JP2007516169A5 - - Google Patents

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Publication number
JP2007516169A5
JP2007516169A5 JP2006516555A JP2006516555A JP2007516169A5 JP 2007516169 A5 JP2007516169 A5 JP 2007516169A5 JP 2006516555 A JP2006516555 A JP 2006516555A JP 2006516555 A JP2006516555 A JP 2006516555A JP 2007516169 A5 JP2007516169 A5 JP 2007516169A5
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JP
Japan
Prior art keywords
alkyl
optionally substituted
heteroaryl
cycloalkyl
aryl
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JP2006516555A
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English (en)
Japanese (ja)
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JP4680897B2 (ja
JP2007516169A (ja
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Priority claimed from PCT/IB2004/001989 external-priority patent/WO2005000303A1/en
Publication of JP2007516169A publication Critical patent/JP2007516169A/ja
Publication of JP2007516169A5 publication Critical patent/JP2007516169A5/ja
Application granted granted Critical
Publication of JP4680897B2 publication Critical patent/JP4680897B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2006516555A 2003-06-27 2004-06-14 Gsk−3阻害薬としてのピラゾロ[3,4−b]ピリジン−6−オン類 Expired - Fee Related JP4680897B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US48348903P 2003-06-27 2003-06-27
PCT/IB2004/001989 WO2005000303A1 (en) 2003-06-27 2004-06-14 Pyrazolo`3,4-b!pyridin-6-ones as gsk-3 inhibitors

Publications (3)

Publication Number Publication Date
JP2007516169A JP2007516169A (ja) 2007-06-21
JP2007516169A5 true JP2007516169A5 (https=) 2007-08-02
JP4680897B2 JP4680897B2 (ja) 2011-05-11

Family

ID=33552061

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006516555A Expired - Fee Related JP4680897B2 (ja) 2003-06-27 2004-06-14 Gsk−3阻害薬としてのピラゾロ[3,4−b]ピリジン−6−オン類

Country Status (11)

Country Link
US (1) US7300943B2 (https=)
EP (1) EP1641454B1 (https=)
JP (1) JP4680897B2 (https=)
AT (1) ATE409480T1 (https=)
BR (1) BRPI0411891A (https=)
CA (1) CA2529083A1 (https=)
DE (1) DE602004016850D1 (https=)
DK (1) DK1641454T3 (https=)
ES (1) ES2313014T3 (https=)
MX (1) MXPA05014201A (https=)
WO (1) WO2005000303A1 (https=)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2006130673A1 (en) 2005-05-31 2006-12-07 Janssen Pharmaceutica, N.V. 3-benzoimidazolyl-pyrazolopyridines useful in treating kinase disorders
EP2258358A3 (en) 2005-08-26 2011-09-07 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
EP2275095A3 (en) 2005-08-26 2011-08-17 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
EP1940389A2 (en) 2005-10-21 2008-07-09 Braincells, Inc. Modulation of neurogenesis by pde inhibition
AU2006308889A1 (en) 2005-10-31 2007-05-10 Braincells, Inc. GABA receptor mediated modulation of neurogenesis
WO2007076055A2 (en) * 2005-12-22 2007-07-05 Entremed, Inc. Compositions and methods comprising proteinase activated receptor antagonists
US8193238B2 (en) * 2006-03-08 2012-06-05 University Of Maryland, Baltimore Inhibition of microtubule protrusion in cancer cells
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
EP2382975A3 (en) 2006-05-09 2012-02-29 Braincells, Inc. Neurogenesis by modulating angiotensin
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
JP2008074788A (ja) * 2006-09-22 2008-04-03 Rohto Pharmaceut Co Ltd エラスチン産生促進剤
WO2008136948A1 (en) * 2007-05-07 2008-11-13 Amgen Inc. Pyrazolo-pyridinone and pyrazolo-pyrazinone compounds as p38 modulators, process for their preparation, and their pharmaceutical use
WO2008137176A1 (en) * 2007-05-07 2008-11-13 Amgen Inc. Pyrazolo-pyridinone compounds, process for their preparation, and their pharmaceutical use
US20100210644A1 (en) * 2007-06-25 2010-08-19 Boehringer Ingelheim International Gmbh Chemical compounds
WO2009017453A1 (en) * 2007-07-30 2009-02-05 Astrazeneca Ab New therapeutic combination of an antipsychotic and a gsk3 inhibitor 958
MX2010002692A (es) 2007-09-13 2010-06-01 Concert Pharmaceuticals Inc Sintesis de catecoles deuterados y derivados de benzo[d][1,3]dioxoles de los mismos.
GB0719299D0 (en) 2007-10-03 2007-11-14 Optinose As Nasal delivery devices
FR2931677B1 (fr) * 2008-06-02 2010-08-20 Sanofi Aventis Association d'un agoniste partiel des recepteurs nicotiniques et d'un inhibiteur d'acetylcholinesterase, composition la contenant et son utilisation dans le traitement des troubles cognitifs
WO2010099217A1 (en) 2009-02-25 2010-09-02 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
US20140206667A1 (en) 2012-11-14 2014-07-24 Michela Gallagher Methods and compositions for treating schizophrenia
CA2945263A1 (en) 2014-04-09 2015-10-15 Christopher Rudd Use of gsk-3 inhibitors or activators which modulate pd-1 or t-bet expression to modulate t cell immunity
WO2023011456A1 (en) * 2021-08-03 2023-02-09 Beigene, Ltd. Pyrazolopyridinone compounds

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE138773C (https=)
US4020072A (en) * 1976-05-04 1977-04-26 E. R. Squibb & Sons, Inc. 5-Aminomethyl-1H-pyrazolo[3,4-b]pyridines
DD138773A1 (de) * 1978-09-15 1979-11-21 Helmut Dorn Verfahren zur herstellung von 6,7-dihydro-6-oxo-pyr&zolo eckige klammer auf 3,4-b eckige klammer zu-pyridinen
US7109199B2 (en) * 2000-09-22 2006-09-19 Smithkline Beecham Corporation Pyrazolopyridines and pyrazolopyridazines as antidiabetics
AU2002222293A1 (en) * 2000-12-19 2002-07-01 Smithkline Beecham P.L.C. Pyrazolo(3,4-c)pyridines as gsk-3 inhibitors
GB0128287D0 (en) * 2001-11-26 2002-01-16 Smithkline Beecham Plc Novel method and compounds

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