ID27833A - METODA UNTUK MENGOBATI ATEROSKLEROSIS DENGAN MENGGUNAKAN INHIBITOR aP2 DAN KOMBINASINYA - Google Patents

METODA UNTUK MENGOBATI ATEROSKLEROSIS DENGAN MENGGUNAKAN INHIBITOR aP2 DAN KOMBINASINYA

Info

Publication number
ID27833A
ID27833A IDW20010626A ID20010626A ID27833A ID 27833 A ID27833 A ID 27833A ID W20010626 A IDW20010626 A ID W20010626A ID 20010626 A ID20010626 A ID 20010626A ID 27833 A ID27833 A ID 27833A
Authority
ID
Indonesia
Prior art keywords
aterosclelerosis
inhibitors
combinations
treatment
methods
Prior art date
Application number
IDW20010626A
Other languages
English (en)
Indonesian (id)
Inventor
Jeffry A Robl
Rex A Parker
Scott A Biller
Haris Jamil
Bruce L Jacobson
Krishna Kudukula
Original Assignee
Bristol Myers Squibb Co
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22280975&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ID27833(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of ID27833A publication Critical patent/ID27833A/id

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/4211,3-Oxazoles, e.g. pemoline, trimethadione
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/42Oxazoles
    • A61K31/422Oxazoles not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00Medicinal preparations containing peptides
    • A61K38/16Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • 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
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/48Drugs for disorders of the endocrine system of the pancreatic hormones
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical & Material Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Diabetes (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Zoology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Immunology (AREA)
  • Endocrinology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Urology & Nephrology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Vascular Medicine (AREA)
  • Cardiology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines Containing Plant Substances (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Steroid Compounds (AREA)
IDW20010626A 1998-09-17 1999-09-13 METODA UNTUK MENGOBATI ATEROSKLEROSIS DENGAN MENGGUNAKAN INHIBITOR aP2 DAN KOMBINASINYA ID27833A (id)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US10067798P 1998-09-17 1998-09-17

Publications (1)

Publication Number Publication Date
ID27833A true ID27833A (id) 2001-04-26

Family

ID=22280975

Family Applications (2)

Application Number Title Priority Date Filing Date
IDW20010626A ID27833A (id) 1998-09-17 1999-09-13 METODA UNTUK MENGOBATI ATEROSKLEROSIS DENGAN MENGGUNAKAN INHIBITOR aP2 DAN KOMBINASINYA
IDW20010624A ID28450A (id) 1998-09-17 1999-09-13 METODA UNTUK MENGOBATI DIABETES DENGAN MENGGUNAKAN INHIBITOR aP2 DAN KOMBINASINYA

Family Applications After (1)

Application Number Title Priority Date Filing Date
IDW20010624A ID28450A (id) 1998-09-17 1999-09-13 METODA UNTUK MENGOBATI DIABETES DENGAN MENGGUNAKAN INHIBITOR aP2 DAN KOMBINASINYA

Country Status (30)

Country Link
US (1) US20020035064A1 (fr)
EP (2) EP1121129B1 (fr)
JP (2) JP2002524518A (fr)
KR (2) KR20010075150A (fr)
CN (2) CN1319012A (fr)
AT (1) ATE406898T1 (fr)
AU (2) AU755563B2 (fr)
BG (2) BG105431A (fr)
BR (2) BR9913831A (fr)
CA (2) CA2344300A1 (fr)
CO (2) CO5130025A1 (fr)
CZ (2) CZ2001964A3 (fr)
DE (1) DE69939481D1 (fr)
EE (2) EE200100155A (fr)
ES (1) ES2311306T3 (fr)
GE (2) GEP20033044B (fr)
HU (2) HUP0104108A2 (fr)
ID (2) ID27833A (fr)
IL (2) IL141786A0 (fr)
LT (2) LT4870B (fr)
LV (2) LV12686B (fr)
NO (2) NO20011351L (fr)
NZ (2) NZ510207A (fr)
PE (2) PE20001047A1 (fr)
PL (2) PL346660A1 (fr)
SK (1) SK3202001A3 (fr)
TR (2) TR200100774T2 (fr)
UY (2) UY25713A1 (fr)
WO (2) WO2000015229A1 (fr)
ZA (2) ZA200207430B (fr)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE69834508T2 (de) * 1997-11-19 2006-11-23 Takeda Pharmaceutical Co. Ltd. Apoptoseinhibitoren
AU2005201289B2 (en) * 1999-02-12 2008-04-17 President And Fellows Of Harvard College Inhibiting formation of atherosclerotic lesions
DE60041246D1 (de) * 1999-02-12 2009-02-12 Harvard College Hemmung der bildung von atherosklerotischen wunden mittels afabp antisens nukleinsäuren
US6548529B1 (en) * 1999-04-05 2003-04-15 Bristol-Myers Squibb Company Heterocyclic containing biphenyl aP2 inhibitors and method
US6586438B2 (en) 1999-11-03 2003-07-01 Bristol-Myers Squibb Co. Antidiabetic formulation and method
CA2396596A1 (fr) 2000-01-28 2001-08-02 Bristol-Myers Squibb Company Inhibiteurs de tetrahydropyrimidone de la proteine de liaison de l'acide gras et procede correspondant
WO2002040448A1 (fr) * 2000-11-20 2002-05-23 Bristol-Myers Squibb Company Derives de pyridones utilises en tant qu'inhibiteurs ap2
US20040143015A1 (en) * 2001-03-12 2004-07-22 Villhauer Edwin Bernard Combination of organic compounds
WO2003006023A1 (fr) 2001-07-13 2003-01-23 Bristol-Myers Squibb Company Inhibiteurs pyrazinones inhibant une proteine de liaison aux acides gras et procede
WO2003007888A2 (fr) * 2001-07-20 2003-01-30 Adipogenix, Inc. Composes de modulation d'accumulation de graisse
EP1443919A4 (fr) 2001-11-16 2006-03-22 Bristol Myers Squibb Co Inhibiteurs doubles de la proteine de liaison des acides gras des adipocytes et de la proteine de liaison des acides gras des keratinocytes
ATE490244T1 (de) 2003-01-27 2010-12-15 Merck Sharp & Dohme Substituierte pyrazole, zusammensetzungen,die solche verbindungen enthalten, und anwendungsverfahren
AU2004224825A1 (en) * 2003-03-26 2004-10-07 Crc For Asthma Limited Therapeutic and prophylactic compositions and uses therefor
WO2004096977A2 (fr) * 2003-04-30 2004-11-11 Pfizer Products Inc. Structure cristalline de la proteine de liaison des lipides dans les adipocytes de l'homo sapiens
WO2005087234A1 (fr) * 2004-03-05 2005-09-22 The Trustees Of The University Of Pennsylvania Traitement a faibles effets secondaires contre des affections liees a l'hyperlipidemie et l'hypercholesterolemie
DK1756064T3 (da) 2004-06-04 2008-09-22 Merck & Co Inc Pyrazolderivater, sammensætninger indeholdende sådanne forbindelser og anvendelsesmetoder
KR101364762B1 (ko) 2005-02-17 2014-02-17 신타 파마슈티칼스 코프. 증식성 장애의 치료를 위한 화합물
CN101300232A (zh) 2005-07-26 2008-11-05 默克公司 合成取代的吡唑的方法
EP1951220A2 (fr) * 2005-10-18 2008-08-06 Aegerion Pharmaceuticals Compositions destinees a l'abbaissement du cholesterol serique et/ou des triglycerides
AU2007254827A1 (en) * 2006-06-02 2007-12-13 San Diego State University Research Foundation Compositions and methods for ameliorating hyperlipidemia
WO2008079398A1 (fr) * 2006-12-21 2008-07-03 Aegerion Pharmaceuticals, Inc. Procédés de traitement de l'obésité à l'aide d'une combinaison comprenant un inhibiteur de mtp et un inhibiteur de l'absorption du cholestérol
EP2358716B1 (fr) * 2008-11-12 2016-01-06 Merck Sharp & Dohme Corp. Inhibiteurs de la protéine de liaison aux acides gras (fabp)
AU2010221182B2 (en) * 2009-03-05 2016-07-28 President And Fellows Of Harvard College Secreted aP2 and methods of inhibiting same
JP6514282B2 (ja) * 2014-03-24 2019-05-15 花王株式会社 Gip上昇抑制剤の評価又は選択方法
JP6223376B2 (ja) * 2014-03-24 2017-11-01 花王株式会社 Gip上昇抑制剤の評価又は選択方法
WO2016176656A2 (fr) 2015-04-30 2016-11-03 President And Fellows Of Harvard College Anticorps anti-ap2 et agents de liaison à l'antigène utilisables en vue du traitement d'affections métaboliques
CN109642908B (zh) * 2016-06-27 2022-08-16 哈佛学院院长及董事 可用于治疗代谢病症的化合物
CA3066733A1 (fr) 2017-06-09 2018-12-13 President And Fellows Of Harvard College Procede d'identification de composes utiles pour traiter une lipogenese deregulee, le diabete et autres troubles apparentes

Family Cites Families (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2129012A1 (de) 1971-06-11 1973-01-04 Merck Patent Gmbh Azol-derivate
FR2156486A1 (en) 1971-10-22 1973-06-01 Roussel Uclaf Oxazolyl oxy or thio acetic acids - analgesics antipyretics and anti-inflammatories
JPS5612114B2 (fr) 1974-06-07 1981-03-18
GB1507032A (en) 1974-08-06 1978-04-12 Serono Lab 2-thiol-4,5-diphenyloxazole s-derivatives
NO154918C (no) 1977-08-27 1987-01-14 Bayer Ag Analogifremgangsmaate til fremstilling av terapeutisk aktive derivater av 3,4,5-trihydroksypiperidin.
US4231938A (en) 1979-06-15 1980-11-04 Merck & Co., Inc. Hypocholesteremic fermentation products and process of preparation
JPS6051189A (ja) 1983-08-30 1985-03-22 Sankyo Co Ltd チアゾリジン誘導体およびその製造法
CA1327360C (fr) 1983-11-14 1994-03-01 William F. Hoffman Analogues oxo d'agents antihypercholesterolemiants ayant les caracteristiques de la mevinoline
DE3543999A1 (de) 1985-12-13 1987-06-19 Bayer Ag Hochreine acarbose
PT87539B (pt) 1987-05-22 1992-09-30 Squibb & Sons Inc Processo para a preparacao de inibidores da reductase de hmg-coa contendo fosforo e novos intermediarios
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
US5218124A (en) * 1989-10-27 1993-06-08 American Home Products Corporation Substituted benzoylbenzene-, biphenyl- and 2-oxazole-alkanoic acid derivatives as inhibitors of pla2 and lipoxygenase
PT95690A (pt) * 1989-10-27 1991-09-13 American Home Prod Processo para a preparacao de derivados substituidos de acidos benzoilbenzo-, bifenil- e 2-oxazol-alcanoicos, uteis como inibidores de pla2 e da lipoxigenase
US5262540A (en) * 1989-12-20 1993-11-16 Bristol-Myers Squibb Company [2(4,5-diaryl-2 oxazoyl substituted phenoxy alkanoic acid and esters
FR2663331B1 (fr) 1990-06-14 1994-05-06 Bellon Laboratoires Nouveaux derives de l'oxazole, leur preparation et les compositions pharmaceutiques qui les contiennent.
GB9019841D0 (en) * 1990-09-11 1990-10-24 Smith Kline French Lab Compounds
US5187188A (en) * 1992-04-03 1993-02-16 Bristol-Myers Squibb Company Oxazole carboxylic acid derivatives
US5348969A (en) * 1992-04-03 1994-09-20 Bristol-Myers Squibb Company Diphenyloxazolyl-oxazoles as platelet aggregation inhibitors
US5254576A (en) * 1992-04-03 1993-10-19 Bristol-Myers Squibb Company Diphenyl-heterocyclic-oxazole as platelet aggregation inhibitors
US5594016A (en) 1992-12-28 1997-01-14 Mitsubishi Chemical Corporation Naphthalene derivatives
US5346701A (en) 1993-02-22 1994-09-13 Theratech, Inc. Transmucosal delivery of macromolecular drugs
US5362879A (en) * 1993-04-15 1994-11-08 Bristol-Myers Squibb Company 4-5-diphenyloxazole derivatives as inhibitors of blood platelet aggregation
US5739135A (en) 1993-09-03 1998-04-14 Bristol-Myers Squibb Company Inhibitors of microsomal triglyceride transfer protein and method
DE4340781C3 (de) 1993-11-30 2000-01-27 Novartis Ag Cyclosporin enthaltende flüssige Zubereitungen und Verfahren zu ihrer Herstellung
PT736018E (pt) * 1993-12-20 2000-10-31 Fujisawa Pharmaceutical Co Derivados de 4,5-diariloxazol
US5599770A (en) 1994-07-15 1997-02-04 Kureha Kagaku Kogyo Kabushiki Kaisha Herbicidal composition containing 2-benzyloxypyrimidine derivatives, processes for producing the derivatives and 2-benzyloxypyrimidine derivatives
WO1996004261A1 (fr) 1994-07-29 1996-02-15 Smithkline Beecham Plc Benzoxoazoles et derives de pryridine destines a etre utilises pour le traitement du diabete tardif
US5612359A (en) * 1994-08-26 1997-03-18 Bristol-Myers Squibb Company Substituted biphenyl isoxazole sulfonamides
UA56992C2 (uk) 1995-05-08 2003-06-16 Фармація Енд Апджон Компані <font face="Symbol">a</font>-ПІРИМІДИНТІОАЛКІЛЗАМІЩЕНІ ТА <font face="Symbol">a</font>-ПІРИМІДИНОКСОАЛКІЛЗАМІЩЕНІ СПОЛУКИ
US5620997A (en) 1995-05-31 1997-04-15 Warner-Lambert Company Isothiazolones
JP3144624B2 (ja) 1995-06-02 2001-03-12 杏林製薬株式会社 N−ベンジルジオキソチアゾリジルベンズアミド誘導体及びその製造法
AU6966696A (en) 1995-10-05 1997-04-28 Warner-Lambert Company Method for treating and preventing inflammation and atherosclerosis
GB9600231D0 (en) 1996-01-05 1996-03-06 Foster Wheeler Petrol Dev Ltd Spacing bouy for flexible risers
AUPO134596A0 (en) 1996-08-01 1996-08-22 Jal Pastoral Co. Pty Ltd Demountable article carrier for motor vehicles
US5760246A (en) 1996-12-17 1998-06-02 Biller; Scott A. Conformationally restricted aromatic inhibitors of microsomal triglyceride transfer protein and method

Also Published As

Publication number Publication date
ZA200207433B (en) 2003-10-27
NO20011352L (no) 2001-05-11
NO20011351D0 (no) 2001-03-16
NZ510209A (en) 2003-07-25
BR9913831A (pt) 2001-05-29
LT2001023A (en) 2001-08-27
UY25714A1 (es) 2001-08-27
BG105431A (en) 2001-12-29
CO5130025A1 (es) 2002-02-27
CA2344309A1 (fr) 2000-03-23
PL346660A1 (en) 2002-02-25
ZA200207430B (en) 2003-09-16
JP2002524518A (ja) 2002-08-06
EE200100154A (et) 2002-12-16
CZ2001964A3 (cs) 2002-01-16
AU6143799A (en) 2000-04-03
EE04356B1 (et) 2004-10-15
EP1113801A1 (fr) 2001-07-11
CO5130026A1 (es) 2002-02-27
BG105432A (en) 2001-12-29
HUP0104240A2 (hu) 2002-03-28
LT4870B (lt) 2001-12-27
US20020035064A1 (en) 2002-03-21
TR200100774T2 (tr) 2001-12-21
EP1121129B1 (fr) 2008-09-03
NO20011352D0 (no) 2001-03-16
EP1121129A1 (fr) 2001-08-08
DE69939481D1 (de) 2008-10-16
UY25713A1 (es) 2001-08-27
AU754488B2 (en) 2002-11-14
EE200100155A (et) 2002-08-15
KR20010075150A (ko) 2001-08-09
LV12687A (en) 2001-07-20
IL141786A0 (en) 2002-03-10
IL141785A0 (en) 2002-03-10
ATE406898T1 (de) 2008-09-15
BR9913833A (pt) 2001-05-29
CN1317970A (zh) 2001-10-17
TR200100773T2 (tr) 2001-07-23
LV12686A (en) 2001-07-20
CZ2001965A3 (cs) 2002-02-13
EP1121129A4 (fr) 2002-10-16
ES2311306T3 (es) 2009-02-01
WO2000015230A1 (fr) 2000-03-23
LT4871B (lt) 2001-12-27
LV12686B (lv) 2001-10-20
PE20001047A1 (es) 2000-12-24
SK3202001A3 (en) 2002-04-04
PL346661A1 (en) 2002-02-25
EP1113801A4 (fr) 2002-10-02
GEP20033045B (en) 2003-08-25
AU755563B2 (en) 2002-12-12
WO2000015229A1 (fr) 2000-03-23
ID28450A (id) 2001-05-24
PE20001056A1 (es) 2000-12-24
LV12687B (lv) 2001-10-20
GEP20033044B (en) 2003-08-25
LT2001022A (en) 2001-08-27
CA2344300A1 (fr) 2000-03-23
NO20011351L (no) 2001-05-11
CN1319012A (zh) 2001-10-24
HUP0104108A2 (hu) 2002-03-28
AU6387799A (en) 2000-04-03
JP2002524517A (ja) 2002-08-06
KR20010079842A (ko) 2001-08-22
NZ510207A (en) 2003-08-29

Similar Documents

Publication Publication Date Title
ID27833A (id) METODA UNTUK MENGOBATI ATEROSKLEROSIS DENGAN MENGGUNAKAN INHIBITOR aP2 DAN KOMBINASINYA
WO2000061167A3 (fr) TRAITEMENT DU SYNDROME MYELOPROLIFERATIF AU MOYEN D&#39;INHIBITEURS DE L&#39;ACTIVITE DES PROTEASOMES ET DE NF-λB
PT971713E (pt) Utilizacao de inibidores da colinesterase para tratamento de desordens da atencao
BR0311375A (pt) Composição farmacêutica, uso da mesma, e, método para o tratamento de demência ou dano cognitivo suave em um mamìfero
ES2172657T3 (es) Inhibidores de trombina.
DK0946166T3 (da) Anvendelse af matrixmetalloproteinaseinhibitorer til fremme af sårheling
DK1427409T3 (da) Fremgangsmåde til behandling eller forhindring af vaskulær inflammation under brug af en eller flere sterolabssorptionsinhibitorer
EA199800988A1 (ru) Бифенилсульфонамидные ингибиторы матричных металлопротеиназ
BR9713522A (pt) Método de uso de inibidores da cicloxigenase-2 como agentes antiangiogênicos.
MX9805290A (es) Utilizacion de inhibidores de la actividad del acido retinoico para tratar las pieles sensibles y/o los daños agudos inducidos por las radiaciones ultravioleta.
EA199901043A1 (ru) ИНГИБИТОРЫ ФАРНЕЗИЛТРАНСФЕРАЗЫ В КОМБИНАЦИИ С ИНГИБИТОРАМИ HMG-CoA-РЕДУКТАЗЫ ДЛЯ ЛЕЧЕНИЯ РАКА
BR9808923B1 (pt) processos para fazer compostos inibidores de ciclooxigenase-2, e, compostos intermediÁrios para fazer inibidores de ciclooxigenase-2.
NO981578D0 (no) FremgangsmÕte for hemming av plasminogenaktivatorhemmer I
MXPA02004699A (es) Derivados de acidos hidroxieicosatetraenoico modificados con cadena omega y metodos de su uso para el tratameinto del ojo reseco.
EE9700350A (et) COMT-inhibiitorite uus kasutamine ja diabeetiliste vaskulaarsete häirete ärahoidmise meetod
ATE234800T1 (de) Verfahren zur synthese von taxanen
MY140504A (en) Statin-mmp inhibitor combinations
DE69824862D1 (de) Zusammenstellungen zur verbesserten wundheilung
BR0112460A (pt) Método para tratamento de sépsis
DE60001932D1 (de) Behandlungsverfahren von kontinuierlich gewalzten stahlbändern und damit hergestellte produkte
AU2177701A (en) Use of hmg-coa reductase inhibitors for treating seborrhea
BR9807920A (pt) Processos para tratamento de uma demência em um sujeito e para prevenção de uma demência
ECSP992885A (es) Combinaciones de estatina-inhibidor de mmp
ECSP961804A (es) Nuevos compuestos monociclicos de b -.lactama