JP2008524328A5 - - Google Patents

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Publication number
JP2008524328A5
JP2008524328A5 JP2007548300A JP2007548300A JP2008524328A5 JP 2008524328 A5 JP2008524328 A5 JP 2008524328A5 JP 2007548300 A JP2007548300 A JP 2007548300A JP 2007548300 A JP2007548300 A JP 2007548300A JP 2008524328 A5 JP2008524328 A5 JP 2008524328A5
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Japan
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optionally substituted
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alkyl
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JP2007548300A
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English (en)
Japanese (ja)
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JP2008524328A (ja
JP5114208B2 (ja
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Priority claimed from US11/019,556 external-priority patent/US7550459B2/en
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Publication of JP2008524328A publication Critical patent/JP2008524328A/ja
Publication of JP2008524328A5 publication Critical patent/JP2008524328A5/ja
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Publication of JP5114208B2 publication Critical patent/JP5114208B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2007548300A 2004-12-21 2005-12-15 ムスカリン作動薬としてのテトラヒドロキノリン類似体 Expired - Fee Related JP5114208B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US11/019,556 2004-12-21
US11/019,556 US7550459B2 (en) 2001-12-28 2004-12-21 Tetrahydroquinoline analogues as muscarinic agonists
PCT/US2005/045313 WO2006068904A1 (en) 2004-12-21 2005-12-15 Tetrahydroquinoline analogues as muscarinic agonists

Publications (3)

Publication Number Publication Date
JP2008524328A JP2008524328A (ja) 2008-07-10
JP2008524328A5 true JP2008524328A5 (enExample) 2009-02-05
JP5114208B2 JP5114208B2 (ja) 2013-01-09

Family

ID=36123554

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007548300A Expired - Fee Related JP5114208B2 (ja) 2004-12-21 2005-12-15 ムスカリン作動薬としてのテトラヒドロキノリン類似体

Country Status (16)

Country Link
US (3) US7550459B2 (enExample)
EP (1) EP1828176A1 (enExample)
JP (1) JP5114208B2 (enExample)
KR (2) KR20130095846A (enExample)
CN (2) CN101124222A (enExample)
AR (1) AR052343A1 (enExample)
AU (1) AU2005319426B2 (enExample)
BR (1) BRPI0517485A (enExample)
CA (1) CA2591766C (enExample)
IL (2) IL184065A (enExample)
MX (1) MX2007007588A (enExample)
NO (1) NO20073183L (enExample)
NZ (1) NZ555994A (enExample)
RU (1) RU2434865C2 (enExample)
TW (2) TW201414731A (enExample)
WO (1) WO2006068904A1 (enExample)

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WO2007134136A2 (en) 2006-05-09 2007-11-22 Braincells, Inc. Neurogenesis by modulating angiotensin
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GB201519352D0 (en) 2015-11-02 2015-12-16 Heptares Therapeutics Ltd Pharmaceutical compounds
GB201617454D0 (en) 2016-10-14 2016-11-30 Heptares Therapeutics Limited Pharmaceutical compounds
GB201810239D0 (en) 2018-06-22 2018-08-08 Heptares Therapeutics Ltd Pharmaceutical compounds
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GB201819961D0 (en) 2018-12-07 2019-01-23 Heptares Therapeutics Ltd Pharmaceutical compounds
GB201819960D0 (en) 2018-12-07 2019-01-23 Heptares Therapeutics Ltd Pharmaceutical compounds
US11384083B2 (en) 2019-02-15 2022-07-12 Incyte Corporation Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
WO2020180959A1 (en) 2019-03-05 2020-09-10 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors
WO2020205560A1 (en) 2019-03-29 2020-10-08 Incyte Corporation Sulfonylamide compounds as cdk2 inhibitors
GB202020191D0 (en) 2020-12-18 2021-02-03 Heptares Therapeutics Ltd Pharmaceutical compounds
WO2020223558A1 (en) 2019-05-01 2020-11-05 Incyte Corporation Tricyclic amine compounds as cdk2 inhibitors
WO2020223469A1 (en) 2019-05-01 2020-11-05 Incyte Corporation N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer
AU2020328025A1 (en) 2019-08-14 2022-03-03 Incyte Corporation Imidazolyl pyrimidinylamine compounds as CDK2 inhibitors
JOP20220087A1 (ar) 2019-10-11 2023-01-30 Incyte Corp أمينات ثنائية الحلقة كمثبطات لـ cdk2
CN115073370B (zh) * 2021-03-10 2024-12-17 成都硕德药业有限公司 新型烷基氨类化合物或盐、异构体、其制备方法及用途
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors
WO2023114224A1 (en) 2021-12-13 2023-06-22 Sage Therapeutics, Inc. Combination of muscarinic receptor positive modulators and nmda positive allosteric modulators

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