AR046783A1 - Compuesto de sal ciclica de amonio cuaternario composicion farmaceutica que lo comprende y su uso para preparar esta ultima - Google Patents

Compuesto de sal ciclica de amonio cuaternario composicion farmaceutica que lo comprende y su uso para preparar esta ultima

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Publication number
AR046783A1
AR046783A1 ARP040104478A ARP040104478A AR046783A1 AR 046783 A1 AR046783 A1 AR 046783A1 AR P040104478 A ARP040104478 A AR P040104478A AR P040104478 A ARP040104478 A AR P040104478A AR 046783 A1 AR046783 A1 AR 046783A1
Authority
AR
Argentina
Prior art keywords
alkyl
lower alkyl
cycloalkyl
group
phenyl
Prior art date
Application number
ARP040104478A
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English (en)
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Glaxo Group Ltd
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Publication date
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of AR046783A1 publication Critical patent/AR046783A1/es

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56Nitrogen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/02Nasal agents, e.g. decongestants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/08Bronchodilators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/36Sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D263/46Sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D277/38Nitrogen atoms
    • C07D277/44Acylated amino or imino radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30Hetero atoms other than halogen
    • C07D333/34Sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • 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
    • C07D401/12Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • C07D413/02Heterocyclic 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
    • 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
    • C07D417/14Heterocyclic 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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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Pulmonology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Immunology (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Hydrogenated Pyridines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Peptides Or Proteins (AREA)
  • Pyridine Compounds (AREA)

Abstract

Un compuesto de sal cíclica de amonio cuaternario caracterizado porque tiene la fórmula (1), en la que: n es 0 ó 1; cuando X es nitrógeno u oxígeno, Y no es nada; cuando Y es nitrógeno u oxígeno, X no es nada; T es un grupo sulfonilo (SO2) o carbonilo (CO); cuando T = CO, X es oxígeno o nitrógeno; Z- se selecciona entre el grupo compuesto por halo, CF3COO-, mesilato, tosilato, o cualquier otro contraión farmacéuticamente aceptable; R1 se selecciona entre el grupo compuesto por alquilo C1-8 ramificado o no ramificado, cicloalquilo C3-8, cicloalquil(C3-8)-alquilo inferior, alquenilo C3-8, fenilo no sustituido o sustituido, o fenil no sustituido o sustituido-alquilo inferior(C1-3); donde, cuando está sustituido, un grupo está sustituido con uno o más radicales seleccionados entre el grupo compuesto por alcoxi C1-8, halo, hidroxi, amino, ciano, trifluorometilo, alquilo C1-8 ramificado o no ramificado, cicloalquilo C3-8, cicloalquil(C3-8)-alquilo inferior, fenilo y fenil- alquilo inferior(C1-3); R2 se selecciona entre el grupo compuesto por alquilo C1-8 ramificado o no ramificado, cicloalquilo C3-8, cicloalquil(C3-8)-alquilo inferior, fenilo no sustituido o sustituido, o fenil no sustituido o sustituido-alquilo inferior(C1-3); donde, cuando está sustituido, un grupo está sustituido con uno o más radicales seleccionados entre el grupo compuesto por alcoxi C1-8, halo, hidroxi, amino, ciano, trifluorometilo, alquilo C1-8 ramificado o no ramificado, cicloalquil C3-8 y cicloalquil(C3-8)-alquilo inferior y anillos heterocíclicos; R3 se selecciona entre el grupo compuesto por uno de los siguientes grupos no sustituidos o sustituidos: fenilo, fenil-alquilo inferior(C1-6) tiofenilo, tiofenil-alquilo inferior(C1-6), furanilo, furanil-alquilo inferior(C1-6), piridinilo, piridinil-alquilo inferior(C1-6), imidazolilo, imidazolilo-alquilo inferior(C1-6), naftilo, naftil-alquilo inferior(C1-6) quinolinilo, quinolinil-alquilo inferior(C1-6), indolilo, indolil-alquilo inferior(C1-6), benzotiofenilo, benzotiofenil-alquilo inferior(C1-6), benzofuranilo, benzofuranil-alquilo inferior(C1-6), benzoimidazolilo, benzoimidazolil-alquilo inferior(C1-6), alquilo C1-8 ramificado o no ramificado, cicloalquilo C3-8, cicloalquil(C3-8)-alquilo inferior(C1-6), o alquenilo C3-8; donde, cuando está sustituido, un grupo está sustituido con uno o más radicales seleccionados entre el grupo compuestos por alcoxi C1-6, fenoxi, fenil-alcoxi(C1-3), halo, hidroxi, amino, ciano, trifluorometilo, metilenodioxi, etilenodioxi, propilenodioxi, butilenodioxi, alquilo C1-8 ramificado o no ramificado, cicloalquilo C3-8, cicloalquil(C3-8)-alquilo inferior, fenilo, fenil-alquilo inferior(C1-3) tiofenilo, tiofenil- alquilo inferior(C1-3), furanilo, furanil-alquilo inferior(C1-3), piridinilo, piridinil-alquilo inferior(C1-3), naftilo, naftil-alquilo inferior(C1-3) quinolinilo, quinolinil-alquilo inferior(C1-3), indolilo, indolil-alquilo inferior(C1-3), benzotiofenilo, benzotiofenil-alquilo inferior(C1-3), benzofuranilo, benzofuranil-alquilo inferior(C1-6), COOH, COR6, COOR6, CONHR6, CON(R6)2, COG, NHR6, N(R6)2, G', OCOR6, OCONHR6, NHCOR6, N(R6)COR6, NHCOOR6 y NHCONHR6; y R4 se selecciona entre el grupo compuesto alquilo C1-8 ramificado o no ramificado, cicloalquilo C3-8 o cicloalquil(C3-8)-alquilo inferior; o una sal farmacéuticamente aceptable del mismo. Composición farmacéutica para el tratamiento de enfermedades mediadas por el receptor muscarínico de acetilcolina, que comprende un compuesto de la fórmula (1) y un vehículo farmacéuticamente aceptable del mismo. Uso de un compuesto de la fórmula (1) para preparar una composición farmacéutica para inhibir la unión de acetilcolina a sus receptores en un mamífero en necesidad del mismo, siendo efectiva preferentemente para tratar una enfermedad mediada por el receptor muscarínico de acetilcolina, donde la acetilcolina se une a dicho receptor. La enfermedad puede ser enfermedad pulmonar obstructiva crónica, bronquitis crónica, asma, obstrucción respiratoria crónica, fibrosis pulmonar, enfisema pulmonar y rinitis alérgica.
ARP040104478A 2003-12-03 2004-12-01 Compuesto de sal ciclica de amonio cuaternario composicion farmaceutica que lo comprende y su uso para preparar esta ultima AR046783A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US52676603P 2003-12-03 2003-12-03

Publications (1)

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AR046783A1 true AR046783A1 (es) 2005-12-21

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ID=34676649

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP040104478A AR046783A1 (es) 2003-12-03 2004-12-01 Compuesto de sal ciclica de amonio cuaternario composicion farmaceutica que lo comprende y su uso para preparar esta ultima

Country Status (20)

Country Link
US (1) US20070179180A1 (es)
EP (1) EP1694327A4 (es)
JP (1) JP2007513182A (es)
KR (1) KR20060123414A (es)
CN (1) CN1913895A (es)
AR (1) AR046783A1 (es)
AU (1) AU2004296208A1 (es)
BR (1) BRPI0417343A (es)
CA (1) CA2549273A1 (es)
IL (1) IL176078A0 (es)
IS (1) IS8522A (es)
MA (1) MA28218A1 (es)
MX (1) MXPA06006256A (es)
NO (1) NO20063032L (es)
PE (1) PE20050861A1 (es)
RU (1) RU2006123418A (es)
TW (1) TW200530226A (es)
UY (1) UY28646A1 (es)
WO (1) WO2005055941A2 (es)
ZA (1) ZA200604485B (es)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20050250A1 (es) * 2003-07-17 2005-04-08 Glaxo Group Ltd Antagonistas de los receptores muscarinicos de la acetilcolina
TW200528448A (en) * 2003-10-17 2005-09-01 Glaxo Group Ltd Muscarinic acetylcholine receptor antagonists
AR046225A1 (es) * 2003-11-04 2005-11-30 Glaxo Group Ltd Compuesto de 8-azoniabiciclo(3.2.1)octano, composicion farmaceutica para el tratamiento de enfermedades mediadas por receptores de acetilcolina muscarinicos que lo comprende y uso del compuesto para preparar dicha composicion
JP2007528420A (ja) * 2004-03-11 2007-10-11 グラクソ グループ リミテッド 新規m3ムスカリン性アセチルコリン受容体アンタゴニスト
US20070185148A1 (en) * 2004-03-17 2007-08-09 Glaxo Group Limited M3 muscarinic acetylchoine receptor antagonists
WO2005095407A1 (en) * 2004-03-17 2005-10-13 Glaxo Group Limited M3 muscarinic acetylcholine receptor antagonists
MY144753A (en) 2004-04-27 2011-10-31 Glaxo Group Ltd Muscarinic acetylcholine receptor antagonists
EP1747219A4 (en) * 2004-05-13 2010-05-26 Glaxo Group Ltd Antagonists of muscarinic acetylcholine receptor
TW200630337A (en) * 2004-10-14 2006-09-01 Euro Celtique Sa Piperidinyl compounds and the use thereof
US7932247B2 (en) * 2004-11-15 2011-04-26 Glaxo Group Limited M3 muscarinic acetylcholine receptor antagonists
WO2007016639A2 (en) * 2005-08-02 2007-02-08 Glaxo Group Limited M3 muscarinic acetylcholine receptor antagonists
JP2009504768A (ja) 2005-08-18 2009-02-05 グラクソ グループ リミテッド ムスカリン性アセチルコリン受容体アンタゴニスト
WO2007110449A1 (en) * 2006-03-29 2007-10-04 Euro-Celtique S.A. Benzenesulfonamide compounds and their use
US8791264B2 (en) * 2006-04-13 2014-07-29 Purdue Pharma L.P. Benzenesulfonamide compounds and their use as blockers of calcium channels
WO2007118854A1 (en) * 2006-04-13 2007-10-25 Euro-Celtique S.A. Benzenesulfonamide compounds and the use thereof
WO2008103426A1 (en) * 2007-02-23 2008-08-28 Theravance, Inc. Quaternary ammonium diphenylmethyl compounds useful as muscarinic receptor antagonists
WO2008124118A1 (en) * 2007-04-09 2008-10-16 Purdue Pharma L.P. Benzenesulfonyl compounds and the use therof
US8765736B2 (en) * 2007-09-28 2014-07-01 Purdue Pharma L.P. Benzenesulfonamide compounds and the use thereof
CL2009000248A1 (es) 2008-02-06 2009-09-11 Glaxo Group Ltd Compuestos derivados de pirazolo [3,4-b] piridin-5-il, inhibidores de la fosfodiesterasa de tipo iv (pde4) y antagonista de receptores muscarinicos de acetilcolina (machr); composicion farmaceutica que los comprende; y su uso en la preparacion de medicamentos utiles en el tratamiento de enferemedades respiratorias y alergicas
UY31637A1 (es) 2008-02-06 2009-08-03 Farmacoforos duales-antagonistas muscarinicos de pde4
UY31636A1 (es) 2008-02-06 2009-08-03 Farmacoforos duales-antagonistas muscarinicos de pde4
WO2010094643A1 (en) 2009-02-17 2010-08-26 Glaxo Group Limited Quinoline derivatives and their uses for rhinitis and urticaria

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6482837B1 (en) * 1998-04-24 2002-11-19 University Of Rochester Antimuscarinic compounds and methods for treatment of bladder diseases
CA2378499A1 (en) * 1999-08-04 2001-02-15 Teijin Limited Cyclic amine ccr3 antagonists
DE10063008A1 (de) * 2000-12-16 2002-06-20 Merck Patent Gmbh Carbonsäureamidderivate
DE10201550A1 (de) * 2002-01-17 2003-07-31 Merck Patent Gmbh Phenoxy-Piperidine

Also Published As

Publication number Publication date
ZA200604485B (en) 2007-11-28
RU2006123418A (ru) 2008-01-10
PE20050861A1 (es) 2005-12-10
EP1694327A2 (en) 2006-08-30
MA28218A1 (fr) 2006-10-02
AU2004296208A1 (en) 2005-06-23
US20070179180A1 (en) 2007-08-02
WO2005055941A3 (en) 2006-02-16
EP1694327A4 (en) 2009-11-25
IL176078A0 (en) 2006-10-05
BRPI0417343A (pt) 2007-03-13
UY28646A1 (es) 2005-06-30
NO20063032L (no) 2006-08-30
MXPA06006256A (es) 2006-08-23
WO2005055941A2 (en) 2005-06-23
TW200530226A (en) 2005-09-16
CN1913895A (zh) 2007-02-14
CA2549273A1 (en) 2005-06-23
KR20060123414A (ko) 2006-12-01
IS8522A (is) 2006-06-26
JP2007513182A (ja) 2007-05-24

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