KR20050105492A - 2형 당뇨병 및 아테롬성경화증 치료용 ppar조절제로서의4-(3-(2-페닐옥사졸-4-일메톡시)-사이클로헥실옥시)-부탄산유도체 및 관련 화합물 - Google Patents

2형 당뇨병 및 아테롬성경화증 치료용 ppar조절제로서의4-(3-(2-페닐옥사졸-4-일메톡시)-사이클로헥실옥시)-부탄산유도체 및 관련 화합물 Download PDF

Info

Publication number
KR20050105492A
KR20050105492A KR1020057015851A KR20057015851A KR20050105492A KR 20050105492 A KR20050105492 A KR 20050105492A KR 1020057015851 A KR1020057015851 A KR 1020057015851A KR 20057015851 A KR20057015851 A KR 20057015851A KR 20050105492 A KR20050105492 A KR 20050105492A
Authority
KR
South Korea
Prior art keywords
alkyl
methyl
ylmethoxy
compound
phenyl
Prior art date
Application number
KR1020057015851A
Other languages
English (en)
Korean (ko)
Inventor
크리스티안 스타퍼
슈테파니 카일
하이너 글롬빅
오이겐 팔크
요헨 괴를리처
디르크 그레츠케
한스-루드빅 쉐퍼
볼프강 벤들러
Original Assignee
사노피-아벤티스 도이칠란트 게엠베하
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 사노피-아벤티스 도이칠란트 게엠베하 filed Critical 사노피-아벤티스 도이칠란트 게엠베하
Publication of KR20050105492A publication Critical patent/KR20050105492A/ko

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/32Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • 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
    • A61P3/06Antihyperlipidemics
    • 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
    • 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
    • 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
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/48Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/12Antidiuretics, e.g. drugs for diabetes insipidus
    • 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
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Diabetes (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Hematology (AREA)
  • Endocrinology (AREA)
  • Obesity (AREA)
  • Emergency Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)
KR1020057015851A 2003-02-27 2004-02-19 2형 당뇨병 및 아테롬성경화증 치료용 ppar조절제로서의4-(3-(2-페닐옥사졸-4-일메톡시)-사이클로헥실옥시)-부탄산유도체 및 관련 화합물 KR20050105492A (ko)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10308355.3 2003-02-27
DE10308355A DE10308355A1 (de) 2003-02-27 2003-02-27 Aryl-cycloalkyl substituierte Alkansäurederivate, Verfahren zu ihrer Herstellung und ihre Anwendung als Arzneimittel

Publications (1)

Publication Number Publication Date
KR20050105492A true KR20050105492A (ko) 2005-11-04

Family

ID=32920629

Family Applications (3)

Application Number Title Priority Date Filing Date
KR1020057015851A KR20050105492A (ko) 2003-02-27 2004-02-19 2형 당뇨병 및 아테롬성경화증 치료용 ppar조절제로서의4-(3-(2-페닐옥사졸-4-일메톡시)-사이클로헥실옥시)-부탄산유도체 및 관련 화합물
KR1020057016023A KR20050106462A (ko) 2003-02-27 2004-02-19 2형 당뇨병 및 죽상동맥경화증 치료용 ppar조절제로서의3-메틸-2-(3-(2-페닐-옥사졸-4-일메톡시)-사이클로헥산카보닐-아미노 부티르산 유도체 및 관련 화합물
KR1020057015995A KR20050106461A (ko) 2003-02-27 2004-02-19 타입 2 당뇨병과 죽상동맥경화증 치료에 ppar 조절제로사용되는 3-(2-페닐-옥사졸-4-일 메톡시)사이클로헥실메톡시 아세트산 유도체 및 이와 관련된화합물

Family Applications After (2)

Application Number Title Priority Date Filing Date
KR1020057016023A KR20050106462A (ko) 2003-02-27 2004-02-19 2형 당뇨병 및 죽상동맥경화증 치료용 ppar조절제로서의3-메틸-2-(3-(2-페닐-옥사졸-4-일메톡시)-사이클로헥산카보닐-아미노 부티르산 유도체 및 관련 화합물
KR1020057015995A KR20050106461A (ko) 2003-02-27 2004-02-19 타입 2 당뇨병과 죽상동맥경화증 치료에 ppar 조절제로사용되는 3-(2-페닐-옥사졸-4-일 메톡시)사이클로헥실메톡시 아세트산 유도체 및 이와 관련된화합물

Country Status (34)

Country Link
US (5) US7259177B2 (US07259177-20070821-C00114.png)
EP (3) EP1599452B1 (US07259177-20070821-C00114.png)
JP (3) JP2006519194A (US07259177-20070821-C00114.png)
KR (3) KR20050105492A (US07259177-20070821-C00114.png)
CN (3) CN100439347C (US07259177-20070821-C00114.png)
AR (3) AR043432A1 (US07259177-20070821-C00114.png)
AT (3) ATE430738T1 (US07259177-20070821-C00114.png)
AU (3) AU2004215677B2 (US07259177-20070821-C00114.png)
BR (3) BRPI0407814A (US07259177-20070821-C00114.png)
CA (3) CA2517386A1 (US07259177-20070821-C00114.png)
CL (2) CL2004000392A1 (US07259177-20070821-C00114.png)
CO (2) CO5690578A2 (US07259177-20070821-C00114.png)
DE (4) DE10308355A1 (US07259177-20070821-C00114.png)
DK (3) DK1599455T3 (US07259177-20070821-C00114.png)
EC (2) ECSP055986A (US07259177-20070821-C00114.png)
ES (3) ES2329366T3 (US07259177-20070821-C00114.png)
HR (3) HRP20050743A2 (US07259177-20070821-C00114.png)
IL (2) IL170316A (US07259177-20070821-C00114.png)
MA (3) MA27737A1 (US07259177-20070821-C00114.png)
MX (3) MXPA05008951A (US07259177-20070821-C00114.png)
NO (3) NO20054408L (US07259177-20070821-C00114.png)
OA (2) OA13034A (US07259177-20070821-C00114.png)
PA (1) PA8596801A1 (US07259177-20070821-C00114.png)
PE (3) PE20040959A1 (US07259177-20070821-C00114.png)
PL (3) PL377735A1 (US07259177-20070821-C00114.png)
PT (3) PT1599452E (US07259177-20070821-C00114.png)
RS (1) RS20050594A (US07259177-20070821-C00114.png)
RU (3) RU2005130002A (US07259177-20070821-C00114.png)
SA (1) SA04250153A (US07259177-20070821-C00114.png)
TN (2) TNSN05204A1 (US07259177-20070821-C00114.png)
TW (3) TW200510352A (US07259177-20070821-C00114.png)
UY (2) UY28210A1 (US07259177-20070821-C00114.png)
WO (3) WO2004076428A1 (US07259177-20070821-C00114.png)
ZA (2) ZA200505765B (US07259177-20070821-C00114.png)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6262118B1 (en) * 1999-06-04 2001-07-17 Metabolex, Inc. Use of (-) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of insulin resistance, type 2 diabetes and hyperlipidemia
US7576131B2 (en) 1999-06-04 2009-08-18 Metabolex, Inc. Use of (-) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of insulin resistance, type 2 diabetes, hyperlipidemia and hyperuricemia
US7399777B2 (en) * 2001-08-31 2008-07-15 Sanofi-Aventis Deutschland Gmbh Diarylcycloalkyl derivatives, processes for their preparation and their use as pharmceuticals
DE10308353A1 (de) * 2003-02-27 2004-12-02 Aventis Pharma Deutschland Gmbh Diarylcycloalkylderivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
DE102004038403B4 (de) * 2004-08-07 2006-08-31 Sanofi-Aventis Deutschland Gmbh Verfahren zur Herstellung der enantiomeren Formen von cis-konfigurierten 3-Hydroxycyclohexancarbonsäure-Derivaten
DE102004039532B4 (de) 2004-08-14 2006-09-21 Sanofi-Aventis Deutschland Gmbh Cyclohexyl-methyloxy substituierte Essigsäurederivate, Verfahren zu ihrer Herstellung und ihre Anwendung als Arzneimittel
DE102004039533B4 (de) * 2004-08-14 2006-09-28 Sanofi-Aventis Deutschland Gmbh Essigsäurederivate mit Cyclohexylmethoxy-Substituenten, Verfahren zu ihrer Herstellung und ihre Anwendung als Arzneimittel
DE102004039509B4 (de) 2004-08-14 2006-09-21 Sanofi-Aventis Deutschland Gmbh Aryl-cycloalkyl substituierte Alkansäurederivate, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
DE102004060227B3 (de) * 2004-12-15 2006-07-20 Sanofi-Aventis Deutschland Gmbh Verfahren zur Herstellung von Oxazolen durch Kondensation von aromatischen Aldehyden mit α-Ketoximen zu N-Oxiden und nachfolgende Reaktion mit aktivierten Säurederivaten
GT200600218A (es) * 2005-06-10 2007-03-28 Formulación y proceso de compresión directa
CN101272784A (zh) 2005-09-29 2008-09-24 塞诺菲-安万特股份有限公司 苯基-和吡啶基-1,2,4-噁二唑酮衍生物、它们的制备方法和它们作为药物的用途
BRPI0621960A2 (pt) 2006-08-10 2011-12-27 Wood One Co Ltd composiÇço hipoglicÊmica contendo derivado da casca de acÁcia
CN101801906A (zh) 2007-08-16 2010-08-11 索尔维公司 制备4-氟取代的3-氧代-烷酸酯的方法
UA104286C2 (uk) * 2008-02-29 2014-01-27 Нисан Кемикал Индастрис, Лтд. Спосіб одержання тіофенової сполуки та її проміжних сполук (варіанти)
US7615661B2 (en) * 2008-03-12 2009-11-10 International Flavors & Fragrances Inc. Thioester compounds and their use in fragrance or flavor applications
CN116224734A (zh) 2017-12-13 2023-06-06 佳能株式会社 盒与图像形成装置
CN109810071B (zh) * 2019-03-28 2023-04-21 中国科学院成都生物研究所 一种miRNA生物合成抑制剂

Family Cites Families (64)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2663336B1 (fr) 1990-06-18 1992-09-04 Adir Nouveaux derives peptidiques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
FR2663464B1 (fr) * 1990-06-19 1992-09-11 Commissariat Energie Atomique Circuit integre en technologie silicium sur isolant comportant un transistor a effet de champ et son procede de fabrication.
IL108634A0 (en) 1993-02-15 1994-05-30 Wellcome Found Hypolipidaemic heterocyclic compounds, their prepatation and pharmaceutical compositions containing them
IL108633A (en) 1993-02-15 1998-07-15 Wellcome Found History of Benzothiazepine Hypolipidemic Preparation and Pharmaceutical Preparations Containing Them
JP3144624B2 (ja) 1995-06-02 2001-03-12 杏林製薬株式会社 N−ベンジルジオキソチアゾリジルベンズアミド誘導体及びその製造法
WO1997026265A1 (en) 1996-01-17 1997-07-24 Novo Nordisk A/S Fused 1,2,4-thiadiazine and fused 1,4-thiazine derivatives, their preparation and use
UA72181C2 (uk) 1996-08-30 2005-02-15 Ново Нордіск А/С Похідна глюкагоноподібного пептиду-1 (варіанти), фармацевтична композиція та спосіб одержання лікувального засобу (варіанти), спосіб лікування діабету (варіанти) і ожиріння
TW492957B (en) 1996-11-07 2002-07-01 Novartis Ag N-substituted 2-cyanopyrrolidnes
HUP0301101A3 (en) 1996-12-31 2009-03-30 Reddy S Res Foundation Novel heterocyclic compounds process for their preparation and pharmaceutical compositions containing them and their use in the treatment of diabetes and related diseases
DE19726167B4 (de) * 1997-06-20 2008-01-24 Sanofi-Aventis Deutschland Gmbh Insulin, Verfahren zu seiner Herstellung und es enthaltende pharmazeutische Zubereitung
CN1264384A (zh) 1997-07-16 2000-08-23 诺沃挪第克公司 稠合1,2,4-噻二嗪衍生物及其制备方法和用途
CO4970713A1 (es) 1997-09-19 2000-11-07 Sanofi Synthelabo Derivados de carboxamidotiazoles, su preparacion, composiciones farmaceuticas que los contienen
ATE451346T1 (de) * 1998-03-10 2009-12-15 Ono Pharmaceutical Co Carbonsäurederivate und medikamente die diese als aktiven wirkstoff enthalten
DE19823831A1 (de) 1998-05-28 1999-12-02 Probiodrug Ges Fuer Arzneim Neue pharmazeutische Verwendung von Isoleucyl Thiazolidid und seinen Salzen
SE9801992D0 (sv) 1998-06-04 1998-06-04 Astra Ab New 3-aryl-2-hydroxypropionic acid derivative I
MA26634A1 (fr) 1998-06-04 2004-12-20 Astra Ab Nouveaux derives de l'acide 3-aryl propionique et analogues
US6221897B1 (en) * 1998-06-10 2001-04-24 Aventis Pharma Deutschland Gmbh Benzothiepine 1,1-dioxide derivatives, a process for their preparation, pharmaceuticals comprising these compounds, and their use
DE19828114A1 (de) 1998-06-24 2000-01-27 Probiodrug Ges Fuer Arzneim Produgs instabiler Inhibitoren der Dipeptidyl Peptidase IV
DE19828113A1 (de) 1998-06-24 2000-01-05 Probiodrug Ges Fuer Arzneim Prodrugs von Inhibitoren der Dipeptidyl Peptidase IV
WO2000012491A1 (fr) * 1998-08-27 2000-03-09 Ono Pharmaceutical Co., Ltd. Derives d'acide carboxylique et medicaments dont ils sont le principe actif
DE19845405C2 (de) * 1998-10-02 2000-07-13 Aventis Pharma Gmbh Arylsubstituierte Propanolaminderivate und deren Verwendung
GB9900416D0 (en) 1999-01-08 1999-02-24 Alizyme Therapeutics Ltd Inhibitors
DE19916108C1 (de) 1999-04-09 2001-01-11 Aventis Pharma Gmbh Mit Zuckerresten substituierte 1,4-Benzothiazepin-1,1-dioxidderivate, Verfahren zu deren Herstellung und deren Verwendung
JP2002542245A (ja) 1999-04-16 2002-12-10 ノボ ノルディスク アクティーゼルスカブ 置換イミダゾール、それらの製造および使用
US6908926B1 (en) * 1999-04-16 2005-06-21 Novo Nordisk A/S Substituted imidazoles, their preparation and use
WO2000064876A1 (en) * 1999-04-28 2000-11-02 Aventis Pharma Deutschland Gmbh Tri-aryl acid derivatives as ppar receptor ligands
DE60035682T2 (de) 1999-04-28 2008-04-30 Sanofi-Aventis Deutschland Gmbh Di-aryl-säurederivate als ppar rezeptor liganden
US6284766B1 (en) 1999-04-30 2001-09-04 Neurogen Corporation 9H-pyrimido [4,5-b] indole derivatives: CRF1 specific ligands
GB9911863D0 (en) 1999-05-21 1999-07-21 Knoll Ag Therapeutic agents
US6399640B1 (en) 1999-06-18 2002-06-04 Merck & Co., Inc. Arylthiazolidinedione and aryloxazolidinedione derivatives
AU5784000A (en) 1999-07-09 2001-01-30 Cohesion Technologies, Inc. Ecarin polypeptides, polynucleotides encoding ecarin, and methods for use thereof
EP1204654B1 (en) 1999-07-29 2003-07-23 Eli Lilly And Company Benzofurylpiperazines: 5-ht2c serotonin receptor agonists
AU774071B2 (en) * 1999-09-01 2004-06-17 Sanofi-Aventis Deutschland Gmbh Sulfonyl carboxamide derivatives, method for their production and their use as medicaments
TWI302149B (en) 1999-09-22 2008-10-21 Bristol Myers Squibb Co Substituted acid derivatives useful as antiodiabetic and antiobesity agents and method
JP2003515582A (ja) 1999-12-03 2003-05-07 アストラゼネカ アクチボラグ (s)−2−エトキシ−3−[4−(2−{4−メタンスルホニルオキシフェニル}エトキシ)フェニル]プロピオン酸の結晶形
SE9904413D0 (sv) 1999-12-03 1999-12-03 Astra Ab Comminuted form
ES2525041T3 (es) 2000-03-31 2014-12-16 Royalty Pharma Collection Trust Método para la mejora de la señalización de islotes en diabetes mellitus y para su prevención
MXPA02010545A (es) 2000-04-25 2004-05-14 Kyorin Seiyaku Kk Cristal estable novedoso de derivado de tiazolidinediona y proceso para producir el mismo.
CN1430603A (zh) 2000-04-28 2003-07-16 旭化成株式会社 新型双环化合物
AU5959201A (en) 2000-05-11 2001-11-20 Bristol Myers Squibb Co Tetrahydroisoquinoline analogs useful as growth hormone secretagogues
AU2001264977B2 (en) 2000-05-30 2005-04-14 Merck & Co., Inc. Melanocortin receptor agonists
SK17252002A3 (sk) * 2000-06-09 2003-05-02 Aventis Pharma Deutschland Gmbh Deriváty acylfenylmočoviny, spôsoby ich výroby a použitie ako liečivo
DE10038709A1 (de) 2000-08-09 2002-02-28 Aventis Pharma Gmbh Substituierte und unsubstituierte Benzooxathiazole sowie daraus abgeleitete Verbindungen
EP1182251A1 (en) * 2000-08-11 2002-02-27 Yissum Research Development Company of the Hebrew University of Jerusalem Methods for identifying compounds that inhibit ubiquitin-mediated proteolysis of IkB
AU2001284658A1 (en) 2000-08-23 2002-03-13 Eli Lilly And Company Oxazolyl-aryloxyacetic acid derivatives and their use as ppar agonists
JP2004506721A (ja) * 2000-08-23 2004-03-04 イーライ・リリー・アンド・カンパニー オキサゾリル−アリールプロピオン酸誘導体およびそのpparアゴニストとしての使用
TWI243162B (en) 2000-11-10 2005-11-11 Taisho Pharmaceutical Co Ltd Cyanopyrrolidine derivatives
WO2002046146A1 (fr) 2000-12-05 2002-06-13 Kyorin Pharmaceutical Co., Ltd. Derives d'acide carboxylique substitues
GB0031103D0 (en) * 2000-12-20 2001-01-31 Glaxo Group Ltd Chemical compounds
ES2277890T3 (es) 2000-12-21 2007-08-01 Sanofi-Aventis Deutschland Gmbh Nuevas difenilazetidinonas, procedimiento para su preparacion, medicamentos que contienen estos compuestos y su uso para el tratamiento de trastornos del metabolismo de lipidos.
PT1354879E (pt) * 2000-12-25 2007-10-29 Ono Pharmaceutical Co Compostos derivados de di-hidronaftaleno e medicamentos que utilizam estes compostos como ingrediente activo
BR0207285A (pt) * 2001-02-15 2004-02-10 Pfizer Producs Inc Agonistas de ppar
PE20021091A1 (es) 2001-05-25 2003-02-04 Aventis Pharma Gmbh Derivados de fenilurea sustituidos con carbonamida y procedimiento para su preparacion
IL159002A0 (en) * 2001-06-07 2004-05-12 Lilly Co Eli Modulators of peroxisome proliferator activated receptors (ppar)
DE10154689A1 (de) 2001-11-09 2003-05-22 Probiodrug Ag Substituierte Aminoketonverbindungen
WO2003005025A1 (en) 2001-07-03 2003-01-16 Biovitrum Ab Methods for identifying compounds modulating the activity of ppar-gamma
FR2827859B1 (fr) 2001-07-30 2005-09-23 Lipha Derives 4-(arylthio) - ou 4-(heteroarylthio) -butyrique dans la preparation de medicaments destines au traitement du diabete
CA2458210C (en) 2001-08-31 2011-09-20 Aventis Pharma Deutschland Gmbh Diaryl cycloalkyl derivatives, method for producing the same and the use thereof as ppar-activators
EP1474385B1 (en) 2002-02-05 2009-06-10 Eli Lilly And Company Urea linker derivatives for use as ppar modulators
DE10215908B4 (de) 2002-04-11 2005-08-18 Aventis Pharma Deutschland Gmbh Acyl-3-carboxyphenyl-harnstoffderivate und deren Verwendung als Arzneimittel
DE10215907A1 (de) 2002-04-11 2003-11-06 Aventis Pharma Gmbh Acyl-4-carboxyphenyl-harnstoffderivate, Verfahren zu deren Herstellung und deren Verwendung
DE10225635C1 (de) 2002-06-07 2003-12-24 Aventis Pharma Gmbh N-Benzoylureido-Zimtsäurederivate, Verfahren zu deren Herstellung und deren Verwendung
PL374860A1 (en) 2002-07-09 2005-11-14 Bristol-Myers Squibb Company Substituted heterocyclic derivatives useful as antidiabetic and antiobesity agents and method
US7148246B2 (en) * 2003-02-27 2006-12-12 Sanofi-Aventis Deutschland Gmbh Cycloalkyl derivatives having bioisosteric carboxylic acid groups, processes for their preparation and their use as pharmaceuticals

Also Published As

Publication number Publication date
EP1599455B1 (de) 2009-07-01
TNSN05206A1 (en) 2007-06-11
PT1599452E (pt) 2007-09-12
ATE435217T1 (de) 2009-07-15
NO20054398D0 (no) 2005-09-22
HRP20050743A2 (en) 2006-08-31
IL170316A (en) 2010-11-30
EP1599455A1 (de) 2005-11-30
MXPA05008951A (es) 2005-11-04
BRPI0407758A (pt) 2006-02-14
EP1599453B1 (de) 2009-05-06
EP1599452A1 (de) 2005-11-30
CA2517386A1 (en) 2004-09-10
RU2005130002A (ru) 2006-01-27
DE502004009690D1 (de) 2009-08-13
BRPI0407907A (pt) 2006-02-14
CN1756748A (zh) 2006-04-05
AU2004215673A1 (en) 2004-09-10
PE20050292A1 (es) 2005-05-24
JP2006519199A (ja) 2006-08-24
PE20040959A1 (es) 2005-01-17
RU2005129992A (ru) 2006-02-10
PL378437A1 (pl) 2006-04-03
AR043427A1 (es) 2005-07-27
OA13034A (en) 2006-11-10
AU2004215673B2 (en) 2009-10-01
NO20054396D0 (no) 2005-09-22
RU2005129995A (ru) 2006-01-27
EP1599453A1 (de) 2005-11-30
US7872034B2 (en) 2011-01-18
PL377735A1 (pl) 2006-02-20
WO2004076428A1 (de) 2004-09-10
DK1599453T3 (da) 2009-08-24
PT1599455E (pt) 2009-09-29
NO20054408D0 (no) 2005-09-22
DE10308355A1 (de) 2004-12-23
ZA200505768B (en) 2005-11-23
TW200508210A (en) 2005-03-01
CA2517381A1 (en) 2004-09-10
US7335671B2 (en) 2008-02-26
KR20050106462A (ko) 2005-11-09
CO5690578A2 (es) 2006-10-31
US20050101637A1 (en) 2005-05-12
US20080167354A1 (en) 2008-07-10
NO20054408L (no) 2005-11-23
PA8596801A1 (es) 2004-09-16
AR043432A1 (es) 2005-07-27
US20040209920A1 (en) 2004-10-21
WO2004076427A1 (de) 2004-09-10
AU2004215677A1 (en) 2004-09-10
HRP20050742A2 (en) 2006-09-30
US20050215596A1 (en) 2005-09-29
HRP20050744A2 (en) 2006-09-30
MXPA05008988A (es) 2005-10-18
TW200510352A (en) 2005-03-16
CL2004000391A1 (es) 2005-01-07
JP2006519194A (ja) 2006-08-24
PT1599453E (pt) 2009-07-14
JP2006519193A (ja) 2006-08-24
DK1599452T3 (da) 2007-10-01
EP1599452B1 (de) 2007-06-20
CA2516620A1 (en) 2004-09-10
ZA200505765B (en) 2006-05-31
ES2326418T3 (es) 2009-10-09
ECSP055986A (es) 2006-01-16
AU2004215672B2 (en) 2010-01-07
US7365084B2 (en) 2008-04-29
DE502004009453D1 (de) 2009-06-18
ATE365159T1 (de) 2007-07-15
CN100398526C (zh) 2008-07-02
CN100439345C (zh) 2008-12-03
UY28210A1 (es) 2004-09-30
CO5690580A2 (es) 2006-10-31
OA13035A (en) 2006-11-10
ES2329366T3 (es) 2009-11-25
ECSP055985A (es) 2006-01-16
AR043433A1 (es) 2005-07-27
IL170314A (en) 2010-11-30
US7259177B2 (en) 2007-08-21
MA27737A1 (fr) 2006-02-01
RS20050594A (en) 2007-12-31
NO20054398L (no) 2005-11-02
TW200500349A (en) 2005-01-01
ATE430738T1 (de) 2009-05-15
AU2004215672A1 (en) 2004-09-10
MA27736A1 (fr) 2006-02-01
AU2004215677B2 (en) 2010-01-07
SA04250153A (ar) 2005-12-03
DK1599455T3 (da) 2009-11-09
WO2004076426A1 (de) 2004-09-10
UY28209A1 (es) 2004-09-30
ES2287700T3 (es) 2007-12-16
BRPI0407814A (pt) 2006-02-14
NO20054396L (no) 2005-11-11
TNSN05204A1 (en) 2007-06-11
CN1753881A (zh) 2006-03-29
PE20050293A1 (es) 2005-05-24
MA27742A1 (fr) 2006-02-01
DE502004004139D1 (de) 2007-08-02
MXPA05008995A (es) 2005-10-18
US20080015238A1 (en) 2008-01-17
CN100439347C (zh) 2008-12-03
CL2004000392A1 (es) 2005-04-22
CN1753879A (zh) 2006-03-29
PL378130A1 (pl) 2006-03-06
KR20050106461A (ko) 2005-11-09

Similar Documents

Publication Publication Date Title
US7872034B2 (en) Arylcycloalkyl-substituted alkanoic acid derivatives, processes for their preparation and their use as pharmaceuticals
US7598281B2 (en) Arylcycloakyl-substituted alkanoic acid derivatives useful as peroxisome proliferator-activated receptor (PPAR) ligands for the treatment of hyperlipidemia and diabetes
US20040204462A1 (en) Diarylcycloalkyl derivatives, process for their preparation and their use as pharmaceuticals
AU2004216519B2 (en) 1,3-substituted cycloalkyl derivatives containing acidic, mainly heterocyclic groups, corresponding production method and use of said derivatives as medicaments
KR20050115255A (ko) 사이클로알킬-치환된 알칸산 유도체, 이의 제조 방법 및약제로서의 이의 용도
AU2004215676B2 (en) Cycloalkyl derivatives comprising bioisosteric carboxylic acid groups, method for the production thereof, and use thereof as a medicament
BRPI0611786A2 (pt) derivados de ácido benzóico substituìdo por 6-oxazol-4-ilmetóxi-alcoximetila formando ligandos de ppar, métodos para produção e o uso dos mesmos na forma de fármacos
KR20070046116A (ko) 고지질혈증 및 당뇨병 치료용 ppar 리간드〔퍼옥시좀증식체-활성화 수용체〕로서 사용된2-〔-3-'2-(페닐)-옥사졸-4-일메톡시메틸-사이클로헥실메톡시〕-프로피온산 유도체
MX2007000913A (es) Derivados del acido 2-{3-2-(fenil)-oxazol-4-ilmetoximetil-ciclohexilmetoxi] propionico utilizados como ligandos de ppar (receptores activados del proliferador de peroxisomas) para el tratamiento de hiperlipidemia y diabetes.

Legal Events

Date Code Title Description
A201 Request for examination
E902 Notification of reason for refusal
E601 Decision to refuse application