ECSP034671A - Inhibidores de aldosa reductasa del grupo de las piridazinonas - Google Patents

Inhibidores de aldosa reductasa del grupo de las piridazinonas

Info

Publication number
ECSP034671A
ECSP034671A EC2003004671A ECSP034671A ECSP034671A EC SP034671 A ECSP034671 A EC SP034671A EC 2003004671 A EC2003004671 A EC 2003004671A EC SP034671 A ECSP034671 A EC SP034671A EC SP034671 A ECSP034671 A EC SP034671A
Authority
EC
Ecuador
Prior art keywords
diabetic
inhibitors
sorbitol
relates
compositions
Prior art date
Application number
EC2003004671A
Other languages
English (en)
Spanish (es)
Inventor
Banavara Lakshman Mylari
Original Assignee
Pfizer Prod 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 Prod Inc filed Critical Pfizer Prod Inc
Publication of ECSP034671A publication Critical patent/ECSP034671A/es

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)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Obesity (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (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)
EC2003004671A 2001-03-30 2003-06-25 Inhibidores de aldosa reductasa del grupo de las piridazinonas ECSP034671A (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US28005101P 2001-03-30 2001-03-30

Publications (1)

Publication Number Publication Date
ECSP034671A true ECSP034671A (es) 2003-08-29

Family

ID=23071435

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2003004671A ECSP034671A (es) 2001-03-30 2003-06-25 Inhibidores de aldosa reductasa del grupo de las piridazinonas

Country Status (43)

Country Link
US (2) US6579879B2 (cg-RX-API-DMAC7.html)
EP (3) EP1373259B1 (cg-RX-API-DMAC7.html)
JP (1) JP2004528319A (cg-RX-API-DMAC7.html)
KR (1) KR100586138B1 (cg-RX-API-DMAC7.html)
CN (1) CN1215067C (cg-RX-API-DMAC7.html)
AP (1) AP2002002461A0 (cg-RX-API-DMAC7.html)
AR (1) AR035798A1 (cg-RX-API-DMAC7.html)
AT (3) ATE348100T1 (cg-RX-API-DMAC7.html)
AU (1) AU2002226634B2 (cg-RX-API-DMAC7.html)
BG (1) BG108179A (cg-RX-API-DMAC7.html)
BR (1) BR0208571A (cg-RX-API-DMAC7.html)
CA (1) CA2442476A1 (cg-RX-API-DMAC7.html)
CZ (1) CZ20032563A3 (cg-RX-API-DMAC7.html)
DE (3) DE60217930T2 (cg-RX-API-DMAC7.html)
DK (2) DK1491540T3 (cg-RX-API-DMAC7.html)
EA (1) EA006023B1 (cg-RX-API-DMAC7.html)
EC (1) ECSP034671A (cg-RX-API-DMAC7.html)
EE (1) EE200300470A (cg-RX-API-DMAC7.html)
ES (2) ES2274369T3 (cg-RX-API-DMAC7.html)
GE (1) GEP20053675B (cg-RX-API-DMAC7.html)
HR (1) HRP20030752A2 (cg-RX-API-DMAC7.html)
HU (1) HUP0303644A3 (cg-RX-API-DMAC7.html)
IL (1) IL156462A0 (cg-RX-API-DMAC7.html)
IS (3) IS2205B (cg-RX-API-DMAC7.html)
MA (1) MA27003A1 (cg-RX-API-DMAC7.html)
MX (1) MXPA03008850A (cg-RX-API-DMAC7.html)
MY (1) MY134304A (cg-RX-API-DMAC7.html)
NO (1) NO20034345D0 (cg-RX-API-DMAC7.html)
NZ (1) NZ528406A (cg-RX-API-DMAC7.html)
OA (1) OA12453A (cg-RX-API-DMAC7.html)
PA (1) PA8541801A1 (cg-RX-API-DMAC7.html)
PE (1) PE20030007A1 (cg-RX-API-DMAC7.html)
PL (1) PL365294A1 (cg-RX-API-DMAC7.html)
PT (2) PT1491540E (cg-RX-API-DMAC7.html)
SI (1) SI1373259T1 (cg-RX-API-DMAC7.html)
SK (1) SK11852003A3 (cg-RX-API-DMAC7.html)
TN (1) TNSN02037A1 (cg-RX-API-DMAC7.html)
TW (1) TWI245762B (cg-RX-API-DMAC7.html)
UA (1) UA73236C2 (cg-RX-API-DMAC7.html)
UY (1) UY27237A1 (cg-RX-API-DMAC7.html)
WO (1) WO2002079198A1 (cg-RX-API-DMAC7.html)
YU (1) YU71403A (cg-RX-API-DMAC7.html)
ZA (1) ZA200304671B (cg-RX-API-DMAC7.html)

Families Citing this family (43)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU714980B2 (en) 1996-07-24 2000-01-13 Warner-Lambert Company Llc Isobutylgaba and its derivatives for the treatment of pain
EP1236720B1 (en) * 2001-02-28 2005-06-15 Pfizer Products Inc. Sulfonyl pyridazinone compounds useful as aldose reductase inhibitors
EE200300470A (et) * 2001-03-30 2004-02-16 Pfizer Products Inc. Aldoosreduktaasi püridasinooninhibiitorid
AU761191B2 (en) * 2001-05-24 2003-05-29 Pfizer Products Inc. Therapies for tissue damage resulting from ischemia
IL162594A0 (en) * 2002-01-09 2005-11-20 Pfizer Prod 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
US8226977B2 (en) 2004-06-04 2012-07-24 Teva Pharmaceutical Industries Ltd. Pharmaceutical composition containing irbesartan
US20050288340A1 (en) * 2004-06-29 2005-12-29 Pfizer Inc Substituted heteroaryl- and phenylsulfamoyl compounds
EP1769088A2 (en) * 2004-06-30 2007-04-04 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
EP1973876A2 (en) * 2006-01-13 2008-10-01 Wyeth Sulfonyl substituted 1h-indoles as ligands for the 5-hydroxytryptamine receptors
RS52307B (sr) * 2006-06-27 2012-12-31 Takeda Pharmaceutical Company Limited Kondenzovana ciklična jedinjenja
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
US8173645B2 (en) * 2007-03-21 2012-05-08 Takeda San Diego, Inc. Glucokinase activators
EP2116618A1 (en) 2008-05-09 2009-11-11 Agency for Science, Technology And Research Diagnosis and treatment of Kawasaki disease
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
EP2763673B1 (en) * 2011-09-15 2018-08-01 Taipei Medical University Use of indolyl hydroxamates for treating heart failure or neuronal injury
US9339542B2 (en) * 2013-04-16 2016-05-17 John L Couvaras Hypertension reducing composition
AU2014255381A1 (en) 2013-04-17 2015-10-08 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
AU2016248080A1 (en) * 2015-04-14 2017-11-02 Board Of Regents Of The University Of Texas System 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
EP3352754B1 (en) 2016-06-21 2020-09-02 The Trustees of Columbia University in the City of New York Aldose reductase inhibitors and methods of use thereof
WO2018002673A1 (en) 2016-07-01 2018-01-04 N4 Pharma Uk Limited Novel formulations of angiotensin ii receptor antagonists
WO2018058109A1 (en) * 2016-09-26 2018-03-29 Nusirt Sciences, Inc. Compositions and methods for treating metabolic disorders
JP7595413B2 (ja) 2016-11-30 2024-12-06 ケース ウエスタン リザーブ ユニバーシティ 15-pgdh阻害剤とコルチコステロイドおよび/またはtnf阻害剤との組み合わせならびにその使用
EP3576737A4 (en) 2017-02-06 2021-04-21 Case Western Reserve University COMPOSITIONS AND METHODS OF MODULATING THE ACTIVITY OF SHORT CHAIN DEHYDROGENASE
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
EP3883577A4 (en) 2018-11-21 2022-06-15 Case Western Reserve University COMPOSITIONS AND METHODS FOR MODULATION OF SHORT CHAIN DEHYDROGENASE ACTIVITY
DK3911648T3 (da) 2019-01-18 2025-01-13 Astrazeneca Ab 6'-[[(1s,3s)-3-[[5-(difluormethoxy)-2-pyrimidinyl]amino]cyclopentyl]amino][1(2h),3'-bipyridin]-2-on som pcsk9-hæmmer og fremgangsmåder til anvendelse deraf
BR112021021939A2 (pt) 2019-05-07 2022-02-22 Ucl Business Ltd Tratamento e detecção de neuropatias herdadas e distúrbios associados
SG11202113129UA (en) 2019-05-31 2021-12-30 Ikena Oncology Inc Tead inhibitors and uses thereof
SG11202113154YA (en) 2019-05-31 2021-12-30 Ikena Oncology Inc Tead inhibitors and uses thereof
WO2022120353A1 (en) * 2020-12-02 2022-06-09 Ikena Oncology, Inc. Tead inhibitors and uses thereof

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
WO1992009594A1 (fr) * 1990-11-30 1992-06-11 Tsumura & Co. Derive de benzopyrone et inhibiteur de reductase d'aldose contenant ce derive en tant qu'ingredient actif
CZ387092A3 (en) 1991-03-28 1994-02-16 Pfizer Pyridazinoacetic acids, their derivatives, process of their preparation and use
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
TW438587B (en) 1995-06-20 2001-06-07 Takeda Chemical Industries Ltd A pharmaceutical composition for prophylaxis and treatment of diabetes
WO1999015523A1 (en) * 1997-09-24 1999-04-01 Orion Corporation Bisethers of 1-oxa, aza and thianaphthalen-2-ones as phospholamban inhibitors
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
EE200300470A (et) * 2001-03-30 2004-02-16 Pfizer Products Inc. Aldoosreduktaasi püridasinooninhibiitorid
AU2002236131B2 (en) * 2001-04-30 2005-04-14 Pfizer Products Inc. Combinations of aldose reductase inhibitors and cyclooxygenase-2 inhibitors
IL162594A0 (en) * 2002-01-09 2005-11-20 Pfizer Prod Inc Process and intermediates for pyridazinone antidiabetic agents

Also Published As

Publication number Publication date
IS8251A (is) 2006-01-23
CN1215067C (zh) 2005-08-17
EA200300673A1 (ru) 2003-12-25
DE60217930T2 (de) 2007-10-18
ATE348100T1 (de) 2007-01-15
IS2205B (is) 2007-02-15
ATE352551T1 (de) 2007-02-15
HRP20030752A2 (en) 2005-06-30
HUP0303644A2 (hu) 2004-03-01
DE60217930D1 (de) 2007-03-15
UA73236C2 (en) 2005-06-15
DK1491540T3 (da) 2007-03-26
DE60202452D1 (de) 2005-02-03
TWI245762B (en) 2005-12-21
DK1373259T3 (da) 2005-03-29
EE200300470A (et) 2004-02-16
DE60202452C5 (de) 2006-11-23
DE60202452T2 (de) 2006-02-09
HUP0303644A3 (en) 2008-06-30
JP2004528319A (ja) 2004-09-16
AP2002002461A0 (en) 2002-06-30
NO20034345L (no) 2003-09-29
US6579879B2 (en) 2003-06-17
US20020143017A1 (en) 2002-10-03
IS8250A (is) 2006-01-23
YU71403A (sh) 2006-05-25
KR100586138B1 (ko) 2006-06-07
AR035798A1 (es) 2004-07-14
US6849629B2 (en) 2005-02-01
US20030162784A1 (en) 2003-08-28
PT1491540E (pt) 2007-01-31
MA27003A1 (fr) 2004-12-20
DE60216823T2 (de) 2007-10-04
EP1373259A1 (en) 2004-01-02
PE20030007A1 (es) 2003-01-28
MY134304A (en) 2007-12-31
IL156462A0 (en) 2004-01-04
OA12453A (en) 2006-05-24
GEP20053675B (en) 2005-11-25
CA2442476A1 (en) 2002-10-10
EP1491541A1 (en) 2004-12-29
HK1061678A1 (en) 2004-09-30
AU2002226634B2 (en) 2007-01-25
PT1373259E (pt) 2005-03-31
SI1373259T1 (en) 2005-04-30
MXPA03008850A (es) 2003-12-04
PA8541801A1 (es) 2002-10-28
WO2002079198A1 (en) 2002-10-10
EA006023B1 (ru) 2005-08-25
BR0208571A (pt) 2004-03-23
DE60216823D1 (de) 2007-01-25
CN1500087A (zh) 2004-05-26
NO20034345D0 (no) 2003-09-29
NZ528406A (en) 2004-03-26
IS6845A (is) 2003-06-16
EP1373259B1 (en) 2004-12-29
ATE286049T1 (de) 2005-01-15
KR20030088484A (ko) 2003-11-19
CZ20032563A3 (cs) 2004-05-12
EP1491540A1 (en) 2004-12-29
BG108179A (en) 2004-09-30
ZA200304671B (en) 2004-06-25
ES2274369T3 (es) 2007-05-16
EP1491540B1 (en) 2006-12-13
UY27237A1 (es) 2002-12-31
TNSN02037A1 (fr) 2005-12-23
ES2231681T3 (es) 2005-05-16
EP1491541B1 (en) 2007-01-24
PL365294A1 (en) 2004-12-27
SK11852003A3 (sk) 2004-07-07

Similar Documents

Publication Publication Date Title
ECSP034671A (es) Inhibidores de aldosa reductasa del grupo de las piridazinonas
NO20073068L (no) Stereoisomere anrikete 3-aminokarbonylbisykloheptenpyrimidindiaminforindelser og deres anvendelse
AR056850A1 (es) MÉTODOS Y KITS PARA DOSIFICAR NUCLEoSIDOS ANTIVIRALES BETA-D-2',3'-DIDEHIDRO-2',3' DIDEOXI-5-FLUOROCITIDINA
AR032403A1 (es) Combinaciones de inhibidor(es) de la absorcion de esterol con modificador(es) sanguineos para tratar cuadros vasculares
ECSP074704A (es) Combinaciones de inhibidor(es) de la absorción de esterol con modificador(es) sanguíneos para tratar cuadros vasculares
TW200609334A (en) Flame-retardants
WO2005123672A3 (en) Kinase inhibitors
NO20064976L (no) Azanidoler som er nyttige som inhibitorer av rock og andre proteinkinaser
GT200800022A (es) Composiciones lhg para reducir el gusto amargo prolongado de los glucósidos de esteviol
PE20080731A1 (es) Derivados espirocetales comoinhibidores de sglt2
AR056832A1 (es) Procedimiento para tratar el crecimiento celular anormal
ECSP044935A (es) Inhibidores de la dipeptidil peptidasa beta-amino heterocíclica para el tratamiento o la prevención de la diabetes
NO20091326L (no) Indazolderivater som modulatorer av interleukin-1-reseptor-assosiert kinase
NI201000156A (es) Compuestos heterocíclicos novedosos y usos de los mismos.
ECSP099465A (es) Polimorfos de sal de succinato 2-[6-(3-amino-piperidin-1-ilo)-3-metil-2,4-dioxo-3,4-dihidro-2h-pirimidin-1-ilmetil]-4-fluoro-benzonitrilo y métodos
AR067469A1 (es) Composiciones con contenido de difluorometano
NO20081973L (no) PDE inhibitorer og kombinasjoner derav i behandlingen av urologiske lidelser
CR9675A (es) Agente desinfectante
BR0318503A (pt) quinolinas substituìdas como inibidores de enzima proteìna tirosina cinase
ES2173433T3 (es) Procedimiento para la cristalizacion de losartan.
AR054666A1 (es) Metodo y composicion para desinfeccion de alto nivel que emplea compuestos de amonio cuaternario
WO2007014008A3 (en) Benzenesulfonamide inhibitor of ccr2 chemokine receptor
WO2005113759A3 (en) Microbial production of xylitol via a hexose phosphate and a pentose phosphate intermediate
AR056945A1 (es) Carboxanilidas como microbiocidas
BRPI0417433A (pt) processo para preparação de compostos