NO20080497L - Pyrrolopyridinderivater og anvendelse av disse som PPAR-reseptormodulatorer - Google Patents

Pyrrolopyridinderivater og anvendelse av disse som PPAR-reseptormodulatorer

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Publication number
NO20080497L
NO20080497L NO20080497A NO20080497A NO20080497L NO 20080497 L NO20080497 L NO 20080497L NO 20080497 A NO20080497 A NO 20080497A NO 20080497 A NO20080497 A NO 20080497A NO 20080497 L NO20080497 L NO 20080497L
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NO
Norway
Prior art keywords
ppar
alkyl
pyrrolopyridine derivatives
salts
new
Prior art date
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NO20080497A
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English (en)
Other versions
NO340681B1 (no
Inventor
Pierre Dodey
Christiane Legendre
Martine Barth
Olivia Poupardin-Olivier
Boubia Benaissa
Jean Binet
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Inventiva
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Publication date
Application filed by Inventiva filed Critical Inventiva
Publication of NO20080497L publication Critical patent/NO20080497L/no
Publication of NO340681B1 publication Critical patent/NO340681B1/no

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    • 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
    • C07D207/46Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
    • C07D207/48Sulfur atoms
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61P25/28Drugs 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
    • 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
    • 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
    • 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
    • A61P9/10Drugs 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
    • 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
    • C07D213/61Halogen atoms or nitro radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

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

Abstract

Oppfinnelsen angår pyrrolopyridinbaserte forbindelser med generell formel (I): (I) slik som definert i kravene, og til de farmasøytisk akseptable addisjonssaltene derav. Oppfinnelsen angår også fremgangsmåten for fremstilling av nevnte forbindelser, til farmasøytiske preparater som inneholder dem og til anvendelse av dem som farmakologisk aktive substanser, spesielt ved behandling av hypertriglyceridemi, hyperlipidemi, hyperkolesterolemi, diabetes, endotel funksjonsforstyrrelse, kardiovaskulære sykdommer, inflammatoriske sykdommer og neurodegenerative sykdommer.
NO20080497A 2005-09-01 2008-01-28 Pyrrolopyridinderivater, framgangsmåte for fremstilling, farmasøytisk praparater omfattende slike, slike forbindelser som farmakologisk aktive substanser samt anvendelse av slike forbindelser og preparater for behandling av sykdom NO340681B1 (no)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US71345905P 2005-09-01 2005-09-01
FR0510482A FR2890072A1 (fr) 2005-09-01 2005-10-14 Nouveaux composesde pyrrolopyridine
PCT/FR2006/050827 WO2007026104A1 (fr) 2005-09-01 2006-08-31 Derives de pyrrolopyridine et leurs utilisations comme modulateurs des recepteurs ppar

Publications (2)

Publication Number Publication Date
NO20080497L true NO20080497L (no) 2008-02-29
NO340681B1 NO340681B1 (no) 2017-05-29

Family

ID=37735036

Family Applications (1)

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NO20080497A NO340681B1 (no) 2005-09-01 2008-01-28 Pyrrolopyridinderivater, framgangsmåte for fremstilling, farmasøytisk praparater omfattende slike, slike forbindelser som farmakologisk aktive substanser samt anvendelse av slike forbindelser og preparater for behandling av sykdom

Country Status (27)

Country Link
US (2) US7557122B2 (no)
EP (1) EP1919474B1 (no)
JP (1) JP5232000B2 (no)
KR (1) KR101289589B1 (no)
CN (1) CN101242833B (no)
AT (1) ATE438396T1 (no)
AU (1) AU2006286348B2 (no)
BR (1) BRPI0615335A2 (no)
CA (1) CA2620662C (no)
DE (1) DE602006008320D1 (no)
DK (1) DK1919474T3 (no)
EA (1) EA014185B1 (no)
ES (1) ES2331336T3 (no)
FR (1) FR2890072A1 (no)
HK (1) HK1116698A1 (no)
HR (1) HRP20090512T1 (no)
IL (1) IL189189A (no)
MX (1) MX2008003038A (no)
MY (1) MY142983A (no)
NO (1) NO340681B1 (no)
PL (1) PL1919474T3 (no)
PT (1) PT1919474E (no)
SI (1) SI1919474T1 (no)
TN (1) TNSN08091A1 (no)
UA (1) UA92026C2 (no)
WO (1) WO2007026104A1 (no)
ZA (1) ZA200801885B (no)

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* Cited by examiner, † Cited by third party
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RU2007145434A (ru) * 2005-05-10 2009-06-20 Вертекс Фармасьютикалз Инкорпорейтед (Us) Бициклические производные в качестве модуляторов ионных каналов
FR2890071B1 (fr) * 2005-08-30 2007-11-09 Fournier Sa Sa Lab Nouveaux composes de l'indole
PE20090159A1 (es) * 2007-03-08 2009-02-21 Plexxikon Inc COMPUESTOS DERIVADOS DE ACIDO INDOL-PROPIONICO COMO MODULADORES PPARs
JP2010528991A (ja) * 2007-05-21 2010-08-26 エスジーエックス ファーマシューティカルズ、インコーポレイテッド 複素環式キナーゼ調節因子
FR2955110A1 (fr) * 2010-01-08 2011-07-15 Fournier Lab Sa Nouveaux derives de type pyrrolopyridine benzoique
FR2955108B1 (fr) 2010-01-08 2012-03-16 Fournier Lab Sa Utilisation de derives de pyrrolopyridine comme activateurs de nurr-1, pour le traitement de la maladie de parkinson
WO2013122897A1 (en) * 2012-02-13 2013-08-22 Amgen Inc. Dihydrobenzoxazine and tetrahydroquinoxaline sodium channel inhibitors
WO2013134518A1 (en) 2012-03-09 2013-09-12 Amgen Inc. Sulfamide sodium channel inhibitors
GB201317363D0 (en) * 2013-10-01 2013-11-13 Eisai Ltd Novel compounds
CN103630519A (zh) * 2013-12-03 2014-03-12 华东理工大学 应用pH敏感的比率荧光蛋白检测酶-前药反应的方法
CN108164528B (zh) * 2018-03-31 2019-03-22 杭州巴洛特生物科技有限公司 一种酰胺类衍生物及其在高血压、高血脂和动脉粥样硬化中的应用
CN108456207B (zh) * 2018-03-31 2020-11-20 浙江药苑生物科技有限公司 一种酰胺类衍生物及其在心脑血管方面的应用
CN108218865B (zh) * 2018-03-31 2020-06-26 济南市儿童医院 一种酰胺类衍生物及其在心脑血管方面的应用
CN108383838B (zh) * 2018-03-31 2020-08-28 浙江药苑生物科技有限公司 一种酰胺类衍生物及其在高血压、高血脂和动脉粥样硬化中的应用
CN111793066B (zh) * 2020-07-17 2022-04-08 瀚海新拓(杭州)生物医药有限公司 苯并五元杂环磺酰胺类化合物、其制备方法、药物组合物及应用

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WO1997028149A1 (en) 1996-02-02 1997-08-07 Merck & Co., Inc. Method for raising hdl cholesterol levels
EA002817B1 (ru) 1996-12-13 2002-10-31 Авентис Фармасьютикалз Продактс Инк. Соединения сульфоновой кислоты или сульфониламино-n-(гетероаралкил)азагетероциклиламида
WO2001060807A1 (en) 2000-02-18 2001-08-23 Merck & Co. Inc. Aryloxyacetic acids for diabetes and lipid disorders
WO2002071827A2 (en) 2001-03-14 2002-09-19 Eli Lilly And Company Retinoid x receptor modulators
MXPA04004711A (es) * 2001-11-19 2005-08-16 Neurogen Corp Amidas del acido 1h-pirrolo(3,2-b(piridin-3-carboxilico.
DE10229777A1 (de) * 2002-07-03 2004-01-29 Bayer Ag Indolin-Phenylsulfonamid-Derivate
DE10300099A1 (de) 2003-01-07 2004-07-15 Bayer Healthcare Ag Indol-Phenylsulfonamid-Derivate
US20050014753A1 (en) * 2003-04-04 2005-01-20 Irm Llc Novel compounds and compositions as protein kinase inhibitors
KR20130023381A (ko) * 2003-07-17 2013-03-07 플렉시콘, 인코퍼레이티드 Ppar 활성 화합물
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Also Published As

Publication number Publication date
HK1116698A1 (en) 2009-01-02
US7557122B2 (en) 2009-07-07
BRPI0615335A2 (pt) 2012-12-11
ATE438396T1 (de) 2009-08-15
ES2331336T3 (es) 2009-12-29
UA92026C2 (uk) 2010-09-27
FR2890072A1 (fr) 2007-03-02
DE602006008320D1 (de) 2009-09-17
DK1919474T3 (da) 2009-11-09
JP5232000B2 (ja) 2013-07-10
AU2006286348A1 (en) 2007-03-08
AU2006286348B2 (en) 2012-04-26
EA200800352A1 (ru) 2008-06-30
EP1919474A1 (fr) 2008-05-14
JP2009507007A (ja) 2009-02-19
CN101242833A (zh) 2008-08-13
US7728002B2 (en) 2010-06-01
NO340681B1 (no) 2017-05-29
ZA200801885B (en) 2009-08-26
CA2620662C (fr) 2015-10-06
WO2007026104A1 (fr) 2007-03-08
IL189189A0 (en) 2008-06-05
IL189189A (en) 2013-10-31
CA2620662A1 (fr) 2007-03-08
CN101242833B (zh) 2012-06-27
PT1919474E (pt) 2009-10-28
KR20080039908A (ko) 2008-05-07
SI1919474T1 (sl) 2009-12-31
EA014185B1 (ru) 2010-10-29
TNSN08091A1 (fr) 2009-07-14
MX2008003038A (es) 2008-03-24
EP1919474B1 (fr) 2009-08-05
MY142983A (en) 2011-02-14
US20090239856A1 (en) 2009-09-24
PL1919474T3 (pl) 2010-03-31
HRP20090512T1 (hr) 2009-12-31
KR101289589B1 (ko) 2013-07-24
US20080200495A1 (en) 2008-08-21

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