JP2007520440A5 - - Google Patents

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Publication number
JP2007520440A5
JP2007520440A5 JP2006518649A JP2006518649A JP2007520440A5 JP 2007520440 A5 JP2007520440 A5 JP 2007520440A5 JP 2006518649 A JP2006518649 A JP 2006518649A JP 2006518649 A JP2006518649 A JP 2006518649A JP 2007520440 A5 JP2007520440 A5 JP 2007520440A5
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JP
Japan
Prior art keywords
group
alkyl
alkoxy
halogen
optionally substituted
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
JP2006518649A
Other languages
English (en)
Japanese (ja)
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JP2007520440A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2004/019094 external-priority patent/WO2005009941A1/en
Publication of JP2007520440A publication Critical patent/JP2007520440A/ja
Publication of JP2007520440A5 publication Critical patent/JP2007520440A5/ja
Pending legal-status Critical Current

Links

JP2006518649A 2003-07-03 2004-06-23 ムスカリン性受容体アゴニストとしてのインダン誘導体 Pending JP2007520440A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US48469603P 2003-07-03 2003-07-03
PCT/US2004/019094 WO2005009941A1 (en) 2003-07-03 2004-06-23 Indane derivates as muscarinic receptor agonists

Publications (2)

Publication Number Publication Date
JP2007520440A JP2007520440A (ja) 2007-07-26
JP2007520440A5 true JP2007520440A5 (cg-RX-API-DMAC10.html) 2007-09-06

Family

ID=34102660

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006518649A Pending JP2007520440A (ja) 2003-07-03 2004-06-23 ムスカリン性受容体アゴニストとしてのインダン誘導体

Country Status (8)

Country Link
US (1) US7265246B2 (cg-RX-API-DMAC10.html)
EP (1) EP1644320B1 (cg-RX-API-DMAC10.html)
JP (1) JP2007520440A (cg-RX-API-DMAC10.html)
AT (1) ATE384039T1 (cg-RX-API-DMAC10.html)
CA (1) CA2529036A1 (cg-RX-API-DMAC10.html)
DE (1) DE602004011348T2 (cg-RX-API-DMAC10.html)
ES (1) ES2298819T3 (cg-RX-API-DMAC10.html)
WO (1) WO2005009941A1 (cg-RX-API-DMAC10.html)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005113002A1 (ja) * 2004-05-21 2005-12-01 Senju Pharmaceutical Co., Ltd. ムスカリン受容体作動薬を含有する眼科用経皮吸収型製剤
EP1973904A2 (en) * 2005-12-27 2008-10-01 University Of Toledo Muscarinic agonists and methods of use thereof
WO2009140483A1 (en) 2008-05-15 2009-11-19 University Of Toledo Muscarinic agonists as cognitive enhancers
WO2010043721A1 (en) 2008-10-17 2010-04-22 Oryzon Genomics, S.A. Oxidase inhibitors and their use
WO2010084160A1 (en) 2009-01-21 2010-07-29 Oryzon Genomics S.A. Phenylcyclopropylamine derivatives and their medical use
WO2010115736A2 (en) 2009-04-02 2010-10-14 Merck Serono S.A. Dihydroorotate dehydrogenase inhibitors
WO2010141690A2 (en) * 2009-06-04 2010-12-09 Dara Biosciences, Inc. Indane analogs and use as pharmaceutical agents and process of making
KR101736218B1 (ko) 2009-09-25 2017-05-16 오리존 지노믹스 에스.에이. 라이신 특이적 디메틸라아제-1 억제제 및 이의 용도
WO2011042217A1 (en) 2009-10-09 2011-04-14 Oryzon Genomics S.A. Substituted heteroaryl- and aryl- cyclopropylamine acetamides and their use
WO2011106106A2 (en) 2010-02-24 2011-09-01 Oryzon Genomics, S.A. Lysine demethylase inhibitors for diseases and disorders associated with hepadnaviridae
WO2011106105A2 (en) 2010-02-24 2011-09-01 Oryzon Genomics, S.A. Inhibitors for antiviral use
JP5868948B2 (ja) 2010-04-19 2016-02-24 オリゾン・ジェノミックス・ソシエダッド・アノニマOryzon Genomics S.A. リジン特異的脱メチル化酵素1阻害薬およびその使用
CN104086528A (zh) 2010-07-15 2014-10-08 拜耳知识产权有限责任公司 作为杀虫剂的新杂环化合物
EP3375775A1 (en) 2010-07-29 2018-09-19 Oryzon Genomics, S.A. Arylcyclopropylamine based demethylase inhibitors of lsd1 and their medical use
EP2598480B1 (en) 2010-07-29 2019-04-24 Oryzon Genomics, S.A. Cyclopropylamine derivatives useful as lsd1 inhibitors
US9061966B2 (en) 2010-10-08 2015-06-23 Oryzon Genomics S.A. Cyclopropylamine inhibitors of oxidases
WO2012072713A2 (en) 2010-11-30 2012-06-07 Oryzon Genomics, S.A. Lysine demethylase inhibitors for diseases and disorders associated with flaviviridae
EP2712315B1 (en) 2011-02-08 2021-11-24 Oryzon Genomics, S.A. Lysine demethylase inhibitors for myeloproliferative disorders
WO2012149524A1 (en) 2011-04-29 2012-11-01 The University Of Toledo Muscarinic agonists as enhancers of working memory and cognitive flexibility
IL264982B (en) 2011-10-20 2022-08-01 Oryzon Genomics Sa Hetero(aryl)cyclopropylamine compounds as lsd1 inhibitors
US9487512B2 (en) 2011-10-20 2016-11-08 Oryzon Genomics S.A. (Hetero)aryl cyclopropylamine compounds as LSD1 inhibitors
CA3001484A1 (en) 2015-10-19 2017-04-27 Board Of Regents, The University Of Texas System Piperazinyl norbenzomorphan compounds and methods for using the same
WO2017160922A1 (en) 2016-03-16 2017-09-21 Kalyra Pharmaceuticals, Inc. Analgesic compounds
US10954217B2 (en) 2016-04-29 2021-03-23 Board Of Regents, The University Of Texas System Sigma receptor binders
US20210323913A1 (en) * 2016-04-29 2021-10-21 Board Of Regents, The University Of Texas System Sigma receptor binders
CN114736128A (zh) * 2022-03-10 2022-07-12 青岛科技大学 一种制备邻氨基苯醚的方法
CN118652255B (zh) * 2024-08-20 2024-10-15 广州市桐晖药业有限公司 一种己酮可可碱的工艺改进方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE290859T1 (de) * 1996-01-22 2005-04-15 Lilly Co Eli Indanderivate für antipsychotische mittel
EP1003495A4 (en) 1997-07-22 2002-08-28 Lilly Co Eli PHARMACEUTICAL COMPOUNDS
TWI241190B (en) * 2001-02-13 2005-10-11 Aventis Pharma Gmbh 4-Fluoro-N-indan-2-yl benzamide and its use as pharmaceutical
NZ531135A (en) * 2001-09-21 2006-09-29 Lilly Co Eli Muscarinic agonists

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