LU90130I2 - Tiagabine anhydre - Google Patents

Tiagabine anhydre

Info

Publication number
LU90130I2
LU90130I2 LU90130C LU90130C LU90130I2 LU 90130 I2 LU90130 I2 LU 90130I2 LU 90130 C LU90130 C LU 90130C LU 90130 C LU90130 C LU 90130C LU 90130 I2 LU90130 I2 LU 90130I2
Authority
LU
Luxembourg
Prior art keywords
tiagabine
anhydrous
carboxytetrahydropyrid
carboxymethylpyrrolidin
carboxypiperidin
Prior art date
Application number
LU90130C
Other languages
English (en)
Original Assignee
Novo Nordisk As
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Novo Nordisk As filed Critical Novo Nordisk As
Publication of LU90130I2 publication Critical patent/LU90130I2/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
LU90130C 1985-06-26 1997-08-29 Tiagabine anhydre LU90130I2 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DK288385A DK288385D0 (da) 1985-06-26 1985-06-26 Aminosyrederivater

Publications (1)

Publication Number Publication Date
LU90130I2 true LU90130I2 (fr) 1997-10-24

Family

ID=8116767

Family Applications (1)

Application Number Title Priority Date Filing Date
LU90130C LU90130I2 (fr) 1985-06-26 1997-08-29 Tiagabine anhydre

Country Status (16)

Country Link
US (1) US5010090A (fr)
EP (1) EP0236342B1 (fr)
JP (1) JPH07103116B2 (fr)
AT (1) ATE67196T1 (fr)
AU (1) AU599326B2 (fr)
CA (1) CA1284503C (fr)
DK (2) DK288385D0 (fr)
ES (1) ES8800927A1 (fr)
FI (1) FI89355C (fr)
GR (1) GR861650B (fr)
IE (1) IE59084B1 (fr)
LU (1) LU90130I2 (fr)
NZ (1) NZ216657A (fr)
PT (1) PT82841B (fr)
WO (1) WO1987000171A1 (fr)
ZA (1) ZA864608B (fr)

Families Citing this family (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DK704488D0 (da) * 1988-12-19 1988-12-19 Novo Industri As Nye n-substituerede azaheterocykliske carboxylsyrer
DK288385D0 (da) * 1985-06-26 1985-06-26 Novo Industri As Aminosyrederivater
DK588189D0 (da) * 1989-11-22 1989-11-22 Novo Nordisk As Nye heterocykliske carboxylsyrer
DK58291D0 (da) * 1991-04-02 1991-04-02 Novo Nordisk As Krystalinsk stof og dets fremstilling
SI0812318T1 (sl) * 1995-02-28 2006-06-30 Lundbeck & Co As H Spojine 4-aminotetrahidrobenzisoksazola ali -izotiazola
US5962449A (en) 1995-04-07 1999-10-05 Novo Nordisk A/S Tricyclic compounds in treating hyperalgesic conditions and NIDDM
MX9708394A (es) * 1995-05-05 1998-02-28 Novo Nordisk As Composicion farmaceutica que contiene clorhidrato de tiagabina y el proceso para su preparacion.
US6191165B1 (en) 1996-05-31 2001-02-20 Allelix Neuroscience Inc. Pharmaceutical for treatment of neurological and neuropsychiatric disorders
UA52661C2 (uk) * 1996-06-14 2003-01-15 Ново Нордіск А/С Безводна кристалічна форма гідрохлориду r(-)-n-(4,4-ди(3-метилтієн-2-іл)бут-3-еніл) ніпекотинової кислоти
US5958951A (en) * 1996-06-14 1999-09-28 Novo Nordiskials Modified form of the R(-)-N-(4,4-di(3-methylthien-2-yl)but-3-enyl)-nipecotic acid hydrochloride
US5914333A (en) * 1996-07-31 1999-06-22 Novo Nordisk A/S Treatment of psychotic disorders
IE970588A1 (en) 1997-08-01 2000-08-23 Elan Corp Plc Controlled release pharmaceutical compositions containing tiagabine
JP2001511450A (ja) * 1997-08-01 2001-08-14 エラン コーポレーシヨン ピーエルシー チアガビンを含有する制御放出性の医薬組成物
US6288083B1 (en) * 1998-09-04 2001-09-11 Millennium Pharmaceuticals, Inc. Chemokine receptor antagonists and methods of use therefor
US6503926B2 (en) * 1998-09-04 2003-01-07 Millennium Pharmaceuticals, Inc. Chemokine receptor antagonists and methods of use therefor
DE19840611A1 (de) * 1998-09-05 2000-03-09 Klaus Wanner GABA-uptake-Inhibitoren mit Pyrrolidinstruktur
EP1142584A4 (fr) * 1999-01-12 2003-04-16 Takeda Chemical Industries Ltd Compositions pour le traitement de la miction frequente et de l'incontinence d'urine
US6872734B2 (en) 2000-10-20 2005-03-29 Abbott Laboratories Use of tiagabine for treatment of diabetic neuropathy and migraine
EA200300432A1 (ru) 2000-11-30 2003-10-30 Пфайзер Продактс Инк. Комбинация гамк-агонистов и ингибиторов сорбитолдегидрогеназы
MXPA03004871A (es) * 2000-11-30 2003-08-19 Pfizer Prod Inc Combinacion de agonistas de gaba e inhibidores de aldosa-reductasa.
NZ527695A (en) 2001-02-16 2005-05-27 Allelix Neuroscience Inc GlyT-1 inhibitors
EP2316468A1 (fr) 2002-02-22 2011-05-04 Shire LLC Système de distribution et méthodes de protection et d'administration de dextroamphetamine
CN1382441A (zh) * 2002-05-21 2002-12-04 中国科学院上海生命科学研究院 γ－氨基丁酸转运蛋白抑制剂在制备镇痛药物中的应用
WO2004100992A2 (fr) * 2003-05-16 2004-11-25 Pfizer Products Inc. Combinaisons therapeutiques d'antipsychotiques atypiques avec des modulateurs de l'acide 4-aminobutanoique et/ou des medicaments anticonvulsivants
PT1691811E (pt) 2003-12-11 2014-10-30 Sunovion Pharmaceuticals Inc Combinação de um sedativo e de um modulador de neurotransmissores e métodos para melhorar a qualidade do sono e tratamento da depressão
WO2005122698A2 (fr) * 2003-12-24 2005-12-29 Sun Pharmaceutical Industries Limited Nouvelles formes polymorphes stables d'un anticonvulsif
CN1314684C (zh) * 2003-12-24 2007-05-09 中国科学院上海有机化学研究所 噻加宾及其消旋体和s－构型的合成方法及其无定形粉末的制法
EP1737466A1 (fr) * 2004-01-29 2007-01-03 Pfizer Products Inc. COMBINAISON DE MODULATEURS D'ACIDE GAMMA-AMINOBUTYRIQUE ET D'ANTAGONISTES DU RECEPTEUR 5-HT-1b
WO2005092886A1 (fr) * 2004-03-29 2005-10-06 Ranbaxy Laboratories Limited Procede de preparation d'une forme amorphe de la tiagabine
WO2006013550A2 (fr) * 2004-08-04 2006-02-09 Ranbaxy Laboratories Limited Procede d'elaboration d'acide carboxylique de piperidine
EP2258357A3 (fr) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenèse avec inhibiteur de l'acetylcholinestérase
EP2275095A3 (fr) 2005-08-26 2011-08-17 Braincells, Inc. Neurogenese par modulation des recepteurs muscariniques
EP2377530A3 (fr) 2005-10-21 2012-06-20 Braincells, Inc. Modulation de neurogénèse par inhibition PDE
EP2314289A1 (fr) 2005-10-31 2011-04-27 Braincells, Inc. Modulation de la neurogenese dont la médiation est assurée par récepteur gaba
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
CA2651862A1 (fr) 2006-05-09 2007-11-22 Braincells, Inc. Neurogenese induite par le recepteur 5ht
WO2007134136A2 (fr) 2006-05-09 2007-11-22 Braincells, Inc. Neurogenèse par modulation de l'angiotensine
US20080051435A1 (en) * 2006-08-18 2008-02-28 Cephalon, Inc. Crystalline and amorphous forms of tiagabine
US20080064727A1 (en) * 2006-08-18 2008-03-13 Cephalon, Inc. Crystalline forms of tiagabine hydrochloride
JP2010502722A (ja) 2006-09-08 2010-01-28 ブレインセルス，インコーポレイティド ４−アシルアミノピリジン誘導体を含む組み合わせ
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
US20090082401A1 (en) * 2007-09-25 2009-03-26 Protia, Llc Deuterium-enriched tiagabine
WO2010099217A1 (fr) 2009-02-25 2010-09-02 Braincells, Inc. Modulation de neurogenèse à l'aide de combinaisons de d-cyclosérine
CN101857591B (zh) * 2009-04-09 2013-06-05 北京京卫燕康药物研究所有限公司 盐酸噻加宾晶型及其制备方法
CN102070624B (zh) * 2011-01-25 2013-04-10 赵学清 一种盐酸噻加宾的合成方法及无水盐酸噻加宾的制备方法
CN102827152B (zh) * 2012-09-17 2014-11-05 扬子江药业集团四川海蓉药业有限公司 噻加宾的制备方法及其前体化合物

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4383999A (en) * 1981-05-26 1983-05-17 Smithkline Beckman Corporation Inhibition of GABA uptake by N-substituted azaheterocyclic carboxylic acids and their esters
US4514414A (en) * 1982-10-25 1985-04-30 Smithkline Beckman Corporation N-Substituted pyrrolidineacetic acids and their esters
DK288385D0 (da) * 1985-06-26 1985-06-26 Novo Industri As Aminosyrederivater
DE3787657T2 (de) * 1986-01-07 1994-02-03 Novo Ind A S Bagsvaerd Aminosäure-Derivate.

Also Published As

Publication number Publication date
EP0236342A1 (fr) 1987-09-16
AU599326B2 (en) 1990-07-19
JPS62503172A (ja) 1987-12-17
ES8800927A1 (es) 1987-12-01
FI870810A0 (fi) 1987-02-25
ES556659A0 (es) 1987-12-01
ATE67196T1 (de) 1991-09-15
DK156398C (da) 1990-01-08
PT82841B (pt) 1989-01-17
CA1284503C (fr) 1991-05-28
IE861702L (en) 1986-12-26
EP0236342B1 (fr) 1991-09-11
IE59084B1 (en) 1994-01-12
ZA864608B (en) 1987-02-25
JPH07103116B2 (ja) 1995-11-08
DK156398B (da) 1989-08-14
DK100887A (da) 1987-02-26
FI870810A (fi) 1987-02-25
AU6133686A (en) 1987-01-30
FI89355C (fi) 1993-09-27
GR861650B (en) 1986-10-30
WO1987000171A1 (fr) 1987-01-15
US5010090A (en) 1991-04-23
FI89355B (fi) 1993-06-15
PT82841A (en) 1986-07-01
DK288385D0 (da) 1985-06-26
DK100887D0 (da) 1987-02-26
NZ216657A (en) 1989-10-27

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