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PE20050690A1 - Derivados de indazol como inhibidores de la lipasa sensible a hormonas - Google Patents

Derivados de indazol como inhibidores de la lipasa sensible a hormonas

Info

Publication number
PE20050690A1
PE20050690A1 PE2005000108A PE2005000108A PE20050690A1 PE 20050690 A1 PE20050690 A1 PE 20050690A1 PE 2005000108 A PE2005000108 A PE 2005000108A PE 2005000108 A PE2005000108 A PE 2005000108A PE 20050690 A1 PE20050690 A1 PE 20050690A1
Authority
PE
Peru
Prior art keywords
alkyl
inhibitors
hormone
sensitive lipase
indazol
Prior art date
Application number
PE2005000108A
Other languages
English (en)
Inventor
Gerhard Zoller
Stefan Petry
Gunter Muller
Hubert Heuer
Karl-Heinz Baringhaus
Original Assignee
Sanofi Aventis Deutschland
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 Deutschland filed Critical Sanofi Aventis Deutschland
Publication of PE20050690A1 publication Critical patent/PE20050690A1/es

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    • C07ORGANIC CHEMISTRY
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    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • 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
    • AHUMAN NECESSITIES
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    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
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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
    • A61P3/06Antihyperlipidemics
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
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    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56Benzopyrazoles; Hydrogenated benzopyrazoles
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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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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    • 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
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    • 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
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    • C07D495/04Ortho-condensed systems

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  • Organic Chemistry (AREA)
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Abstract

REFERIDA A UN COMPUESTO DE FORMULAS I O II DONDE W ES C=O, S=O, SO2; X ES =CH, =CF, =N, ENTRE OTROS; Y ES O, NH, N(R1); R1 ES H, ALQUILO C1-C6, BENCILO; R2 ES H, ALQUILO C1-C6, ALQUIL(C1-C4)-FENILO, ENTRE OTROS; R3 ES H, ALQUILO(C1-C6), O JUNTO A R2 SON UN SISTEMA DE 4-7 MIEMBROS, ENTRE OTROS. TAMBIEN REFERIDA A LA PREPARACION DE MEDICAMENTOS CUYOS COMPUESTOS PREFERIDOS SON: ESTER DE 1H-INDAZOL-3-ILO DEL ACIDO 3-METILPIPERIDINA-1-CARBOXILICO, (3,4-DIHIDRO-2H-QUINOLIN-1-IL)-(3-HIDROXI-INDAZOL-1-IL)-METANONA Y METIL-FENIL-AMIDA DEL ACIDO 3-HIDROXI-INDAZOL-1-CARBOXILICO, ENTRE OTROS. DICHOS COMPUESTOS SON INHIBIDORES DE LA LIPASA SENSIBLE A HORMONAS (HSL)
PE2005000108A 2004-02-02 2005-01-28 Derivados de indazol como inhibidores de la lipasa sensible a hormonas PE20050690A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102004005172A DE102004005172A1 (de) 2004-02-02 2004-02-02 Indazolderivate als Inhibitoren der Hormon Sensitiven Lipase

Publications (1)

Publication Number Publication Date
PE20050690A1 true PE20050690A1 (es) 2005-11-07

Family

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Application Number Title Priority Date Filing Date
PE2005000108A PE20050690A1 (es) 2004-02-02 2005-01-28 Derivados de indazol como inhibidores de la lipasa sensible a hormonas

Country Status (27)

Country Link
US (2) US7528155B2 (es)
EP (1) EP1713779B1 (es)
JP (1) JP4714158B2 (es)
KR (1) KR20060128958A (es)
CN (1) CN1914180A (es)
AR (1) AR047520A1 (es)
AT (1) ATE505460T1 (es)
AU (1) AU2005209366A1 (es)
BR (1) BRPI0507370A (es)
CA (1) CA2554524A1 (es)
CR (1) CR8487A (es)
DE (2) DE102004005172A1 (es)
DO (1) DOP2005000011A (es)
EC (1) ECSP066750A (es)
HN (1) HN2005000039A (es)
IL (1) IL176912A (es)
MA (1) MA28338A1 (es)
MY (1) MY143407A (es)
NO (1) NO20063925L (es)
NZ (1) NZ548872A (es)
PE (1) PE20050690A1 (es)
RU (1) RU2370491C2 (es)
SG (1) SG149891A1 (es)
TW (1) TW200536535A (es)
UY (1) UY28735A1 (es)
WO (1) WO2005073199A1 (es)
ZA (1) ZA200605311B (es)

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EP1586573B1 (en) 2004-04-01 2007-02-07 Sanofi-Aventis Deutschland GmbH Oxadiazolones, processes for their preparation and their use as pharmaceuticals
DE102005026808A1 (de) 2005-06-09 2006-12-14 Sanofi-Aventis Deutschland Gmbh Benzooxazol-2-on-derivate als Inhibitoren von Lipasen und Phospholipasen
DE102005026762A1 (de) 2005-06-09 2006-12-21 Sanofi-Aventis Deutschland Gmbh Azolopyridin-2-on-derivate als Inhibitoren von Lipasen und Phospholipasen
DE102005048897A1 (de) 2005-10-12 2007-04-19 Sanofi-Aventis Deutschland Gmbh Diacylindazol-derivate als Inhibitoren von Lipasen und Phospholipasen
DE102005049954A1 (de) 2005-10-19 2007-05-31 Sanofi-Aventis Deutschland Gmbh Triazolopyridin-derivate als Inhibitoren von Lipasen und Phospholipasen
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BRPI0810044A2 (pt) 2007-04-05 2014-10-14 Sanofi Aventis 5-oxoisoxazóis como inibidores de lipases e fosfolipases
FR2915197B1 (fr) 2007-04-18 2009-06-12 Sanofi Aventis Sa Derives de triazolopyridine-carboxamides, leur preparation et leur application therapeutique.
FR2915199B1 (fr) * 2007-04-18 2010-01-22 Sanofi Aventis Derives de triazolopyridine-carboxamides et triazolopyrimidine-carboxamides, leur preparation et leur application en therapeutique.
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WO2012031383A1 (zh) * 2010-09-06 2012-03-15 中国科学院广州生物医药与健康研究院 酰胺类化合物
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