PE20070820A1 - Derivados de triazolopiridina en calidad de inhibidores de lipasas y fosfolipasas - Google Patents

Derivados de triazolopiridina en calidad de inhibidores de lipasas y fosfolipasas

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Publication number
PE20070820A1
PE20070820A1 PE2006001256A PE2006001256A PE20070820A1 PE 20070820 A1 PE20070820 A1 PE 20070820A1 PE 2006001256 A PE2006001256 A PE 2006001256A PE 2006001256 A PE2006001256 A PE 2006001256A PE 20070820 A1 PE20070820 A1 PE 20070820A1
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PE
Peru
Prior art keywords
lipase
methanone
triazolo
pyridin
quality
Prior art date
Application number
PE2006001256A
Other languages
English (en)
Inventor
Hubert Heuer
Stefan Petry
Karl-Heinz Baringhaus
Gunter Muller
Gerhard Zoller
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.)
Filing date
Publication date
Application filed by Sanofi Aventis filed Critical Sanofi Aventis
Publication of PE20070820A1 publication Critical patent/PE20070820A1/es

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    • 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
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

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Abstract

SE REFIERE A UN COMPUESTO DE FORMULA I, DONDE X =C(-R)-, =N-, EN LA QUE AL MENOS 1 O A LO SUMO 2 X ES/SON =N-; W ES -(C=O)-, -(S=O)-, -(SO2)-; R ES H, HALOGENO, HALOALQUILO C1-C3, ALQUILOXI C1-C3, ENTRE OTROS; R1 ES ALQUILO C5-C16, CICLOALQUILO C5-C12, BICICLO, TRIFLUOROMETOXI, ENTRE OTROS; R2 ES H, ALQUILO C4-C12, O R1 Y R2 PUEDEN FORMAR UN SISTEMA DE ANILLO DE 4 A 7 MIEMBROS, MONOCICLICO, SATURADO O PARCIALMENTE INSATURADO, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: (5-CLORO-[1,2,3]TRIAZOLO[4,5-b]PIRIDIN-1-IL)-(3,4-DIHIDRO-1H-ISOQUINOLIN-2-IL)-METANONA; (5-CLORO-[1,2,3]TRIAZOLO[4,5-b]PIRIDIN-1-IL)-(3,4-DIHIDRO-1H-ISOQUINOLIN-2-IL)-METANONA; (4-METILPIPERIDIN-1-IL)-[1,2,3]TRIAZOLO[4,5-c]PIRIDIN-1-IL-METANONA. REFERIDA TAMBIEN A UNA COMPOSICION FARMACEUTICA Y A UN PROCEDIMIENTO DE PREPARACION. DICHOS COMPUESTOS SON INHIBIDORES DE LIPASA SENSIBLE A HORMONAS O DE LIPASA ENDOTELIAL UTILES EN TRASTORNOS DEL METABOLISMO DE LOS ACIDOS GRASOS Y TRASTORNOS DE UTILIZACION DE GLUCOSA, SINDROME METABOLICO, DIABETES, ENTRE OTROS
PE2006001256A 2005-10-19 2006-10-17 Derivados de triazolopiridina en calidad de inhibidores de lipasas y fosfolipasas PE20070820A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102005049954A DE102005049954A1 (de) 2005-10-19 2005-10-19 Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen

Publications (1)

Publication Number Publication Date
PE20070820A1 true PE20070820A1 (es) 2007-09-04

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US (2) US7718669B2 (es)
EP (1) EP1940838B1 (es)
JP (1) JP2009512649A (es)
KR (1) KR20080057299A (es)
CN (1) CN101291932A (es)
AR (1) AR058095A1 (es)
AU (1) AU2006303551A1 (es)
BR (1) BRPI0617712A2 (es)
CA (1) CA2625442A1 (es)
CR (1) CR9851A (es)
DE (1) DE102005049954A1 (es)
DO (1) DOP2006000227A (es)
EC (1) ECSP088376A (es)
HN (1) HN2006035237A (es)
IL (1) IL190715A0 (es)
MA (1) MA29857B1 (es)
MY (1) MY140514A (es)
NO (1) NO20082159L (es)
NZ (1) NZ567574A (es)
PE (1) PE20070820A1 (es)
RU (1) RU2008119435A (es)
TN (1) TNSN08178A1 (es)
TW (1) TW200800987A (es)
UY (1) UY29878A1 (es)
WO (1) WO2007045392A1 (es)
ZA (1) ZA200802369B (es)

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ES2614090T3 (es) 2005-12-29 2017-05-29 Celtaxsys, Inc. Derivados de diamina como inhibidores de leucotrieno A4 hidrolasa
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FR2915197B1 (fr) 2007-04-18 2009-06-12 Sanofi Aventis Sa Derives de triazolopyridine-carboxamides, leur preparation et leur application therapeutique.
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
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US9333202B2 (en) 2012-05-01 2016-05-10 The Trustees Of Columbia University In The City Of New York Non-retinoid antagonists for treatment of age-related macular degeneration and stargardt disease
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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
US9637450B2 (en) 2013-03-14 2017-05-02 The Trustees Of Columbia University In The City Of New York Octahydrocyclopentapyrroles, their preparation and use
US9580422B2 (en) * 2013-10-22 2017-02-28 Bristol-Myers Squibb Company Isotopically labeled triazolopyridine 11-beta hydroxysteroid dehydrogenase type I inhibitors
KR102429220B1 (ko) 2014-04-30 2022-08-04 더 트러스티이스 오브 콜롬비아 유니버시티 인 더 시티 오브 뉴욕 치환 4-페닐피페리딘, 그 제조 및 사용
KR20190043437A (ko) 2017-10-18 2019-04-26 씨제이헬스케어 주식회사 단백질 키나제 억제제로서의 헤테로고리 화합물
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KR20080057299A (ko) 2008-06-24
RU2008119435A (ru) 2009-11-27
TNSN08178A1 (en) 2009-10-30
AR058095A1 (es) 2008-01-23
MA29857B1 (fr) 2008-10-03
CR9851A (es) 2008-07-29
MY140514A (en) 2009-12-31
BRPI0617712A2 (pt) 2011-08-02
DE102005049954A1 (de) 2007-05-31
EP1940838B1 (de) 2012-08-22
CA2625442A1 (en) 2007-04-26
DOP2006000227A (es) 2007-05-15
IL190715A0 (en) 2008-11-03
JP2009512649A (ja) 2009-03-26
HN2006035237A (es) 2010-03-11
NZ567574A (en) 2010-03-26
WO2007045392A1 (de) 2007-04-26
AU2006303551A1 (en) 2007-04-26
ZA200802369B (en) 2009-01-28
US20100190801A1 (en) 2010-07-29
UY29878A1 (es) 2007-05-31
EP1940838A1 (de) 2008-07-09
US20090030011A1 (en) 2009-01-29
CN101291932A (zh) 2008-10-22
TW200800987A (en) 2008-01-01
NO20082159L (no) 2008-05-08
ECSP088376A (es) 2008-05-30
US7718669B2 (en) 2010-05-18

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