PE20080188A1 - Derivados del acido benzoazepin-oxi-acetico como agonistas de ppar-delta usados para aumentar hdl-c, reducir ldl-c y reducir colesterol - Google Patents

Derivados del acido benzoazepin-oxi-acetico como agonistas de ppar-delta usados para aumentar hdl-c, reducir ldl-c y reducir colesterol

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Publication number
PE20080188A1
PE20080188A1 PE2007000463A PE2007000463A PE20080188A1 PE 20080188 A1 PE20080188 A1 PE 20080188A1 PE 2007000463 A PE2007000463 A PE 2007000463A PE 2007000463 A PE2007000463 A PE 2007000463A PE 20080188 A1 PE20080188 A1 PE 20080188A1
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PE
Peru
Prior art keywords
reduce
ppar
acetic acid
benzoazepine
oxy
Prior art date
Application number
PE2007000463A
Other languages
English (en)
Inventor
Gee-Hong Kuo
Yan Zhang
Lan Shen
Songfeng Lu
Keith T Demarest
Patricia Pelton
Original Assignee
Janssen Pharmaceutica Nv
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=38610435&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20080188(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of PE20080188A1 publication Critical patent/PE20080188A1/es

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    • C07ORGANIC CHEMISTRY
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    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/06Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms
    • C07D233/08Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms
    • C07D233/12Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to ring carbon atoms with alkyl radicals, containing more than four carbon atoms, directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
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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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    • A61P3/00Drugs for disorders of the metabolism
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    • A61P3/06Antihyperlipidemics
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    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
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    • C07D223/14Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D223/16Benzazepines; Hydrogenated benzazepines
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    • 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
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    • C07D417/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms

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  • Diabetes (AREA)
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Abstract

SE REFIERE A UN COMPUESTO DE FORMULA I DONDE X ES UN ENLACE COVALENTE, O, S; R1 y R2 SON CADA UNO H, ALQUILO C1-C8 SUSTITUIDO O NO O FORMAN JUNTO AL ATOMO DE CARBONO CICLOALQUILO C3-C7; R3 ES H; R4 y R5 SON CADA UNO H, HALO, ALQUILO C1-C8, ENTRE OTROS; R6 y R7 SON CADA UNO H, HALO, ALQUILO C1-C3, ALCOXI C1-C3, ENTRE OTROS; n ES 1; Q ES 1,2-TIAZOL, TIAZOL, TIOFENO, 3-METILTIAZOL, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: ACIDO {3-[3-(4-TRIFLUOROMETIL-FENIL)ISOTIAZOL-5-ILMETIL]-2,3,4,5-TETRAHIDRO-1H-BENZO[d]AZEPIN-7-ILOXI)-ACETICO; ACIDO 2-METIL-2-{3-[3-(4-TRIFLUOROMETIL-FENIL)-ISOTIAZOL-5-ILMETIL} 2,3,4,5-TETRAHIDRO-1H-BENZO[d]AZEPIN-7-ILOXI}-PROPIONICO; ENTRE OTROS. SE REFIERE TAMBIEN UNA COMPOSICION FARMACEUTICA Y UN PROCEDIMIENTO DE PREPARACION. LOS COMPUESTOS DESCRITOS SON AGONISTAS DE RECEPTORES ACTIVADOS POR EL PROLIFERADOR DE PEROXISOMA (PPAR), UTILES EN EL TRATAMIENTO DE NEUROPATIA, RETINOPATIA, NEFROPATIA, CATARATAS, ATEROSCLEROSIS Y OTROS TRASTORNOS RELACIONADOS
PE2007000463A 2006-04-18 2007-04-16 Derivados del acido benzoazepin-oxi-acetico como agonistas de ppar-delta usados para aumentar hdl-c, reducir ldl-c y reducir colesterol PE20080188A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US79300106P 2006-04-18 2006-04-18

Publications (1)

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PE20080188A1 true PE20080188A1 (es) 2008-03-10

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ID=38610435

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PE2007000463A PE20080188A1 (es) 2006-04-18 2007-04-16 Derivados del acido benzoazepin-oxi-acetico como agonistas de ppar-delta usados para aumentar hdl-c, reducir ldl-c y reducir colesterol

Country Status (30)

Country Link
US (2) US7678786B2 (es)
EP (1) EP2010289B1 (es)
JP (1) JP5232771B2 (es)
KR (1) KR101472370B1 (es)
CN (1) CN101479008B (es)
AR (1) AR060489A1 (es)
AT (1) ATE535282T1 (es)
AU (1) AU2007237928B2 (es)
BR (1) BRPI0711695A2 (es)
CA (1) CA2649700C (es)
CO (1) CO6160296A2 (es)
CR (1) CR10447A (es)
EA (1) EA016583B1 (es)
EC (1) ECSP088841A (es)
ES (1) ES2375754T3 (es)
GT (1) GT200800226A (es)
HK (1) HK1124797A1 (es)
HN (1) HN2008001559A (es)
IL (1) IL194850A (es)
JO (1) JO3444B1 (es)
MX (1) MX2008013534A (es)
MY (1) MY144637A (es)
NO (1) NO344334B1 (es)
NZ (1) NZ571998A (es)
PE (1) PE20080188A1 (es)
TW (1) TWI404712B (es)
UA (1) UA96150C2 (es)
UY (1) UY30288A1 (es)
WO (1) WO2007121432A2 (es)
ZA (1) ZA200809790B (es)

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