NO20081829L - Biarylsubstituerte heterosykliske inhibitorer av LTA4H for behandling av inflammasjon - Google Patents

Biarylsubstituerte heterosykliske inhibitorer av LTA4H for behandling av inflammasjon

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Publication number
NO20081829L
NO20081829L NO20081829A NO20081829A NO20081829L NO 20081829 L NO20081829 L NO 20081829L NO 20081829 A NO20081829 A NO 20081829A NO 20081829 A NO20081829 A NO 20081829A NO 20081829 L NO20081829 L NO 20081829L
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NO
Norway
Prior art keywords
lta4h
biaryl
treatment
inflammation
substituted heterocyclic
Prior art date
Application number
NO20081829A
Other languages
English (en)
Inventor
Jasbir Singh
Mark Gurney
Peng Yu
Vincent Sandanayaka
Louis Bedell
Bjorn Mamat
Lei Zhao
Rama K Mishra
Original Assignee
Decode Genetics Ehf
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Publication date
Application filed by Decode Genetics Ehf filed Critical Decode Genetics Ehf
Publication of NO20081829L publication Critical patent/NO20081829L/no

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    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
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    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
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    • C07D211/20Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pulmonology (AREA)
  • Cardiology (AREA)
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  • Immunology (AREA)
  • Rheumatology (AREA)
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  • Urology & Nephrology (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
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  • Hydrogenated Pyridines (AREA)
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Abstract

Foreliggende oppfinnelse angår en kjemisk type biarylsubstituerte heterosykelinhibitorer av LTA4H (leukotrien A4-hydrolase) anvendelig for behandling og hindring og profylakse av infiammatoriske sykdommer og forstyrrelser. Forbindelsene har generell formel x¥.
NO20081829A 2005-09-21 2008-04-15 Biarylsubstituerte heterosykliske inhibitorer av LTA4H for behandling av inflammasjon NO20081829L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US71901605P 2005-09-21 2005-09-21
PCT/US2006/024393 WO2007040682A1 (en) 2005-09-21 2006-06-23 Biaryl substituted heterocycle inhibitors of lta4h for treating inflammation

Publications (1)

Publication Number Publication Date
NO20081829L true NO20081829L (no) 2008-06-19

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NO20081829A NO20081829L (no) 2005-09-21 2008-04-15 Biarylsubstituerte heterosykliske inhibitorer av LTA4H for behandling av inflammasjon

Country Status (15)

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US (3) US20070078263A1 (no)
EP (1) EP1926708B1 (no)
JP (1) JP5133889B2 (no)
KR (1) KR101328306B1 (no)
CN (1) CN101312948B (no)
AU (1) AU2006297798B2 (no)
BR (1) BRPI0616187A2 (no)
CA (1) CA2623348A1 (no)
EA (1) EA017618B1 (no)
IL (1) IL190372A0 (no)
NO (1) NO20081829L (no)
NZ (1) NZ566788A (no)
SG (1) SG166769A1 (no)
UA (1) UA101943C2 (no)
WO (2) WO2007040681A1 (no)

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JP4999923B2 (ja) * 2006-06-13 2012-08-15 中国科学院上海薬物研究所 複素環非ヌクレオシド系化合物、抗ウィルス医薬組成物、及びウィルス性疾病治療薬物
WO2008019302A1 (en) * 2006-08-04 2008-02-14 Decode Genetics Ehf Pyrazolylphenyl and pyrrolylphenyl inhibitors of lta4h for treating inflammation
CA2694362A1 (en) * 2007-07-27 2009-02-05 F. Hoffmann-La Roche Ag 2-azetidinemethaneamines and 2-pyrrolidinemethaneamines as taar-ligands
UY31443A1 (es) * 2007-10-31 2009-04-30 Diaminas en puente o fusionadas sustituidas con arilo como moduladores de leucotrieno a4 hidrolasa
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US20100112606A1 (en) * 2008-10-17 2010-05-06 Michael Armstrong Measurement and analysis of leukotrienes
CN102459251B (zh) * 2009-05-14 2015-05-20 詹森药业有限公司 作为白三烯a4水解酶的调节剂的具有两个稠合双环杂芳基部分的化合物
WO2011011598A1 (en) 2009-07-24 2011-01-27 Decode Genetics Ehf Process for preparing 4- { (s) -2- (4-(4-chlorophenoxy) phenoxymethyl) pyrrolidin-1-yl) } butyric acid and salts thereof
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US9139567B2 (en) 2011-07-19 2015-09-22 Boehringer Ingelheim International Gmbh Arylpyrazole ethers as inhibitors of leukotriene A4 hydrolase
US8946203B2 (en) 2012-03-06 2015-02-03 Boehringer Ingelheim International Gmbh Benzodioxane inhibitors of leukotriene production
AU2013229560A1 (en) 2012-03-06 2014-08-28 Boehringer Ingelheim International Gmbh Benzodioxanes in combination with other actives for inhibiting leukotriene production
AR090847A1 (es) * 2012-04-27 2014-12-10 Glaxo Group Ltd Compuestos moduladores del receptor huerfano retinoideo (ror)
JP6256467B2 (ja) * 2012-07-17 2018-01-10 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング ロイコトリエン生成を阻害するピラゾール誘導体
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BR112015022227A2 (pt) 2013-03-14 2017-07-18 Celtaxsys Inc inibidores de leucotrieno a4 hidrolase
RU2678196C2 (ru) 2013-03-14 2019-01-24 Селтакссис, Инк. Производные 2-фениламино-3-цианопиразоло[1,5-а]пиримидина, полезные в качестве ингибитора лейкотриен-a4-гидролазы
BR112015022226A2 (pt) 2013-03-14 2017-07-18 Celtaxsys Inc inibidores de leucotrieno a4 hidrolase
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