CN1741999A - 用作GSK-3β抑制剂的哒嗪酮衍生物 - Google Patents

用作GSK-3β抑制剂的哒嗪酮衍生物 Download PDF

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Publication number
CN1741999A
CN1741999A CNA2003801050578A CN200380105057A CN1741999A CN 1741999 A CN1741999 A CN 1741999A CN A2003801050578 A CNA2003801050578 A CN A2003801050578A CN 200380105057 A CN200380105057 A CN 200380105057A CN 1741999 A CN1741999 A CN 1741999A
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alkyl
aryl
oxo
heteroaryl
heterocyclyl
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CNA2003801050578A
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Chinese (zh)
Inventor
S·赫尔德
T·瑙曼
K·舍纳芬格
D·W·威尔
H·马特
G·米勒
D·勒叙斯
B·博杜安
T·鲁尼
F·阿莱
G·蒂拉博斯奇
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Sanofi Aventis Deutschland GmbH
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Aventis Pharma Deutschland GmbH
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    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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CNA2003801050578A 2002-11-19 2003-11-19 用作GSK-3β抑制剂的哒嗪酮衍生物 Pending CN1741999A (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0214443 2002-11-19
FR0214443A FR2847253B1 (fr) 2002-11-19 2002-11-19 Nouveaux derives de pyridazinones a titre de medicaments et compositions pharmaceutiques les renfermant

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CN1741999A true CN1741999A (zh) 2006-03-01

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EP (2) EP1581505B1 (cg-RX-API-DMAC7.html)
JP (1) JP2006509748A (cg-RX-API-DMAC7.html)
KR (1) KR20050083918A (cg-RX-API-DMAC7.html)
CN (1) CN1741999A (cg-RX-API-DMAC7.html)
AR (2) AR042089A1 (cg-RX-API-DMAC7.html)
AT (2) ATE369356T1 (cg-RX-API-DMAC7.html)
AU (2) AU2003283414A1 (cg-RX-API-DMAC7.html)
BR (1) BR0316720A (cg-RX-API-DMAC7.html)
CA (2) CA2506022A1 (cg-RX-API-DMAC7.html)
CO (1) CO5700722A2 (cg-RX-API-DMAC7.html)
DE (2) DE60315516T2 (cg-RX-API-DMAC7.html)
FR (1) FR2847253B1 (cg-RX-API-DMAC7.html)
MA (1) MA27814A1 (cg-RX-API-DMAC7.html)
MX (1) MXPA05005270A (cg-RX-API-DMAC7.html)
NO (1) NO20052887L (cg-RX-API-DMAC7.html)
PL (1) PL376129A1 (cg-RX-API-DMAC7.html)
RU (1) RU2005119151A (cg-RX-API-DMAC7.html)
TW (2) TW200418478A (cg-RX-API-DMAC7.html)
WO (2) WO2004046117A1 (cg-RX-API-DMAC7.html)

Cited By (9)

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CN102731379A (zh) * 2009-03-02 2012-10-17 Irm责任有限公司 用作wnt信号调节剂的n-(杂)芳基、2-(杂)芳基取代的乙酰胺类
CN102958917A (zh) * 2010-06-29 2013-03-06 Irm责任有限公司 用于调节wnt信号通路的组合物和方法
US8501731B2 (en) 2008-03-18 2013-08-06 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Derivatives of 6[3-(trifluoromethyl)phenyl]pyridazin-3(2H)-one having antitumor activity
US9212146B2 (en) 2008-03-18 2015-12-15 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Substituted pyridazinones for the treatment of tumors
CN106458910A (zh) * 2014-02-19 2017-02-22 亚倍生技制药公司 线粒体醛脱氢酶2(aldh2)结合多环酰胺和其用于治疗癌症的用途
CN108558889A (zh) * 2013-10-18 2018-09-21 赛尔基因昆蒂赛尔研究公司 布罗莫结构域抑制剂
CN109863140A (zh) * 2016-05-25 2019-06-07 拜耳医药股份有限公司 3-氧代-2,6-二苯基-2,3-二氢哒嗪-4-甲酰胺
CN110577564A (zh) * 2012-01-20 2019-12-17 医药研究委员会 多肽和方法
CN111533697A (zh) * 2020-05-07 2020-08-14 成都大学 4-氨基哒嗪酮类化合物及其制备方法

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DE102004010207A1 (de) 2004-03-02 2005-09-15 Aventis Pharma S.A. Neue 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate
DE102004010194A1 (de) 2004-03-02 2005-10-13 Aventis Pharma Deutschland Gmbh 4-Benzimidazol-2-yl-pyridazin-3-on-Derivate, ihre Herstellung und Verwendung in Arzneimitteln
EP1598348A1 (en) 2004-05-18 2005-11-23 Aventis Pharma Deutschland GmbH Novel pyridazinone derivatives as inhibitors of CDK2
EP1604988A1 (en) 2004-05-18 2005-12-14 Sanofi-Aventis Deutschland GmbH Pyridazinone derivatives, methods for producing them and their use as pharmaceuticals
EP1799664A1 (en) 2004-09-20 2007-06-27 Xenon Pharmaceuticals Inc. Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors
EP1799667B1 (en) 2004-09-20 2013-03-20 Xenon Pharmaceuticals Inc. Heterocyclic derivatives and their use as therapeutic agents
AU2005286728A1 (en) 2004-09-20 2006-03-30 Xenon Pharmaceuticals Inc. Heterocyclic derivatives and their use as mediators of stearoyl-CoA desaturase
CA2580845A1 (en) 2004-09-20 2006-03-30 Xenon Pharmaceuticals Inc. Pyridazine derivatives for inhibiting human stearoyl-coa-desaturase
BRPI0515505A (pt) 2004-09-20 2008-07-29 Xenon Pharmaceuticals Inc derivados heterocìclicos e sua utilização como inibidores da estearoil-coa desaturase
WO2006101521A2 (en) 2004-09-20 2006-09-28 Xenon Pharmaceuticals Inc. Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors
AR051026A1 (es) 2004-09-20 2006-12-13 Xenon Pharmaceuticals Inc Derivados heterociclicos y su uso como inhibidores de la estearoil-coa desaturasa
ATE523199T1 (de) 2004-11-02 2011-09-15 Univ Northwestern Pyridazinverbindungen und verfahren
CN101087766B (zh) 2004-11-02 2011-09-07 西北大学 哒嗪化合物、组合物和方法
CA2618646A1 (en) 2005-06-03 2007-11-15 Xenon Pharmaceuticals Inc. Aminothiazole derivatives as human stearoyl-coa desaturase inhibitors
EP1928437A2 (en) 2005-08-26 2008-06-11 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
EP2258357A3 (en) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
WO2007047978A2 (en) 2005-10-21 2007-04-26 Braincells, Inc. Modulation of neurogenesis by pde inhibition
WO2007053596A1 (en) 2005-10-31 2007-05-10 Braincells, Inc. Gaba receptor mediated modulation of neurogenesis
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
WO2007127475A2 (en) * 2006-04-28 2007-11-08 Northwestern University Pyridazines for demyelinating diseases and neuropathic pain
EP2015750A2 (en) * 2006-04-28 2009-01-21 Northwestern University Compositions and treatments using pyridazine compounds and cholinesterase inhibitors
US20090325973A1 (en) 2006-04-28 2009-12-31 Watterson D Martin Formulations containing pyridazine compounds
EP2021000A2 (en) 2006-05-09 2009-02-11 Braincells, Inc. Neurogenesis by modulating angiotensin
MX2009001043A (es) 2006-08-08 2009-02-06 Sanofi Aventis Imidazolidina-2,4-dionas sustituidas con arilaminoarilalquilo, procedimiento para preparalas, medicamentos que comprenden estos compuestos y su uso.
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
EP2310372B1 (en) 2008-07-09 2012-05-23 Sanofi Heterocyclic compounds, processes for their preparation, medicaments comprising these compounds, and the use thereof
WO2010068601A1 (en) 2008-12-08 2010-06-17 Sanofi-Aventis A crystalline heteroaromatic fluoroglycoside hydrate, processes for making, methods of use and pharmaceutical compositions thereof
US20100216805A1 (en) 2009-02-25 2010-08-26 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
AU2012203023C1 (en) * 2009-03-02 2013-11-07 Novartis Ag N-(hetero)aryl, 2- (hetero)aryl-substituted acetamides for use as Wnt signaling modulators
US8785608B2 (en) 2009-08-26 2014-07-22 Sanofi Crystalline heteroaromatic fluoroglycoside hydrates, pharmaceuticals comprising these compounds and their use
WO2011107494A1 (de) 2010-03-03 2011-09-09 Sanofi Neue aromatische glykosidderivate, diese verbindungen enthaltende arzneimittel und deren verwendung
WO2011157827A1 (de) 2010-06-18 2011-12-22 Sanofi Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen
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