EA200401614A1 - O-замещённые гидроксиарильные производные - Google Patents

O-замещённые гидроксиарильные производные

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Publication number
EA200401614A1
EA200401614A1 EA200401614A EA200401614A EA200401614A1 EA 200401614 A1 EA200401614 A1 EA 200401614A1 EA 200401614 A EA200401614 A EA 200401614A EA 200401614 A EA200401614 A EA 200401614A EA 200401614 A1 EA200401614 A1 EA 200401614A1
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Eurasian Patent Office
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group
substituted
formula
defined above
meaning defined
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EA200401614A
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EA009051B1 (ru
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Сусуму Муто
Акико Итай
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Инститьют Оф Медисинал Молекьюлар Дизайн. Инк.
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Publication of EA200401614A1 publication Critical patent/EA200401614A1/ru
Publication of EA009051B1 publication Critical patent/EA009051B1/ru

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    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
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    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
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    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/16Amides, e.g. hydroxamic acids
    • A61K31/165Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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    • 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
    • A61K31/425Thiazoles
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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    • 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
    • C07D211/60Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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    • C07D265/241,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with hetero atoms directly attached in positions 2 and 4
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    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
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Abstract

Лекарственное средство, обладающее ингибирующей активностью, направленной на активацию NF-κB, и содержащее в качестве активного ингредиента вещество, выбранное из группы, состоящей из соединений, представленных нижеследующей общей формулой (I), и их фармацевтически приемлемой соли, гидрата и сольвата:где X представляет собой связывающую группу, у которой число атомов в главной цепи составляет 2-5 (где указанная связывающая группа может быть замещенной),A представляет собой ацильную группу, которая может быть замещенной (при условии, что исключаются незамещенная ацетильная группа и незамещенная акрилоильная группа), или C-C-алкильную группу, которая может быть замещенной, либо A связана со связывающей группой X с образованием циклической структуры, которая может быть замещенной,E представляет собой арильную группу, которая может быть замещенной, или гетероарильную группу, которая может быть замещенной,кольцо Z представляет собой арен, который может иметь один или несколько заместителей помимо группы, представленной формулой -O-A, где A имеет значение, определенное выше, и группы, представленной формулой -X-E, где каждый из X и E имеет значение, определенное выше; или гетероарен, который может иметь один или несколько заместителей помимо группы, представленной формулой -O-A, где A имеет значение, определенное выше, и группы, представленной формулой -X-E, где каждый из X и E имеет значение, определенное выше.Международная заявка была опубликована вместе с отчетом о международном поиске.
EA200401614A 2002-06-06 2003-06-05 О-замещенные гидроксиарильные производные EA009051B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2002165482 2002-06-06
PCT/JP2003/007127 WO2003103656A1 (ja) 2002-06-06 2003-06-05 O−置換ヒドロキシアリール誘導体

Publications (2)

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EA200401614A1 true EA200401614A1 (ru) 2005-06-30
EA009051B1 EA009051B1 (ru) 2007-10-26

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US (2) US7626042B2 (ru)
EP (1) EP1512397B1 (ru)
JP (1) JP4743382B2 (ru)
KR (2) KR101118807B1 (ru)
CN (1) CN1658855B (ru)
AU (1) AU2003242118B2 (ru)
CA (1) CA2488363C (ru)
EA (1) EA009051B1 (ru)
TW (1) TW200406198A (ru)
WO (1) WO2003103656A1 (ru)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA82827C2 (en) * 2000-12-18 2008-05-26 Inhibitors against the production and release of inflammatory cytokines
CA2489091A1 (en) * 2002-06-10 2003-12-18 Institute Of Medicinal Molecular Design, Inc. Inhibitors against activation of nf-kappab
US8076352B2 (en) 2004-03-15 2011-12-13 Ptc Therapeutics, Inc. Administration of carboline derivatives useful in the treatment of cancer and other diseases
US8076353B2 (en) 2004-03-15 2011-12-13 Ptc Therapeutics, Inc. Inhibition of VEGF translation
AU2005222632B2 (en) 2004-03-15 2012-02-09 Ptc Therapeutics, Inc. Carboline derivatives useful in the inhibition of angiogenesis
US7767689B2 (en) 2004-03-15 2010-08-03 Ptc Therapeutics, Inc. Carboline derivatives useful in the treatment of cancer
EP1886681A3 (en) * 2004-10-07 2008-11-19 Sulfidris S.r.l. 5-(p-hydroxyphenyl)-3H-1,2-dithiol-3-thione valproate ester
CA2588389A1 (en) * 2004-11-23 2006-06-22 Ptc Therapeutics, Inc. Substituted phenols as active agents inhibiting vegf production
US7671058B2 (en) 2006-06-21 2010-03-02 Institute Of Medicinal Molecular Design, Inc. N-(3,4-disubstituted phenyl) salicylamide derivatives
US8211882B2 (en) * 2008-03-08 2012-07-03 Richard Delarey Wood Glutamate receptor modulators and therapeutic agents
EP2760844B1 (fr) * 2011-09-29 2018-11-21 Ecole Normale Superieure De Lyon Substrat de peptidase fluorogene
AU2013259526B2 (en) * 2012-05-08 2018-02-15 Aeromics, Inc. New methods
EP2767832A1 (en) * 2013-02-18 2014-08-20 Imabiotech Photo or chemolabile conjugates for molecules detection
US9974860B2 (en) 2013-09-13 2018-05-22 Akiko Itai Aqueous solution formulation and method for manufacturing same
WO2015069948A1 (en) 2013-11-06 2015-05-14 Aeromics, Llc Novel methods
WO2016077787A1 (en) * 2014-11-13 2016-05-19 Aeromics, Llc Novel methods
US10525021B2 (en) 2014-11-18 2020-01-07 Rutgers, The State University Of New Jersey Mitochondrial uncouplers for treatment of metabolic diseases and cancer
CZ2014915A3 (cs) * 2014-12-16 2016-02-24 Univerzita Karlova v Praze, Farmaceutická fakulta v Hradci Králové Substituovaný derivát kyslíkatých kyselin fosforu, jeho použití a farmaceutický přípravek ho obsahující
CN105777808B (zh) * 2014-12-23 2018-11-09 中国人民解放军军事医学科学院毒物药物研究所 替唑尼特磷酸酯和烷基磺酸酯及其在药学中的应用
CA3011289A1 (en) * 2016-01-12 2017-07-20 Taipei Medical University Compounds for inhibiting cancer and virus
CN115093443A (zh) 2016-05-13 2022-09-23 埃罗米克斯公司 晶体
EP3458454B1 (en) 2016-05-18 2021-11-24 Rutgers, The State University of New Jersey 2-hydroxy-n-(benzo[d]thiazol-2-yl)benzamide derivatives as mitochondrial uncouplers for the treatment of metabolic diseases and cancer
CN106748914B (zh) * 2016-11-18 2019-04-09 浙江工业大学 O-苯磺酰-4-三氟甲基水杨酰胺类化合物及其在制备抗胃癌药物中的应用
CN106588716B (zh) * 2016-11-18 2019-04-09 浙江工业大学 O-苯磺酰-4-三氟甲基水杨酰胺类化合物及其在制备抗肺癌药物中的应用
CN113382736A (zh) * 2018-11-01 2021-09-10 加利福尼亚大学董事会 用于治疗雄激素介导的疾病的化合物、组合物和方法
US20230015875A1 (en) * 2019-12-14 2023-01-19 Shanghai East Hospital Ion Channel Antagonists/Blockers and Uses Thereof
MX2023001493A (es) * 2020-08-05 2023-06-23 Jiangsu Simcere Pharm Co Ltd Composicion farmaceutica de un inhibidor de la acuaporina y metodo para la preparacion de la misma.

Family Cites Families (95)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US87650A (en) * 1869-03-09 Improvement in the manufacture of artificial fuel
US69267A (en) * 1867-09-24 Improved means for extinguishing fire in steamships
US157844A (en) * 1874-12-15 Improvement in steam x c cylinder lubricators
US122244A (en) * 1871-12-26 Improvement in fire-extinguishers
US48891A (en) * 1865-07-25 Improved vessel for holding petroleum
US165398A (en) * 1875-07-06 Improvement in processes for cleansing gas-retorts
US2199A (en) * 1841-07-29 Improvement in the manufacture of buttons
US19412A (en) * 1858-02-23 Improvement in shovel-plows
US259877A (en) * 1882-06-20 Under-garment for infants
US19958A (en) * 1858-04-13 Improvement in raking attachments to harvesters
US14811A (en) * 1856-05-06 Process of preparing elastic india-rubber cloth
JPS37225B1 (ru) 1958-07-23 1962-01-23
NL292958A (ru) 1962-05-29 1900-01-01
GB1099865A (en) 1965-10-11 1968-01-17 Stecker Internat S P A Benzoazinediones and germicidal compositions made therewith
FR1481713A (fr) 1965-10-11 1967-05-19 Stecker Internat S P A Benzoazinediones et compositions germicides qui les contiennent
DE2120862A1 (de) * 1971-04-28 1972-11-09 Farbenfabriken Bayer Ag, 5090 Leverkusen 3,5-Disubstituierte 2-Acyloxybenzoesäureanilide, Verfahren zu ihrer Herstellung und ihre insektizide und akarizide Verwendung
JPS52110835A (en) 1976-03-11 1977-09-17 Microbial Chem Res Found Remedy for immunological diseases containing benzanilide derivative as active ingredient
FR2434158A1 (fr) 1978-08-25 1980-03-21 Esteve Int Prod Nouveaux derives de 1,3-benzoxazine-2,4-dione, leur preparation et leur application en tant que medicaments
JPS5673054A (en) * 1979-11-20 1981-06-17 Hodogaya Chem Co Ltd Benzamide derivative and herbicide containing the same
US4358443A (en) 1980-04-14 1982-11-09 The Research Foundation Of State University Of New York Method and composition for controlling the growth of microorganisms
JPS56156251A (en) * 1980-05-06 1981-12-02 Hodogaya Chem Co Ltd Benzamide derivative and herbicide comprising it
CA1219587A (en) 1981-12-14 1987-03-24 Norman P. Jensen Hydroxybenzylaminobenzenes as anti-inflammatory agents
JPS59118750A (ja) 1982-12-27 1984-07-09 Eisai Co Ltd カルボン酸アミド化合物およびその誘導体
US4725590A (en) 1983-08-24 1988-02-16 Lever Brothers Company Method of relieving pain and inflammatory conditions employing substituted salicylamides
JPS6299329A (ja) * 1983-08-24 1987-05-08 ユニリ−バ−・ナ−ムロ−ゼ・ベンノ−トシヤ−プ 皮膚用抗炎症組成物
US4560549A (en) 1983-08-24 1985-12-24 Lever Brothers Company Method of relieving pain and inflammatory conditions employing substituted salicylamides
US4742083A (en) 1983-08-24 1988-05-03 Lever Brothers Company Method of relieving pain and inflammatory conditions employing substituted salicylamides
JPS6230780A (ja) 1985-04-17 1987-02-09 Ss Pharmaceut Co Ltd 1,7−ナフチリジン誘導体及びこれを含有する薬剤
US4939133A (en) 1985-10-01 1990-07-03 Warner-Lambert Company N-substituted-2-hydroxy-α-oxo-benzeneacetamides and pharmaceutical compositions having activity as modulators of the arachidonic acid cascade
JPH0755902B2 (ja) 1986-10-21 1995-06-14 株式会社ツムラ アルド−スリダクタ−ゼ阻害剤
JPS6487491A (en) 1987-09-30 1989-03-31 Hitachi Ltd Guide apparatus for passenger conveyor
JPH01121225A (ja) 1987-11-02 1989-05-12 Agency Of Ind Science & Technol エチレン性不飽和化合物の製造方法
US4952588A (en) 1987-11-27 1990-08-28 Hoechst-Roussel Pharmaceuticals Inc. 1-aryl-3-quinoline-and 1-aryl-3-isoquinoline-carboxamides
US4966906A (en) 1987-11-27 1990-10-30 Hoechst-Roussel Pharmaceuticals Inc. 1-aryl-3-isoquinolinecarboxamides
US4786644A (en) 1987-11-27 1988-11-22 Hoechst-Roussel Pharmaceuticals Inc. 1-aryl-3-quinolinecarboxamide
JP2988739B2 (ja) 1990-04-16 1999-12-13 協和醗酵工業株式会社 1,8−ナフチリジン−2−オン誘導体
JPH04217916A (ja) 1990-06-21 1992-08-07 Japan Tobacco Inc 抗炎症剤
CA2054339C (en) 1990-11-02 2002-12-24 Francesco G. Salituro 3-amidoindolyl derivatives
US5192753A (en) 1991-04-23 1993-03-09 Mcgeer Patrick L Anti-rheumatoid arthritic drugs in the treatment of dementia
US6159988A (en) 1992-01-16 2000-12-12 Hoeschst Aktiengesellschaft Arylcycloalkyl derivatives, their production and their use
CZ285937B6 (cs) 1992-01-16 1999-12-15 Hoechst Aktiengesellschaft Arylcykloalkylové deriváty, způsob přípravy těchto derivátů a jejich použití
JP2546622B2 (ja) 1994-02-14 1996-10-23 オリエント時計株式会社 複合混合多層膜
AU4152296A (en) 1994-12-07 1996-06-26 Warner-Lambert Company Novel glutamate receptor antagonists: fused cycloalkylquinoxalinediones
JPH08175990A (ja) 1994-12-19 1996-07-09 Mitsubishi Chem Corp Pi3キナーゼ阻害剤とその製造法
DE19505751A1 (de) * 1995-02-20 1996-08-22 Basf Ag Wäßrige Alkyldiketen-Dispersionen und ihre Verwendung als Leimungsmittel für Papier
US5811428A (en) 1995-12-18 1998-09-22 Signal Pharmaceuticals, Inc. Pyrimidine carboxamides and related compounds and methods for treating inflammatory conditions
US5852028A (en) 1995-12-18 1998-12-22 Signal Pharmaceuticals, Inc. Pyrimidine carboxylates and related compounds and methods for treating inflammatory conditions
CA2230894A1 (en) 1995-09-01 1997-03-13 Signal Pharmaceuticals, Inc. Pyrimidine carboxamides and related compounds and methods for treating inflammatory conditions
US5935966A (en) 1995-09-01 1999-08-10 Signal Pharmaceuticals, Inc. Pyrimidine carboxylates and related compounds and methods for treating inflammatory conditions
JPH09169747A (ja) 1995-12-18 1997-06-30 Kyorin Pharmaceut Co Ltd 新規置換フェニルチアゾリジン−2,4−ジオン誘導体及びその製造法
JPH09203951A (ja) 1996-01-26 1997-08-05 Minolta Co Ltd カートリッジホルダーの防水機構
JPH09227561A (ja) 1996-02-21 1997-09-02 Tanabe Seiyaku Co Ltd キサンチン誘導体
JPH1045738A (ja) 1996-07-29 1998-02-17 Microbial Chem Res Found 抗生物質エポキシキノマイシンcおよびdとその製造法ならびに抗リウマチ剤
ITMI962356A1 (it) 1996-11-13 1998-05-13 Uni Degli Studi Di Brescia D I Uso di composti derivati da molecole ad attivita' antinfiammatoria di tipo non steroideo per la prevenzione e il trattamento di
DK0960335T3 (da) 1997-01-15 2005-06-20 Telik Inc Modulatorer af insulinreceptoraktivitet
JPH1121243A (ja) 1997-05-06 1999-01-26 Tanabe Seiyaku Co Ltd 医薬組成物
JP3840317B2 (ja) 1997-08-01 2006-11-01 シーケーディ株式会社 手動機構付エアオペレイト弁
US6117859A (en) 1997-11-04 2000-09-12 The Research Foundation Of State University Of New York Method of relieving chronic inflammation by using 5-alkylsulfonylsalicylanilides
US6022884A (en) 1997-11-07 2000-02-08 Amgen Inc. Substituted pyridine compounds and methods of use
US6262096B1 (en) * 1997-11-12 2001-07-17 Bristol-Myers Squibb Company Aminothiazole inhibitors of cyclin dependent kinases
JPH11180873A (ja) 1997-12-22 1999-07-06 Kaken Shoyaku Kk NF−κB活性阻害剤
JPH11217361A (ja) 1998-01-29 1999-08-10 Fuji Photo Film Co Ltd ナフトキノン化合物及び該化合物からなる医薬
AU2662899A (en) * 1998-02-13 1999-08-30 Medinox, Inc. Methods for the controlled delivery of carbon disulfide for the treatment of inflammatory conditions
JP2000080041A (ja) 1998-03-09 2000-03-21 Tanabe Seiyaku Co Ltd 医薬組成物
WO1999046267A1 (en) * 1998-03-12 1999-09-16 Novo Nordisk A/S Modulators of protein tyrosine phosphatases (ptpases)
US6262044B1 (en) 1998-03-12 2001-07-17 Novo Nordisk A/S Modulators of protein tyrosine phosphatases (PTPASES)
ATE308546T1 (de) 1998-03-12 2005-11-15 Novo Nordisk As Modulatoren der protein tyrosin phosphatase (ptpases)
AU2713699A (en) * 1998-03-12 1999-09-27 Novo Nordisk A/S Modulators of protein tyrosine phosphatases (ptpases)
US6225329B1 (en) 1998-03-12 2001-05-01 Novo Nordisk A/S Modulators of protein tyrosine phosphatases (PTPases)
US20020019412A1 (en) 1998-03-12 2002-02-14 Henrik Sune Andersen Modulators of protein tyrosine phosphatases (ptpases)
US20020002199A1 (en) 1998-03-12 2002-01-03 Lone Jeppesen Modulators of protein tyrosine phosphatases (ptpases)
AU2713799A (en) * 1998-03-12 1999-09-27 Novo Nordisk A/S Modulators of protein tyrosine phosphatases (ptpases)
CN1181817C (zh) * 1998-03-20 2004-12-29 第一三得利制药株式会社 以苯基甲苯醌为有效成分的NF-kB抑制剂
HUP0102782A3 (en) * 1998-06-19 2002-12-28 Smithkline Beecham Corp Salycilanilide as inhibitors of transcription factor nf-kb
ES2219033T3 (es) 1998-07-22 2004-11-16 Daiichi Suntory Pharma Co., Ltd. Inhibidores de nf-kappa b que contienen derivados de indano como ingrediente activo.
CA2343101A1 (en) * 1998-09-11 2000-03-23 Ajinomoto Co., Inc. Benzene derivatives and medicinal use thereof
JP2000169479A (ja) * 1998-12-09 2000-06-20 Kyowa Hakko Kogyo Co Ltd NF−κB活性化阻害剤
US6653309B1 (en) 1999-04-26 2003-11-25 Vertex Pharmaceuticals Incorporated Inhibitors of IMPDH enzyme technical field of the invention
US6498165B1 (en) * 1999-06-30 2002-12-24 Merck & Co., Inc. Src kinase inhibitor compounds
WO2001010865A1 (fr) 1999-08-06 2001-02-15 Takeda Chemical Industries, Ltd. INHIBITEURS DE p38MAP KINASE
WO2001012588A1 (fr) * 1999-08-11 2001-02-22 Mercian Corporation Derives de salicylamide
EP1088819B1 (en) 1999-09-30 2005-06-15 Pfizer Products Inc. 6-azauracil derivatives as thyroid receptor ligands
US6787652B1 (en) 1999-09-30 2004-09-07 Pfizer, Inc. 6-Azauracil derivatives as thyroid receptor ligands
US6706766B2 (en) 1999-12-13 2004-03-16 President And Fellows Of Harvard College Small molecules used to increase cell death
US6414013B1 (en) 2000-06-19 2002-07-02 Pharmacia & Upjohn S.P.A. Thiophene compounds, process for preparing the same, and pharmaceutical compositions containing the same background of the invention
EP1182251A1 (en) * 2000-08-11 2002-02-27 Yissum Research Development Company of the Hebrew University of Jerusalem Methods for identifying compounds that inhibit ubiquitin-mediated proteolysis of IkB
UA82827C2 (en) * 2000-12-18 2008-05-26 Inhibitors against the production and release of inflammatory cytokines
CA2432713C (en) 2000-12-22 2009-10-27 Ishihara Sangyo Kaisha, Ltd. Aniline derivatives or salts thereof and cytokine production inhibitors containing the same
JPWO2002076918A1 (ja) * 2001-03-27 2004-07-15 第一サントリーファーマ株式会社 置換安息香酸誘導体を有効成分とするNF−κB阻害剤
AU2003242131A1 (en) 2002-06-05 2003-12-22 Institute Of Medicinal Molecular Design, Inc. Immunity-related protein kinase inhibitors
AU2003242127A1 (en) 2002-06-05 2003-12-22 Institute Of Medicinal Molecular Design, Inc. Inhibitors against the activation of ap-1 and nfat
WO2003103665A1 (ja) 2002-06-06 2003-12-18 株式会社医薬分子設計研究所 抗アレルギー薬
CA2489091A1 (en) * 2002-06-10 2003-12-18 Institute Of Medicinal Molecular Design, Inc. Inhibitors against activation of nf-kappab
EP1535610A4 (en) 2002-06-10 2008-12-31 Inst Med Molecular Design Inc THERAPEUTIC CANCER
AU2003242124A1 (en) * 2002-06-11 2003-12-22 Institute Of Medicinal Molecular Design, Inc. Medicament for treatment of neurodegenerative diseases

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KR101118807B1 (ko) 2012-04-12
US20060094718A1 (en) 2006-05-04
AU2003242118B2 (en) 2008-09-11
JP4743382B2 (ja) 2011-08-10
CA2488363C (en) 2011-01-04
US20100113770A1 (en) 2010-05-06
JPWO2003103656A1 (ja) 2005-10-06
US7626042B2 (en) 2009-12-01
TW200406198A (en) 2004-05-01
KR20110028554A (ko) 2011-03-18
AU2003242118A1 (en) 2003-12-22
EP1512397A1 (en) 2005-03-09
CN1658855B (zh) 2010-04-28
EP1512397B1 (en) 2014-10-08
WO2003103656A1 (ja) 2003-12-18
KR20050023288A (ko) 2005-03-09
CA2488363A1 (en) 2003-12-18
CN1658855A (zh) 2005-08-24
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