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SE0400850D0 - Novel Compounds - Google Patents

Novel Compounds

Info

Publication number
SE0400850D0
SE0400850D0 SE0400850A SE0400850A SE0400850D0 SE 0400850 D0 SE0400850 D0 SE 0400850D0 SE 0400850 A SE0400850 A SE 0400850A SE 0400850 A SE0400850 A SE 0400850A SE 0400850 D0 SE0400850 D0 SE 0400850D0
Authority
SE
Sweden
Prior art keywords
novel compounds
compounds
metalloproteinase
mmp
inhibitors
Prior art date
Application number
SE0400850A
Other languages
English (en)
Swedish (sv)
Inventor
Anders Eriksson
Matti Lepistoe
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Priority to SE0400850A priority Critical patent/SE0400850D0/xx
Publication of SE0400850D0 publication Critical patent/SE0400850D0/xx
Priority to JP2007506108A priority patent/JP2007530672A/ja
Priority to ES05722275T priority patent/ES2320679T3/es
Priority to CNA2005800176722A priority patent/CN1960979A/zh
Priority to EP05722275A priority patent/EP1732903B1/fr
Priority to AT05722275T priority patent/ATE423105T1/de
Priority to HK07105624.6A priority patent/HK1099751B/en
Priority to PCT/SE2005/000448 priority patent/WO2005095362A1/fr
Priority to DE602005012811T priority patent/DE602005012811D1/de
Priority to US10/593,543 priority patent/US20070219217A1/en
Priority to US12/538,522 priority patent/US20090299066A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C07D249/101,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
    • C07D249/12Oxygen or sulfur atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • 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
    • 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
    • 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
    • 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
    • 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

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
SE0400850A 2004-03-30 2004-03-30 Novel Compounds SE0400850D0 (sv)

Priority Applications (11)

Application Number Priority Date Filing Date Title
SE0400850A SE0400850D0 (sv) 2004-03-30 2004-03-30 Novel Compounds
US10/593,543 US20070219217A1 (en) 2004-03-30 2005-03-29 Triazolone Derivatives as Mmp Inhibitors for the Treatment of Asthma and Copd
EP05722275A EP1732903B1 (fr) 2004-03-30 2005-03-29 Derives de la triazolone utilises comme inhibiteurs de la mmp dans le traitement de l'asthme et de la bpco
ES05722275T ES2320679T3 (es) 2004-03-30 2005-03-29 Derivados de triazolona como inhibidores de mmp para el tratamiento del asma y epoc.
CNA2005800176722A CN1960979A (zh) 2004-03-30 2005-03-29 作为mmp抑制剂用于治疗哮喘和慢性阻塞性肺病的三唑酮衍生物
JP2007506108A JP2007530672A (ja) 2004-03-30 2005-03-29 喘息およびcopdの処置のためのmmp阻害剤としてのトリアゾロン誘導体
AT05722275T ATE423105T1 (de) 2004-03-30 2005-03-29 Triazolonderivate als mmp-inhibitoren zur behandlung von asthma und copd
HK07105624.6A HK1099751B (en) 2004-03-30 2005-03-29 Triazolone derivatives as mmp inhibitors for the treatment of asthma and copd
PCT/SE2005/000448 WO2005095362A1 (fr) 2004-03-30 2005-03-29 Derives de la triazolone utilises comme inhibiteurs de la mmp dans le traitement de l'asthme et de la bpco
DE602005012811T DE602005012811D1 (de) 2004-03-30 2005-03-29 Triazolonderivate als mmp-inhibitoren zur behandlung von asthma und copd
US12/538,522 US20090299066A1 (en) 2004-03-30 2009-08-10 Triazolone derivatives as mmp inhibitors for the treatment of asthma and copd

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE0400850A SE0400850D0 (sv) 2004-03-30 2004-03-30 Novel Compounds

Publications (1)

Publication Number Publication Date
SE0400850D0 true SE0400850D0 (sv) 2004-03-31

Family

ID=32105805

Family Applications (1)

Application Number Title Priority Date Filing Date
SE0400850A SE0400850D0 (sv) 2004-03-30 2004-03-30 Novel Compounds

Country Status (9)

Country Link
US (2) US20070219217A1 (fr)
EP (1) EP1732903B1 (fr)
JP (1) JP2007530672A (fr)
CN (1) CN1960979A (fr)
AT (1) ATE423105T1 (fr)
DE (1) DE602005012811D1 (fr)
ES (1) ES2320679T3 (fr)
SE (1) SE0400850D0 (fr)
WO (1) WO2005095362A1 (fr)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2331853T3 (es) 2005-06-28 2010-01-18 Sanofi-Aventis Derivados de isoquinolina como inhibidores de rho-cinasa.
ES2372067T3 (es) 2005-07-26 2012-01-13 Sanofi Derivados de ciclohexilamina isoquinolona como inhibidores de la rho-quinasa.
NZ565668A (en) 2005-07-26 2010-09-30 Sanofi Aventis Piperidinyl-substituted isoquinolone derivatives as RHO-kinase inhibitors
KR101517154B1 (ko) 2006-12-27 2015-04-30 사노피 Rho-키나제의 억제제로서의 치환된 이소퀴놀린 및 이소퀴놀리논 유도체
ATE502027T1 (de) 2006-12-27 2011-04-15 Sanofi Aventis Substituierte isochinoline und ihre verwendung als rho-kinase-inhibitoren
HRP20100705T1 (hr) 2006-12-27 2011-01-31 Sanofi-Aventis Cikloalkilaminski supstituirani izokinolinski i izokinolinonski derivati
RU2009128693A (ru) 2006-12-27 2011-02-10 Санофи-Авентис (Fr) Замещенные производные изохинолина и изохинолинона
CN101595094B (zh) 2006-12-27 2013-02-20 塞诺菲-安万特股份有限公司 环烷基胺取代的异喹诺酮衍生物
CA2673920C (fr) 2006-12-27 2015-03-24 Sanofi-Aventis Derives d'isoquinoline substitues par une cycloalkylamine
AU2009241365B2 (en) 2008-04-28 2015-01-22 Revalesio Corporation Compositions and methods for treating multiple sclerosis
AU2009262517B2 (en) 2008-06-24 2014-01-09 Sanofi Substituted isoquinolines and isoquinolinones as Rho kinase inhibitors
AU2009262509B2 (en) 2008-06-24 2014-01-30 Sanofi Bi-and polycyclic substituted isoquinoline and isoquinoline derivatives as Rho kinase inhibitors
ES2436531T3 (es) 2008-06-24 2014-01-02 Sanofi Isoquinolinas e isoquinolinonas sustituidas en posición 6
GB0813142D0 (en) 2008-07-17 2008-08-27 Glaxo Group Ltd Novel compounds
GB0813144D0 (en) 2008-07-17 2008-08-27 Glaxo Group Ltd Novel compounds
CN102858175A (zh) * 2010-02-22 2013-01-02 葛兰素史密斯克莱有限责任公司 作为脂肪酸合成酶抑制剂的三唑酮
EP2575815A4 (fr) 2010-06-04 2013-12-25 Albany Molecular Res Inc Inhibiteurs du transporteur 1 de la glycine, procédés de fabrication associés, et utilisations associées
WO2013134562A1 (fr) 2012-03-09 2013-09-12 Inception 2, Inc. Composés de triazolone et leurs utilisations
MX376108B (es) 2012-12-20 2025-03-07 Tempest Therapeutics Inc Compuestos de triazolona y usos de los mismos.
KR20160048988A (ko) 2013-09-06 2016-05-04 인셉션 2 인코퍼레이티드 트라이아졸론 화합물 및 이의 용도
CN104876917B (zh) * 2015-06-16 2017-09-19 上海皓元医药股份有限公司 用作脂肪酸合成酶抑制剂的三唑酮的合成方法

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19504627A1 (de) * 1995-02-13 1996-08-14 Bayer Ag Verfahren und neue Zwischenprodukte zur Herstellung von Triazolinonen
EP1187614A4 (fr) * 1999-06-04 2005-06-22 Merck & Co Inc Piperidines substituees en tant qu'agonistes du recepteur de melanocortine-4
AU1196601A (en) * 1999-10-12 2001-04-23 Board Of Trustees Of The Leland Stanford Junior University Methods of diagnosing and treating urinary incontinence
EP1110958A1 (fr) * 1999-12-20 2001-06-27 Ucb, S.A. Derivés de pipérazines-alpha-aryléthyles comme antagonistes de neurokinines
WO2001070734A2 (fr) * 2000-03-17 2001-09-27 Bristol-Myers Squibb Pharma Company DERIVES DE β-AMINOACIDES EN TANT QU'INHIBITEURS DE METALLOPROTEASES MATRICIELLES ET DE TNF-$g(a)
GB0203412D0 (en) * 2002-02-13 2002-04-03 Pharmagene Lab Ltd 5-HT 2B receptor antagonists
DE60332816D1 (de) * 2002-03-13 2010-07-15 Schering Corp Nk1-antagonisten
AR039625A1 (es) * 2002-04-18 2005-03-02 Merck & Co Inc Proceso para la preparacion de 5-((2(r)--(1(r)- (3,5-bis (trifluormetil) fenil)etoxi-3 (s) - (4-fluorfenil) -4-morfolinil) metil) -1,2-dihidro-3h-1,2,4-triazol-3-ona
US20040010010A1 (en) * 2002-04-30 2004-01-15 Ebetino Frank Hallock Melanocortin receptor ligands
AU2003241903A1 (en) * 2002-05-31 2003-12-19 Takeda Pharmaceutical Company Limited Piperidine derivative, process for producing the same, and use
SE0202539D0 (sv) * 2002-08-27 2002-08-27 Astrazeneca Ab Compounds
KR20060106106A (ko) * 2005-04-06 2006-10-12 삼성전자주식회사 고속 레벨 쉬프터

Also Published As

Publication number Publication date
ATE423105T1 (de) 2009-03-15
HK1099751A1 (en) 2007-08-24
EP1732903A1 (fr) 2006-12-20
US20070219217A1 (en) 2007-09-20
EP1732903B1 (fr) 2009-02-18
US20090299066A1 (en) 2009-12-03
WO2005095362A1 (fr) 2005-10-13
DE602005012811D1 (de) 2009-04-02
JP2007530672A (ja) 2007-11-01
CN1960979A (zh) 2007-05-09
ES2320679T3 (es) 2009-05-27

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