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TN2009000204A1 - Spirocetones servant d'inhibiteurs d'acetyl-coa-carboxylase - Google Patents

Spirocetones servant d'inhibiteurs d'acetyl-coa-carboxylase

Info

Publication number
TN2009000204A1
TN2009000204A1 TNP2009000204A TN2009000204A TN2009000204A1 TN 2009000204 A1 TN2009000204 A1 TN 2009000204A1 TN P2009000204 A TNP2009000204 A TN P2009000204A TN 2009000204 A TN2009000204 A TN 2009000204A TN 2009000204 A1 TN2009000204 A1 TN 2009000204A1
Authority
TN
Tunisia
Prior art keywords
spirocetones
carboxylase
coa
acetyl
inhibitors
Prior art date
Application number
TNP2009000204A
Other languages
English (en)
Inventor
Jeffrey Wayne Corbett
Richard Louis Elliott
Andrew Simon Bell
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 TN2009000204A1 publication Critical patent/TN2009000204A1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/38Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/39Heterocyclic compounds having sulfur as a ring hetero atom having oxygen in the same ring
    • 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
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Diabetes (AREA)
  • Cardiology (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Endocrinology (AREA)
  • Urology & Nephrology (AREA)
  • Emergency Medicine (AREA)
  • Hospice & Palliative Care (AREA)
  • Vascular Medicine (AREA)
  • Child & Adolescent Psychology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La présente invention propose des composés de formule (I) ou un sel pharmaceutiquement acceptable d'un tel composé, formule dans laquelle R1, R2, R3 R4, R5, R6, R7, R8 et R9 répondent aux définitions figurant dans le présent mémoire ; des compositions pharmaceutiques les contenant ; et leur utilisation dans le traitement de mammifères souffrant d'un état de surcharge pondérale.
TNP2009000204A 2006-11-29 2009-05-22 Spirocetones servant d'inhibiteurs d'acetyl-coa-carboxylase TN2009000204A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US86177906P 2006-11-29 2006-11-29
PCT/IB2007/003639 WO2008065508A1 (fr) 2006-11-29 2007-11-16 Inhibiteurs de la spirocétoneacétyl-coa carboxylase

Publications (1)

Publication Number Publication Date
TN2009000204A1 true TN2009000204A1 (fr) 2010-10-18

Family

ID=39126209

Family Applications (1)

Application Number Title Priority Date Filing Date
TNP2009000204A TN2009000204A1 (fr) 2006-11-29 2009-05-22 Spirocetones servant d'inhibiteurs d'acetyl-coa-carboxylase

Country Status (23)

Country Link
US (1) US20090270435A1 (fr)
EP (1) EP2097420B1 (fr)
JP (1) JP2010511035A (fr)
KR (1) KR20090083956A (fr)
CN (1) CN101541809A (fr)
AP (1) AP2009004880A0 (fr)
AT (1) ATE552262T1 (fr)
AU (1) AU2007326950B2 (fr)
BR (1) BRPI0721053A2 (fr)
CA (1) CA2670422C (fr)
CO (1) CO6180424A2 (fr)
CR (1) CR10831A (fr)
EA (1) EA200900613A1 (fr)
EC (1) ECSP099371A (fr)
IL (1) IL198779A0 (fr)
MA (1) MA30932B1 (fr)
MX (1) MX2009005604A (fr)
NO (1) NO20091889L (fr)
RS (1) RS20090249A (fr)
SV (1) SV2009003281A (fr)
TN (1) TN2009000204A1 (fr)
WO (1) WO2008065508A1 (fr)
ZA (1) ZA200903268B (fr)

Families Citing this family (72)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20081559A1 (es) 2007-01-12 2008-11-20 Merck & Co Inc DERIVADOS DE ESPIROCROMANONA SUSTITUIDOS COMO INHIBIDORES DE ACETIL CoA CARBOXILASA
US8138197B2 (en) 2007-01-12 2012-03-20 Msd K.K. Spirochromanon derivatives
CN100550853C (zh) * 2007-01-25 2009-10-14 华为技术有限公司 一种基于输出队列的流控实现方法及装置
DE102007028521A1 (de) * 2007-06-21 2008-12-24 Merck Patent Gmbh Indazolamidderivate
EP2297164A1 (fr) * 2008-05-28 2011-03-23 Pfizer Inc. Inhibiteurs de la pyrazolospirocétone acétyl-coa carboxylase
ES2545231T3 (es) 2008-05-28 2015-09-09 Pfizer Inc. Inhibidores de pirazoloespirocetona acetil-CoA carboxilasa
AU2009266730B2 (en) * 2008-07-04 2013-07-18 Msd K.K. Novel spirochromanone carboxylic acids
US8110570B2 (en) 2008-07-14 2012-02-07 Cropsolution, Inc. Modulators of acetyl-coenzyme A carboxylase and methods of use thereof
DE102008038222A1 (de) 2008-08-18 2010-02-25 Merck Patent Gmbh Indazol-5-carbonsäurehydrazid-derivate
EP2184276A1 (fr) 2008-11-07 2010-05-12 Universite Paul Cezanne Aix-Marseille Iii Procédé de préparation de nouvelles 1H-benzo(d) imidazol-2(3h)-ones substituées, de nouveaux intermédiaires et leur utilisation en tant qu'inhibiteurs de bace 1
WO2011058473A1 (fr) * 2009-11-10 2011-05-19 Pfizer Inc. Inhibiteurs de n2-pyrazolospirocétone acétyl-coa carboxylase
ES2444543T3 (es) * 2009-11-10 2014-02-25 Pfizer Inc Inhibidores de la N1-pirazoloespirocetona acetil-CoA carboxilasa
JP5496409B2 (ja) 2010-03-19 2014-05-21 ファイザー・インク 2,3ジヒドロ−1h−インデン−1−イル−2,7−ジアザスピロ[3.5]ノナン誘導体およびグレリン受容体のアンタゴニストまたは逆アゴニストとしてのそれらの使用
WO2011140425A1 (fr) 2010-05-06 2011-11-10 Vertex Pharmaceuticals Incorporated Amides de chromène hétérocyclique-pipéridine spirocyclique utiles comme modulateurs des canaux ioniques
EP2582709B1 (fr) 2010-06-18 2018-01-24 Sanofi Dérivés d'azolopyridin-3-one en tant qu'inhibiteurs de lipases et de phospholipases
US8859577B2 (en) 2010-09-30 2014-10-14 Pfizer Inc. N1-pyrazolospiroketone acetyl-CoA carboxylase inhibitors
ES2546465T3 (es) 2010-10-29 2015-09-23 Pfizer Inc Inhibidores de N1/N2-lactama acetil-CoA carboxilasa
CN106008504A (zh) 2011-02-02 2016-10-12 沃泰克斯药物股份有限公司 作为离子通道调节剂的吡咯并吡嗪-螺环哌啶酰胺
CA2827311A1 (fr) * 2011-02-18 2012-08-23 Vertex Pharmaceuticals Incorporated Amides de piperidine spirocyclique chromanique en tant que modulateurs des canaux ioniques
AU2012229187B2 (en) 2011-03-14 2016-11-10 Vertex Pharmaceuticals Incorporated Morpholine-spirocyclic piperidine amides as modulators of ion channels
WO2012143813A1 (fr) 2011-04-22 2012-10-26 Pfizer Inc. Dérivés de pyrazolospirocétone destinés à être utilisés comme inhibiteurs d'acétyl-coa carboxylase
US9169198B2 (en) 2011-07-08 2015-10-27 Bayer Intellectual Property Gmbh Method for the production of 2-amino-5-cyano-N,3-dimethylbenzamide
CA2841757A1 (fr) 2011-07-15 2013-01-24 Etzer Darout Modulateurs de gpr 119
AU2012288493B2 (en) 2011-07-22 2015-08-06 Pfizer Inc. Quinolinyl glucagon receptor modulators
BR112014003496B1 (pt) 2011-08-18 2022-02-22 Nippon Shinyaku Co., Ltd Derivado heterocíclico, usos do mesmo e composição farmacêutica
ES2605565T3 (es) 2011-08-31 2017-03-15 Pfizer Inc Compuestos de hexahidropirano [3,4-D][1,3]tiazin-2-amina
MX351299B (es) 2011-11-11 2017-10-10 Pfizer 2-tiopirimidinonas.
HK1206735A1 (en) 2012-04-06 2016-01-15 辉瑞公司 Diacylglycerol acyltransferase 2 inhibitors
US8889730B2 (en) 2012-04-10 2014-11-18 Pfizer Inc. Indole and indazole compounds that activate AMPK
WO2013164730A1 (fr) 2012-05-04 2013-11-07 Pfizer Inc. Composés d'hexahydropyrano[3,4-d][1,3]thiazin-2-amine substitués par des hétérocycliques à titre d'inhibiteurs d'app, bace1 et bace2
US9260455B2 (en) 2012-09-20 2016-02-16 Pfizer Inc. Alkyl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds
EP2931731A1 (fr) 2012-12-11 2015-10-21 Pfizer Inc. Composés d'hexahydropyrano [3,4-d][1,3]thiazin-2-amine en tant qu'inhibiteurs de bace1
JP6162820B2 (ja) 2012-12-19 2017-07-12 ファイザー・インク 炭素環式および複素環式置換ヘキサヒドロピラノ[3,4−d][1,3]チアジン−2−アミン化合物
CA2897678A1 (fr) 2013-02-13 2014-08-21 Pfizer Inc. Composes hexahydropyrano [3,4-d][1,3] thiazin-2-amine substitues par un heteroaryle
US9233981B1 (en) 2013-02-15 2016-01-12 Pfizer Inc. Substituted phenyl hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds
JP6348582B2 (ja) 2013-10-09 2018-06-27 ファイザー・インク プロスタグランジンep3受容体の拮抗薬
DK3119757T3 (en) 2014-03-17 2018-06-18 Pfizer DIACYLGYLERIC-ACYL TRANSFERASE-2 INHIBITORS TO USE IN THE TREATMENT OF METABOLIC AND RELATED DISEASES
CN106458912B (zh) 2014-04-04 2020-10-27 辉瑞公司 双环稠合的杂芳基或芳基化合物以及它们作为irak4拟制剂的用途
CN106459088A (zh) 2014-04-10 2017-02-22 辉瑞公司 2‑氨基‑6‑甲基‑4,4a,5,6‑四氢吡喃并[3,4‑d][1,3]噻嗪‑8a(8H)‑基‑1,3‑噻唑‑4‑基酰胺
WO2016092413A1 (fr) 2014-12-10 2016-06-16 Pfizer Inc. Composés indoliques et indazoliques qui activent l'ampk
EP3237401B1 (fr) 2014-12-22 2019-03-06 Pfizer Inc Antagonistes de récepteur ep3 de prostaglandine
CN107531647A (zh) 2015-05-05 2018-01-02 辉瑞大药厂 2‑硫代嘧啶酮类
EP3303303A1 (fr) 2015-05-29 2018-04-11 Pfizer Inc Nouveaux composés hétérocycliques utilisés en tant qu'inhibiteurs de l'enzyme vanine-1
PT3766885T (pt) 2015-06-17 2022-08-09 Pfizer Compostos tricíclicos e a sua utilização como inibidores de fosfodiesterase
WO2016203335A1 (fr) 2015-06-18 2016-12-22 Pfizer Inc. Nouvelles pyrido [2,3-b] pyrazinones utilisées en tant qu'inhibiteurs de bromodomaines de la famille bet
CA2995153A1 (fr) 2015-08-13 2017-02-16 Pfizer Inc. Composes aryle ou heteroaryle condenses bicycliques
DK3341367T3 (da) 2015-08-27 2021-04-12 Pfizer Bicyklisk-fusionerede heteroaryl- eller arylforbindelser som irak4-modulatorer
WO2017037567A1 (fr) 2015-09-03 2017-03-09 Pfizer Inc. Régulateurs de la frataxine
WO2017051294A1 (fr) 2015-09-24 2017-03-30 Pfizer Inc. N-[2-(3-amino-2,5-diméthyl-1,1-dioxido-5,6-dihydro-2h-1,2,4-thiadiazin-5-yl)-1,3-thiazol-4-yl] amides utiles comme inhibiteurs de bace
WO2017051303A1 (fr) 2015-09-24 2017-03-30 Pfizer Inc. Dérivés de tétrahydropyrano[3,4-d] [1,3]oxazine et leur utilisation en tant qu'inhibiteurs de bace
AU2016325665A1 (en) 2015-09-24 2018-03-08 Pfizer Inc. N-[2-(2-amino-6,6-disubstituted-4, 4a, 5, 6-tetrahydropyrano [3,4-d][1,3] thiazin-8a (8h)-yl) -1, 3-thiazol-4-yl] amides
US9809579B2 (en) 2015-12-29 2017-11-07 Pfizer Inc. Substituted 3-azabicyclo[3.1.0]hexanes as ketohexokinase inhibitors
US10906888B2 (en) 2016-07-14 2021-02-02 Pfizer Inc. Pyrimidine carboxamides as inhibitors of Vanin-1 enzyme
AR109179A1 (es) 2016-08-19 2018-11-07 Pfizer Inhibidores de diacilglicerol aciltransferasa 2
WO2019133445A1 (fr) 2017-12-28 2019-07-04 Inception Ibd, Inc. Aminothiazoles utilisés en tant qu'inhibiteurs de vanin-1
CN108658938B (zh) * 2018-06-15 2021-03-23 上海现代制药股份有限公司 一种甲磺酸达比加群酯工艺杂质的合成方法
CN108774242B (zh) * 2018-08-22 2020-10-27 牡丹江医学院 一种防治冠心病的药物及其制备方法
TWI718644B (zh) 2018-08-31 2021-02-11 美商輝瑞股份有限公司 用於治療nash/nafld和相關疾病之組合
CN109400618B (zh) * 2018-11-09 2021-08-10 中国药科大学 一种色满衍生物及其制备方法和应用
WO2020102575A1 (fr) 2018-11-16 2020-05-22 Inception Ibd, Inc. Aminothiazoles hétérocycliques et leurs utilisations
CN109809992A (zh) * 2019-02-16 2019-05-28 安徽华胜医药科技有限公司 一种2-(2-氟-3-甲氧基苯基)-2-羟基乙酸乙酯的合成方法
EP3972596B1 (fr) 2019-05-20 2025-07-16 Pfizer Inc. Combinaisons comprenant du benzodioxol en tant qu'agonistes de glp-1r destinées à être utilisées dans le traitement de la nash/nafld et de maladies associées
CN110128347A (zh) 2019-06-17 2019-08-16 韶远科技(上海)有限公司 一种1-甲基-1h-吲唑-6-甲酸的合成方法
GB201910304D0 (en) 2019-07-18 2019-09-04 Ctxt Pty Ltd Compounds
HUE068174T2 (hu) 2020-02-07 2024-12-28 Gasherbrum Bio Inc Heterociklusos GLP-1 agonisták
CN114437096B (zh) * 2020-11-06 2025-09-12 上海医药集团股份有限公司 一种螺杂环类化合物、其制备方法及应用
WO2023169456A1 (fr) 2022-03-09 2023-09-14 Gasherbrum Bio , Inc. Agonistes hétérocycliques de glp-1
EP4508047A1 (fr) 2022-04-14 2025-02-19 Gasherbrum Bio, Inc. Agonistes hétérocycliques de glp-1
WO2024118524A1 (fr) 2022-11-28 2024-06-06 Cerevel Therapeutics, Llc Composés d'azaindole et leur utilisation en tant qu'inhibiteurs de phosphodiestérase
AU2023396387A1 (en) 2022-12-15 2025-06-26 Gasherbrum Bio, Inc. Salts and solid forms of a compound having glp-1 agonist activity
WO2025036472A1 (fr) * 2023-08-16 2025-02-20 Pharmaengine, Inc. Inhibiteur de prmt5 mta-coopératif spirocyclique
WO2025133948A1 (fr) * 2023-12-21 2025-06-26 Pfizer Inc. Inhibiteurs de l'acétyl coa-carboxylase (acc)

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL96507A0 (en) * 1989-12-08 1991-08-16 Merck & Co Inc Nitrogen-containing spirocycles and pharmaceutical compositions containing them
JP2001516330A (ja) * 1995-06-06 2001-09-25 メルク エンド カンパニー インコーポレーテッド アルファ1aアドレナリンレセプターアンタゴニスト
WO2002020509A2 (fr) * 2000-09-06 2002-03-14 Bayer Aktiengesellschaft Medicament pour lutter contre des maladies virales
WO2004092179A1 (fr) * 2003-04-14 2004-10-28 Nippon Soda Co. Ltd. Derive spiro, procede de production et antioxydant
JP2005119987A (ja) * 2003-10-15 2005-05-12 Ajinomoto Co Inc アシルスルホンアミド誘導体
US8138342B2 (en) * 2004-10-12 2012-03-20 High Point Pharmacueticals, LLC 11β-hydroxysteroid dehydrogenase type 1 active spiro compounds
US20090215742A1 (en) * 2005-05-03 2009-08-27 Pfizer, Inc. Amide resorcinol compounds
ATE509023T1 (de) * 2005-07-19 2011-05-15 Merck Sharp & Dohme Spirochromanon-derivate als acetyl-koenzym-a- carboxylase-hemmer

Also Published As

Publication number Publication date
CO6180424A2 (es) 2010-07-19
JP2010511035A (ja) 2010-04-08
ATE552262T1 (de) 2012-04-15
IL198779A0 (en) 2010-02-17
EP2097420B1 (fr) 2012-04-04
AU2007326950B2 (en) 2010-10-14
CA2670422C (fr) 2011-09-06
MA30932B1 (fr) 2009-11-02
NO20091889L (no) 2009-06-17
ZA200903268B (en) 2010-07-28
CN101541809A (zh) 2009-09-23
MX2009005604A (es) 2009-06-08
RS20090249A (sr) 2010-06-30
AU2007326950A1 (en) 2008-06-05
CR10831A (es) 2009-06-18
ECSP099371A (es) 2009-06-30
BRPI0721053A2 (pt) 2014-07-29
EA200900613A1 (ru) 2009-10-30
CA2670422A1 (fr) 2008-06-05
SV2009003281A (es) 2010-08-17
AP2009004880A0 (en) 2009-06-30
EP2097420A1 (fr) 2009-09-09
WO2008065508A1 (fr) 2008-06-05
KR20090083956A (ko) 2009-08-04
US20090270435A1 (en) 2009-10-29

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MA30999B1 (fr) Composés.
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