UY29163A1 - Derivados de piridina, su preparación y su aplicación en terapéutica - Google Patents

Derivados de piridina, su preparación y su aplicación en terapéutica

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Publication number
UY29163A1
UY29163A1 UY29163A UY29163A UY29163A1 UY 29163 A1 UY29163 A1 UY 29163A1 UY 29163 A UY29163 A UY 29163A UY 29163 A UY29163 A UY 29163A UY 29163 A1 UY29163 A1 UY 29163A1
Authority
UY
Uruguay
Prior art keywords
piridine
therapeutics
preparation
derivatives
application
Prior art date
Application number
UY29163A
Other languages
English (en)
Inventor
Lionel Barre
Francis Barth
Christian Congy
Philippe Pointeau
Murielle Rinaldo-Carmona
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 UY29163A1 publication Critical patent/UY29163A1/es

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    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/36—Radicals substituted by singly-bound nitrogen atoms
    • C07D213/40—Acylated substituent nitrogen atom
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    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
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Abstract

La presente invención tiene como objetivo compuestos que responden a la fórmula : en la que: - Z, X, R1, R2, R´2 y R3 son como fueron definidas en la memoria descriptiva y reivindicaciones y a procedimiento de preparación y aplicaciones.
UY29163A 2004-10-18 2005-10-14 Derivados de piridina, su preparación y su aplicación en terapéutica UY29163A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0411030A FR2876691B1 (fr) 2004-10-18 2004-10-18 Derives de pyridine, leur preparation, leur application en therapeutique

Publications (1)

Publication Number Publication Date
UY29163A1 true UY29163A1 (es) 2006-04-28

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ID=34950592

Family Applications (1)

Application Number Title Priority Date Filing Date
UY29163A UY29163A1 (es) 2004-10-18 2005-10-14 Derivados de piridina, su preparación y su aplicación en terapéutica

Country Status (22)

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US (1) US20080021070A1 (es)
EP (1) EP1805143A1 (es)
JP (1) JP2008516934A (es)
KR (1) KR20070063008A (es)
CN (1) CN101039912A (es)
AR (1) AR051221A1 (es)
AU (1) AU2005296959A1 (es)
BR (1) BRPI0516926A (es)
CA (1) CA2582778A1 (es)
EA (1) EA200700891A1 (es)
EC (1) ECSP077400A (es)
FR (1) FR2876691B1 (es)
IL (1) IL182385A0 (es)
MA (1) MA29016B1 (es)
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FR2899899A1 (fr) * 2006-04-14 2007-10-19 Sanofi Aventis Sa Derives d'aminomethyl pyridine, leur preparation et leur application en therapeutique
TW200815438A (en) * 2006-06-13 2008-04-01 Bayer Schering Pharma Ag Substituted pyrazolopyridines and salts thereof, pharmaceutical compositions comprising same, methods of preparing same and uses of same
US7781593B2 (en) 2006-09-14 2010-08-24 Hoffmann-La Roche Inc. 5-phenyl-nicotinamide derivatives
FR2922209B1 (fr) 2007-10-12 2010-06-11 Sanofi Aventis 5,6-DIARYLES PYRIDINES SUBSTITUES EN POSITION 2 et 3, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE.
BRPI1010600A2 (pt) 2009-05-15 2016-03-15 Novartis Ag aril piridina como inibidores de aldosterona sintase
BR112018076800A2 (pt) * 2016-07-29 2019-04-02 Toray Industries, Inc. derivado de guanidina, medicamento, inibidor da proteína 1 da translocação de linfoma de tecido linfóide associado com mucosa, e, agente terapêutico ou profilático.
WO2018159650A1 (ja) * 2017-02-28 2018-09-07 東レ株式会社 グアニジン誘導体及びその医薬用途

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FR2198737B1 (es) * 1972-09-13 1975-11-28 Serdex
US5686470A (en) * 1995-02-10 1997-11-11 Weier; Richard M. 2, 3-substituted pyridines for the treatment of inflammation
JP2004517870A (ja) * 2001-01-02 2004-06-17 藤沢薬品工業株式会社 シクロオキシゲナーゼ阻害剤
WO2003082191A2 (en) * 2002-03-28 2003-10-09 Merck & Co., Inc. Substituted 2,3-diphenyl pyridines
FR2838438A1 (fr) * 2002-04-11 2003-10-17 Sanofi Synthelabo Derives de diphenylpyridine,leur preparation, les compositions pharmaceutiques en contenant
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TNSN07114A1 (fr) 2008-06-02
IL182385A0 (en) 2007-07-24
NZ554952A (en) 2009-08-28
US20080021070A1 (en) 2008-01-24
PE20060584A1 (es) 2006-08-18
MX2007004482A (es) 2007-06-13
KR20070063008A (ko) 2007-06-18
EA200700891A1 (ru) 2007-08-31
BRPI0516926A (pt) 2008-09-23
CN101039912A (zh) 2007-09-19
JP2008516934A (ja) 2008-05-22
EP1805143A1 (fr) 2007-07-11
TW200628450A (en) 2006-08-16
ECSP077400A (es) 2007-05-30
NO20072454L (no) 2007-05-14
AU2005296959A1 (en) 2006-04-27
WO2006042955A1 (fr) 2006-04-27
MA29016B1 (fr) 2007-11-01
AR051221A1 (es) 2006-12-27
CA2582778A1 (fr) 2006-04-27
FR2876691A1 (fr) 2006-04-21
FR2876691B1 (fr) 2006-12-29

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