ATE528307T1 - Imidazopyridin-2-onderivate als inhibitoren von endothellipase - Google Patents

Imidazopyridin-2-onderivate als inhibitoren von endothellipase

Info

Publication number
ATE528307T1
ATE528307T1 AT07723584T AT07723584T ATE528307T1 AT E528307 T1 ATE528307 T1 AT E528307T1 AT 07723584 T AT07723584 T AT 07723584T AT 07723584 T AT07723584 T AT 07723584T AT E528307 T1 ATE528307 T1 AT E528307T1
Authority
AT
Austria
Prior art keywords
alkyl
cycloalkyl
aryl
bicyclic
ocoa
Prior art date
Application number
AT07723584T
Other languages
English (en)
Inventor
Gerhard Zoller
Stefan Petry
Markus Follmann
Guenter Mueller
Norbert Tennagels
Original Assignee
Sanofi Sa
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 Sanofi Sa filed Critical Sanofi Sa
Application granted granted Critical
Publication of ATE528307T1 publication Critical patent/ATE528307T1/de

Links

Classifications

    • 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
    • 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
    • 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
    • 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
    • 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
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Diabetes (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Emergency Medicine (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
AT07723584T 2006-03-28 2007-03-26 Imidazopyridin-2-onderivate als inhibitoren von endothellipase ATE528307T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102006014685A DE102006014685A1 (de) 2006-03-28 2006-03-28 Imidazo-pyridin-2-on-derivate als Inhibitoren von Lipasen und Phospholiphasen
PCT/EP2007/002637 WO2007110215A1 (en) 2006-03-28 2007-03-26 Imidazopyridin-2-one derivatives as inhibitors of endothelial lipase

Publications (1)

Publication Number Publication Date
ATE528307T1 true ATE528307T1 (de) 2011-10-15

Family

ID=38179814

Family Applications (1)

Application Number Title Priority Date Filing Date
AT07723584T ATE528307T1 (de) 2006-03-28 2007-03-26 Imidazopyridin-2-onderivate als inhibitoren von endothellipase

Country Status (14)

Country Link
US (1) US7897616B2 (de)
EP (1) EP2001878B1 (de)
JP (1) JP2009531356A (de)
KR (1) KR20080104341A (de)
CN (1) CN101405288A (de)
AT (1) ATE528307T1 (de)
AU (1) AU2007229708A1 (de)
BR (1) BRPI0709211A2 (de)
CA (1) CA2647422A1 (de)
DE (1) DE102006014685A1 (de)
MX (1) MX2008012126A (de)
NO (1) NO20084419L (de)
TW (1) TW200815434A (de)
WO (1) WO2007110215A1 (de)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2025674A1 (de) 2007-08-15 2009-02-18 sanofi-aventis Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
UY31968A (es) 2008-07-09 2010-01-29 Sanofi Aventis Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos
EP2351744B1 (de) 2008-10-17 2015-01-07 Shionogi & Co., Ltd. Essigsäureamidderivat mit hemmender wirkung auf vaskuläre endothellipase
WO2011034741A1 (en) * 2009-09-15 2011-03-24 Merck Sharp & Dohme Corp. Imidazopyridin-2-one derivatives
US9556201B2 (en) * 2009-10-29 2017-01-31 Glaxosmithkline Llc Bicyclic pyridines and analogs as sirtuin modulators
US8754113B2 (en) 2009-12-15 2014-06-17 Shionogi & Co., Ltd. Oxadiazole derivative having endothelial lipase inhibitory activity
EP2582709B1 (de) 2010-06-18 2018-01-24 Sanofi Azolopyridin-3-on-derivate als inhibitoren von lipasen und phospholipasen
WO2012030165A2 (ko) 2010-08-31 2012-03-08 서울대학교산학협력단 P P A R δ 활성물질의 태자재프로그래밍용도
WO2013048928A1 (en) 2011-09-27 2013-04-04 Bristol-Myers Squibb Company Pyrrolinone carboxamide compounds useful as endothelial lipase inhibitors
WO2013049096A1 (en) 2011-09-27 2013-04-04 Bristol-Myers Squibb Company Pyrrolinone carboxamide compounds useful as endothelial lipase inhibitors
WO2013048982A1 (en) 2011-09-27 2013-04-04 Bristol-Myers Squibb Company Pyrrolinone carboxamide compounds useful as endothelial lipase inhibitors
WO2013048942A1 (en) 2011-09-30 2013-04-04 Bristol-Myers Squibb Company Quinolinone carboxamide inhibitors of endothelial lipase
US8993557B2 (en) 2011-09-30 2015-03-31 Bristol-Myers Squibb Company Pyridinedione carboxamide inhibitors of endothelial lipase
US8933235B2 (en) 2011-09-30 2015-01-13 Bristol-Myers Squibb Company Pyridinedione carboxamide inhibitors of endothelial lipase
WO2013151877A1 (en) 2012-04-03 2013-10-10 Bristol-Myers Squibb Company Pyrimidinedione carboxamide inhibitors of endothelial lipase
WO2013151923A1 (en) 2012-04-03 2013-10-10 Bristol-Myers Squibb Company Pyrimidinone carboxamides as inhibitors of endothelial lipase
WO2014011513A1 (en) 2012-07-09 2014-01-16 Bristol-Myers Squibb Company Sulfonyl containing benzothiazole inhibitors of endothelial lipase
EP2870152B1 (de) 2012-07-09 2016-09-28 Bristol-Myers Squibb Company Amid- oder harnstoff-substituierte benzothiazolderivate als inhibitoren von endothellipase
EP2875007B1 (de) 2012-07-19 2016-08-24 Bristol-Myers Squibb Company Amid-, harnstoff- oder sulfonamidgebundene benzothiazolinhibitoren der endothellipase
WO2014042939A1 (en) 2012-09-11 2014-03-20 Bristol-Myers Squibb Company Ketone linked benzothiazole inhibitors of endothelial lipase
WO2015105749A1 (en) 2014-01-07 2015-07-16 Bristol-Myers Squibb Company Sulfone amide linked benzothiazole inhibitors of endothelial lipase
US10597370B2 (en) 2016-06-06 2020-03-24 Bristol-Myers Squibb Company 2-(benzothiazol-2-yl)-2-cyano-acetamide derivatives and their use as endothelial lipase inhibitors

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE422799B (sv) * 1975-05-28 1982-03-29 Merck & Co Inc Analogiforfarande for framstellning av 1,3-dihydroimidazo (4,5-b)pyridin-2-oner
WO2002030886A2 (en) * 2000-10-12 2002-04-18 Matthews Barry R Heterocyclic angiogenesis inhibitors
DE102004005172A1 (de) * 2004-02-02 2005-08-18 Aventis Pharma Deutschland Gmbh Indazolderivate als Inhibitoren der Hormon Sensitiven Lipase
CN101076334A (zh) * 2004-05-28 2007-11-21 默克公司 具有抗糖尿病活性的苯并脲类化合物
EP1861377B1 (de) * 2005-03-15 2010-12-29 Pfizer, Inc. Benzimidazolonderivate als cb2-rezeptor-liganden
DE102005026762A1 (de) * 2005-06-09 2006-12-21 Sanofi-Aventis Deutschland Gmbh Azolopyridin-2-on-derivate als Inhibitoren von Lipasen und Phospholipasen

Also Published As

Publication number Publication date
AU2007229708A1 (en) 2007-10-04
US20090076068A1 (en) 2009-03-19
KR20080104341A (ko) 2008-12-02
NO20084419L (no) 2008-11-26
JP2009531356A (ja) 2009-09-03
US7897616B2 (en) 2011-03-01
CA2647422A1 (en) 2007-10-04
DE102006014685A1 (de) 2007-10-04
MX2008012126A (es) 2008-10-03
EP2001878A1 (de) 2008-12-17
EP2001878B1 (de) 2011-10-12
TW200815434A (en) 2008-04-01
BRPI0709211A2 (pt) 2011-06-28
CN101405288A (zh) 2009-04-08
WO2007110215A1 (en) 2007-10-04

Similar Documents

Publication Publication Date Title
ATE528307T1 (de) Imidazopyridin-2-onderivate als inhibitoren von endothellipase
PE20120120A1 (es) DERIVADOS DE 2H-PIRAZOLO[3,4-d]PIRIMIDINA-4,6(5H,7H)-DIONA, COMO INHIBIDORES DE PDE1
SG151286A1 (en) 5-substituted-2-phenylamino-benzamide as mek inhibitor
PE20091573A1 (es) Derivados heterociclicos de urea como inhibidores de adn girasa y/o topoisomerasa
PE20090773A1 (es) Derivados de morfolina pirimidina
PE20061124A1 (es) Compuestos y derivados de dibencil amina
PE20060691A1 (es) Serinamidas sustituidas por benzoilo
ATE432259T1 (de) Pyridinderivate als dipeptedyl-peptidase-hemmer
PE20091201A1 (es) AMIDAS SUSTITUIDAS COMO INHIBIDORES DE LA TIROSINA QUINASA DE BRUTON (Btk)
AR079541A1 (es) Compuestos sustituidos de n-(1h-indazol-4-il) imidazo (1,2-a) piridin-3-carboxamida como inhibidores de cfms
PT1539734E (pt) Derivados da quinolil propil piperidina e sua utilizacao como agentes antimicrobianos
PE20071176A1 (es) Derivados diamina como inhibidores de leucotrieno a4 hidrolasa
CA2412718A1 (en) Viral polymerase inhibitors
MX2008013836A (es) Derivados de 2-piridona para el tratamiento de enfermedades o condiciones en las cuales es benefica la inhibicion de la actividad de elastasa de neutrofilos.
NO20075059L (no) Nye forbindelser II 2-pyridinderivater som inhibitorer av neutrofil elastase
ATE420639T1 (de) Antimykotische mittel
NZ612544A (en) Heterocyclic compounds suitable for the treatment of dyslipidemia
TW200640879A (en) Amide derivatives
EP1921077A4 (de) Mittel zur behandlung und/oder prävention von schlafstörungen
GT200600105A (es) Derivados de pirimidina para el tratamiento de trastornos hiperproliferativos.
PE20061394A1 (es) Metabolitos de n-(2-cloro-6-metilfenil)-2-[[6-[4-(2-hidroxietil)-1-piperazinil]-2-metil-4-pirimidinil]amino]-5-tiazolcarboxamidas
ATE476431T1 (de) Piperidin- und azetidinderivate als glyt1- inhibitoren
PE20091455A1 (es) Triazolopiridazinas como inhibidores de par1, su preparacion y uso como medicamentos
HRP20090264T1 (hr) Derivati fenil-piperazin metanona
RU2007139928A (ru) Производное бензимидазола и применение в качестве антагониста ангиотензина

Legal Events

Date Code Title Description
RER Ceased as to paragraph 5 lit. 3 law introducing patent treaties