MA29260B1 - Derives d'oxindole servant d'agonistes du recepteur 5ht4 - Google Patents

Derives d'oxindole servant d'agonistes du recepteur 5ht4

Info

Publication number
MA29260B1
MA29260B1 MA30153A MA30153A MA29260B1 MA 29260 B1 MA29260 B1 MA 29260B1 MA 30153 A MA30153 A MA 30153A MA 30153 A MA30153 A MA 30153A MA 29260 B1 MA29260 B1 MA 29260B1
Authority
MA
Morocco
Prior art keywords
disease
gastric
dyspepsy
oeso
compounds
Prior art date
Application number
MA30153A
Other languages
English (en)
Inventor
Kiyoshi Kawamura
Hiroki Sone
Chikara Uchida
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
Application filed by Pfizer filed Critical Pfizer
Publication of MA29260B1 publication Critical patent/MA29260B1/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
    • C07D401/02—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 two hetero rings
    • C07D401/12—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 two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/10—Laxatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/12—Antidiarrhoeals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • 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
    • 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
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • 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
    • A61P25/06—Antimigraine agents
    • 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
    • A61P25/28—Drugs 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/06—Antiarrhythmics
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Cardiology (AREA)
  • Diabetes (AREA)
  • Hospice & Palliative Care (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Pulmonology (AREA)
  • Nutrition Science (AREA)
  • Otolaryngology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)

Abstract

L'INVENTION CONCERNE DES COMPOSÉS DE FORMULE (I) OU UN DE LEURS SELS PHARMACEUTIQUEMENT ACCEPTABLES OÙ : A, R1, R2, R3, R4 ET R5 SONT DÉCRITS DANS LA DESCRIPTION, OU UN SEL PHARMACEUTIQUEMENT ACCEPTABLE, ET DES COMPOSITIONS CONTENANT CES COMPOSÉS AINSI QUE LEUR UTILISATION DANS LE TRAITEMENT D'UN ÉTAT À MÉDIATION PAR UNE ACTIVITÉ DE RÉCEPTEUR 5-HT4 TEL QUE (MAIS DE FAÇON NON RESTRICTIVE) LE REFLUX OESO-GASTRIQUE, LA MALADIE GASTRO-INTESTINALE, LE TROUBLE DE MOTILITÉ GASTRIQUE, LA DYSPEPSIE NON ULCÉREUSE, LA DYSPEPSIE FONCTIONNELLE, LE SYNDROME DU CÔLON IRRITABLE (IBS), LA CONSTIPATION, LA DYSPEPSIE, L'OESOPHAGITE, LA MALADIE OESO-GASTRIQUE, LA NAUSÉE, LA MALADIE DU SYSTÈME NERVEUX CENTRAL, LA MALADIE D'ALZHEIMER, LE TROUBLE COGNITIF, LE VOMISSEMENT, LA MIGRAINE, LE TROUBLE NEUROLOGIQUE, LA DOULEUR, LES TROUBLES CARDIOVASCULAIRES, L'INSUFFISANCE CARDIAQUE, L'ARYTHMIE, LE DIABÈTE ET LE SYNDROME D'APNÉE
MA30153A 2005-02-22 2007-08-22 Derives d'oxindole servant d'agonistes du recepteur 5ht4 MA29260B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US65527605P 2005-02-22 2005-02-22

Publications (1)

Publication Number Publication Date
MA29260B1 true MA29260B1 (fr) 2008-02-01

Family

ID=36579484

Family Applications (1)

Application Number Title Priority Date Filing Date
MA30153A MA29260B1 (fr) 2005-02-22 2007-08-22 Derives d'oxindole servant d'agonistes du recepteur 5ht4

Country Status (31)

Country Link
US (2) US7589109B2 (fr)
EP (1) EP1856110B1 (fr)
JP (1) JP4130220B1 (fr)
KR (1) KR100908547B1 (fr)
CN (1) CN101522668B (fr)
AP (1) AP2007004067A0 (fr)
AR (1) AR053548A1 (fr)
AT (1) ATE513827T1 (fr)
AU (1) AU2006217534B8 (fr)
BR (1) BRPI0607456A2 (fr)
CA (1) CA2598536C (fr)
DK (1) DK1856110T3 (fr)
DO (1) DOP2006000046A (fr)
EA (1) EA012615B1 (fr)
ES (1) ES2366375T3 (fr)
GE (1) GEP20094727B (fr)
GT (1) GT200600083A (fr)
HN (1) HN2006007884A (fr)
IL (1) IL184505A0 (fr)
MA (1) MA29260B1 (fr)
MX (1) MX2007010139A (fr)
NL (1) NL1031218C2 (fr)
NO (1) NO20073566L (fr)
NZ (1) NZ556627A (fr)
PE (1) PE20061096A1 (fr)
TN (1) TNSN07319A1 (fr)
TW (1) TW200640915A (fr)
UA (1) UA86301C2 (fr)
UY (1) UY29389A1 (fr)
WO (1) WO2006090279A1 (fr)
ZA (1) ZA200706420B (fr)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0934061B3 (fr) 1996-07-24 2015-01-21 Warner-Lambert Company LLC Isobutylgaba et ses derives utilises pour le traitement de la douleur
AU2006217534B8 (en) * 2005-02-22 2011-12-08 Pfizer Inc. Oxyindole derivatives as 5HT4 receptor agonists
JP2009500340A (ja) * 2005-06-29 2009-01-08 メルク エンド カムパニー インコーポレーテッド 4−フルオロ−ピペリジンt型カルシウムチャネルアンタゴニスト
GB0525068D0 (en) 2005-12-08 2006-01-18 Novartis Ag Organic compounds
JP5205971B2 (ja) * 2006-01-27 2013-06-05 宇部興産株式会社 テトラヒドロピラン化合物の製造方法
US20080051585A1 (en) * 2006-08-17 2008-02-28 Wyeth Process for the preparation of indolin-2-one derivatives useful as PR modulators
MX2008010233A (es) * 2008-03-10 2009-11-10 Eurodrug Lab B V Composicion de liberacion modificada, que comprende doxofilina.
US8642772B2 (en) 2008-10-14 2014-02-04 Sk Biopharmaceuticals Co., Ltd. Piperidine compounds, pharmaceutical composition comprising the same and its use
JP5663743B2 (ja) * 2009-02-27 2015-02-04 ラクオリア創薬株式会社 モチリン受容体作動活性を有するオキシインドール誘導体
CN102421288B (zh) * 2009-05-07 2015-04-22 联合治疗公司 前列环素类似物的固体剂型
SG178557A1 (en) 2009-09-14 2012-03-29 Suven Life Sciences Ltd L -dihydro-2-oxoquinoline compounds a 5-ht4 receptor ligands
CN107260736A (zh) 2010-02-12 2017-10-20 株式会社AskAt 用于治疗痴呆的5‑ht4受体激动剂
DK2758394T3 (en) 2011-09-19 2015-04-20 Suven Life Sciences Ltd HETEROARYL COMPOUNDS AS 5-HT4 RECEPTOR LIGANDS
KR101692578B1 (ko) * 2013-04-18 2017-01-03 삼진제약주식회사 레바미피드 또는 이의 전구체를 포함하는 안구건조증의 예방 또는 치료를 위한 경구용 약제학적 조성물
LT3105218T (lt) 2014-02-13 2019-12-10 Incyte Corp Ciklopropilaminai kaip lsd1 inhibitoriai
US9527835B2 (en) 2014-02-13 2016-12-27 Incyte Corporation Cyclopropylamines as LSD1 inhibitors
WO2015123424A1 (fr) 2014-02-13 2015-08-20 Incyte Corporation Cyclopropylamines en tant qu'inhibiteurs de lsd1
EP3392244A1 (fr) 2014-02-13 2018-10-24 Incyte Corporation Cyclopropylamines en tant qu'inhibiteurs de lsd1
US9758523B2 (en) 2014-07-10 2017-09-12 Incyte Corporation Triazolopyridines and triazolopyrazines as LSD1 inhibitors
WO2016007731A1 (fr) 2014-07-10 2016-01-14 Incyte Corporation Imidazopyridines et imidazopyrazines à utiliser en tant qu'inhibiteurs de lsd1
WO2016007736A1 (fr) 2014-07-10 2016-01-14 Incyte Corporation Imidazopyrazines en tant qu'inhibiteurs de lsd1
WO2016007722A1 (fr) 2014-07-10 2016-01-14 Incyte Corporation Triazolopyridines et triazolopyrazines utilisables comme inhibiteurs de lsd1
EA201792205A1 (ru) 2015-04-03 2018-02-28 Инсайт Корпорейшн Гетероциклические соединения как ингибиторы lsd1
DK3334709T3 (da) 2015-08-12 2025-02-03 Incyte Holdings Corp Salte af en lsd1-hæmmer
CA3014406A1 (fr) * 2016-02-16 2017-08-24 Strongbridge Biopharma plc Veldoreotide de faible solubilite dans des conditions physiologiques destine a etre utilise dans le traitement d'une acromegalie, d'un cancer associe a une acromegalie, de tumeurs exprimant le sst-r5, du diabete de type 2, d'une hyperglycemie, et de tumeurs associees aux hormones
CA3021678A1 (fr) 2016-04-22 2017-10-26 Incyte Corporation Formulations d'un inhibiteur de lsd1
US10968200B2 (en) 2018-08-31 2021-04-06 Incyte Corporation Salts of an LSD1 inhibitor and processes for preparing the same
CN114105863B (zh) * 2021-12-07 2023-11-28 江苏汉拓光学材料有限公司 酸扩散抑制剂、含酸扩散抑制剂的化学放大型光刻胶及其制备与使用方法

Family Cites Families (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5223511A (en) 1987-09-23 1993-06-29 Boehringer Ingelheim Italia S.P.A. Benzimidazoline-2-oxo-1-carboxylic acid compounds useful as 5-HT receptor antagonists
US5552408A (en) 1987-09-23 1996-09-03 Boehringer Ingelheim Italia S.P.A. Benzimidazoline-2-oxo-1-carboxylic acid derivatives useful as 5-ht receptor antagonists
GB8829079D0 (en) 1988-12-13 1989-01-25 Beecham Group Plc Novel compounds
GB9020927D0 (en) 1990-09-26 1990-11-07 Beecham Group Plc Pharmaceuticals
AU1161292A (en) 1991-01-09 1992-08-17 Smithkline Beecham Plc Azabicydic and azatricydic derivatives, process and intermediates for their preparation and pharmaceutical compositions containing them
US5955470A (en) 1991-06-11 1999-09-21 Merrell Pharmaceuticals, Inc. Derivatives of amide analogs of certain methano bridged quinolizines
IT1251144B (it) 1991-07-30 1995-05-04 Boehringer Ingelheim Italia Derivati del benzimidazolone
GB9121170D0 (en) 1991-10-05 1991-11-20 Smithkline Beecham Plc Pharmaceuticals
GB9204565D0 (en) * 1992-03-03 1992-04-15 Smithkline Beecham Plc Pharmaceuticals
US5300512A (en) 1992-06-24 1994-04-05 G. D. Searle & Co. Benzimidazole compounds
US5521193A (en) 1992-06-24 1996-05-28 G. D. Searle & Co. Benzimidazole compounds
US5280028A (en) 1992-06-24 1994-01-18 G. D. Searle & Co. Benzimidazole compounds
FR2694292B1 (fr) 1992-07-29 1994-10-21 Esteve Labor Dr Dérivés de benzimidazole-2-thione-, leur préparation et leur application en tant que médicament.
US5705498A (en) 1992-11-05 1998-01-06 Smithkline Beecham Plc. Piperidine derivatives as 5-HT4 receptor antagonists
TW251287B (fr) 1993-04-30 1995-07-11 Nissei Co Ltd
GB9312348D0 (en) 1993-06-16 1993-07-28 Smithkline Beecham Plc Pharmaceuticals
US5534521A (en) 1993-06-23 1996-07-09 G. D. Searle & Co. Benzimidazole compounds
CA2134192A1 (fr) 1993-11-12 1995-05-13 Michael L. Denney Antagonistes iib/iiia de la glycoproteine 5, 6-bicyclique
US5399562A (en) * 1994-02-04 1995-03-21 G. D. Searle & Co. Indolones useful as serotonergic agents
GB9414139D0 (en) 1994-07-13 1994-08-31 Smithkline Beecham Plc Novel compounds
DE4440675A1 (de) 1994-11-14 1996-05-15 Basf Ag Verfahren zur Herstellung von kautschukmodifizierten Formmassen mittels in den Kautschuk eingebauten, bei thermischer Zersetzung Radikale bildenden Gruppen
IT1275903B1 (it) 1995-03-14 1997-10-24 Boehringer Ingelheim Italia Esteri e ammidi della 1,4-piperidina disostituita
WO1999012903A1 (fr) 1997-09-09 1999-03-18 Du Pont Pharmaceuticals Company BENZIMIDAZOLINONES, BENZOXAZOLINONES, BENZOPIPERAZINONES, INDANONES ET LEURS DERIVES EN TANT QU'INHIBITEURS DU FACTEUR Xa
US6069152A (en) 1997-10-07 2000-05-30 Eli Lilly And Company 5-HT4 agonists and antagonists
US6362371B1 (en) 1998-06-08 2002-03-26 Advanced Medicine, Inc. β2- adrenergic receptor agonists
US6492375B2 (en) 1998-06-30 2002-12-10 Neuromed Technologies, Inc. Partially saturated calcium channel blockers
US6310059B1 (en) 1998-06-30 2001-10-30 Neuromed Technologies, Inc. Fused ring calcium channel blockers
WO2000026197A1 (fr) 1998-10-29 2000-05-11 Bristol-Myers Squibb Company Nouveaux inhibiteurs de l'enzyme impdh
MXPA02006137A (es) 1999-12-20 2002-12-05 Neuromed Tech Inc Bloqueadores del canal de calcio parcialmente saturados.
WO2002030886A2 (fr) 2000-10-12 2002-04-18 Matthews Barry R Inhibiteurs d'angiogenese heterocycliques
AU3950802A (en) 2000-12-07 2002-06-18 Cv Therapeutics Inc Abca-1 elevating compounds
DOP2003000703A (es) * 2002-09-20 2004-03-31 Pfizer Compuestos de imidazopiradina como agonistas del receptor 5-ht4
WO2004113300A1 (fr) 2003-06-23 2004-12-29 Ono Pharmaceutical Co., Ltd. Nouveau compose heterocyclique tricyclique
PL1664036T3 (pl) 2003-09-03 2012-04-30 Pfizer Związki benzimidazolonu wykazujące działanie agonistyczne względem receptora 5-ht4
EA200801607A1 (ru) * 2004-06-15 2008-10-30 Пфайзер Инк. Производные бензимидазолонкарбоновой кислоты
US7737163B2 (en) 2004-06-15 2010-06-15 Pfizer Inc. Benzimidazolone carboxylic acid derivatives
AU2006217534B8 (en) * 2005-02-22 2011-12-08 Pfizer Inc. Oxyindole derivatives as 5HT4 receptor agonists

Also Published As

Publication number Publication date
CN101522668A (zh) 2009-09-02
MX2007010139A (es) 2007-09-27
EA200701552A1 (ru) 2007-12-28
US20060194842A1 (en) 2006-08-31
GEP20094727B (en) 2009-07-10
AU2006217534B2 (en) 2011-08-11
PE20061096A1 (es) 2006-11-09
US20100173925A1 (en) 2010-07-08
TW200640915A (en) 2006-12-01
WO2006090279A1 (fr) 2006-08-31
NO20073566L (no) 2007-08-08
HN2006007884A (es) 2010-01-18
IL184505A0 (en) 2007-10-31
AU2006217534A8 (en) 2011-12-08
US7589109B2 (en) 2009-09-15
NL1031218A1 (nl) 2006-08-23
EA012615B1 (ru) 2009-10-30
NZ556627A (en) 2010-09-30
BRPI0607456A2 (pt) 2009-09-08
CN101522668B (zh) 2012-06-06
HK1135966A1 (en) 2010-06-18
AP2007004067A0 (en) 2007-08-31
DK1856110T3 (da) 2011-08-15
GT200600083A (es) 2006-11-07
ATE513827T1 (de) 2011-07-15
AU2006217534B8 (en) 2011-12-08
CA2598536A1 (fr) 2006-08-31
JP2008531543A (ja) 2008-08-14
CA2598536C (fr) 2011-04-05
UA86301C2 (en) 2009-04-10
DOP2006000046A (es) 2006-08-31
UY29389A1 (es) 2006-10-02
KR20070098936A (ko) 2007-10-05
KR100908547B1 (ko) 2009-07-20
ES2366375T3 (es) 2011-10-19
AR053548A1 (es) 2007-05-09
NL1031218C2 (nl) 2007-01-23
EP1856110B1 (fr) 2011-06-22
JP4130220B1 (ja) 2008-08-06
TNSN07319A1 (fr) 2008-12-31
AU2006217534A1 (en) 2006-08-31
ZA200706420B (en) 2009-04-29
EP1856110A1 (fr) 2007-11-21

Similar Documents

Publication Publication Date Title
TNSN07319A1 (fr) Derives d'oxindole servant d'agonistes du recepteur 5ht4
MA28021A1 (fr) Dérivés de benzimidazolone à activité agoniste des récepteurs 5-HT4
UY29421A1 (es) Nuevos compuestos de n-(n-sulfonilaminoarilmetil) ciclopropanocarboxanida sustituidos, comoposiciones farmacéuticas que los contienen a aplicaciones.
EA200602122A1 (ru) Производные бензимидазолонкарбоновой кислоты
JP2008110984A (ja) 2−(1h−インドリルスルファニル)−ベンジルアミン誘導体
ATE449092T1 (de) Indazolcarbonsäureamidderivate als agonisten des 5ht4-rezeptors
ZA200600427B (en) 1-sulfonylindole derivatives, their preparation and their use as 5-HT6 ligands
ES2202348T3 (es) Derivados del azabicicloheptano n-substituidos, como por ejemplo neurolepticos.
CZ282054B6 (cs) 1-/Pyrido/3,4-b/-1,4-oxazin-4-yl/-1H-indoly, meziprodukty a způsob jejich přípravy a jejich použití jako léčiv
HRP950438A2 (en) N-substituted 3-azabicyclo (3.2.0) heptane derivatives, their preparation and use
US20060183902A1 (en) Dihydroindolyl methanones as alpha 1a/1d adrenoreceptor modulators for the treatment of benign prostatic hypertrophy and lower urinary tract symptoms
TH81015B (th) อนุพันธ์ออกซิอินโดล
CA2176962C (fr) Derives d'azabicycloheptane avec substituant sur l'atome d'azote, leur preparation et leur utilisation
CU20070183A7 (es) Derivados de oxindol
TH76314A (th) สารอนุพันธ์แบบซิมิดาโซโลน คาร์บอกซิลิก แอซิด
TH80288A (th) อนุพันธ์เบนซ์ไดออกเซนพิเพอราซีนที่มีการรวมของสัพรรคภาพสำหรับตัวรับโดพามีน-d2 และตำแหน่งการดูดซ้ำของเซอโรโทนิน
CZ284463B6 (cs) N-Substituované azabicykloheptanové deriváty
TH107679A (th) อนุพันธ์อินโดล