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IS6845A - Pýridasínón aldósa afsýringarkljúfshindrar - Google Patents

Pýridasínón aldósa afsýringarkljúfshindrar

Info

Publication number
IS6845A
IS6845A IS6845A IS6845A IS6845A IS 6845 A IS6845 A IS 6845A IS 6845 A IS6845 A IS 6845A IS 6845 A IS6845 A IS 6845A IS 6845 A IS6845 A IS 6845A
Authority
IS
Iceland
Prior art keywords
antacids
pyridazinone aldose
pyridazinone
aldose
aldose antacids
Prior art date
Application number
IS6845A
Other languages
English (en)
Other versions
IS2205B (is
Inventor
Lakshman Mylari Banavara
Original Assignee
Pfizer Products Inc.
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 Pfizer Products Inc. filed Critical Pfizer Products Inc.
Publication of IS6845A publication Critical patent/IS6845A/is
Publication of IS2205B publication Critical patent/IS2205B/is

Links

Classifications

    • 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
    • C07D409/12Heterocyclic 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 chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/12Antidiuretics, e.g. drugs for diabetes insipidus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/78Benzo [b] furans; Hydrogenated benzo [b] furans
    • C07D307/82Benzo [b] furans; Hydrogenated benzo [b] furans 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 carbon atoms of the hetero ring
    • 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
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 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
    • C07D405/12Heterocyclic 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 chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hematology (AREA)
  • Cardiology (AREA)
  • Obesity (AREA)
  • Endocrinology (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Emergency Medicine (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
IS6845A 2001-03-30 2003-06-16 Pýridasínón aldósa afsýringarkljúfshindrar IS2205B (is)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US28005101P 2001-03-30 2001-03-30
PCT/IB2002/000320 WO2002079198A1 (en) 2001-03-30 2002-01-31 Pyridazinone aldose reductase inhibitors

Publications (2)

Publication Number Publication Date
IS6845A true IS6845A (is) 2003-06-16
IS2205B IS2205B (is) 2007-02-15

Family

ID=23071435

Family Applications (3)

Application Number Title Priority Date Filing Date
IS6845A IS2205B (is) 2001-03-30 2003-06-16 Pýridasínón aldósa afsýringarkljúfshindrar
IS8251A IS8251A (is) 2001-03-30 2006-01-23 Pýridasínón aldósa afsýringarkljúfshindrar
IS8250A IS8250A (is) 2001-03-30 2006-01-23 Pýridasínón aldósa afsýringarkljúfshindrar

Family Applications After (2)

Application Number Title Priority Date Filing Date
IS8251A IS8251A (is) 2001-03-30 2006-01-23 Pýridasínón aldósa afsýringarkljúfshindrar
IS8250A IS8250A (is) 2001-03-30 2006-01-23 Pýridasínón aldósa afsýringarkljúfshindrar

Country Status (43)

Country Link
US (2) US6579879B2 (is)
EP (3) EP1373259B1 (is)
JP (1) JP2004528319A (is)
KR (1) KR100586138B1 (is)
CN (1) CN1215067C (is)
AP (1) AP2002002461A0 (is)
AR (1) AR035798A1 (is)
AT (3) ATE352551T1 (is)
AU (1) AU2002226634B2 (is)
BG (1) BG108179A (is)
BR (1) BR0208571A (is)
CA (1) CA2442476A1 (is)
CZ (1) CZ20032563A3 (is)
DE (3) DE60216823T2 (is)
DK (2) DK1373259T3 (is)
EA (1) EA006023B1 (is)
EC (1) ECSP034671A (is)
EE (1) EE200300470A (is)
ES (2) ES2274369T3 (is)
GE (1) GEP20053675B (is)
HR (1) HRP20030752A2 (is)
HU (1) HUP0303644A3 (is)
IL (1) IL156462A0 (is)
IS (3) IS2205B (is)
MA (1) MA27003A1 (is)
MX (1) MXPA03008850A (is)
MY (1) MY134304A (is)
NO (1) NO20034345L (is)
NZ (1) NZ528406A (is)
OA (1) OA12453A (is)
PA (1) PA8541801A1 (is)
PE (1) PE20030007A1 (is)
PL (1) PL365294A1 (is)
PT (2) PT1373259E (is)
SI (1) SI1373259T1 (is)
SK (1) SK11852003A3 (is)
TN (1) TNSN02037A1 (is)
TW (1) TWI245762B (is)
UA (1) UA73236C2 (is)
UY (1) UY27237A1 (is)
WO (1) WO2002079198A1 (is)
YU (1) YU71403A (is)
ZA (1) ZA200304671B (is)

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AU714980B2 (en) 1996-07-24 2000-01-13 Warner-Lambert Company Llc Isobutylgaba and its derivatives for the treatment of pain
DE60204611T2 (de) * 2001-02-28 2006-05-11 Pfizer Products Inc., Groton Sulfonyl-pyridazinon-derivate zur Verwendung als Aldose-reduktase-inhibitoren
PT1373259E (pt) * 2001-03-30 2005-03-31 Pfizer Prod Inc Inibidores piridazinona de aldose reductase
AU761191B2 (en) * 2001-05-24 2003-05-29 Pfizer Products Inc. Therapies for tissue damage resulting from ischemia
AU2003200847A1 (en) * 2002-01-09 2003-07-24 Pfizer Products Inc. Process and intermediates for pyridazinone antidiabetic agents
US20040092522A1 (en) * 2002-08-15 2004-05-13 Field Mark John Synergistic combinations
US7419981B2 (en) * 2002-08-15 2008-09-02 Pfizer Inc. Synergistic combinations of an alpha-2-delta ligand and a cGMP phosphodieterse 5 inhibitor
US6872833B2 (en) * 2003-04-14 2005-03-29 Hoffmann-La Roche Inc. Adenosine receptor ligands
US8017634B2 (en) 2003-12-29 2011-09-13 President And Fellows Of Harvard College Compositions for treating obesity and insulin resistance disorders
US7262318B2 (en) * 2004-03-10 2007-08-28 Pfizer, Inc. Substituted heteroaryl- and phenylsulfamoyl compounds
AR049384A1 (es) 2004-05-24 2006-07-26 Glaxo Group Ltd Derivados de purina
CA2568640C (en) 2004-06-04 2011-08-09 Teva Pharmaceutical Industries Ltd. Pharmaceutical composition containing irbesartan
US20050288340A1 (en) * 2004-06-29 2005-12-29 Pfizer Inc Substituted heteroaryl- and phenylsulfamoyl compounds
US20060035251A1 (en) * 2004-06-30 2006-02-16 Whitehead Institute For Biomedical Research Novel methods for high-throughput genome-wide location analysis
GB0514809D0 (en) 2005-07-19 2005-08-24 Glaxo Group Ltd Compounds
US7741317B2 (en) 2005-10-21 2010-06-22 Bristol-Myers Squibb Company LXR modulators
US7888376B2 (en) 2005-11-23 2011-02-15 Bristol-Myers Squibb Company Heterocyclic CETP inhibitors
AU2007206016A1 (en) * 2006-01-13 2007-07-26 Wyeth Sulfonyl substituted 1H-indoles as ligands for the 5-hydroxytryptamine receptors
EP2431367A3 (en) 2006-06-27 2012-07-04 Takeda Pharmaceutical Company Limited Fused cyclic compounds as GPR40 receptor modulators
ATE547394T1 (de) 2006-12-01 2012-03-15 Bristol Myers Squibb Co N-((3-benzyl)-2,2-(bis-phenyl)-propan-1- aminderivate als cetp-hemmer für die behandlung von atherosklerose und herz-kreislauf- erkrankungen
WO2008116107A2 (en) * 2007-03-21 2008-09-25 Takeda San Diego, Inc. Piperazine derivatives as glucokinase activators
JP2010043063A (ja) 2008-05-09 2010-02-25 Agency For Science Technology & Research 川崎病の診断及び治療
CA2783699C (en) 2009-12-08 2019-01-15 Case Western Reserve University Primary amine compounds for treating ocular disorders
US8916563B2 (en) 2010-07-16 2014-12-23 The Trustees Of Columbia University In The City Of New York Aldose reductase inhibitors and uses thereof
RU2615767C2 (ru) * 2011-09-15 2017-04-11 Тайпей Медикл Юнивесити Способ лечения сердечной недостаточности и поражения нервных клеток
US9339542B2 (en) * 2013-04-16 2016-05-17 John L Couvaras Hypertension reducing composition
CA2909442A1 (en) 2013-04-17 2014-10-23 Pfizer Inc. N-piperidin-3-ylbenzamide derivatives for treating cardiovascular diseases
CN103739547B (zh) * 2014-01-03 2015-09-02 沈阳药科大学 2-[6-甲氧基-3-(2,3-二氯苯基)甲基-4-氧代-1,4-二氢-1(4h)-喹啉基]乙酸的合成方法
WO2016055901A1 (en) 2014-10-08 2016-04-14 Pfizer Inc. Substituted amide compounds
EP3283074A4 (en) * 2015-04-14 2018-12-05 Case Western Reserve University Compositions and methods of modulating short-chain dehydrogenase activity
WO2017168174A1 (en) 2016-04-02 2017-10-05 N4 Pharma Uk Limited New pharmaceutical forms of sildenafil
CN109310674B (zh) 2016-06-21 2022-07-08 纽约市哥伦比亚大学理事会 醛糖还原酶抑制剂及其使用方法
WO2018002673A1 (en) 2016-07-01 2018-01-04 N4 Pharma Uk Limited Novel formulations of angiotensin ii receptor antagonists
US10344002B2 (en) 2016-09-26 2019-07-09 Nusirt Sciences, Inc. Compositions and methods for treating metabolic disorders
EP3548035A4 (en) 2016-11-30 2020-07-22 Case Western Reserve University COMBINATIONS OF 15-PGDH INHIBITORS WITH CORCOSTEROIDS AND / OR TNF INHIBITORS AND THEIR USES
CN110573154A (zh) 2017-02-06 2019-12-13 卡斯西部储备大学 调节短链脱氢酶活性的组合物和方法
IL272246B1 (en) 2017-07-28 2025-09-01 Applied Therapeutics Inc Derivatives of 2-(4-oxo/thioketone/azo-3-((substituted)benzo[d]thiazol-2-yl)methyl)- 3,4-dihydrothieno[3,4-d]pyridazin-1-yl)acetic acid for use as aldose reductase inhibitors in treating galactosemia or preventing complications associated with galactosemia
SG11202105345TA (en) 2018-11-21 2021-06-29 Univ Case Western Reserve Compositions and methods of modulating short-chain dehydrogenase activity
EP4470609A3 (en) 2019-01-18 2025-03-12 Astrazeneca AB Pcsk9 inhibitors and methods of use thereof
CN113966396A (zh) 2019-05-07 2022-01-21 迈阿密大学 遗传性神经病和相关障碍的治疗和检测
MX2021014441A (es) 2019-05-31 2022-01-06 Ikena Oncology Inc Inhibidores del dominio asociado mejorador de la transcripcion (tead) y usos de los mismos.
WO2020243415A2 (en) 2019-05-31 2020-12-03 Ikena Oncology, Inc. Tead inhibitors and uses thereof
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IE47592B1 (en) 1977-12-29 1984-05-02 Ici Ltd Enzyme inhibitory phthalazin-4-ylacetic acid derivatives, pharmaceutical compositions thereof,and process for their manufacture
US4939140A (en) 1985-11-07 1990-07-03 Pfizer Inc. Heterocyclic oxophthalazinyl acetic acids
US4996204A (en) 1989-05-11 1991-02-26 Pfizer Inc. Pyrido[2,3-d]pyridazinones as aldose reductase inhibitors
FR2647676A1 (fr) 1989-06-05 1990-12-07 Union Pharma Scient Appl Nouveaux derives de pyridazinone, leurs procedes de preparation, medicaments les contenant, utiles notamment comme inhibiteurs de l'aldose reductase
KR950001039B1 (ko) * 1990-11-30 1995-02-08 가부시끼가이샤 쓰무라 크로몬 유도체 및 이 화합물을 유효성분으로 하는 아르도스 리덕타제 저해제
FI934222A7 (fi) 1991-03-28 1993-09-27 Pfizer Pyridatsinonietikkahappoja
US5834466A (en) 1994-12-22 1998-11-10 The Regents Of The University Of California Method for protecting of heart by limiting metabolic and ionic abnormalities developed during ischemia, following ischemia or resulting from ischemia
TWI238064B (en) 1995-06-20 2005-08-21 Takeda Chemical Industries Ltd A pharmaceutical composition for prophylaxis and treatment of diabetes
EE04494B1 (et) * 1997-09-24 2005-06-15 Orion Corporation 1-oksa-, asa- ja tianaftaleen-2-oon biseetrid fosfolambaani inhibiitoritena
FR2822827B1 (fr) * 2001-03-28 2003-05-16 Sanofi Synthelabo Nouveaux derives de n-(arylsulfonyl) beta-aminoacides comportant un groupe aminomethyle substitue, leur procede de preparation et les compositions pharmaceutiques en contenant
PT1373259E (pt) * 2001-03-30 2005-03-31 Pfizer Prod Inc Inibidores piridazinona de aldose reductase
CN1505514A (zh) * 2001-04-30 2004-06-16 �Ʒ� 醛糖还原酶抑制剂与环加氧酶-2抑制剂的组合
AU2003200847A1 (en) * 2002-01-09 2003-07-24 Pfizer Products Inc. Process and intermediates for pyridazinone antidiabetic agents

Also Published As

Publication number Publication date
EP1491541B1 (en) 2007-01-24
DE60202452C5 (de) 2006-11-23
EP1491540B1 (en) 2006-12-13
EP1491541A1 (en) 2004-12-29
IS2205B (is) 2007-02-15
UY27237A1 (es) 2002-12-31
GEP20053675B (en) 2005-11-25
ATE348100T1 (de) 2007-01-15
SI1373259T1 (en) 2005-04-30
AU2002226634B2 (en) 2007-01-25
AP2002002461A0 (en) 2002-06-30
DE60217930T2 (de) 2007-10-18
CA2442476A1 (en) 2002-10-10
DE60202452T2 (de) 2006-02-09
OA12453A (en) 2006-05-24
IL156462A0 (en) 2004-01-04
BG108179A (en) 2004-09-30
DE60216823T2 (de) 2007-10-04
HK1061678A1 (en) 2004-09-30
MA27003A1 (fr) 2004-12-20
EE200300470A (et) 2004-02-16
EA006023B1 (ru) 2005-08-25
PA8541801A1 (es) 2002-10-28
DK1373259T3 (da) 2005-03-29
EP1373259B1 (en) 2004-12-29
IS8250A (is) 2006-01-23
ECSP034671A (es) 2003-08-29
KR100586138B1 (ko) 2006-06-07
BR0208571A (pt) 2004-03-23
CN1500087A (zh) 2004-05-26
DK1491540T3 (da) 2007-03-26
JP2004528319A (ja) 2004-09-16
UA73236C2 (en) 2005-06-15
ATE352551T1 (de) 2007-02-15
DE60202452D1 (de) 2005-02-03
PE20030007A1 (es) 2003-01-28
ES2231681T3 (es) 2005-05-16
US6849629B2 (en) 2005-02-01
ZA200304671B (en) 2004-06-25
DE60216823D1 (de) 2007-01-25
NZ528406A (en) 2004-03-26
TWI245762B (en) 2005-12-21
MY134304A (en) 2007-12-31
NO20034345D0 (no) 2003-09-29
WO2002079198A1 (en) 2002-10-10
CN1215067C (zh) 2005-08-17
KR20030088484A (ko) 2003-11-19
EP1491540A1 (en) 2004-12-29
ES2274369T3 (es) 2007-05-16
AR035798A1 (es) 2004-07-14
IS8251A (is) 2006-01-23
TNSN02037A1 (fr) 2005-12-23
NO20034345L (no) 2003-09-29
PT1491540E (pt) 2007-01-31
US6579879B2 (en) 2003-06-17
HRP20030752A2 (en) 2005-06-30
EP1373259A1 (en) 2004-01-02
HUP0303644A2 (hu) 2004-03-01
MXPA03008850A (es) 2003-12-04
US20030162784A1 (en) 2003-08-28
EA200300673A1 (ru) 2003-12-25
HUP0303644A3 (en) 2008-06-30
YU71403A (sh) 2006-05-25
PL365294A1 (en) 2004-12-27
CZ20032563A3 (cs) 2004-05-12
SK11852003A3 (sk) 2004-07-07
ATE286049T1 (de) 2005-01-15
US20020143017A1 (en) 2002-10-03
PT1373259E (pt) 2005-03-31
DE60217930D1 (de) 2007-03-15

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