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NO20081369L - Fenyl- og pyridinyl-1,2,4-oksadiazolonderivater, fremgangsmate for deres fremstilling og deres anvendelse som farmasoytika - Google Patents

Fenyl- og pyridinyl-1,2,4-oksadiazolonderivater, fremgangsmate for deres fremstilling og deres anvendelse som farmasoytika

Info

Publication number
NO20081369L
NO20081369L NO20081369A NO20081369A NO20081369L NO 20081369 L NO20081369 L NO 20081369L NO 20081369 A NO20081369 A NO 20081369A NO 20081369 A NO20081369 A NO 20081369A NO 20081369 L NO20081369 L NO 20081369L
Authority
NO
Norway
Prior art keywords
disorders
phenyl
processes
pyridinyl
pharmaceuticals
Prior art date
Application number
NO20081369A
Other languages
English (en)
Inventor
Patrick Bernardelli
Stefanie Keil
Matthias Urmann
Wolfgang Wendler
Maike Glien
Karen Chandross
Lan Lee
Original Assignee
Sanofi Aventis
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.)
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35788653&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO20081369(L) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Sanofi Aventis filed Critical Sanofi Aventis
Publication of NO20081369L publication Critical patent/NO20081369L/no

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    • 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4245Oxadiazoles
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    • CCHEMISTRY; METALLURGY
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    • 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

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  • Health & Medical Sciences (AREA)
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Abstract

Oppfinnelsen angår fenyl-l,2,4-oksadiazolonderivater i alle deres stereoisomere former og blandinger i et hvilket som helst forhold og deres fysiologisk akseptable salter og tautomere former som viser PPAR5-agonistaktivitet. Det som er beskrevet er forbindelser med formel (I) hvori radikalene er som definert, og deres fysiologisk akseptable salter og fremgangsmåter for deres fremstillinger. Forbindelsene er egnet for behandling og/eller hindring av forstyrrelser vedrørende fettsyremetabolisme og glukoseutnyttingsforstyrrelser, så vel som forstyrrelser hvori insulinresistens er involvert og demyelinerende og andre neurodegenerative forstyrrelser i det sentrale og periferale nervesystemet.
NO20081369A 2005-09-29 2008-03-14 Fenyl- og pyridinyl-1,2,4-oksadiazolonderivater, fremgangsmate for deres fremstilling og deres anvendelse som farmasoytika NO20081369L (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP05021277 2005-09-29
PCT/EP2006/009303 WO2007039177A2 (en) 2005-09-29 2006-09-26 Phenyl- and pyridinyl- 1, 2 , 4 - oxadiazolone derivatives, processes for their preparation and their use as pharmaceuticals

Publications (1)

Publication Number Publication Date
NO20081369L true NO20081369L (no) 2008-05-28

Family

ID=35788653

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20081369A NO20081369L (no) 2005-09-29 2008-03-14 Fenyl- og pyridinyl-1,2,4-oksadiazolonderivater, fremgangsmate for deres fremstilling og deres anvendelse som farmasoytika

Country Status (23)

Country Link
US (1) US7709481B2 (no)
EP (1) EP1931337B1 (no)
JP (1) JP2009509988A (no)
KR (1) KR20080048504A (no)
CN (1) CN101272784A (no)
AR (1) AR056095A1 (no)
AU (1) AU2006299091A1 (no)
BR (1) BRPI0617207A2 (no)
CA (1) CA2624102A1 (no)
CR (1) CR9785A (no)
DO (1) DOP2006000203A (no)
EC (1) ECSP088322A (no)
IL (1) IL190231A0 (no)
MA (1) MA29805B1 (no)
NO (1) NO20081369L (no)
NZ (1) NZ566877A (no)
PE (1) PE20070620A1 (no)
RU (1) RU2008112198A (no)
TN (1) TNSN08148A1 (no)
TW (1) TW200806658A (no)
UY (1) UY29831A1 (no)
WO (1) WO2007039177A2 (no)
ZA (1) ZA200801629B (no)

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CN104640869B (zh) 2012-04-26 2017-12-12 百时美施贵宝公司 作为用于治疗血小板聚集的蛋白酶激活受体4(par4)抑制剂的咪唑并噻二唑和咪唑并哒嗪衍生物
CN104583218B (zh) 2012-04-26 2018-04-24 百时美施贵宝公司 作为蛋白酶活化受体4(par4)抑制剂用于治疗血小板聚集的咪唑并噻二唑和咪唑并吡嗪的衍生物
JP6181744B2 (ja) 2012-04-26 2017-08-16 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company 血小板凝集を治療するためのプロテアーゼ活性化受容体4(par4)阻害剤としてのイミダゾチアジアゾール誘導体
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