JP2007530601A5 - - Google Patents

Download PDF

Info

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
Authority
JP
Japan
Prior art keywords
compound
formula
optionally substituted
alkyl
disease
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
JP2007505341A
Other languages
English (en)
Japanese (ja)
Other versions
JP4937111B2 (ja
JP2007530601A (ja
Filing date
Publication date
Application filed filed Critical
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

Links

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
AU2004901802A AU2004901802A0 (en) 2004-04-02 Process for the preparation of intermediates
AU2004901804A AU2004901804A0 (en) 2004-04-02 Neurologically-active compounds
AU2004901804 2004-04-02
AU2004901802 2004-04-02
AU2004907359 2004-12-24
AU2004907359A AU2004907359A0 (en) 2004-12-24 Neurologically-active compounds
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 (enExample) 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 (enExample)
EP (1) EP1737831B1 (enExample)
JP (1) JP4937111B2 (enExample)
BR (1) BRPI0508183B8 (enExample)
CA (1) CA2563038C (enExample)
DK (1) DK1737831T3 (enExample)
ES (1) ES2425476T3 (enExample)
IL (1) IL178330A (enExample)
MX (1) MXPA06011236A (enExample)
NZ (1) NZ551004A (enExample)
WO (1) WO2005095360A1 (enExample)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7692011B2 (en) * 2002-10-04 2010-04-06 Prana Biotechnology Limited 8-hydroxy and 8-mercapto quinazolinones
DK1737831T3 (da) 2004-04-02 2013-08-19 Prana Biotechnology Ltd Neurologisk aktive forbindelser
EP2001875A2 (en) * 2006-03-08 2008-12-17 Takeda San Diego, Inc. Glucokinase activators
CN101987849B (zh) * 2006-04-14 2013-05-08 普拉纳生物技术有限公司 治疗与年龄相关的黄斑变性(amd)的方法
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
EP2164834A2 (en) * 2007-07-06 2010-03-24 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
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
AR103297A1 (es) 2014-12-30 2017-05-03 Forma Therapeutics Inc Pirrolo y pirazolopirimidinas como inhibidores de la proteasa 7 específica de ubiquitina
WO2016126935A1 (en) 2015-02-05 2016-08-11 Forma Therapeutics, Inc. Isothiazolopyrimidinones, pyrazolopyrimidinones, and pyrrolopyrimidinones as ubiquitin-specific protease 7 inhibitors
JP2018504431A (ja) 2015-02-05 2018-02-15 フォーマ セラピューティクス,インコーポレイテッド ユビキチン特異的プロテアーゼ7阻害物質としてのチエノピリミジノン
EP3253738A1 (en) 2015-02-05 2017-12-13 Forma Therapeutics, Inc. Quinazolinones and azaquinazolinones as ubiquitin-specific protease 7 inhibitors
WO2017027064A1 (en) 2015-08-12 2017-02-16 The General Hospital Corporation 8-hydroxyquinoline derivatives as diagnostic and therapeutic agents
WO2019062803A1 (zh) * 2017-09-28 2019-04-04 基石药业 作为a2a受体抑制剂的并环类衍生物
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
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
MX2022013838A (es) 2020-05-04 2023-02-22 Amgen Inc Compuestos heterociclicos como agonistas del receptor de activacion expresado en las celulas mieloides 2 y metodos de uso.
CA3219215A1 (en) * 2021-05-04 2022-11-10 Vigil Neuroscience, Inc. Heterocyclic compounds as triggering receptor expressed on myeloid cells 2 agonists and methods of use
TW202325290A (zh) * 2021-11-09 2023-07-01 美商維佳神經科學有限公司 作為骨髓細胞上表現之觸發受體2促效劑之雜環化合物及其使用方法
JP2024544553A (ja) * 2021-11-09 2024-12-03 ビジル・ニューロサイエンス・インコーポレイテッド ミエロイド細胞に発現するトリガー受容体2アゴニストとしての複素環化合物及び使用方法
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 (enExample) 1950-09-09
US5756502A (en) 1994-08-08 1998-05-26 Warner-Lambert Company Quinazolinone derivatives as cholyecystokinin (CCK) ligands
WO1997010221A1 (en) 1995-09-15 1997-03-20 Torrey Pines Institute For Molecular Studies Synthesis of quinazolinone libraries
CA2271116A1 (en) 1996-11-13 1998-05-22 Gregory J. Wells Benzothiazo and related heterocyclic group-containing cysteine and serine protease inhibitors
JP2002513394A (ja) 1996-12-17 2002-05-08 イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー 殺菌・殺カビ性のキナゾリノン類
US6337332B1 (en) * 1998-09-17 2002-01-08 Pfizer Inc. Neuropeptide Y receptor antagonists
ATE286021T1 (de) * 1998-10-22 2005-01-15 Neurosearch As Substituierte phenylderivate, ihre herstellung und verwendung
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
CA2388646C (en) 1999-10-27 2009-01-27 Cytokinetics, Inc. Methods and compositions utilizing quinazolinones
US6667300B2 (en) 2000-04-25 2003-12-23 Icos Corporation Inhibitors of human phosphatidylinositol 3-kinase delta
IL152275A0 (en) 2000-04-25 2003-05-29 Icos Corp Inhibitors of human phosphatidyl-inositol 3-kinase delta
JP2004515543A (ja) 2000-12-11 2004-05-27 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー 有害無脊椎動物を防除するためのキナゾリノン類およびピリジニルピリミジノン類
JP2005511581A (ja) 2001-11-07 2005-04-28 メルク エンド カムパニー インコーポレーテッド 有糸分裂キネシン阻害剤
WO2003043961A2 (en) 2001-11-19 2003-05-30 Iconix Pharmaceuticals, Inc. Modulators of rho c activity
AU2002346471A1 (en) 2001-11-20 2003-06-10 Cytokinetics, Inc. Process for the racemization of chiral quinazolinones
CA2475879A1 (en) 2002-02-15 2003-08-28 Cytokinetics, Inc. Synthesis of quinazolinones
US20080070864A1 (en) * 2002-03-07 2008-03-20 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
EP1539180A4 (en) 2002-08-21 2006-08-30 Cytokinetics Inc COMPOUNDS, COMPOSITIONS AND METHODS
US7692011B2 (en) 2002-10-04 2010-04-06 Prana Biotechnology Limited 8-hydroxy and 8-mercapto quinazolinones
US9301829B2 (en) 2003-07-30 2016-04-05 Boston Scientific Scimed, Inc. Embolic protection aspirator
US20050043239A1 (en) 2003-08-14 2005-02-24 Jason Douangpanya Methods of inhibiting immune responses stimulated by an endogenous factor
WO2005016349A1 (en) 2003-08-14 2005-02-24 Icos Corporation Methods of inhibiting leukocyte accumulation
CN1886384A (zh) 2003-11-25 2006-12-27 希龙公司 喹唑酮化合物作为抗癌药剂
WO2005067901A2 (en) 2004-01-08 2005-07-28 Michigan State University Methods for treating and preventing hypertension and hypertension-related disorders
DK1737831T3 (da) 2004-04-02 2013-08-19 Prana Biotechnology Ltd Neurologisk aktive forbindelser
CA2730540A1 (en) 2004-05-13 2005-12-01 Vanderbilt University Phosphoinositide 3-kinase delta selective inhibitors for inhibiting angiogenesis
EP1757594A4 (en) 2004-05-31 2007-12-12 Banyu Pharma Co Ltd quinazoline derivative
JP2008501707A (ja) 2004-06-04 2008-01-24 アイコス、コーポレーション マスト細胞障害を処置するための方法
US20050282834A1 (en) 2004-06-09 2005-12-22 Fady Malik Compositions, devices and methods for treating cardiovascular disease

Similar Documents

Publication Publication Date Title
JP2007530601A5 (enExample)
CA2078578C (en) Medical use for tachykinin antagonists
DE60017898T2 (de) Neuartige heterocyclische carboxamidderivate
EP2813498B1 (en) Compounds for Alzheimer's disease
CA2500952A1 (en) Neurologically-active compounds
JPH07324076A (ja) 新規なピラゾール−3−カルボキサミド誘導体、これらを製造するための方法及びこれらが存在する薬学的組成物
DE69529418T2 (de) Cyclopropachromencarbonsäure derivate
WO2002012189A1 (en) Fused bicyclic amide compounds and medicinal use thereof
JP6261011B2 (ja) 眼疾患処置薬
BG65193B1 (bg) Производно на пиразолкарбоксилна киселина, неговото използване и фармацевтични състави, които го съдържат
RU2005100842A (ru) Производные 8-гидроксихинолина
JP2011507878A5 (enExample)
CN103781753B (zh) 用于治疗ape1介导的疾病的醌化合物
JP2005531488A5 (enExample)
JP2006507220A5 (enExample)
MXPA04002338A (es) Derivados de carbazol y su uso como antagonistas receptores del npy5.
JP2011507879A5 (enExample)
JP2007523909A5 (enExample)
KR101233289B1 (ko) 지양제
JP2004507527A5 (enExample)
JPH02503909A (ja) 6.11‐ジヒドロ‐11‐(4‐ピペリジリデン)‐5H‐ベンゾ[5,6]シクロヘプタ[1,2‐b]ピリジン類ならびに組成物および使用法
JP6219955B2 (ja) ベンゾフラザン抗アミロイド化合物および方法
RU2003101396A (ru) Замещенные нитрированные катехолы, их применение в лечении некоторых расстройств центральной и периферической нервной системы и содержащие их фармацевтические композиции
JP5341521B2 (ja) タンパク質と結合パートナーとの相互作用を阻害するための化合物及び方法
CA2589744A1 (en) Pyrrolinidium derivatives as m3 muscarinic receptors