JP2008518969A5 - - Google Patents

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Publication number
JP2008518969A5
JP2008518969A5 JP2007539354A JP2007539354A JP2008518969A5 JP 2008518969 A5 JP2008518969 A5 JP 2008518969A5 JP 2007539354 A JP2007539354 A JP 2007539354A JP 2007539354 A JP2007539354 A JP 2007539354A JP 2008518969 A5 JP2008518969 A5 JP 2008518969A5
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JP
Japan
Prior art keywords
group
alkyl
aryl
halogen
hydrogen
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.)
Pending
Application number
JP2007539354A
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English (en)
Japanese (ja)
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JP2008518969A (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2005/039932 external-priority patent/WO2006060109A1/en
Publication of JP2008518969A publication Critical patent/JP2008518969A/ja
Publication of JP2008518969A5 publication Critical patent/JP2008518969A5/ja
Pending legal-status Critical Current

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JP2007539354A 2004-10-29 2005-10-25 アルツハイマー病を治療するためのβ−セクレターゼ阻害薬として有用な2−アミノピリジン化合物 Pending JP2008518969A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US62344104P 2004-10-29 2004-10-29
PCT/US2005/039932 WO2006060109A1 (en) 2004-10-29 2005-10-25 2-aminopyridine compounds useful as beta-secretase inhibitors for the treatment of alzheimer's disease

Publications (2)

Publication Number Publication Date
JP2008518969A JP2008518969A (ja) 2008-06-05
JP2008518969A5 true JP2008518969A5 (enExample) 2008-10-30

Family

ID=36565355

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007539354A Pending JP2008518969A (ja) 2004-10-29 2005-10-25 アルツハイマー病を治療するためのβ−セクレターゼ阻害薬として有用な2−アミノピリジン化合物

Country Status (7)

Country Link
US (1) US7932275B2 (enExample)
EP (1) EP1807396B1 (enExample)
JP (1) JP2008518969A (enExample)
CN (1) CN101052618A (enExample)
AU (1) AU2005310239A1 (enExample)
CA (1) CA2585279A1 (enExample)
WO (1) WO2006060109A1 (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7763609B2 (en) 2003-12-15 2010-07-27 Schering Corporation Heterocyclic aspartyl protease inhibitors
WO2007050348A2 (en) * 2005-10-21 2007-05-03 Merck & Co., Inc. Potassium channel inhibitors
SI2402317T1 (sl) 2006-03-31 2013-10-30 Novartis Ag DGAT inhibitor
JP5379692B2 (ja) 2006-11-09 2013-12-25 プロビオドルグ エージー 潰瘍、癌及び他の疾患の治療のためのグルタミニルシクラーゼの阻害薬としての3−ヒドロキシ−1,5−ジヒドロ−ピロール−2−オン誘導体
SI2091948T1 (sl) 2006-11-30 2012-07-31 Probiodrug Ag Novi inhibitorji glutaminil ciklaze
ZA200905537B (en) 2007-03-01 2010-10-27 Probiodrug Ag New use of glutaminyl cyclase inhibitors
EP2865670B1 (en) 2007-04-18 2017-01-11 Probiodrug AG Thiourea derivatives as glutaminyl cyclase inhibitors
AR066169A1 (es) 2007-09-28 2009-07-29 Novartis Ag Derivados de benzo-imidazoles, utiles para trastornos asociados con la actividad de dgat
AU2009217518A1 (en) 2008-02-28 2009-09-03 Merck Sharp & Dohme Corp. 2-aminoimidazole beta-secretase inhibitors for the treatment of Alzheimer's disease
EP2475428B1 (en) 2009-09-11 2015-07-01 Probiodrug AG Heterocylcic derivatives as inhibitors of glutaminyl cyclase
UA108363C2 (uk) 2009-10-08 2015-04-27 Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування
WO2011107530A2 (en) 2010-03-03 2011-09-09 Probiodrug Ag Novel inhibitors
BR112012022478B1 (pt) 2010-03-10 2021-09-21 Probiodrug Ag Inibidores heterocíclicos de glutaminil ciclase (qc, ec 2.3.2.5), seu processo de preparação, e composição farmacêutica
JP5945532B2 (ja) 2010-04-21 2016-07-05 プロビオドルグ エージー グルタミニルシクラーゼの阻害剤としてのベンゾイミダゾール誘導体
ES2570167T3 (es) 2011-03-16 2016-05-17 Probiodrug Ag Derivados de benzimidazol como inhibidores de glutaminil ciclasa
WO2012138590A1 (en) 2011-04-07 2012-10-11 Merck Sharp & Dohme Corp. Pyrrolidine-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use
EP2694489B1 (en) 2011-04-07 2017-09-06 Merck Sharp & Dohme Corp. C5-c6 oxacyclic-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use
KR20140054295A (ko) 2011-08-22 2014-05-08 머크 샤프 앤드 돔 코포레이션 Bace 억제제로서의 2-스피로-치환된 이미노티아진 및 그의 모노- 및 디옥시드, 조성물 및 그의 용도
EP3461819B1 (en) 2017-09-29 2020-05-27 Probiodrug AG Inhibitors of glutaminyl cyclase
US11339161B2 (en) * 2017-12-19 2022-05-24 Boehringer Ingelheim International Gmbh Triazolo pyridines as modulators of gamma-secretase
CN111533684B (zh) * 2020-05-29 2021-10-29 四川大学 一种吡啶化合物烯基化的方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IE82916B1 (en) * 1990-11-02 2003-06-11 Elan Corp Plc Formulations and their use in the treatment of neurological diseases
AU2001277741B2 (en) * 2000-08-11 2005-12-22 Eisai R&D Management Co., Ltd. 2-aminopyridine compounds and use thereof as drugs
US6951946B2 (en) * 2002-03-19 2005-10-04 Lexicon Pharmaceuticals, Inc. Large scale synthesis of 1,2,4- and 1,3,4-oxadiazole carboxylates
WO2003106405A1 (en) 2002-06-01 2003-12-24 Sunesis Pharmaceuticals, Inc. Aspartyl protease inhibitors
GB0305918D0 (en) * 2003-03-14 2003-04-23 Glaxo Group Ltd Novel compounds
CA2529739A1 (en) 2003-06-16 2005-01-20 Sunesis Pharmaceuticals, Inc. Aspartyl protease inhibitors
JP2008523139A (ja) 2004-12-14 2008-07-03 アストラゼネカ・アクチエボラーグ 置換アミノピリジン類及びその使用

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