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MA31779B1 - Activateurs de glucokinase - Google Patents

Activateurs de glucokinase

Info

Publication number
MA31779B1
MA31779B1 MA32775A MA32775A MA31779B1 MA 31779 B1 MA31779 B1 MA 31779B1 MA 32775 A MA32775 A MA 32775A MA 32775 A MA32775 A MA 32775A MA 31779 B1 MA31779 B1 MA 31779B1
Authority
MA
Morocco
Prior art keywords
glucokinase
glucokinase activators
gily
glycemia
affection
Prior art date
Application number
MA32775A
Other languages
Arabic (ar)
English (en)
Inventor
Thomas Daniel Aicher
Steven Armen Boyd
Mark Joseph Chicarelli
Kevin Ronald Condroski
Jay Bradford Fell
John P Fischer
Indrani W Gunawardana
Ronald Jay Hinklin
Ajay Singh
Timothy M Turner
Eli M Wallace
Original Assignee
Array Biopharma 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 Array Biopharma Inc filed Critical Array Biopharma Inc
Publication of MA31779B1 publication Critical patent/MA31779B1/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D401/14Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/72Nitrogen atoms
    • C07D213/75Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D417/02Heterocyclic 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • C07D417/14Heterocyclic 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 three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

CETTE INVENTION CONCERNE DES COMPOSÉS DE FORMULE I OÙ R2, R3, R13, L ET D2 SONT TELS QUE DÉFINIS DANS LA DESCRIPTION, QUI SONT UTILISÉS DANS LE TRAITEMENT ET/OU LA PRÉVENTION DES MALADIES OU DES AFFECTIONS ASSOCIÉES AVEC DES TAUX DÉFICITAIRES DE L'ACTIVITÉ GLUCOKINASE, OU QUI PEUVENT ÊTRE TRAITÉES PAR ACTIVATION DE LA GLUCOKINASE Y COMPRIS, MAIS SANS Y ÊTRE LIMITÉS, LE DIABÈTE SUCRÉ, L'INTOLÉRANCE AU GLUCOSE, L'HYPERGLYCÉMIE MODÉRÉE À JEUN, LA GLYCÉMIE À JEUN ANORMALE, ET TOUTE AUTRE MALADIE ET AFFECTION COMME CELLES ÉVOQUÉES ICI.
MA32775A 2007-09-21 2010-04-14 Activateurs de glucokinase MA31779B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US97422507P 2007-09-21 2007-09-21
PCT/US2008/076401 WO2009042435A1 (fr) 2007-09-21 2008-09-15 Activateurs de glucokinase

Publications (1)

Publication Number Publication Date
MA31779B1 true MA31779B1 (fr) 2010-10-01

Family

ID=40250949

Family Applications (1)

Application Number Title Priority Date Filing Date
MA32775A MA31779B1 (fr) 2007-09-21 2010-04-14 Activateurs de glucokinase

Country Status (29)

Country Link
US (3) US8212045B2 (fr)
EP (4) EP2727910B1 (fr)
JP (1) JP5722037B2 (fr)
KR (1) KR101566042B1 (fr)
CN (1) CN101868459B (fr)
AR (1) AR068628A1 (fr)
AU (1) AU2008305294B2 (fr)
BR (1) BRPI0816881A2 (fr)
CA (1) CA2699718C (fr)
CO (1) CO6270223A2 (fr)
CR (2) CR11383A (fr)
DK (1) DK2209778T3 (fr)
EA (1) EA019104B1 (fr)
ES (2) ES2393824T3 (fr)
HK (2) HK1145498A1 (fr)
HR (1) HRP20120814T1 (fr)
IL (1) IL204264A (fr)
MA (1) MA31779B1 (fr)
MX (1) MX2010002772A (fr)
MY (1) MY180558A (fr)
NZ (1) NZ583538A (fr)
PL (1) PL2209778T3 (fr)
PT (1) PT2209778E (fr)
SI (1) SI2209778T1 (fr)
TN (1) TN2010000100A1 (fr)
TW (1) TWI423799B (fr)
UA (1) UA101166C2 (fr)
WO (1) WO2009042435A1 (fr)
ZA (2) ZA201002206B (fr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008061108A2 (fr) * 2006-11-15 2008-05-22 Forest Laboratories Holdings Limited Dérivés de phtalazine
MX2010002772A (es) 2007-09-21 2010-03-31 Array Biopharma Inc Derivados de piridin-2-il-amino-1,2,4-tiadiazol como activadores de glucocinasa para el tratamiento de diabetes mellitus.
WO2011107494A1 (fr) 2010-03-03 2011-09-09 Sanofi Nouveaux dérivés aromatiques de glycoside, médicaments contenants ces composés, et leur utilisation
JP5909482B2 (ja) 2010-03-31 2016-04-26 ザ スクリプス リサーチ インスティテュート 細胞の再プログラム
US8530413B2 (en) 2010-06-21 2013-09-10 Sanofi Heterocyclically substituted methoxyphenyl derivatives with an oxo group, processes for preparation thereof and use thereof as medicaments
TW201215387A (en) 2010-07-05 2012-04-16 Sanofi Aventis Spirocyclically substituted 1,3-propane dioxide derivatives, processes for preparation thereof and use thereof as a medicament
TW201215388A (en) 2010-07-05 2012-04-16 Sanofi Sa (2-aryloxyacetylamino)phenylpropionic acid derivatives, processes for preparation thereof and use thereof as medicaments
TW201221505A (en) 2010-07-05 2012-06-01 Sanofi Sa Aryloxyalkylene-substituted hydroxyphenylhexynoic acids, process for preparation thereof and use thereof as a medicament
WO2012027261A1 (fr) 2010-08-23 2012-03-01 Amgen Inc. Dérivés de sulfonylpipérazine qui interagissent avec la protéine régulatrice de la glucokinase pour le traitement du diabète
KR20140051834A (ko) 2011-03-09 2014-05-02 다이이찌 산쿄 가부시키가이샤 디피리딜아민 유도체
MX2013011561A (es) 2011-04-05 2014-02-28 Amgen Inc Compuestos de benzodioxepina y benzodioxina que interactuan con la proteina reguladora de glucocinasa para el tratamiento de diabetes.
WO2013037390A1 (fr) 2011-09-12 2013-03-21 Sanofi Dérivés amides d'acide 6-(4-hydroxyphényl)-3-styryl-1h-pyrazolo[3,4-b]pyridine-4-carboxylique en tant qu'inhibiteurs de kinase
WO2013045413A1 (fr) 2011-09-27 2013-04-04 Sanofi Dérivés d'amide d'acide 6-(4-hydroxyphényl)-3-alkyl-1h-pyrazolo[3,4-b] pyridine-4-carboxylique utilisés comme inhibiteurs de kinase
WO2013123444A1 (fr) 2012-02-17 2013-08-22 Amgen Inc. Composés de sulfonyle qui interagissent avec la protéine régulatrice de la glucokinase
WO2013173382A1 (fr) 2012-05-15 2013-11-21 Amgen Inc. Benzothiophène sulfonamides et autres composés qui interagissent avec une protéine régulatrice de la glucokinase
WO2013173672A1 (fr) 2012-05-18 2013-11-21 Array Biopharma Inc. Procédé pour la préparation de thiadiazoles
JP2015536993A (ja) * 2012-11-09 2015-12-24 アムジェン インコーポレイテッド (1s)−1−[5−({3−[(2−メチルピリジン−3−イル)オキシ]−5−(ピリジン−2−イルスルファニル)ピリジン−2−イル}アミノ)−1,2,4−チアジアゾール−3−イル]エタン−1,2−ジオールの結晶形態
WO2016059647A2 (fr) * 2014-10-13 2016-04-21 SHRI CHHATRAPTI SHIVAJI COLLEGE Maharashtra, India) Dérivés de triaminotriazine et de picolinonitrile utilisables en tant qu'inhibiteurs efficaces de la transcriptase inverse du vih-1
GB201714777D0 (en) 2017-09-14 2017-11-01 Univ London Queen Mary Agent
SG11202003879RA (en) 2017-10-30 2020-05-28 Neuropore Therapies Inc Substituted phenyl sulfonyl phenyl triazole thiones and uses thereof
KR20240091095A (ko) 2018-05-31 2024-06-21 후아 메디슨 (상하이) 엘티디. 글루코키나제 활성화제 및 α-글루코시다제 억제제를 함유하는 약제학적 병용물, 조성물 및 제제, 및 이들의 제조 방법 및 용도

Family Cites Families (82)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3983246A (en) 1974-04-04 1976-09-28 Fmc Corporation N-(sulfonyloxy) benzimidoyl halides as bactericidal or fungicidal agents
DE2949913A1 (de) * 1979-12-12 1981-06-25 Basf Ag, 6700 Ludwigshafen Azofarbstoffe
EP0300688A1 (fr) 1987-07-21 1989-01-25 FISONS plc Dérivés de pyrrole, procédé de préparation et compositions pharmaceutiques les contenant
JPH0228168A (ja) * 1988-04-14 1990-01-30 Sankyo Co Ltd チアゾール誘導体
US5326776A (en) * 1992-03-02 1994-07-05 Abbott Laboratories Angiotensin II receptor antagonists
AU4090093A (en) 1992-05-29 1993-12-30 Yamanouchi Pharmaceutical Co., Ltd. Medicine containing benzoic acid derivative and novel benzoic acid derivative
ATE217865T1 (de) 1994-06-24 2002-06-15 Euro Celtique Sa Verbindungen zur hemmung von phosphodiesrerase iv
GB9908410D0 (en) * 1999-04-13 1999-06-09 Pfizer Ltd Pyridines
TR200102969T2 (tr) 1999-04-15 2002-08-21 Bristol-Myers Squibb Company Siklik protein tirozin kinaz önleyicileri.
US7125875B2 (en) 1999-04-15 2006-10-24 Bristol-Myers Squibb Company Cyclic protein tyrosine kinase inhibitors
DK1177187T3 (da) 1999-04-28 2007-10-15 Sanofi Aventis Deutschland Diarylsyrederivater som PPAR-receptorligander
KR100722090B1 (ko) 1999-05-21 2007-05-25 바이오비트럼 에이비 신규 화합물, 이의 용도 및 이의 제조 방법
US6465467B1 (en) * 1999-05-21 2002-10-15 Biovitrum Ab Certain aryl-aliphatic and heteroaryl-aliphatic piperazinyl pyrazines and their use in the treatment of serotonin-related diseases
JP4144978B2 (ja) 1999-09-09 2008-09-03 富士フイルム株式会社 1,2,4−チアジアゾール誘導体の合成法
MXPA02002559A (es) * 1999-09-10 2002-07-30 Merck & Co Inc Inhibidores de tirosina cinasa.
US20020065270A1 (en) 1999-12-28 2002-05-30 Moriarty Kevin Joseph N-heterocyclic inhibitors of TNF-alpha expression
ES2335265T3 (es) 1999-12-28 2010-03-24 Pharmacopeia, Inc. Inhibidores de citoquina, especialmente de tnf-alfa.
US6906067B2 (en) 1999-12-28 2005-06-14 Bristol-Myers Squibb Company N-heterocyclic inhibitors of TNF-α expression
US7345051B2 (en) 2000-01-31 2008-03-18 Genaera Corporation Mucin synthesis inhibitors
US20050209297A1 (en) * 2000-08-31 2005-09-22 Pfizer Inc Pyrazole derivatives
JP2004507526A (ja) 2000-08-31 2004-03-11 ファイザー・プロダクツ・インク ピラゾール誘導体及びそのプロテインキナーゼ阻害剤としての使用
US20020132836A1 (en) 2000-10-11 2002-09-19 Chemocentryx Inc. Compounds and methods for modulating CCR4 function
AU2002213467A1 (en) 2000-10-11 2002-04-22 Chemocentryx, Inc. Modulation of ccr4 function
RU2003120061A (ru) 2000-12-07 2004-11-27 Си Ви Терапьютикс, Инк. (Us) Замещенные 1,3,5-триазины и пиримидины в качестве повышающих авса-1 соединений против заболевания коронарной артерии или атеросклероза
CN100408573C (zh) 2000-12-21 2008-08-06 沃泰克斯药物股份有限公司 可用作蛋白激酶抑制剂的吡唑化合物
WO2002064096A2 (fr) 2001-02-16 2002-08-22 Tularik Inc. Procedes d'utilisation d'agents antiviraux a base de pyrimidine
US7144903B2 (en) * 2001-05-23 2006-12-05 Amgen Inc. CCR4 antagonists
CA2450934A1 (fr) 2001-06-19 2002-12-27 Marco Dodier Inhibiteurs pyrimidine de la phosphodiesterase (pde) 7
PE20030008A1 (es) 2001-06-19 2003-01-22 Bristol Myers Squibb Co Inhibidores duales de pde 7 y pde 4
EP1404672B1 (fr) * 2001-06-22 2006-01-18 Merck & Co., Inc. Inhibiteurs de tyrosine kinase
JP4505228B2 (ja) 2002-01-10 2010-07-21 バイエル・シェーリング・ファルマ・アクチェンゲゼルシャフト Rho−キナーゼ阻害剤
EP1479397B1 (fr) 2002-02-05 2011-06-08 Astellas Pharma Inc. Derives de 2,4,6-triamino-1,3,5-triazine
EP1485100B1 (fr) 2002-03-15 2010-05-05 Vertex Pharmaceuticals Incorporated Azinylaminoazoles utilises comme inhibiteurs de proteine kinases
WO2003078426A1 (fr) 2002-03-15 2003-09-25 Vertex Pharmaceuticals, Inc. Azolylaminoazines en tant qu'inhibiteurs de proteines kinases
AU2003220300A1 (en) 2002-03-15 2003-09-29 Binch, Hayley Compositions useful as inhibitors of protein kinases
WO2003078427A1 (fr) 2002-03-15 2003-09-25 Vertex Pharmaceuticals, Inc. Azolylaminoazines inhibitrices des proteines kinases
ATE447404T1 (de) 2002-03-29 2009-11-15 Novartis Vaccines & Diagnostic Substituierte benzazole und ihre verwendung als raf-kinase-hemmer
US8299108B2 (en) * 2002-03-29 2012-10-30 Novartis Ag Substituted benzazoles and methods of their use as inhibitors of raf kinase
WO2003091213A1 (fr) * 2002-04-25 2003-11-06 Yamanouchi Pharmaceutical Co., Ltd. Derives d'amide ou sels de ces derives
AU2003249369A1 (en) 2002-06-21 2004-01-06 Cellular Genomics, Inc. Certain amino-substituted monocycles as kinase modulators
AR041508A1 (es) 2002-08-09 2005-05-18 Astra Ab Compuestos con actividad en los receptores de glutamato metabotropicos
AU2003272324A1 (en) 2002-09-10 2004-04-30 Scios Inc. INHIBITORS OF TFGBeta
JP2006509774A (ja) 2002-10-03 2006-03-23 ノバルティス アクチエンゲゼルシャフト 2型糖尿病の処置において有用なグルコキナーゼアクチベーターとしての置換(チアゾール−2−イル)−アミドまたはスルホンアミド
EP1558609A4 (fr) 2002-10-30 2008-05-28 Merck & Co Inc Inhibiteurs de kinase
RU2351590C2 (ru) 2003-02-10 2009-04-10 Вертекс Фармасьютикалз Инкорпорейтед Способ получения диариламина
WO2004071426A2 (fr) 2003-02-11 2004-08-26 Kemia Inc. Composes destines au traitement d'une infection virale
JP4400563B2 (ja) 2003-02-13 2010-01-20 萬有製薬株式会社 新規2−ピリジンカルボキサミド誘導体
ATE396731T1 (de) 2003-03-25 2008-06-15 Vertex Pharma Thiazole zur verwendung als inhibitoren von protein-kinasen
US7244763B2 (en) 2003-04-17 2007-07-17 Warner Lambert Company Llc Compounds that modulate PPAR activity and methods of preparation
CA2537141A1 (fr) * 2003-09-02 2005-03-10 Merck And Co., Inc. Amines et ethers de bipyridyle utilises comme modulateurs du recepteur 5 metabotropique au glutamate
US7470712B2 (en) 2004-01-21 2008-12-30 Bristol-Myers Squibb Company Amino-benzazoles as P2Y1 receptor inhibitors
WO2005077373A2 (fr) 2004-02-03 2005-08-25 Astrazeneca Ab Nouveau traitement du reflux gastro-oesophagien pathologique ii
AR049418A1 (es) 2004-02-27 2006-08-02 Bayer Pharmaceuticals Corp Derivados de heteroarilaminopirazol y composiciones farmaceuticas para el tratamiento de la diabetes.
KR20050091462A (ko) 2004-03-12 2005-09-15 한국과학기술연구원 푸로피리미딘 화합물 및 이를 포함하는 ddr2 티로신키나아제 활성 저해제
CA2560286A1 (fr) 2004-03-23 2005-09-29 Banyu Pharmaceutical Co., Ltd. Derive de la quinazoline ou de la pyridopyrimidine substituee
EP1737870A1 (fr) 2004-04-02 2007-01-03 Novartis AG Derives thiazolopyridine, compositions pharmaceutiques les contenant et procedes de traitement de troubles a mediation par glucokinase
US20080108600A1 (en) 2004-04-13 2008-05-08 Icagen, Inc. Polycyclic Pyridines as Potassium Ion Channel Modulators
ATE458730T1 (de) 2004-04-13 2010-03-15 Icagen Inc Polycyclische pyrazine als kaliumionenkanal- modulatoren
TW200606129A (en) * 2004-07-26 2006-02-16 Chugai Pharmaceutical Co Ltd Novel cyclohexane derivative, its prodrug, its salt and diabetic therapeutic agent containing the same
EP1844023A1 (fr) 2004-12-31 2007-10-17 Sk Chemicals Co., Ltd. Dérivés de quinazoline pour le traitement prophylactique et thérapeutique du diabète et de l'obésité
ATE499370T1 (de) 2005-01-19 2011-03-15 Bristol Myers Squibb Co 2-phenoxy-n-(1,3,4-thiadizol-2-yl)pyridin-3- aminderivate und verwandte verbindungen als p2y1- rezeptor-hemmer zur behandlung thromboembolischer erkrankungen
DE102005025161A1 (de) 2005-06-01 2006-12-07 Phenion Gmbh & Co. Kg Derivate des Pyrimidins und Triazins und deren Verwendung
AU2006279376B2 (en) * 2005-08-18 2011-04-14 Vertex Pharmaceuticals Incoporated Pyrazine kinase inhibitors
AU2006285834A1 (en) * 2005-08-31 2007-03-08 Astellas Pharma Inc. Thiazole derivative
US9018209B2 (en) 2005-09-23 2015-04-28 Yale University Compounds and methods for the treatment of viruses and cancer
ATE521608T1 (de) 2005-11-01 2011-09-15 Array Biopharma Inc Glucokinaseaktivatoren
EP1954277B1 (fr) 2005-11-03 2017-01-18 Vertex Pharmaceuticals Incorporated Aminopyrimidines utiles en tant qu'inhibiteurs de kinases
KR20070052207A (ko) 2005-11-16 2007-05-21 주식회사 엘지생명과학 신규한 kdr 억제제
CA2629781A1 (fr) * 2005-11-16 2007-05-24 Vertex Pharmaceuticals Incorporated Aminopyrimidines utiles en tant qu'inhibiteurs de la kinase
US8022222B2 (en) 2006-01-27 2011-09-20 Array Biopharma, Inc. Glucokinase activators
DK2013204T3 (en) * 2006-03-24 2015-04-20 Array Biopharma Inc 2-aminopyridinanaloger as glucokinase activators
US8080669B2 (en) * 2006-05-12 2011-12-20 Ab Science Process for the synthesis of 2-aminoxazole compounds
WO2008024963A1 (fr) 2006-08-24 2008-02-28 Serenex, Inc. Dérivés de benzène, de pyridine et de pyridazine
CL2007003061A1 (es) 2006-10-26 2008-08-01 Astrazeneca Ab Compuestos derivados de 3,5-dioxi-benzamida; proceso de preparacion; composicion farmaceutica que comprende a dichos compuestos; y su uso para tratar una enfermedad mediada a traves de glk, tal como la diabetes tipo 2.
PT2091918E (pt) 2006-12-08 2014-11-24 Irm Llc Compostos e composições como inibidores de proteína cinase
WO2008091770A1 (fr) 2007-01-24 2008-07-31 Array Biopharma Inc. Dérivés de 2-aminopyridine utilisés comme activateurs de la glucokinase
EP2173745A2 (fr) * 2007-03-23 2010-04-14 Array Biopharma, Inc. Analogues de la 2-aminopyridine comme activateurs de la glucokinase
WO2008124083A2 (fr) 2007-04-05 2008-10-16 Amgen Inc. Modulateurs de la kinase aurora et méthode d'utilisation
US20090012091A1 (en) 2007-07-02 2009-01-08 Kinagen, Inc. Oximide derivatives and their therapeutical application
UY31281A1 (es) 2007-08-13 2009-03-31 Aminas, benzamidas y sulfonamidas {[4-(5,6-dimetil-2-piridin-2-il-piridin-3-il) oxipiridin-2-il]amino} sustituidas, sus sales farmacéuticamente aceptables, composiciones contenniéndolas y aplicaciones.
MX2010002772A (es) 2007-09-21 2010-03-31 Array Biopharma Inc Derivados de piridin-2-il-amino-1,2,4-tiadiazol como activadores de glucocinasa para el tratamiento de diabetes mellitus.
KR20100090250A (ko) 2007-10-09 2010-08-13 메르크 파텐트 게엠베하 글루코키나제 활성체로서 유용한 피리딘 유도체

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MX2010002772A (es) 2010-03-31
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UA101166C2 (ru) 2013-03-11
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