MA26732A1 - Composition pharmaceutique nouvelle comprenant un inhibiteur de nos, et procede pour sa preparation - Google Patents

Composition pharmaceutique nouvelle comprenant un inhibiteur de nos, et procede pour sa preparation

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Publication number
MA26732A1
MA26732A1 MA25976A MA25976A MA26732A1 MA 26732 A1 MA26732 A1 MA 26732A1 MA 25976 A MA25976 A MA 25976A MA 25976 A MA25976 A MA 25976A MA 26732 A1 MA26732 A1 MA 26732A1
Authority
MA
Morocco
Prior art keywords
preparation
inhibitor
pharmaceutical composition
novel pharmaceutical
treatment
Prior art date
Application number
MA25976A
Other languages
English (en)
Inventor
David Saltarelli Mario
Adams Lowe John Iii
Original Assignee
Pfizer Prod Inc
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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of MA26732A1 publication Critical patent/MA26732A1/fr

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    • 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
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    • A61K31/13Amines
    • A61K31/135Amines having aromatic rings, e.g. ketamine, nortriptyline
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    • A61K31/138Aryloxyalkylamines, e.g. propranolol, tamoxifen, phenoxybenzamine
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    • A61K31/15Oximes (>C=N—O—); Hydrazines (>N—N<); Hydrazones (>N—N=) ; Imines (C—N=C)
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    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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  • Hydrogenated Pyridines (AREA)

Abstract

L'INVENTION CONCERNE DES COMPOSITIONS PHARMACEUTIQUES COMPRENANT UN COMPOSÉ INHIBITEUR DE NOS, SEUL OU EN ASSOCIATION AVEC UN ANTAGONISTE DES RÉCEPTEURS DE NK-1 OU UN SSRI. ELLE CONCERNE ÉGALEMENT UN PROCÉDÉ POUR LEUR PRÉPARATION. - APPLICATION : UTILISATION DE CES COMPOSITIONS POUR LE TRAITEMENT DE DIVERS TROUBLES DONT LE TRAITEMENT PEUT eTRE EFFECTUÉ OU FACILITÉ PAR LA MODOFICATION DES RYTHMES CIRCADIENS.
MA25976A 1999-05-21 2000-05-17 Composition pharmaceutique nouvelle comprenant un inhibiteur de nos, et procede pour sa preparation MA26732A1 (fr)

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DE10001785A1 (de) * 2000-01-18 2001-07-19 Boehringer Ingelheim Pharma NK¶1¶-Rezeptor-Antagonisten zur Behandlung des Restless Legs Syndroms
GB0019006D0 (en) * 2000-08-04 2000-09-20 Astrazeneca Ab Novel compounds
US20030045449A1 (en) * 2001-08-15 2003-03-06 Pfizer, Inc. Pharmaceutical combinations for the treatment of neurodegenerative diseases
US6803470B2 (en) * 2001-10-10 2004-10-12 Pfizer Inc 2-amino-6-(2,4,5-substituted-phenyl)-pyridines
DOP2002000467A (es) * 2001-10-10 2003-04-15 Pfizer Prod Inc 2-amino-6 (fenilo sustituido en las posiciones 2,4,5)-piridinas
BRPI0411608A (pt) * 2003-06-24 2006-08-08 Neurosearch As derivado de 8-aza-biciclo [3.2.1] octano, composição farmacêutica, uso do composto, e, método de tratamento, prevenção ou alìvio de uma doença, um distúrbio ou uma condição de um organismo animal vivo
EP1634598A1 (fr) * 2004-09-07 2006-03-15 Laboratorios Del Dr. Esteve, S.A. Utilisation de dérivés de piperazine et ses analogues pour prevenir et traiter des désordres liés à l'ingestion de nourriture
ES2483898T3 (es) 2007-06-08 2014-08-08 Janssen Pharmaceutica, N.V. Derivados de piperidina/piperazina
MX2009013335A (es) 2007-06-08 2010-01-20 Janssen Pharmaceutica Nv Derivados de piperidina/piperazina.
JO2972B1 (en) 2007-06-08 2016-03-15 جانسين فارماسوتيكا ان. في Piperidine / piperazine derivatives
JP5443342B2 (ja) 2007-06-08 2014-03-19 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ ピペリジン/ピペラジン誘導体
UY31863A (es) 2008-06-05 2010-01-05 Janssen Pharmaceutica Nv Combinaciones de drogas que comprenden un inhibidor de dgat y un agonista de ppar
US8889674B2 (en) 2009-03-05 2014-11-18 Shionogi & Co., Ltd. Piperidine and pyrrolidine derivatives having NPY Y5 receptor antagonism
US10154988B2 (en) 2012-11-14 2018-12-18 The Johns Hopkins University Methods and compositions for treating schizophrenia
EP3983392A4 (fr) * 2019-06-14 2023-12-06 SRX Cardio, LLC Composés pour la modulation de la proprotéine convertase subtilisine/kexine de type 9 (pcsk9)

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TNSN00106A1 (fr) 2005-11-10
DZ3041A1 (fr) 2004-03-27
AR022640A1 (es) 2002-09-04
NO20015651L (no) 2002-01-18
HN2000000045A (es) 2001-03-02
WO2000071107A2 (fr) 2000-11-30
PE20010157A1 (es) 2001-02-16
MXPA01011978A (es) 2002-05-06
EA200101110A1 (ru) 2002-08-29
TR200103351T2 (tr) 2002-06-21
PL358538A1 (en) 2004-08-09
HRP20010862A2 (en) 2003-06-30
GT200000071A (es) 2001-11-08
NO20015651D0 (no) 2001-11-20
PA8494601A1 (es) 2002-08-29
IS6126A (is) 2001-10-26
HUP0301287A2 (hu) 2003-08-28
SK16602001A3 (sk) 2003-03-04
ZA200109555B (en) 2004-04-07
OA11943A (en) 2006-04-12
CO5160295A1 (es) 2002-05-30
JP2003523941A (ja) 2003-08-12
UY26148A1 (es) 2000-12-29
BR0010820A (pt) 2002-03-05
WO2000071107A8 (fr) 2002-01-24
HUP0301287A3 (en) 2005-03-29
EE200100611A (et) 2003-02-17
CA2374668A1 (fr) 2000-11-30
IL145955A0 (en) 2002-07-25
CN1617743A (zh) 2005-05-18
BG106208A (en) 2002-09-30
AU2935300A (en) 2000-12-12
EP1178784A1 (fr) 2002-02-13
KR20020010916A (ko) 2002-02-06
AP2001002326A0 (en) 2001-12-31

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