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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JP2007505341A
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English (en)
Japanese (ja)
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JP4937111B2 (ja
JP2007530601A (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
AU2004901804 2004-04-02
AU2004901802 2004-04-02
AU2004901804A AU2004901804A0 (en) 2004-04-02 Neurologically-active compounds
AU2004901802A AU2004901802A0 (en) 2004-04-02 Process for the preparation of intermediates
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 (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)

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ES2634492T3 (es) * 2008-12-24 2017-09-28 Prana Biotechnology Ltd Compuestos de quinazolinona
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HK1248220A1 (zh) 2015-02-05 2018-10-12 Forma Therapeutics, Inc. 喹唑啉酮和偶氮喹唑啉作为泛特丁胺蛋白酶7抑制剂
HK1248222A1 (zh) 2015-02-05 2018-10-12 Forma Therapeutics, Inc. 噻吩并嘧啶酮作为泛素特异性蛋白酶7抑制剂
US10781178B2 (en) 2015-08-12 2020-09-22 The General Hospital Corporation 8-hydroxyquinoline derivatives as diagnostic and therapeutic agents
AU2018341781B2 (en) 2017-09-28 2023-03-30 Cstone Pharmaceuticals Fused ring derivative 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
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
JP7741100B2 (ja) * 2020-05-04 2025-09-17 アムジェン 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
KR20240026911A (ko) * 2021-05-04 2024-02-29 비질 뉴로사이언스 인코포레이티드 골수성 세포 2 작용제 상에서 발현되는 유발 수용체로서의 헤테로고리 화합물 및 사용 방법
EP4430022A4 (en) * 2021-11-09 2025-09-10 Vigil Neuroscience Inc HETEROCYCLIC COMPOUNDS USED AS AGONISTS OF THE TRIGGER RECEPTOR EXPRESSED ON MYELOID CELLS 2 AND METHODS OF USE
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
WO2026011223A1 (en) * 2024-07-12 2026-01-15 Alterity Therapeutics Limited Novel salt and crystalline form
WO2026020054A1 (en) * 2024-07-18 2026-01-22 Neumora Therapeutics, Inc. Compounds and methods for treating neurological disorders

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