JP2012514006A5 - - Google Patents

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Publication number
JP2012514006A5
JP2012514006A5 JP2011543717A JP2011543717A JP2012514006A5 JP 2012514006 A5 JP2012514006 A5 JP 2012514006A5 JP 2011543717 A JP2011543717 A JP 2011543717A JP 2011543717 A JP2011543717 A JP 2011543717A JP 2012514006 A5 JP2012514006 A5 JP 2012514006A5
Authority
JP
Japan
Prior art keywords
optionally substituted
disorder
hydrogen
carbons
compound
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
JP2011543717A
Other languages
English (en)
Japanese (ja)
Other versions
JP2012514006A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2009/069716 external-priority patent/WO2010078348A1/en
Publication of JP2012514006A publication Critical patent/JP2012514006A/ja
Publication of JP2012514006A5 publication Critical patent/JP2012514006A5/ja
Pending legal-status Critical Current

Links

JP2011543717A 2008-12-29 2009-12-29 3.1.0二環式GlyT1阻害剤ならびにその作製および使用の方法 Pending JP2012514006A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US14103008P 2008-12-29 2008-12-29
US61/141,030 2008-12-29
PCT/US2009/069716 WO2010078348A1 (en) 2008-12-29 2009-12-29 3.1.0 bicyclic glyt1 inhibitors and methods of making and using same

Publications (2)

Publication Number Publication Date
JP2012514006A JP2012514006A (ja) 2012-06-21
JP2012514006A5 true JP2012514006A5 (enExample) 2013-01-31

Family

ID=42310195

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011543717A Pending JP2012514006A (ja) 2008-12-29 2009-12-29 3.1.0二環式GlyT1阻害剤ならびにその作製および使用の方法

Country Status (12)

Country Link
US (1) US8497289B2 (enExample)
EP (1) EP2381941A4 (enExample)
JP (1) JP2012514006A (enExample)
KR (1) KR20110117087A (enExample)
CN (1) CN102271677A (enExample)
AU (1) AU2009335120A1 (enExample)
BR (1) BRPI0923878A2 (enExample)
CA (1) CA2747602A1 (enExample)
IL (1) IL213541A0 (enExample)
MX (1) MX2011006845A (enExample)
RU (1) RU2011124709A (enExample)
WO (1) WO2010078348A1 (enExample)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9012489B2 (en) * 2011-08-03 2015-04-21 Boehringer Ingelheim International Gmbh Phenyl-3-aza-bicyclo[3.1.0]hex-3-yl-methanones and the use thereof as medicament
BR112016025910A8 (pt) * 2014-05-06 2021-07-13 Univ Northwestern uso de uma quantidade eficaz de glyx-13, uso de glyx-13 e um antagonista de nmdar e composição farmaceuticamente aceitável compreendendo os mesmos
US9987242B2 (en) 2015-05-05 2018-06-05 Northwestern University Treatment of Levodopa-induced Dyskinesias
CR20210545A (es) * 2019-05-01 2021-12-23 Boehringer Ingelheim Int Formas sólidas de un inhibidor de glyt1
CA3188340A1 (en) 2020-08-13 2022-02-17 Boehringer Ingelheim International Gmbh Treatment of cognitive impairement associated with schizophrenia
KR20230088761A (ko) 2020-10-13 2023-06-20 베링거 인겔하임 인터내셔날 게엠베하 재가공하는 방법
JP2025528779A (ja) 2022-08-09 2025-09-02 シーザン ハイスーク ファーマシューティカル カンパニー リミテッド Pde4b阻害剤及びその用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5981168A (en) * 1998-05-15 1999-11-09 The University Of British Columbia Method and composition for modulating amyloidosis
EA009903B1 (ru) * 2003-10-14 2008-04-28 Пфайзер Продактс Инк. Бициклические [3.1.0] производные в качестве ингибиторов переносчиков глицина
AU2005317846B2 (en) * 2004-12-21 2011-12-08 Merck Sharp & Dohme Limited Piperidine and azetidine derivatives as GlyT1 inhibitors
US20080319043A1 (en) * 2005-05-03 2008-12-25 Mohammad Salman 3,6-Disubstituted Azabicyclo (3.1.0) Hexane Derivatives as Muscarinic Receptor Antagonists
GB0523998D0 (en) * 2005-11-25 2006-01-04 Merck Sharp & Dohme Therapeutic agents
CL2007002809A1 (es) * 2006-09-29 2008-04-18 Actelion Pharmaceuticals Ltd Compuestos derivados de 3-aza biciclo [3.1.0]hexano; y su uso en el tratamiento de enfermedades tales como desordenes psicoticos y de ansiedad, desordenes del sueno, uso y abuso de sustancias psicoactivas, demencia y deterioro de funciones cognitivas

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