JP2006523694A5 - - Google Patents

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Publication number
JP2006523694A5
JP2006523694A5 JP2006509747A JP2006509747A JP2006523694A5 JP 2006523694 A5 JP2006523694 A5 JP 2006523694A5 JP 2006509747 A JP2006509747 A JP 2006509747A JP 2006509747 A JP2006509747 A JP 2006509747A JP 2006523694 A5 JP2006523694 A5 JP 2006523694A5
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JP
Japan
Prior art keywords
group
ethyl
disorder
dioxo
carbon atoms
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JP2006509747A
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English (en)
Japanese (ja)
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JP2006523694A (ja
JP4621659B2 (ja
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Priority claimed from PCT/US2004/010596 external-priority patent/WO2004092189A1/en
Publication of JP2006523694A publication Critical patent/JP2006523694A/ja
Publication of JP2006523694A5 publication Critical patent/JP2006523694A5/ja
Application granted granted Critical
Publication of JP4621659B2 publication Critical patent/JP4621659B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2006509747A 2003-04-09 2004-04-07 [2−(8,9−ジオキソ−2,6−ジアザビシクロ[5.2.0]ノナ−1(7)−エン−2−イル)アルキル]ホスホン酸の誘導体およびn−メチル−d−アスパルテート(nmda)受容体アンタゴニストとしてのその使用 Expired - Fee Related JP4621659B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US46149003P 2003-04-09 2003-04-09
PCT/US2004/010596 WO2004092189A1 (en) 2003-04-09 2004-04-07 Derivatives of 2-(8,9-dioxo-2,6-diazabicyclo(5.2.0)non-1(7)-en-2-yl)alkyl phosphonic acid and their use as n-methyl-d-aspartate (nmda) recetor antagonists

Publications (3)

Publication Number Publication Date
JP2006523694A JP2006523694A (ja) 2006-10-19
JP2006523694A5 true JP2006523694A5 (enExample) 2007-06-14
JP4621659B2 JP4621659B2 (ja) 2011-01-26

Family

ID=33299828

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2006509747A Expired - Fee Related JP4621659B2 (ja) 2003-04-09 2004-04-07 [2−(8,9−ジオキソ−2,6−ジアザビシクロ[5.2.0]ノナ−1(7)−エン−2−イル)アルキル]ホスホン酸の誘導体およびn−メチル−d−アスパルテート(nmda)受容体アンタゴニストとしてのその使用

Country Status (19)

Country Link
US (2) US7253153B2 (enExample)
EP (1) EP1611144B1 (enExample)
JP (1) JP4621659B2 (enExample)
CN (1) CN1863810B (enExample)
AR (1) AR044013A1 (enExample)
AT (1) ATE481103T1 (enExample)
AU (1) AU2004230895B2 (enExample)
BR (1) BRPI0409255A (enExample)
CA (1) CA2521313A1 (enExample)
CL (1) CL2004000769A1 (enExample)
CY (1) CY1110863T1 (enExample)
DE (1) DE602004029146D1 (enExample)
DK (1) DK1611144T3 (enExample)
ES (1) ES2350449T3 (enExample)
MX (1) MXPA05010760A (enExample)
PL (1) PL1611144T3 (enExample)
PT (1) PT1611144E (enExample)
TW (1) TWI349674B (enExample)
WO (1) WO2004092189A1 (enExample)

Families Citing this family (24)

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US7687080B2 (en) * 2002-11-25 2010-03-30 Taraxos Inc. Treatment of neuropathy
US7732162B2 (en) 2003-05-05 2010-06-08 Probiodrug Ag Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases
TW200514775A (en) 2003-10-22 2005-05-01 Wyeth Corp Methods for the preparation of {2-[(8,9)-dioxo-2,6-diaza-bicyclo[5.2.0]-non-1(7)-en-2-yl]ethyl} phosphonic acid and esters thereof
CN101072784B (zh) * 2004-10-08 2011-05-04 惠氏公司 [2-(8,9-二氧代-2,6-二氮杂二环[5.2.0]壬-1(7)-烯-2-基)烷基]膦酸衍生物及其制备方法
JP5379692B2 (ja) 2006-11-09 2013-12-25 プロビオドルグ エージー 潰瘍、癌及び他の疾患の治療のためのグルタミニルシクラーゼの阻害薬としての3−ヒドロキシ−1,5−ジヒドロ−ピロール−2−オン誘導体
SI2091948T1 (sl) 2006-11-30 2012-07-31 Probiodrug Ag Novi inhibitorji glutaminil ciklaze
CN101668525A (zh) 2007-03-01 2010-03-10 前体生物药物股份公司 谷氨酰胺酰环化酶抑制剂的新用途
EP2142514B1 (en) 2007-04-18 2014-12-24 Probiodrug AG Thiourea derivatives as glutaminyl cyclase inhibitors
KR20100049663A (ko) * 2007-08-27 2010-05-12 와이어쓰 엘엘씨 마취제-절감 효과를 달성하기 위해 nmda 길항제를 사용하는 조성물 및 방법
HRP20120735T1 (hr) 2007-11-29 2012-10-31 Actelion Pharmaceuticals Ltd. Derivati fosfonske kiseline i njihova uporaba kao antagonista p2y12 receptora
AR071653A1 (es) 2008-04-11 2010-07-07 Actelion Pharmaceuticals Ltd Derivados 2-fenil-4-ciclopropil-pirimidina
AR071652A1 (es) 2008-04-11 2010-07-07 Actelion Pharmaceuticals Ltd Derivados 2- fenil-piridina substituidos
AU2009296457A1 (en) * 2008-09-27 2010-04-01 Taraxos Inc. Topical formulations for treatment of neuropathy
NZ596213A (en) 2009-04-08 2013-05-31 Actelion Pharmaceuticals Ltd 6-(3-aza-bicyclo[3.1.0]hex-3-yl)-2-phenyl-pyrimidines as adenosine 5'-diphosphate (ADP) receptor antagonists
PL2475428T3 (pl) 2009-09-11 2015-12-31 Probiodrug Ag Pochodne heterocykliczne jako inhibitory cyklazy glutaminowej
WO2011107530A2 (en) 2010-03-03 2011-09-09 Probiodrug Ag Novel inhibitors
KR101790806B1 (ko) 2010-03-10 2017-11-20 프로비오드룩 아게 글루타미닐 사이클라제(qc, ec 2.3.2.5)의 헤테로사이클릭 억제제
WO2011131748A2 (en) 2010-04-21 2011-10-27 Probiodrug Ag Novel inhibitors
WO2012123563A1 (en) 2011-03-16 2012-09-20 Probiodrug Ag Benz imidazole derivatives as inhibitors of glutaminyl cyclase
CN103607888A (zh) 2011-04-08 2014-02-26 斯法尔制药私人有限公司 取代的甲基甲酰基试剂以及使用所述试剂改进化合物的物理化学性质和/或药代动力学性质的方法
TWI752086B (zh) 2016-09-22 2022-01-11 瑞士商愛杜西亞製藥有限公司 結晶型式
KR102510832B1 (ko) 2017-03-15 2023-03-15 이도르시아 파마슈티컬스 리미티드 P2y12 수용체 안타고니스트의 피하 투여
DK3461819T3 (da) 2017-09-29 2020-08-10 Probiodrug Ag Inhibitorer af glutaminylcyklase
US10902020B2 (en) * 2018-06-08 2021-01-26 International Business Machines Corporation Multiple cache processing of streaming data

Family Cites Families (15)

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US5624898A (en) * 1989-12-05 1997-04-29 Ramsey Foundation Method for administering neurologic agents to the brain
US5168103A (en) * 1991-01-22 1992-12-01 American Home Products Corporation [[2-(amino-3,4-dioxo-1-cyclobuten-1-yl) amino]alkyl]-acid derivatives
US5124319A (en) * 1991-10-11 1992-06-23 American Home Products Corporation Benzimidazole phosphono-amino acids
DK124393D0 (da) 1993-11-03 1993-11-03 Lundbeck & Co As H Compounds
TW427904B (en) 1995-12-07 2001-04-01 American Home Prod Neuroprotective agents
UA52698C2 (uk) 1996-10-04 2003-01-15 Х. Луннбек А/С Похідні (3-алкоксіізоксазол-4-іл)заміщеної 2-амінокарбонової кислоти та їх сірковмісні аналоги, фармацевтична композиція на їх основі
DK1000072T3 (da) 1997-08-01 2003-04-22 Wyeth Corp Fremgangsmåde til fremstilling af [2-((8,9)- dioxo-2,6-diazabicylo-[5.2.0]non-1(7)-en-2-yl)ethyl]phosphonsyre
US5990307A (en) * 1997-08-01 1999-11-23 American Home Products Corporation Process for the preparation of [2-((8.9)-Dioxo-2,6-Diazabicyclo [5.2.0]-Non-1(7)-en-2yl) Ethyl]Phosphonic acid
US6541669B1 (en) 1998-06-08 2003-04-01 Theravance, Inc. β2-adrenergic receptor agonists
US6225343B1 (en) * 1999-06-16 2001-05-01 Nastech Pharmaceutical Company, Inc. Compositions and methods comprising morphine gluconate
UA78529C2 (en) 2001-10-10 2007-04-10 Wyeth Corp Derivatives of [[2-(amino-3,4-dioxo-1-cyclobutene-1-yl)amino]alkyl] acid for treating pain
US20040082543A1 (en) 2002-10-29 2004-04-29 Pharmacia Corporation Compositions of cyclooxygenase-2 selective inhibitors and NMDA receptor antagonists for the treatment or prevention of neuropathic pain
US20050004079A1 (en) * 2003-04-09 2005-01-06 Wyeth Pharmaceutical compositions for intranasal administration of [2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)alkyl] phosphonic acid and derivatives and methods of use thereof
US6933289B2 (en) 2003-07-01 2005-08-23 Allergan, Inc. Inhibition of irritating side effects associated with use of a topical ophthalmic medication
US20050142192A1 (en) 2003-10-15 2005-06-30 Wyeth Oral administration of [2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7)-en-2-yl)alkyl] phosphonic acid and derivatives

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