JP2003513071A5 - - Google Patents

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Publication number
JP2003513071A5
JP2003513071A5 JP2001534771A JP2001534771A JP2003513071A5 JP 2003513071 A5 JP2003513071 A5 JP 2003513071A5 JP 2001534771 A JP2001534771 A JP 2001534771A JP 2001534771 A JP2001534771 A JP 2001534771A JP 2003513071 A5 JP2003513071 A5 JP 2003513071A5
Authority
JP
Japan
Prior art keywords
disease
disorder
pharmaceutical composition
composition according
nicotine
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.)
Abandoned
Application number
JP2001534771A
Other languages
English (en)
Japanese (ja)
Other versions
JP2003513071A (ja
Filing date
Publication date
Priority claimed from SE9903997A external-priority patent/SE9903997D0/xx
Application filed filed Critical
Publication of JP2003513071A publication Critical patent/JP2003513071A/ja
Publication of JP2003513071A5 publication Critical patent/JP2003513071A5/ja
Abandoned legal-status Critical Current

Links

JP2001534771A 1999-11-03 2000-11-01 ニコチン受容体作用薬の正のモジュレーター Abandoned JP2003513071A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
SE9903997A SE9903997D0 (sv) 1999-11-03 1999-11-03 New compounds
SE9903997-6 1999-11-03
PCT/SE2000/002148 WO2001032619A1 (en) 1999-11-03 2000-11-01 Positive modulators of nicotinic receptor agonists

Publications (2)

Publication Number Publication Date
JP2003513071A JP2003513071A (ja) 2003-04-08
JP2003513071A5 true JP2003513071A5 (enExample) 2007-11-22

Family

ID=20417607

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001534771A Abandoned JP2003513071A (ja) 1999-11-03 2000-11-01 ニコチン受容体作用薬の正のモジュレーター

Country Status (16)

Country Link
US (1) US6750242B1 (enExample)
EP (1) EP1230216A1 (enExample)
JP (1) JP2003513071A (enExample)
KR (1) KR20020063176A (enExample)
CN (1) CN1239482C (enExample)
AU (1) AU783507B2 (enExample)
BR (1) BR0015195A (enExample)
CA (1) CA2387745A1 (enExample)
CO (1) CO5251458A1 (enExample)
IL (1) IL149098A0 (enExample)
MX (1) MXPA02004232A (enExample)
NO (1) NO323076B1 (enExample)
NZ (2) NZ518450A (enExample)
SE (1) SE9903997D0 (enExample)
WO (1) WO2001032619A1 (enExample)
ZA (1) ZA200203171B (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE9903998D0 (sv) * 1999-11-03 1999-11-03 Astra Ab New compounds
DE10164139A1 (de) 2001-12-27 2003-07-10 Bayer Ag 2-Heteroarylcarbonsäureamide
DE10234424A1 (de) * 2002-07-29 2004-02-12 Bayer Ag Benzothiophen-, Benzofuran- und Indolharnstoffe
JP2006501246A (ja) 2002-08-30 2006-01-12 メモリー・ファーマシューティカルズ・コーポレイション 神経変性疾患の治療において有用なアナバセイン誘導体
AU2003276919B2 (en) 2002-09-25 2013-05-16 Memory Pharmaceuticals Corporation Indazoles, benzothiazoles, and benzoisothiazoles, and preparation and uses thereof
US20050234095A1 (en) 2004-03-25 2005-10-20 Wenge Xie Indazoles, benzothiazoles, benzoisothiazoles, benzisoxazoles, and preparation and uses thereof
CN101247853B (zh) * 2005-04-13 2014-11-12 轴突公司 具有nos抑制活性的取代的吲哚化合物
US20070134169A1 (en) * 2005-12-11 2007-06-14 Rabinoff Michael D Methods for smoking cessation or alcohol cessation or other addiction cessation
US7989447B2 (en) 2006-04-13 2011-08-02 Neuraxon, Inc. 1,5 and 3,6-substituted indole compounds having NOS inhibitory activity
AU2008321353A1 (en) * 2007-11-16 2009-05-22 The Arizona Board Of Regents On Behalf Of The University Of Arizona Methods for treating visceral pain
MX2010005343A (es) * 2007-11-16 2010-08-09 Neuraxon Inc Compuestos indola 3, 5-sustituidos que tienen actividad inhibidora de la re-absorcion y el reciclo de nos y norepinefrina.
JP2011503120A (ja) * 2007-11-16 2011-01-27 ニューラクソン,インコーポレーテッド 内臓痛を治療するためのインドール化合物および方法
US8383657B2 (en) 2007-12-21 2013-02-26 Abbott Laboratories Thiazolylidine urea and amide derivatives and methods of use thereof
AU2009212259A1 (en) * 2008-02-07 2009-08-13 Abbott Laboratories Amide derivatives as positive allosteric modulators and methods of use thereof
UY31769A1 (es) 2008-04-17 2009-09-30 Derivados del indol con actividad modulatoria del receptor nicotínico de acetilcolina
JP5642154B2 (ja) * 2009-04-16 2014-12-17 プロキシマジェン エルティーディーProximagen Ltd. α7nAChRのインドール誘導体モジュレータ
JP5749797B2 (ja) * 2010-05-17 2015-07-15 フォルム ファーマシューティカルズ、インコーポレイテッド (r)−7−クロロ−n−(キヌクリジン−3−イル)ベンゾ[b]チオフェン−2−カルボキサミド塩酸塩一水和物の結晶形
TW201245185A (en) 2011-04-01 2012-11-16 Lundbeck & Co As H New positive allosteric modulators of nicotinic acetylcholine receptor
AR086791A1 (es) 2011-07-01 2014-01-22 Lundbeck & Co As H Moduladores alostericos positivos del receptor de acetilcolina nicotinico
CA2872005A1 (en) 2012-05-08 2013-11-14 Forum Pharmaceuticals, Inc. Methods of maintaining, treating or improving cognitive function
WO2020045982A1 (ko) * 2018-08-29 2020-03-05 숙명여자대학교산학협력단 치환된 인돌 유도체, 이의 제조방법 및 이를 유효성분으로 포함하는 PPARα, PPARγ 및 PPARδ 관련 질환의 예방 또는 치료용 약학적 조성물

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2787551A (en) * 1954-02-24 1957-04-02 Eastman Kodak Co Compositions stabilized with hydroxyindole
BE758766A (fr) * 1969-11-17 1971-05-10 Ici Ltd Nouveaux derives de la morpholine et de la
US4704390A (en) * 1986-02-13 1987-11-03 Warner-Lambert Company Phenyl and heterocyclic tetrahydropyridyl alkoxy-benzheterocyclic compounds as antipsychotic agents
KR930702334A (ko) * 1990-09-13 1993-09-08 데이비드 로버트 5 하이드록시트립타민 수용체 길항제로서의 인돌우레아
RU2126399C1 (ru) * 1991-11-25 1999-02-20 Пфайзер Инк. Производные индола, замещенные индолы и способ ингибирования 5ht1 рецептора серотонина
WO1993018026A1 (en) * 1992-03-04 1993-09-16 Beecham Group Plc Indole ureas as 5-ht1c receptor antogonists
US5504101A (en) * 1994-05-06 1996-04-02 Allelix Biopharmaceuticals, Inc. 5-HT-1D receptor ligands
FR2722686B1 (fr) * 1994-07-22 1996-08-30 Oreal Set, procede, dispositif et composition de teinture des fibres keratiniques
US5576321A (en) * 1995-01-17 1996-11-19 Eli Lilly And Company Compounds having effects on serotonin-related systems

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