CA2322136A1 - Inhibiteurs du transport de la glycine - Google Patents

Inhibiteurs du transport de la glycine Download PDF

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Publication number
CA2322136A1
CA2322136A1 CA002322136A CA2322136A CA2322136A1 CA 2322136 A1 CA2322136 A1 CA 2322136A1 CA 002322136 A CA002322136 A CA 002322136A CA 2322136 A CA2322136 A CA 2322136A CA 2322136 A1 CA2322136 A1 CA 2322136A1
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Prior art keywords
formula
4alkyl
radical
hydrogen
aryl
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Abandoned
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CA002322136A
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Inventor
Ludo Edmond Josephine Kennis
Frans Eduard Janssens
Walter Herman Maria Louis Luyten
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Janssen Pharmaceutica NV
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Individual
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    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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 two hetero rings
    • C07D401/04Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
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    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/451Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
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    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • C07D211/30Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
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    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
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    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

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  • Nitrogen Condensed Heterocyclic Rings (AREA)
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Abstract

La présente invention concerne l'utilisation des .alpha.,.alpha.-diphényl-1-pipéridinebutanamides, inhibiteurs du transport de la glycine, pour la préparation de médicaments destinés aux traitements des troubles du système nerveux périphérique et du système nerveux central, en particulier, des psychoses, de la douleur, de l'épilepsie, des maladies neurodégénératives (maladie d'Alzheimer), de l'ictus, du trauma crânien, de la sclérose multiple et des troubles de même genre. La présente invention concerne aussi de nouveaux composés, leur préparation et leurs formes galéniques.
CA002322136A 1998-03-06 1999-02-26 Inhibiteurs du transport de la glycine Abandoned CA2322136A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP98200700 1998-03-06
EP98200700.7 1998-03-06
PCT/EP1999/001308 WO1999045011A1 (fr) 1998-03-06 1999-02-26 Inhibiteurs du transport de la glycine

Publications (1)

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CA2322136A1 true CA2322136A1 (fr) 1999-09-10

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CA002322136A Abandoned CA2322136A1 (fr) 1998-03-06 1999-02-26 Inhibiteurs du transport de la glycine

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EP (1) EP1058684A1 (fr)
JP (1) JP2002505332A (fr)
KR (1) KR20010032967A (fr)
CN (1) CN1291984A (fr)
AU (1) AU3254499A (fr)
BG (1) BG104686A (fr)
BR (1) BR9907953A (fr)
CA (1) CA2322136A1 (fr)
EE (1) EE200000483A (fr)
HR (1) HRP20000524A2 (fr)
HU (1) HUP0101281A3 (fr)
IL (1) IL138227A0 (fr)
NO (1) NO20004432L (fr)
PL (1) PL342818A1 (fr)
SK (1) SK13092000A3 (fr)
TR (1) TR200002570T2 (fr)
WO (1) WO1999045011A1 (fr)

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AU2001288896A1 (en) 2000-09-08 2002-03-22 Gliatech, Inc. Substituted hydrazine derivatives
US20020082283A1 (en) 2000-09-14 2002-06-27 Gliatech, Inc. Nitrogen-containing compounds and their use as glycine transport inhibitors
US20040034104A1 (en) * 2000-10-12 2004-02-19 Susumu Sato 2,2-Diphenylbutanamide derivatives and medicines containing the same
AR032653A1 (es) 2001-02-09 2003-11-19 Telik Inc Inhibidores heterociclicos del trasportador de glicina 2 composiciones farmaceuticas, uso y metodos.
JPWO2003082819A1 (ja) * 2002-04-01 2005-08-04 日本ケミファ株式会社 N−フェニル−n−(4−ピペリジニル)アミド誘導体
FR2838739B1 (fr) * 2002-04-19 2004-05-28 Sanofi Synthelabo Derives de n-[phenyl(piperidin-2-yl)methyl)benzamide, leur preparation et leur application en therapeutique
US6995168B2 (en) * 2002-05-31 2006-02-07 Euro-Celtique S.A. Triazaspiro compounds useful for treating or preventing pain
FR2842805A1 (fr) * 2002-07-29 2004-01-30 Sanofi Synthelabo Derives de n-[phenyl(piperidin-2-yl)methyl]benzamide,leur preparation et leur application et therapeutique
FR2842804B1 (fr) * 2002-07-29 2004-09-03 Sanofi Synthelabo Derives de n-[phenyl(piperidin-2-yl)methyl]benzamide, leur preparation et leur application en therapeutique
US7202259B2 (en) 2002-11-18 2007-04-10 Euro-Celtique S.A. Therapeutic agents useful for treating pain
EP1594840B1 (fr) * 2003-02-17 2006-09-27 F. Hoffmann-La Roche Ag Dérivés de piperidine-benzenesulfonamide
KR100774622B1 (ko) * 2003-08-11 2007-11-08 에프. 호프만-라 로슈 아게 Or-치환된 페닐 그룹을 갖는 피페라진 및 glyt1억제제로서 그의 용도
FR2861076B1 (fr) * 2003-10-17 2006-01-06 Sanofi Synthelabo Derives de n-heterocyclymethylbenzamide, leur preparation et leur application en therapeutique
FR2861070B1 (fr) * 2003-10-17 2006-01-06 Sanofi Synthelabo Derives de n-[phenyl(pyrrolidin-2-yl)methyl]benzamide et n-[(azepan-2-yl)phenylmethyl]benzamide, leur preparation et leur application en therapeutique
FR2861071B1 (fr) 2003-10-17 2006-01-06 Sanofi Synthelabo Derives de n-[phenyl(alkylpiperidin-2-yl) methyl]benzamide, leur prepartation et leur application en therapeutique
WO2005058317A1 (fr) * 2003-12-18 2005-06-30 Glaxo Group Limited Inhibiteurs du transporteur-1 de la glycine
CA2720312A1 (fr) * 2004-01-30 2005-08-18 Euro-Celtique S.A. Procedes d'elaboration de composes de 4-tetrazolyl-4-phenylpiperidine
GB0408774D0 (en) * 2004-04-20 2004-05-26 Glaxo Group Ltd Compounds
ATE430142T1 (de) 2004-12-09 2009-05-15 Hoffmann La Roche Phenylpiperazin-methanon-derivate
DE602005019465D1 (de) 2004-12-15 2010-04-01 Hoffmann La Roche Bi- und trizyklische substituierte phenyl-methanone als inhibitoren von glycin-i (glyt-1)-transportern zur behandlung der alzheimer-krankheit
US7485637B2 (en) 2005-01-04 2009-02-03 Hoffmann-La Roche Inc. Benzoyl-tetrahydropiperidine derivatives
RU2396270C2 (ru) 2005-01-07 2010-08-10 Ф.Хоффманн-Ля Рош Аг Производные [4-(гетероарил)пиперазин-1-ил]-(2,5-замещенный фенил)метанона в качестве ингибиторов переносчика глицина-1 (glyt-1) для лечения неврологических и психоневрологических заболеваний
MX2007008616A (es) 2005-01-18 2007-09-11 Hoffmann La Roche Derivados de fenil metanona 2,5-disubstituidos como inhibidores del transportador de glicina 1 para tratamiento de trastornos neurologicos y neuropsiquiatricos.
ES2332529T3 (es) 2005-01-26 2010-02-08 F. Hoffmann-La Roche Ag Derivados de fenil-metanona y su empleo como inhibidores del transportador 1 de glicina.
EP1848694B1 (fr) 2005-02-07 2009-11-25 F. Hoffmann-Roche AG Phenylmethanones heterocycliques substituees servant d'inhibiteurs du transporteur 1 de la glycine
CA2603939C (fr) 2005-04-08 2013-08-27 Pfizer Products Inc. Heteroarylamides bicycliques [3.1.0 ] comme inhibiteurs de transport de la glycine
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CA2745690A1 (fr) * 2008-12-04 2010-06-10 Evgeny Zlotinikov Nouvelles formes polymorphes d'un derive d'azabicyclo-trifluoromethyl benzamide
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AU3254499A (en) 1999-09-20
EP1058684A1 (fr) 2000-12-13
SK13092000A3 (sk) 2001-03-12
HUP0101281A2 (hu) 2001-09-28
BR9907953A (pt) 2000-10-24
TR200002570T2 (tr) 2000-12-21
BG104686A (en) 2001-04-30
CN1291984A (zh) 2001-04-18
WO1999045011A8 (fr) 1999-10-14
IL138227A0 (en) 2001-10-31
JP2002505332A (ja) 2002-02-19
HUP0101281A3 (en) 2001-11-28
HRP20000524A2 (en) 2001-02-28
NO20004432L (no) 2000-11-02
WO1999045011A1 (fr) 1999-09-10
NO20004432D0 (no) 2000-09-05
EE200000483A (et) 2002-02-15
PL342818A1 (en) 2001-07-02
KR20010032967A (ko) 2001-04-25

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