JP2007530601A5 - - Google Patents

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Publication number
JP2007530601A5
JP2007530601A5 JP2007505341A JP2007505341A JP2007530601A5 JP 2007530601 A5 JP2007530601 A5 JP 2007530601A5 JP 2007505341 A JP2007505341 A JP 2007505341A JP 2007505341 A JP2007505341 A JP 2007505341A JP 2007530601 A5 JP2007530601 A5 JP 2007530601A5
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JP
Japan
Prior art keywords
compound
formula
optionally substituted
alkyl
disease
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Application number
JP2007505341A
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English (en)
Japanese (ja)
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JP2007530601A (ja
JP4937111B2 (ja
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Priority claimed from PCT/AU2005/000477 external-priority patent/WO2005095360A1/en
Publication of JP2007530601A publication Critical patent/JP2007530601A/ja
Publication of JP2007530601A5 publication Critical patent/JP2007530601A5/ja
Application granted granted Critical
Publication of JP4937111B2 publication Critical patent/JP4937111B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2007505341A 2004-04-02 2005-04-01 神経学的に活性な化合物 Expired - Fee Related JP4937111B2 (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
AU2004901804A AU2004901804A0 (en) 2004-04-02 Neurologically-active compounds
AU2004901802A AU2004901802A0 (en) 2004-04-02 Process for the preparation of intermediates
AU2004901804 2004-04-02
AU2004901802 2004-04-02
AU2004907359A AU2004907359A0 (en) 2004-12-24 Neurologically-active compounds
AU2004907359 2004-12-24
PCT/AU2005/000477 WO2005095360A1 (en) 2004-04-02 2005-04-01 Neurologically-active compounds

Publications (3)

Publication Number Publication Date
JP2007530601A JP2007530601A (ja) 2007-11-01
JP2007530601A5 true JP2007530601A5 (OSRAM) 2009-06-25
JP4937111B2 JP4937111B2 (ja) 2012-05-23

Family

ID=35063693

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007505341A Expired - Fee Related JP4937111B2 (ja) 2004-04-02 2005-04-01 神経学的に活性な化合物

Country Status (11)

Country Link
US (1) US8084459B2 (OSRAM)
EP (1) EP1737831B1 (OSRAM)
JP (1) JP4937111B2 (OSRAM)
BR (1) BRPI0508183B8 (OSRAM)
CA (1) CA2563038C (OSRAM)
DK (1) DK1737831T3 (OSRAM)
ES (1) ES2425476T3 (OSRAM)
IL (1) IL178330A (OSRAM)
MX (1) MXPA06011236A (OSRAM)
NZ (1) NZ551004A (OSRAM)
WO (1) WO2005095360A1 (OSRAM)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1558585B1 (en) * 2002-10-04 2013-09-25 Prana Biotechnology Limited Neurologically-active compounds
CA2563038C (en) 2004-04-02 2013-10-29 Gaik Beng Kok Neurologically-active compounds
JP5302012B2 (ja) * 2006-03-08 2013-10-02 タケダ カリフォルニア インコーポレイテッド グルコキナーゼ活性剤
NZ572591A (en) * 2006-04-14 2012-01-12 Prana Biotechnology Ltd 3N-substituted 8-hydroxy-quinazolin-4-ones
JP4876690B2 (ja) * 2006-04-21 2012-02-15 三菱瓦斯化学株式会社 キナゾリン−4−オン誘導体の製造法
CA2687750C (en) * 2007-07-06 2016-10-18 Boehringer Ingelheim International Gmbh Substituted amino-quinazolinones, medicaments comprising said compound, their use and their method of manufacture
CA2704710C (en) * 2007-09-26 2016-02-02 Celgene Corporation 6-, 7-, or 8-substituted quinazolinone derivatives and compositions comprising the same
ES2634492T3 (es) 2008-12-24 2017-09-28 Prana Biotechnology Ltd Compuestos de quinazolinona
US8592485B2 (en) * 2010-06-17 2013-11-26 Healthpartners Research Foundation Methods and pharmaceutical compositions for treating the animal central nervous system for psychiatric disorders
WO2012066330A1 (en) 2010-11-17 2012-05-24 Heptares Therapeutics Limited Compounds useful as a2a receptor inhibitors
EP2565186A1 (en) 2011-09-02 2013-03-06 Hybrigenics S.A. Selective and reversible inhibitors of ubiquitin specific protease 7
US10260089B2 (en) 2012-10-29 2019-04-16 The Research Foundation Of The State University Of New York Compositions and methods for recognition of RNA using triple helical peptide nucleic acids
US8877766B2 (en) * 2013-02-15 2014-11-04 Peter F. Kador Neuroprotective multifunctional antioxidants and their monofunctional analogs
TWI698436B (zh) 2014-12-30 2020-07-11 美商佛瑪治療公司 作為泛素特異性蛋白酶7抑制劑之吡咯并及吡唑并嘧啶
MA41291A (fr) 2014-12-30 2017-11-07 Forma Therapeutics Inc Dérivés de la pyrrolotriazinone et de l'imidazotriazinone en tant qu'inhibiteurs de la protéase spécifique de l'ubiquitine n° 7 (usp7) pour le traitement d'un cancer
US9932351B2 (en) 2015-02-05 2018-04-03 Forma Therapeutics, Inc. Thienopyrimidinones as ubiquitin-specific protease 7 inhibitors
EP3253738A1 (en) 2015-02-05 2017-12-13 Forma Therapeutics, Inc. Quinazolinones and azaquinazolinones as ubiquitin-specific protease 7 inhibitors
WO2016126935A1 (en) 2015-02-05 2016-08-11 Forma Therapeutics, Inc. Isothiazolopyrimidinones, pyrazolopyrimidinones, and pyrrolopyrimidinones as ubiquitin-specific protease 7 inhibitors
US10781178B2 (en) 2015-08-12 2020-09-22 The General Hospital Corporation 8-hydroxyquinoline derivatives as diagnostic and therapeutic agents
CA3077267C (en) 2017-09-28 2021-02-16 Cstone Pharmaceuticals (Suzhou) Co., Ltd. Fused heteroaryl ring derivatives useful as a2a receptor inhibitor
CN110330487B (zh) * 2019-07-31 2023-03-24 西南大学 喹唑酮噻唑化合物及其制备方法和应用
CU20220065A7 (es) 2020-05-04 2023-06-13 Amgen Inc Compuestos heterocíclicos como agonistas del receptor de activación expresado en las células mieloides 2
TW202208355A (zh) 2020-05-04 2022-03-01 美商安進公司 作為骨髓細胞觸發受體2促效劑之雜環化合物及使用方法
IL308167A (en) * 2021-05-04 2023-12-01 Vigil Neuroscience Inc Heterocyclic compounds as agonists for an excitatory receptor expressed on myeloid cells 2 and methods of use
WO2023086801A1 (en) * 2021-11-09 2023-05-19 Vigil Neuroscience, Inc. Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use
US20250042897A1 (en) * 2021-11-09 2025-02-06 Vigil Neuroscience, Inc. Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use
WO2025059726A1 (en) * 2023-09-22 2025-03-27 Alterity Therapeutics Limited Novel therapy

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE505711A (OSRAM) * 1950-09-09
US5756502A (en) * 1994-08-08 1998-05-26 Warner-Lambert Company Quinazolinone derivatives as cholyecystokinin (CCK) ligands
AU4858596A (en) 1995-09-15 1997-04-01 Torrey Pines Institute For Molecular Studies Synthesis of quinazolinone libraries
WO1998021186A1 (en) 1996-11-13 1998-05-22 Cephalon, Inc. Benzothiazo and related heterocyclic group-containing cysteine and serine protease inhibitors
AU5380398A (en) 1996-12-17 1998-07-15 E.I. Du Pont De Nemours And Company Fungicidal quinazolinones
US6337332B1 (en) * 1998-09-17 2002-01-08 Pfizer Inc. Neuropeptide Y receptor antagonists
EP1123274B1 (en) * 1998-10-22 2004-12-29 Neurosearch A/S Substituted phenyl derivatives, their preparation and use
US6559160B1 (en) 1999-08-27 2003-05-06 Chemocentryx, Inc. Compounds and methods for modulating cxcr3 function
US6545004B1 (en) 1999-10-27 2003-04-08 Cytokinetics, Inc. Methods and compositions utilizing quinazolinones
EP1686120A3 (en) 1999-10-27 2007-05-30 Cytokinetics, Inc. Methods and compositions utilizing quinazolinones
US6667300B2 (en) * 2000-04-25 2003-12-23 Icos Corporation Inhibitors of human phosphatidylinositol 3-kinase delta
EP1278748B1 (en) 2000-04-25 2011-03-23 ICOS Corporation Inhibitors of human phosphatidyl-inositol 3-kinase delta
WO2002048115A2 (en) 2000-12-11 2002-06-20 E. I. Du Pont De Nemours And Company Quinazolinones and pyridinopyrimidinones for controlling invertebrate pests
WO2003039460A2 (en) 2001-11-07 2003-05-15 Merck & Co., Inc. Mitotic kinesin inhibitors
US7053216B2 (en) 2001-11-19 2006-05-30 Iconix Pharmaceuticals, Inc. Modulators of Rho C activity
WO2003043995A1 (en) 2001-11-20 2003-05-30 Cytokinetics, Inc. Process for the racemization of chiral quinazolinones
WO2003070701A2 (en) 2002-02-15 2003-08-28 Cytokinetics, Inc. Syntheses of quinazolinones
AU2003228283A1 (en) * 2002-03-07 2003-09-22 X-Ceptor Therapeutics, Inc. Quinazolinone modulators of nuclear receptors
EP1513534A2 (en) 2002-04-04 2005-03-16 Cv Therapeutics, Inc. Compounds for increasing abca-1 expression useful for treating coronary artery disease and atherosclerosis
AU2002950217A0 (en) * 2002-07-16 2002-09-12 Prana Biotechnology Limited 8- Hydroxy Quinoline Derivatives
AU2003262747A1 (en) * 2002-08-21 2004-03-11 Cytokinetics, Inc. Compounds, compositions, and methods
EP1558585B1 (en) 2002-10-04 2013-09-25 Prana Biotechnology Limited Neurologically-active compounds
US9301829B2 (en) 2003-07-30 2016-04-05 Boston Scientific Scimed, Inc. Embolic protection aspirator
US20050054614A1 (en) 2003-08-14 2005-03-10 Diacovo Thomas G. Methods of inhibiting leukocyte accumulation
US20050043239A1 (en) * 2003-08-14 2005-02-24 Jason Douangpanya Methods of inhibiting immune responses stimulated by an endogenous factor
US7939539B2 (en) 2003-11-25 2011-05-10 Novartis Vaccines And Diagnostics, Inc. Quinazolinone compounds as anticancer agents
US20050239809A1 (en) 2004-01-08 2005-10-27 Watts Stephanie W Methods for treating and preventing hypertension and hypertension-related disorders
CA2563038C (en) 2004-04-02 2013-10-29 Gaik Beng Kok Neurologically-active compounds
CA2566436C (en) 2004-05-13 2011-05-10 Vanderbilt University Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis
JPWO2005115993A1 (ja) 2004-05-31 2008-03-27 萬有製薬株式会社 キナゾリン誘導体
WO2005120511A1 (en) 2004-06-04 2005-12-22 Icos Corporation Methods for treating mast cell disorders
US20050282834A1 (en) * 2004-06-09 2005-12-22 Fady Malik Compositions, devices and methods for treating cardiovascular disease

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