MA27885A1 - Derives de n-pyrrolidine-3-ylamide servant d'inhibiteurs de reabsorption de serotonine et de noradrenaline - Google Patents

Derives de n-pyrrolidine-3-ylamide servant d'inhibiteurs de reabsorption de serotonine et de noradrenaline

Info

Publication number
MA27885A1
MA27885A1 MA28674A MA28674A MA27885A1 MA 27885 A1 MA27885 A1 MA 27885A1 MA 28674 A MA28674 A MA 28674A MA 28674 A MA28674 A MA 28674A MA 27885 A1 MA27885 A1 MA 27885A1
Authority
MA
Morocco
Prior art keywords
alkyl
aryl
het
alkoxy
serotonin
Prior art date
Application number
MA28674A
Other languages
English (en)
Inventor
Paul Vincent Fish
Michael Jonathan Fray
Deborah Jane Lovering
Alan Stobie
Florian Wakenhut
Gavin Alistair Whitlock
Original Assignee
Pfizer
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
Priority claimed from GBGB0314048.0A external-priority patent/GB0314048D0/en
Application filed by Pfizer filed Critical Pfizer
Publication of MA27885A1 publication Critical patent/MA27885A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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
    • C07D207/10Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D207/14Nitrogen atoms not forming part of a nitro radical
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/10Drugs for genital or sexual disorders; Contraceptives for impotence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Endocrinology (AREA)
  • Addiction (AREA)
  • Reproductive Health (AREA)
  • Psychology (AREA)
  • Urology & Nephrology (AREA)
  • Obesity (AREA)
  • Hospice & Palliative Care (AREA)
  • Hematology (AREA)
  • Anesthesiology (AREA)
  • Rheumatology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Gynecology & Obstetrics (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

DEPOSANT Société dite : PFIZER INC. REVENDICATION DE PRIORITES GB 17 Juin 2003 GB 0314048.0 US 6 Août 2003 60/493,126 Dérivés de N-pyrrolidine-3-ylamide servant d'inhibiteurs de réabsorption de sérotonine et de noradrénaline Un composé de formule (I) et ses dérivés acceptables du point de vue pharmaceutique et/ou vétérinaire, formule dans laquelle R1 représente H, un groupe alkyle en C1 à C6, -C(X)Y, cycloalkyle en C3 à C8, aryle, het, aryl (alkyle en C1 à C4) ou het (alkyle en C1 à C4) , dans lequel les groupes cycloalkyle, aryle ou het sont facultativement substitués avec au moins un substituant choisi indépendamment entre des substituants alkyle en C1 à C8, alkoxy en C1 à C8, OH, halogéno, CF3, OCF3, SCF3, hydroxyalkyle en C1 à C6, (alkoxy en C1 à C4) (alkyle en C1 à C6) et (alkyle en C1 à C4) S (alkyle en C1 à C4) , R2 représente un groupe aryle ou hétéroaryle, chacun facultativement substitué avec au moins un substituant choisi indépendamment entre des substituants alkyle en C1 à C8, alkoxy en C1 à C8, OH, halogéno, CF3, OCF3, SCF3, hydroxyalkyle en C1 à C6, (alkoxy en C1 à C4) (alkyle en C1 à C6) et (alkyle en C1 à C4) S (alkyle en C1 à C4) ; R3 représente un groupe alkyle en C1 à C6, cycloalkyle en C3 à C8, (cycloalkyle en C3 à C8) (alkyle en C1 à C6) , aryle, het, aryl (alkyle en C8 à C4) ou het (alkyle en C1 à C4) , dans lequel les groupes cycloalkyle, aryle ou het sont facultativement substitués avec au moins un substituant choisi indépendamment entre des substituants alkyle en C1 à C6, alkoxy en C1 à C6, OH, halogéno, CF3, OCF3, SCF3, hydroxyalkyle en C1 à C6, (alkoxy en C1 à C6) (alkyle en C1 à C6) et (alkyle en C1 à C4) S (alkyle en C1 à C4) ; X représente S ou O ; Y représente H, un groupe alkyle en C1 à C6, aryle, het, aryl (alkyle en C1 à C4) ou het (alkyle en C1 à C4) ; et n est égal à 1 ou 2 ; sous réserve que, lorsque n est égal à 1, m est égal à 0 ou 1 et, lorsque n est égal à 2, m est égal à 0, oé, si m est égal à 0, alors * représente un centre chiral. Les composés de la présente invention ont une activité comme inhibiteurs de réabsorption de sérotonine et de noradrénaline et, en conséquence, sont utiles dans divers domaines thérapeutiques, par exemple l'incontinence urinaire.
MA28674A 2003-06-17 2005-12-16 Derives de n-pyrrolidine-3-ylamide servant d'inhibiteurs de reabsorption de serotonine et de noradrenaline MA27885A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB0314048.0A GB0314048D0 (en) 2003-06-17 2003-06-17 Novel compounds
US49312603P 2003-08-06 2003-08-06

Publications (1)

Publication Number Publication Date
MA27885A1 true MA27885A1 (fr) 2006-05-02

Family

ID=33554153

Family Applications (1)

Application Number Title Priority Date Filing Date
MA28674A MA27885A1 (fr) 2003-06-17 2005-12-16 Derives de n-pyrrolidine-3-ylamide servant d'inhibiteurs de reabsorption de serotonine et de noradrenaline

Country Status (31)

Country Link
US (2) US7378436B2 (fr)
EP (1) EP1638933B1 (fr)
JP (1) JP4137159B2 (fr)
KR (1) KR100803796B1 (fr)
AP (1) AP2005003467A0 (fr)
AR (1) AR044715A1 (fr)
AT (1) ATE398107T1 (fr)
AU (1) AU2004247487B2 (fr)
BR (1) BRPI0411594A (fr)
CA (1) CA2530159C (fr)
CY (1) CY1110434T1 (fr)
DE (1) DE602004014372D1 (fr)
DK (1) DK1638933T3 (fr)
EA (1) EA009881B1 (fr)
EC (1) ECSP056232A (fr)
ES (1) ES2305776T3 (fr)
HR (2) HRP20050993A2 (fr)
IL (1) IL172063A0 (fr)
IS (1) IS8136A (fr)
MA (1) MA27885A1 (fr)
MX (1) MXPA05013960A (fr)
NL (1) NL1026438C2 (fr)
NZ (1) NZ544046A (fr)
PA (1) PA8605301A1 (fr)
PE (1) PE20050631A1 (fr)
PL (1) PL1638933T3 (fr)
PT (1) PT1638933E (fr)
SI (1) SI1638933T1 (fr)
TW (1) TW200505852A (fr)
UY (1) UY28360A1 (fr)
WO (1) WO2004110995A1 (fr)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ524396A (en) * 2000-07-31 2003-09-26 Nycomed Danmark As Fentanyl composition for nasal administration comprising water as a solvent
DK1638933T3 (da) * 2003-06-17 2008-07-28 Pfizer N-pyrrolidin-3-yl-amid-derivater som serotonin- og noradrenalin-genoptagelses inhibitorer
ATE452130T1 (de) 2004-10-18 2010-01-15 Lilly Co Eli 1-(hetero)aryl-3-aminopyrrolidinderivate zur verwendung als antagonisten des mglur3-rezeptors
GB0425766D0 (en) * 2004-11-23 2004-12-22 Pfizer Ltd Novel compounds
US7122683B2 (en) 2004-11-23 2006-10-17 Pfizer Inc. Amides useful as monoamine re-uptake inhibitors
WO2006064332A1 (fr) * 2004-12-14 2006-06-22 Pfizer Limited Derives de n-pyrrolidin-3yl-amide en tant qu'inhibiteurs de recaptage de la serotonine et de la noradrenaline
WO2006064336A2 (fr) * 2004-12-14 2006-06-22 Pfizer Limited Nouveaux composes
TWI439452B (zh) 2005-05-13 2014-06-01 Otsuka Pharma Co Ltd 吡咯烷化合物(二)
WO2006128803A1 (fr) * 2005-06-02 2006-12-07 F. Hoffmann-La Roche Ag Derives de la piperidin-4-yl-amide et leur utilisation comme antagonistes du sous type 5 du recepteur sst
WO2007135530A2 (fr) * 2006-05-22 2007-11-29 Pfizer Limited Sel adapté à un usage pharmaceutique et vétérinaire
US20080014152A1 (en) * 2006-07-13 2008-01-17 Di Mauro Thomas M Intranasal delivery of clenbuterol across the cribriform plate and into the brain
JP5219465B2 (ja) * 2006-11-10 2013-06-26 大塚製薬株式会社 医薬
US20100056497A1 (en) * 2007-01-31 2010-03-04 Dainippon Sumitomo Pharma Co., Ltd Amide derivative
JP2010189275A (ja) * 2007-06-14 2010-09-02 Dainippon Sumitomo Pharma Co Ltd ナフタレン誘導体
US8263652B2 (en) * 2007-10-31 2012-09-11 Sk Biopharmaceuticals Co., Ltd. Stabilized pediatric suspension of carisbamate
CN101952280B (zh) * 2007-12-19 2014-04-23 大日本住友制药株式会社 双环杂环衍生物
WO2010011811A2 (fr) * 2008-07-24 2010-01-28 Theravance, Inc. Composés de 3-(phénoxyphénylméthyl)pyrrolidine
US8247433B2 (en) 2008-11-14 2012-08-21 Theravance, Inc. Process for preparing 4-[2-(2-fluorophenoxymethyl)phenyl]piperidine compounds
US20100267743A1 (en) * 2009-04-15 2010-10-21 Stangeland Eric L 3-(phenoxypyrrolidin-3-yl-methyl)heteroaryl, 3-(phenylpyrrolidin-3-ylmethoxy)heteroaryl, and 3-(heteroarylpyrrolidin-3-ylmethoxy)heteroaryl compounds
AU2010263641A1 (en) 2009-06-24 2012-01-19 Sumitomo Dainippon Pharma Co., Ltd. N-substituted-cyclic amino derivative
CN105254552A (zh) * 2009-07-13 2016-01-20 施万生物制药研发Ip有限责任公司 3-苯氧基甲基吡咯烷化合物
WO2011011231A1 (fr) 2009-07-21 2011-01-27 Theravance, Inc. Composés de la 3-phénoxyméthylpyrrolidine
US8778949B2 (en) 2010-01-11 2014-07-15 Theravance Biopharma R&D Ip, Llc 1-(2-phenoxymethylphenyl)piperazine compounds
ES2543064T3 (es) * 2010-03-22 2015-08-14 Theravance Biopharma R&D Ip, Llc Compuestos de 1-(2-fenoximetilheteroaril)piperidina y piperazina
WO2012051103A1 (fr) 2010-10-11 2012-04-19 Theravance, Inc. Inhibiteurs de la réabsorption de sérotonine
US8501964B2 (en) 2010-12-03 2013-08-06 Theravance, Inc. Serotonin reuptake inhibitors

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE138773C (fr)
US3963745A (en) * 1972-04-03 1976-06-15 A. H. Robins Company, Incorporated Method for controlling emesis with N-(1-substituted-3-pyrrolidinyl)benzamides and thiobenzamides
US4002757A (en) * 1974-12-26 1977-01-11 A. H. Robins Company, Incorporated N-(1-substituted-3-pyrrolidinyl)-4-quinolinecarboxamides
US4020072A (en) * 1976-05-04 1977-04-26 E. R. Squibb & Sons, Inc. 5-Aminomethyl-1H-pyrazolo[3,4-b]pyridines
GB1574419A (en) * 1977-11-11 1980-09-03 Anphar Sa Piperidine compounds
CH628885A5 (en) * 1978-01-01 1982-03-31 Anphar Sa Piperidine derivative
US5130312A (en) * 1987-07-17 1992-07-14 Janssen Pharmaceutica N.V. Substituted N-(3-hydroxy-4-piperidinyl)benzamides
FR2642069B1 (fr) 1989-01-20 1991-04-12 Rhone Poulenc Sante Nouveaux derives du benzopyranne, leur preparation et les compositions pharmaceutiques qui les contiennent
WO1997018813A1 (fr) 1995-11-22 1997-05-29 Merck & Co., Inc. Inhibiteurs de la farnesyl-proteine transferase
WO1999065881A1 (fr) 1998-06-19 1999-12-23 Nissan Chemical Industries, Ltd. Composes heterocycliques utilises comme agents hypoglecymiques
US6670299B1 (en) * 1999-07-03 2003-12-30 Northwestern University Cyclopentadienyl-containing low-valent early transition metal olefin polymerization catalysts
FR2802206B1 (fr) * 1999-12-14 2005-04-22 Sod Conseils Rech Applic Derives de 4-aminopiperidine et leur utilisation en tant que medicament
EP2140868A1 (fr) 2000-03-03 2010-01-06 Eisai R&D Management Co., Ltd. Usage d'un inhibitor de cholinésterase pour la traitement de la démence et de la trouble de la perception associé avec ou provoqué par chimiothérapie
IL151164A0 (en) * 2000-03-06 2003-04-10 Acadia Pharm Inc Azacyclic compounds for use in the treatment of serotonin related diseases
JP2004509891A (ja) 2000-09-22 2004-04-02 スミスクライン ビーチャム パブリック リミテッド カンパニー 抗糖尿病薬としてのピラゾロピリジンおよびピラゾロピリダジン
BR0113989A (pt) 2000-09-25 2004-01-27 Actelion Pharmaceuticals Ltd Compostos, composições farmacêuticas, processo para a preparação de uma composição farmacêutica, e, uso de pelo menos um dos compostos
DE60237528D1 (de) 2001-09-14 2010-10-14 High Point Pharmaceuticals Llc Neue aminoazetidin-, aminopyrrolidin- und aminopiperidinderivative
US20050228017A1 (en) 2001-10-31 2005-10-13 Morphochem Aktiengesellschaft Fur Kombinatorische Chemie Novel anticancer compounds
GB0128287D0 (en) 2001-11-26 2002-01-16 Smithkline Beecham Plc Novel method and compounds
RU2320646C2 (ru) * 2002-06-24 2008-03-27 Акадиа Фармасьютикалз Инк. N-замещенные производные пиперидина в качестве агентов серотонинового рецептора
WO2004009549A2 (fr) 2002-07-18 2004-01-29 Actelion Pharmaceuticals Ltd Piperidines utiles pour traiter des maladies du systeme nerveux central
AU2003263393A1 (en) 2002-09-04 2004-03-29 Glenmark Pharmaceuticals Limited New heterocyclic amide compounds useful for the treatment of inflammatory and allergic disorders: process for their preparation and pharmaceutical compositions containing them
CA2511242C (fr) 2002-12-20 2010-01-12 Anita Melikian Inhibiteurs de ccxckr2 d'expression tumorale humaine
DK1638933T3 (da) * 2003-06-17 2008-07-28 Pfizer N-pyrrolidin-3-yl-amid-derivater som serotonin- og noradrenalin-genoptagelses inhibitorer

Also Published As

Publication number Publication date
NZ544046A (en) 2009-08-28
IS8136A (is) 2005-11-21
ECSP056232A (es) 2006-04-19
SI1638933T1 (sl) 2008-10-31
IL172063A0 (en) 2009-02-11
JP2006527758A (ja) 2006-12-07
NL1026438C2 (nl) 2005-09-20
ES2305776T3 (es) 2008-11-01
US20050137229A1 (en) 2005-06-23
US7378436B2 (en) 2008-05-27
AP2005003467A0 (en) 2006-12-31
CA2530159A1 (fr) 2004-12-23
EA200501730A1 (ru) 2006-08-25
NL1026438A1 (nl) 2004-12-20
KR20060036927A (ko) 2006-05-02
PA8605301A1 (es) 2005-02-04
ATE398107T1 (de) 2008-07-15
EA009881B1 (ru) 2008-04-28
WO2004110995A8 (fr) 2005-04-21
HRP20050993A2 (en) 2006-03-31
KR100803796B1 (ko) 2008-02-14
DK1638933T3 (da) 2008-07-28
JP4137159B2 (ja) 2008-08-20
EP1638933B1 (fr) 2008-06-11
AR044715A1 (es) 2005-09-21
UY28360A1 (es) 2005-01-31
EP1638933A1 (fr) 2006-03-29
PT1638933E (pt) 2008-07-22
PL1638933T3 (pl) 2008-10-31
PE20050631A1 (es) 2005-09-14
HRP20080339T3 (en) 2008-08-31
AU2004247487A1 (en) 2004-12-23
CA2530159C (fr) 2010-02-02
DE602004014372D1 (de) 2008-07-24
CY1110434T1 (el) 2015-04-29
TW200505852A (en) 2005-02-16
AU2004247487B2 (en) 2010-05-20
US20080306123A1 (en) 2008-12-11
MXPA05013960A (es) 2006-02-24
WO2004110995A1 (fr) 2004-12-23
BRPI0411594A (pt) 2006-08-29

Similar Documents

Publication Publication Date Title
MA27885A1 (fr) Derives de n-pyrrolidine-3-ylamide servant d'inhibiteurs de reabsorption de serotonine et de noradrenaline
RU2328486C2 (ru) Производные 2-пиридона в качестве ингибиторов нейтрофильной эластазы
MA32164B1 (fr) Derive heterocyclique fusionne et son utilisation
PE20040164A1 (es) Mimeticos de glucocorticoides, procedimientos para su preparacion y composiciones farmaceuticas
WO2003080580A3 (fr) Composes
DK0794949T3 (da) Hidtil ukendte 3,5-dioxo-(2H,4H)-1,2,4-triazinderivater, fremstilling heraf og deres anvendelse som lægemidler
WO2005092858A3 (fr) Composes alpha-aryle ou heteroaryle methyle beta piperidino propanamide en tant qu'antagoniste du recepteur orl1
MA26983A1 (fr) Derives biaryliques de nicotinamide utiles comme inhibiteurs d'iso-enzymes pde4
PL247096A1 (en) Agent for fighting against and/or preventing paralyzing effects of microorganisms and method of obtaining new derivatives of n-/2-nitrophenylo/-4-aminopyrimidines
CA2481461A1 (fr) Derives de n-[phenyl(piperidin-2-yl) methyl] benzamide, leur preparation et leur application en therapeutique
MA27573A1 (fr) Sinomenine et derives de sinomenine, synthese et utilisation.
CA2489209A1 (fr) Nouveaux derives d'arylsulfonamides et leur utilisation en therapeutique
WO2002074726A3 (fr) Inhibiteurs de phosphodiesterase 4
HUP0201953A2 (hu) Benzolszármazékok, eljárás a vegyületek előállítására és a vegyületeket tartalmazó gyógyászati készítmények
TW200616954A (en) N-(1h-indolyl)-1h-indole-2-carboxamide derivatives, their preparation and their application in therapeutics
WO2004004730A3 (fr) Composes pharmaceutiques
MA31674B1 (fr) Dérivés de 7 -alkynyl-1,8-naphthyridones, leur préparation et leur application en thérapeutique
MEP11508A (en) Piperazinylacylpiperidine derivatives, their preparation and therapeutic use thereof
CA2423007A1 (fr) Composes spiro et inhibiteurs de molecules d'adhesion contenant ces composes comme ingredient actif
MA27795A1 (fr) Derives d'amine cycliques, procedes de preparation de ceux-ci et compositions pharmaceutiques les contenant
FI971353A0 (fi) N-(orto-substituoidut bentsyylioksi)imiinijohdannaiset ja niiden käyttö fungisideina, akarisiseina tai insektisideinä
MA29559B1 (fr) Derives de 4,5-diarylpyrrole, leur preparation et leur application en therapeutique
CA2422703A1 (fr) Procede de preparation de mesylates de derives de piperazine
TNSN05321A1 (fr) Derives de n-pyrrolidine-3-ylamide servant d'inhibiteurs de reabsorption de serotonine et de noradrenaline
ATE445619T1 (de) Pyridinylpyrazolopyrimidinon-derivate als pde 7 inhibitoren