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
Authority
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)
Other versions
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 (enExample) 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 (enExample)
EP (1) EP1644320B1 (enExample)
JP (1) JP2007520440A (enExample)
AT (1) ATE384039T1 (enExample)
CA (1) CA2529036A1 (enExample)
DE (1) DE602004011348T2 (enExample)
ES (1) ES2298819T3 (enExample)
WO (1) WO2005009941A1 (enExample)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE459351T1 (de) * 2004-05-21 2010-03-15 Senju Pharma Co Ophthalmologische perkutan absorbierbare zubereitung enthaltend einen muscarin-rezeptor- agonist
WO2007075297A2 (en) * 2005-12-27 2007-07-05 University Of Toledo Muscarinic agonists and methods of use thereof
EP2296471A4 (en) 2008-05-15 2012-03-14 Univ Toledo MUSCARIC ACID AGONISTS AS COGNITIVE ENHANCERS
EP2361242B1 (en) 2008-10-17 2018-08-01 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
CN102574786A (zh) 2009-04-02 2012-07-11 默克雪兰诺有限公司 二氢乳清酸脱氢酶抑制剂
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
EP2486002B1 (en) 2009-10-09 2019-03-27 Oryzon Genomics, S.A. Substituted heteroaryl- and aryl- cyclopropylamine acetamides and their use
WO2011106574A2 (en) 2010-02-24 2011-09-01 Oryzon Genomics, S.A. Inhibitors for antiviral use
US9186337B2 (en) 2010-02-24 2015-11-17 Oryzon Genomics S.A. Lysine demethylase inhibitors for diseases and disorders associated with Hepadnaviridae
ES2607081T3 (es) 2010-04-19 2017-03-29 Oryzon Genomics, S.A. Inhibidores de desmetilasa específica de lisina-1 y su uso
ES2603032T3 (es) 2010-07-15 2017-02-23 Bayer Intellectual Property Gmbh Compuestos de 3-piridil-heteroarilcarboxamida como pesticidas
US9006449B2 (en) 2010-07-29 2015-04-14 Oryzon Genomics, S.A. Cyclopropylamine derivatives useful as LSD1 inhibitors
LT2598482T (lt) 2010-07-29 2018-07-10 Oryzon Genomics, S.A. Demetilazės lsd1 inhibitoriai arilciklopropilamino pagrindu ir jų medicininis panaudojimas
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
WO2012107498A1 (en) 2011-02-08 2012-08-16 Oryzon Genomics S.A. Lysine demethylase inhibitors for myeloproliferative disorders
US9549928B2 (en) 2011-04-29 2017-01-24 The University Of Toledo Muscarinic agonists as enhancers of cognitive flexibility
SI2776394T1 (sl) 2011-10-20 2019-05-31 Oryzon Genomics, S.A. Spojine (hetero)aril ciklopropilamina kot inhibitorji LSD1
EP3736265A1 (en) 2011-10-20 2020-11-11 Oryzon Genomics, S.A. (hetero)aryl cyclopropylamine compounds as lsd1 inhibitors
US11046670B2 (en) 2015-10-19 2021-06-29 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
WO2017190107A1 (en) * 2016-04-29 2017-11-02 Board Of Regents, The University Of Texas System Sigma receptor binders
US10954217B2 (en) 2016-04-29 2021-03-23 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
AU1582197A (en) * 1996-01-22 1997-08-11 Eli Lilly And Company Combinatorial process for preparing substituted indane libraries
CA2297906A1 (en) 1997-07-22 1999-02-04 Bret Eugene Huff 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
UA76492C2 (en) * 2001-09-21 2006-08-15 Lilly Co Eli Muscarinic agonists, a pharmaceutical composition on their basis

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