical composition and use thereof
JP3782011B2 (ja) 置換8−アリールキノリン系ホスホジエステラーゼ−4阻害薬
HUP0000189A2 (hu) Biciklusos aril-karboxamid-származékok, e vegyületeket tartalmazó gyógyszerkészítmények és alkalmazásuk terápiás célokra
TW201014852A (en) Indolizine inhibitors of leukotriene production
JP2020502252A5 (enExample)
CA2403423A1 (en) Tri-aryl-substituted-ethane pde4 inhibitors
JP2020500192A5 (enExample)
US9096531B2 (en) Fused imidazole derivative
SK7732003A3 (en) Pharmaceutically acceptable salts of substituted 8-arylquinoline compounds, pharmaceutical composition comprising same and their use