ES2569660T3 - Inhibidores de la IRE-1alfa - Google Patents

Inhibidores de la IRE-1alfa Download PDF

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Publication number
ES2569660T3
ES2569660T3 ES12171206.1T ES12171206T ES2569660T3 ES 2569660 T3 ES2569660 T3 ES 2569660T3 ES 12171206 T ES12171206 T ES 12171206T ES 2569660 T3 ES2569660 T3 ES 2569660T3
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ire
compound
nmr
compounds
hydrogen
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Spanish (es)
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John Bruce Patterson
David Gregory Lonergan
Gary A. Flynn
Qingping Zeng
Peter V. Pallai
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Mannkind Corp
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Mannkind Corp
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    • A61K31/166—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the carbon of a carboxamide group directly attached to the aromatic ring, e.g. procainamide, procarbazine, metoclopramide, labetalol
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MX (1) MX2009013332A (enExample)
WO (1) WO2008154484A1 (enExample)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103450077B (zh) * 2007-06-08 2016-07-06 满康德股份有限公司 IRE-1α抑制剂
JP2013500265A (ja) * 2009-07-23 2013-01-07 ザ トラスティーズ オブ プリンストン ユニバーシティ 抗ウイルス剤として用いられるｍＴＯＲキナーゼ阻害剤
EP2496230B1 (en) * 2009-11-03 2020-02-26 Fosun Orinove Pharmatech, Inc. Ire-1 alpha inhibitors
MX2012011504A (es) 2010-04-05 2013-01-18 Mannkind Corp Inhibidores de enzima 1 dependiente de inositol (ire-1 alfa).
TWI622573B (zh) * 2010-11-05 2018-05-01 拜耳知識產權公司 藉由亞胺氫化製備經取代ｎ－（苄基）環丙胺之方法
US9956236B2 (en) 2011-02-07 2018-05-01 Cornell University Methods for increasing immune responses using agents that directly bind to and activate IRE-1
WO2012138715A2 (en) 2011-04-04 2012-10-11 Georgetown University Small molecule inhibitors of xbp1 splicing
JP6367712B2 (ja) 2011-08-19 2018-08-01 グラクソ グループ リミテッドＧｌａｘｏ Ｇｒｏｕｐ Ｌｉｍｉｔｅｄ Ｃ型肝炎ウイルス感染の治療のためのベンゾフラン化合物
US20150018406A1 (en) 2012-03-09 2015-01-15 Cornell University Modulation of breast cancer growth by modulation of xbp1 activity
EP2841449B1 (en) 2012-04-23 2016-12-28 IMBA-Institut für Molekulare Biotechnologie GmbH Archease as rna ligase complex member
RU2015115631A (ru) 2012-09-26 2016-11-20 Дзе Риджентс Оф Дзе Юниверсити Оф Калифорния Модулирование ire1
EP3521431A1 (en) 2013-09-25 2019-08-07 Cornell University Compounds for inducing anti-tumor immunity and methods thereof
CN114380700A (zh) * 2013-10-08 2022-04-22 卢庆彬 用于靶向化疗的非铂基抗癌化合物
WO2015136887A1 (ja) * 2014-03-10 2015-09-17 国立大学法人広島大学 滑膜細胞増殖抑制剤及び滑膜細胞の増殖抑制方法
US20160106687A1 (en) 2014-10-21 2016-04-21 Life Plus, LLC Human therapeutic agents
US9907786B2 (en) 2014-10-21 2018-03-06 Ions Pharmaceutical S.À R.L. Therapeutic compositions containing harmine and isovanillin components, and methods of use thereof
US10092550B2 (en) 2014-10-21 2018-10-09 Ions Pharmaceutical S.À R.L. Therapeutic compositions containing curcumin, harmine, and isovanillin components, and methods of use thereof
EP3573608A1 (en) 2017-01-30 2019-12-04 Université de Liège Perk and ire-1a inhibitors against neurodevelopmental disorders
CN106974908B (zh) * 2017-03-02 2019-11-12 深圳大学 含有hdac抑制剂和ire1抑制剂的药物组合物及用途
CN106822904B (zh) * 2017-03-08 2019-10-25 暨南大学 含akt抑制剂和ire1抑制剂的药物组合物及其应用
CN107308178B (zh) * 2017-07-31 2020-11-10 苏州大学附属儿童医院 一种用于肠外营养相关性肝病药物
KR20200138323A (ko) 2018-03-27 2020-12-09 뉴로포레 테라피스, 인코포레이티드 Tlr2 신호전달의 조절제로서의 화합물
CA3103958A1 (en) 2018-07-03 2020-01-09 The Board Of Trustees Of The University Of Illinois Activators of the unfolded protein response
WO2020019107A1 (en) * 2018-07-23 2020-01-30 Fosun Orinove Pharmatech, Inc. IRE1α INHIBITOR IN COMBINATION WITH CANCER THERAPEUTIC AGENT FOR CANCER TREATMENT
US20210260069A1 (en) * 2018-07-23 2021-08-26 Fosun Orinove Pharmatech, Inc. IRE1a INHIBITOR IN COMBINATION WITH CANCER THERAPEUTIC AGENT FOR CANCER TREATMENT
AU2018447495A1 (en) * 2018-11-02 2021-06-17 Fosun Orinove Pharmatech, Inc. IRE1α inhibitor in combination with cancer therapeutic agent for cancer treatment
CN114025847B (zh) * 2019-03-26 2024-05-24 神经孔疗法股份有限公司 作为tlr信号传导的调节剂的化合物和组合物
US12129265B2 (en) 2020-07-21 2024-10-29 Ankh Life Sciences Limited Therapeutic agents and uses thereof
CN118576600A (zh) * 2024-05-31 2024-09-03 中山大学附属第三医院 IRE1α抑制剂KIRA8在制备治疗复发难治多发性骨髓瘤的药物中的应用

Family Cites Families (403)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE209910C (enExample) *
US675543A (en) 1899-08-05 1901-06-04 Farbenfabriken Elberfeld Co Derivatives of aromatic oxy-aldehydes and process of making same.
US2346662A (en) * 1940-04-08 1944-04-18 Universal Oil Prod Co Suppression of metal catalysis
US2282907A (en) 1941-05-01 1942-05-12 Us Rubber Co Parasiticide
US2649444A (en) 1948-10-19 1953-08-18 Burroughs Wellcome Co Process for the preparation of amino ketones
US2778853A (en) 1952-09-10 1957-01-22 Merck & Co Inc Deamination process
US2771391A (en) 1953-08-20 1956-11-20 Allied Lab Inc Physiologically active p-alkoxy-beta-piperidinopropiophenones causing cns depressantand anesthetic effects in animals
US2712031A (en) * 1953-10-27 1955-06-28 Lasdon Foundation Inc Monosubstituted salicylaldehyde alkoximes
US3080372A (en) 1960-03-25 1963-03-05 Res Lab Dr C Janssen 1-aroylalkyl-4-arylpiperidine derivatives
CH402859A (de) 1960-05-24 1965-11-30 Wander Ag Dr A Verfahren zur Herstellung von a-Pyrrolidino-valerophenonen
US3252996A (en) 1962-10-02 1966-05-24 Ciba Geigy Corp Alpha-pyrrolidinomethyl valero and caprophenones
US3151124A (en) 1961-11-20 1964-09-29 Ciba Geigy Corp Alpha oxy-beta alkyl-gamma tertiary amino-alpha phenyl propanes
NL293782A (enExample) 1962-06-11
US3203962A (en) 1962-10-11 1965-08-31 Ciba Geigy Corp Alpha-phenyl-beta pyrrolidino-propiophenones
US3148997A (en) 1963-01-04 1964-09-15 Dow Chemical Co Catechol compounds in improving clays and clay-containing materials
US3211613A (en) 1963-01-14 1965-10-12 Merck & Co Inc Anticoccidial compositions and method of using same
FR1453234A (fr) 1964-02-18 1966-06-03 Pechiney Progil Sa Nouveaux composés fongicides à usage agricole
US3340300A (en) 1964-10-05 1967-09-05 American Cyanamid Co Trimethoxy benzoylacetaldehyde oximes
CH445193A (de) 1964-12-14 1967-10-15 Agripat Sa Fungizides Mittel und seine Verwendung
FR1437423A (fr) * 1964-12-29 1966-05-06 Pechiney Progil Sa Composés fongicides nouveaux à usage agricole dérivés de l'aldéhyde salicylique
US3816433A (en) 1965-03-24 1974-06-11 Ferrosan Ab 4-fluoro-ypsilon-(4-methylpiperidino)-butyrophenone and its pharmaceutically acceptable salts
US3325521A (en) 1965-07-19 1967-06-13 Parke Davis & Co Halogenated cresol compounds and methods for their production
US3417087A (en) 1965-12-27 1968-12-17 Research Corp 3(aminopropionyl)benzothiophenes
CH479246A (de) 1966-10-28 1969-10-15 Ciba Geigy Mittel zur Bekämpfung von phytopathogenen Pilzen und Bakterien
FR1588756A (enExample) 1967-05-26 1970-03-16 Pepro
DE1679900A1 (de) * 1967-09-07 1971-04-08 Agfa Gevaert Ag Verfahren zum Verkleben von Polyesterfilmen
US3681445A (en) 1968-01-19 1972-08-01 Merck & Co Inc Substituted phenyl benzoic acid compounds
DE1989548U (de) 1968-03-29 1968-07-18 Karl Muenkel K G Zwei- oder mehrteiliger badezimmerschrank aus kunststoff.
US3721741A (en) 1968-10-28 1973-03-20 Ciba Geigy Ag Combatting phytopathogenic fungi on plants with sub-phytoloxic fungicidally effective amounts of herbicidal n-phenyl derivatives of 3,5-dihalo-salicylaldehyde
US3536809A (en) 1969-02-17 1970-10-27 Alza Corp Medication method
US3598123A (en) 1969-04-01 1971-08-10 Alza Corp Bandage for administering drugs
US3651085A (en) 1969-04-14 1972-03-21 Robins Co Inc A H 1-(omega-benzoylalkyl)-3-substituted pyrrolidines
US3703527A (en) 1969-06-04 1972-11-21 Hoffmann La Roche Preparation of mannich-bases
DE2021470A1 (de) 1970-05-02 1971-11-25 Cassella Farbwerke Mainkur Ag Piperazinderivate
FR2092133B1 (enExample) 1970-05-06 1974-03-22 Orsymonde
US3714226A (en) 1970-06-09 1973-01-30 Merck & Co Inc Phenyl benzoic acid compounds
DE2142245C3 (de) * 1971-08-24 1980-09-04 Basf Ag, 6700 Ludwigshafen Farbstoffe auf der Basis von Imino-isoindolin, deren Herstellung und Verwendung als Pigmente für Lacke und zum Anfärben von Polyestermaterialien
US3969356A (en) 1971-09-13 1976-07-13 Kali-Chemie Aktiengesellschaft N-[3-(p-f-benzoyl)-propyl]-N'-[2.(nitro,nitro-el, or methoxyphenyl)-ethyl]-p
US3806526A (en) 1972-01-28 1974-04-23 Richardson Merrell Inc 1-aroylalkyl-4-diphenylmethyl piperidines
US3845770A (en) 1972-06-05 1974-11-05 Alza Corp Osmatic dispensing device for releasing beneficial agent
US3916899A (en) 1973-04-25 1975-11-04 Alza Corp Osmotic dispensing device with maximum and minimum sizes for the passageway
US3962459A (en) 1973-09-04 1976-06-08 Sandoz, Inc. Lipidemia treatment with p-phenoxy-alkylphenone compositions
US3873539A (en) 1973-10-03 1975-03-25 Sandoz Ag Substituted-4-aminoacetyl alkanoylphenones
US3992546A (en) 1973-10-18 1976-11-16 Ciba-Geigy Corporation 4-Piperidinobutyrophenones as neuroleptics
US4054570A (en) 1973-10-18 1977-10-18 Ciba-Geigy Corporation 4-Piperidinobutyrophenones
US3944064A (en) 1973-10-26 1976-03-16 Alza Corporation Self-monitored device for releasing agent at functional rate
US3995047A (en) 1973-12-14 1976-11-30 Eisai Co., Ltd. Propiophenone derivatives in the treatment of pathological muscular conditions
US3912755A (en) 1974-01-30 1975-10-14 Lilly Co Eli Preparation of pharmaceutical intermediates
US3931197A (en) 1974-02-08 1976-01-06 Richardson-Merrell Inc. Substituted piperidine derivatives
IL48319A0 (en) 1974-10-26 1975-12-31 Merck Patent Gmbh Araliphatic nitrogen compounds and a process for their preparation
US4028366A (en) 1975-01-20 1977-06-07 Sterling Drug Inc. 2-Naphthyl-lower-alkanoylamines
US4169892A (en) 1975-04-03 1979-10-02 Innothera 1-(benzothien-2'-yl)-3-morpholino propanones and therapeutic compositions containing same
US4066788A (en) 1975-10-03 1978-01-03 Richardson-Merrell Inc. Substituted benzaldehyde hypolipidemic agents
DE2557341A1 (de) 1975-12-19 1977-06-30 Hoechst Ag Basisch substituierte indolderivate und verfahren zu ihrer herstellung
US4333941A (en) 1975-12-22 1982-06-08 The Dow Chemical Company Inhibition of enveloped viruses with phenyl ketones
US4008719A (en) 1976-02-02 1977-02-22 Alza Corporation Osmotic system having laminar arrangement for programming delivery of active agent
US4015014A (en) 1976-03-17 1977-03-29 The Dow Chemical Company Method for the use of aryl azines as anthelmintics
DE2620254C2 (de) * 1976-05-07 1984-03-15 Bayer Ag, 5090 Leverkusen Verfahren zur Herstellung von Hydroxybenzaldehyden
IT1068110B (it) 1976-08-13 1985-03-21 Montedison Spa Processo per la preparazione di aldeidi 2 idrossibenzoiche
US4072852A (en) * 1976-08-23 1978-02-07 Honeywell Inc. Digital computer monitoring and restart circuit
US4072582A (en) 1976-12-27 1978-02-07 Columbia Chemical Corporation Aqueous acid plating bath and additives for producing bright electrodeposits of tin
US4183553A (en) * 1977-02-04 1980-01-15 Ciba-Geigy Corporation Pressure- or heat-sensitive recording material and novel chromano compounds used therein
DE2718405A1 (de) 1977-04-26 1978-11-02 Boehringer Sohn Ingelheim Neue n- eckige klammer auf 1-(3-benzoylpropyl)-4-piperidyl eckige klammer zu -sulfonsaeureamide und verfahren zu deren herstellung
US4176198A (en) 1977-10-06 1979-11-27 William H. Rorer, Inc. Method of treatment
US4311841A (en) * 1977-11-21 1982-01-19 Petrolite Corporation Process of preparing hexahydropyrimidines
JPS54110321A (en) 1978-02-20 1979-08-29 Ajinomoto Co Inc Insecticide
JPS54125630A (en) 1978-02-22 1979-09-29 Nippon Zoki Pharmaceutical Co Novel propanone derivative*its manufacture and medical composition containing it as active component
JPS54163538A (en) 1978-06-13 1979-12-26 Sumitomo Chemical Co Production of salycilaldehydes
US4230727A (en) 1979-04-02 1980-10-28 William H. Rorer, Inc. Compositions and method of treatment
JPS606339B2 (ja) 1979-04-28 1985-02-18 ダイキン工業株式会社 フツ素化方法
FR2475044A1 (fr) * 1980-02-04 1981-08-07 Anvar Derives de nitro-2 naphtofurannes, leur preparation et leur application notamment comme regulateurs de la croissance cellulaire
DE3019496A1 (de) 1980-05-22 1981-11-26 Bayer Ag, 5090 Leverkusen Aminopropanol-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE3019497A1 (de) 1980-05-22 1981-11-26 Bayer Ag, 5090 Leverkusen Aminopropiophenon-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
FR2486523A1 (fr) 1980-07-11 1982-01-15 Rhone Poulenc Ind Procede de preparation de polyphenols comportant eventuellement un groupement aldehyde
SG56656G (en) * 1980-07-28 1987-03-27 Pfizer Hypoglycemic 5-substituted oxazolidine-2, 4-diones
DE3101750A1 (de) 1981-01-21 1982-08-26 Basf Ag, 6700 Ludwigshafen Verfahren zur kontinuierlichen herstellung von ethanol
US4381308A (en) 1981-04-23 1983-04-26 Pfizer Inc. Hypoglycemic 5-substituted oxazolidine-2,4-diones
US4507268A (en) * 1982-01-25 1985-03-26 Henkel Corporation Solvent extraction
JPS58181971A (ja) 1982-04-15 1983-10-24 松下電器産業株式会社 自動車用キ−レスエントリ装置
JPS5944371A (ja) 1982-09-07 1984-03-12 Dainippon Pharmaceut Co Ltd １―フエニル―２―メチル―３―（１―ピロリジニル）―１―プロパノン誘導体
FR2534912B1 (fr) 1982-10-26 1985-06-28 Lafon Labor Nouveaux derives de (2,4,6-trimethoxyphenyl) - (3-piperidinopropyl) -cetone, utilisation en therapeutique et procede de preparation
DE3332780A1 (de) 1983-09-10 1985-03-28 Hoechst Ag, 6230 Frankfurt 6-sulfoxyphenolderivate, ihre herstellung und ihre verwendung als cytoprotekiva
US4686235A (en) 1983-10-12 1987-08-11 Merck & Co., Inc. Substituted cinnamyl-2,3-dihydrobenzofuran and analogs useful as anti-inflammatory agents
HU33131A (enExample) 1984-01-26 1984-10-29
US4544663A (en) 1984-05-07 1985-10-01 Sandoz, Inc. Indolamine derivatives as anti-fertility agents
DE3436450A1 (de) 1984-10-05 1986-04-10 Bayer Ag, 5090 Leverkusen Verfahren zur herstellung von p-aminoethylketonen
US5057535A (en) 1985-04-11 1991-10-15 Nippon Kayaku Kabushiki Kaisha Derivatives of an aminoketone
FR2584715B1 (fr) 1985-07-10 1987-10-09 Lafon Labor Phenyl-(3-hexamethyleneiminopropyl)-cetone, procede de preparation et utilisation en therapeutique
FR2597864B1 (fr) 1986-04-28 1990-11-16 Lafon Labor Nouveaux derives de la n-((trimethoxy-2,4,6-benzoyl)-3 propyl) piperidine, leurs procedes de preparation et leur application en therapeutique
US5571886A (en) 1986-12-23 1996-11-05 Shipley Company, Inc. Aromatic novolak resins
JPH0637389B2 (ja) 1986-12-26 1994-05-18 北陸製薬株式会社 頻尿治療剤
JPS63243085A (ja) * 1987-03-30 1988-10-07 Toray Ind Inc 新規スピロナフトピラン化合物
FR2618145B1 (fr) 1987-07-17 1989-11-24 Rhone Poulenc Chimie Procede de chloration selective de composes phenoliques
US4847429A (en) 1987-08-03 1989-07-11 Eastman Kodak Company Synthesis of phenylhydroquinones
US4927956A (en) 1987-09-16 1990-05-22 Hoechst Celanese Corporation 3,5-disubstituted-4-acetoxystyrene and process for its production
US5025036A (en) 1987-10-01 1991-06-18 Hoffmann-La Roche Inc. Catechol carboxylic acids
JPH0256469A (ja) * 1987-12-08 1990-02-26 Kumiai Chem Ind Co Ltd ピリミジン誘導体及び除草剤
JPH02264946A (ja) 1989-04-05 1990-10-29 Fuji Photo Film Co Ltd ハロゲン化銀カラー写真感光材料
JPH085780B2 (ja) 1989-04-28 1996-01-24 呉羽化学工業株式会社 変形性関節症治療剤
EP0435827A3 (en) 1989-12-28 1991-11-13 Ciba-Geigy Ag Diaza compounds
DE4012008A1 (de) 1990-04-13 1991-10-17 Bayer Ag Verfahren zur herstellung von o-hydroxy-benzaldehyden
US5025006A (en) 1990-06-26 1991-06-18 Merck & Co., Inc. 2-biphenyl-carbapenem antibacterial agents
EP0467434A1 (en) 1990-06-26 1992-01-22 Merck & Co. Inc. 2-Biphenyl-carbapenem antibacterial agents
EP0464900A3 (en) 1990-06-26 1992-07-22 Merck & Co. Inc. 2-biphenyl-carbapenems
US5202355A (en) 1991-06-12 1993-04-13 Takasago Institute For Interdisciplinary Science Inc. Method of inhibiting aldose reductase in diabetic hosts using phenol derivatives
GB9119920D0 (en) 1991-09-18 1991-10-30 Glaxo Group Ltd Chemical compounds
JPH05127335A (ja) 1991-10-14 1993-05-25 Fuji Photo Film Co Ltd 熱現像拡散転写型カラー感光材料
JPH05127330A (ja) 1991-11-06 1993-05-25 Fuji Photo Film Co Ltd ハロゲン化銀カラー写真感光材料の処理方法
JPH05255089A (ja) 1991-12-18 1993-10-05 Sanwa Kagaku Kenkyusho Co Ltd 抗ウイルス剤
GB9127279D0 (en) 1991-12-23 1992-02-19 Ici Plc Heterocyclic derivatives
FR2689505B1 (fr) 1992-04-03 1995-06-09 Rhone Poulenc Chimie Procede d'hydroxylation de composes phenoliques.
CA2093778A1 (en) 1992-04-10 1993-10-11 George R. Brown Heterocyclic compounds
US5198422A (en) 1992-06-11 1993-03-30 Smithkline Beecham Corporation Stabilized somatotropin for parenteral administration
GB9217723D0 (en) 1992-08-20 1992-09-30 Ici Plc Chemical process
JPH06135153A (ja) 1992-10-29 1994-05-17 Fuji Photo Film Co Ltd 感熱記録材料
FR2698353B1 (fr) 1992-11-25 1995-02-17 Rhone Poulenc Chimie Procédé de O-alkylation des composés phénoliques.
WO1994020473A1 (fr) 1993-03-11 1994-09-15 Yamanouchi Pharmaceutical Co., Ltd. Compose avec action antagoniste de la vasopressine
GB2276162A (en) 1993-03-17 1994-09-21 Glaxo Group Ltd Aniline and benazilide derivatives
KR100238346B1 (ko) 1993-04-07 2000-03-02 오쓰까 아끼히꼬 피페리딘 유도체를 유효성분으로 하는 말초혈관확장제
GB9307527D0 (en) 1993-04-13 1993-06-02 Fujisawa Pharmaceutical Co New venzamide derivatives,processes for the preparation thereof and pharmaceutical composition comprising the same
GB9308652D0 (en) 1993-04-27 1993-06-09 Wellcome Found Anti-inflammatory compounds
JPH06332264A (ja) 1993-05-24 1994-12-02 Hodogaya Chem Co Ltd 静電荷像現像用トナー
JPH0784415A (ja) 1993-06-25 1995-03-31 Hodogaya Chem Co Ltd 正帯電性トナー用摩擦帯電付与部材
DK77393D0 (da) 1993-06-29 1993-06-29 Novo Nordisk As Aktivering af enzymer
US5776951A (en) 1993-06-30 1998-07-07 Glaxo Wellcome Inc. Anti-atherosclerotic diaryl compounds
IT1266582B1 (it) 1993-07-30 1997-01-09 Recordati Chem Pharm Derivati (di)azacicloesanici e diazacicloeptanici
EP0714389B1 (en) 1993-08-20 1998-06-17 Smithkline Beecham Plc Amide and urea derivatives as 5ht1d receptor antagonists
IS4208A (is) 1993-09-22 1995-03-23 Glaxo Group Limited 3-(tetrazólýl-benzyl)amínó-piperadidín afleiður
US5420362A (en) 1993-10-08 1995-05-30 Clairol, Inc. Synthesis of 2-methyl-1-naphthol
WO1995015954A1 (en) 1993-12-07 1995-06-15 Smithkline Beecham Plc Heterocyclic biphenylylamides useful as 5ht1d antagonists
EP0658807B1 (en) 1993-12-17 2000-04-05 Fuji Photo Film Co., Ltd. Positive-working photoresist composition
EP0736023B1 (en) 1993-12-21 1998-07-08 Smithkline Beecham Plc Indole, indoline and quinoline derivatives with 5ht 1d (anti-depressive) activity
GB9326008D0 (en) 1993-12-21 1994-02-23 Smithkline Beecham Plc Novel compounds
US5565416A (en) 1994-01-10 1996-10-15 Phillips Petroleum Company Corrosion inhibitor for wellbore applications
US5654260A (en) 1994-01-10 1997-08-05 Phillips Petroleum Company Corrosion inhibitor for wellbore applications
WO1995026328A1 (en) 1994-03-26 1995-10-05 Smithkline Beecham Plc Biphenyl derivatives as 5ht1d antagonists
GB9408577D0 (en) 1994-04-29 1994-06-22 Fujisawa Pharmaceutical Co New compound
EP0758330A1 (en) 1994-05-06 1997-02-19 Smithkline Beecham Plc Biphenylcarboxamides useful as 5-ht1d antagonists
EP0763034A1 (en) 1994-05-28 1997-03-19 Smithkline Beecham Plc Amide derivatives having 5ht1d-antagonist activity
US20010020100A1 (en) 1994-06-14 2001-09-06 G.D. Searle & Co. N-substituted-1, 2, 4-triazolone compounds for treatment of cardiovascular disorders
DE4423061C1 (de) 1994-07-01 1996-01-18 Hoechst Ag Verfahren zur Herstellung von Biphenylen mit Palladacyclen als Katalysatoren
US5612359A (en) 1994-08-26 1997-03-18 Bristol-Myers Squibb Company Substituted biphenyl isoxazole sulfonamides
US5579110A (en) 1994-08-31 1996-11-26 Honeywell Inc. In-line multiple rotation sensor assembly
CA2158191A1 (en) 1994-09-16 1996-03-17 Junji Yokoi Method for preventing settlement of aquatic fouling organisms
US5599974A (en) 1994-09-19 1997-02-04 Center For Innovative Technology Aldehydic agents for allosteric modification of hemoglobin
US5593994A (en) 1994-09-29 1997-01-14 The Dupont Merck Pharmaceutical Company Prostaglandin synthase inhibitors
GB9421003D0 (en) 1994-10-18 1994-12-07 Smithkline Beecham Plc Novel compounds
US6214994B1 (en) 1997-04-21 2001-04-10 Molecular Geriatrics Corporation Certain substituted 1-aryl-3-piperazin-1′-yl propanones
US5705501A (en) 1994-11-17 1998-01-06 Molecular Geriatrics Corporation Certain substituted 1-aryl-3-morpholinopropanones to treat Alzheimer's Disease
DE4444244A1 (de) * 1994-12-13 1996-06-20 Basf Ag Photochrome Spiroindoline
FI972583L (fi) 1994-12-22 1997-08-19 Smithkline Beecham Plc Tetrasyklisiä spiroyhdisteitä, menetelmä niiden valmistamiseksi ja niiden käyttö 5HT1D-reseptoriantagonisteina
ATE279406T1 (de) * 1995-01-12 2004-10-15 Glaxo Group Ltd Piperidinderivate mit tachykinin-antagonistischer wirkung
CZ294097B6 (cs) 1995-02-02 2004-10-13 Smithklineábeechamáplc Indolový derivátŹ způsob jeho přípravy a farmaceutická kompozice s jeho obsahem
US6008219A (en) 1995-03-27 1999-12-28 Smithkline Beech P.L.C. Bicyclic amine derivatives and their use as anti-psychotic agents
EP1048657A1 (en) 1995-04-04 2000-11-02 Texas Biotechnology Corporation Thienyl-, furyl-, pyrrolyl- and biphenylsulfonamides and derivatives thereof that modulate the activity of endothelin
GB9507203D0 (en) 1995-04-07 1995-05-31 Smithkline Beecham Plc Novel compounds
GB9508637D0 (en) 1995-04-28 1995-06-14 Fujisawa Pharmaceutical Co New use
US5741818A (en) 1995-06-07 1998-04-21 University Of Saskatchewan Semicarbazones having CNS activity and pharmaceutical preparations containing same
GB9512697D0 (en) 1995-06-22 1995-08-23 Zeneca Ltd Heterocyclic compounds
JPH10507205A (ja) 1995-08-02 1998-07-14 ホータ．ウリアッヒ イ シイア．エセ．アー． 抗真菌活性を有する新規カルボンアミド
GB9519033D0 (en) 1995-09-18 1995-11-15 Smithkline Beecham Plc Treatment
FR2739098B1 (fr) 1995-09-25 1997-11-28 Rhone Poulenc Chimie Procede d'acylation d'un compose aromatique
GB9522845D0 (en) 1995-11-08 1996-01-10 Smithkline Beecham Plc Novel compounds
WO1997019070A1 (en) 1995-11-22 1997-05-29 Smithkline Beecham Plc Tricyclic spiro compounds as 5ht1d receptor antagonists
US5763496A (en) 1995-11-27 1998-06-09 The Research Foundation Of State University Of New York Prevention of atherosclerosis using NADPH oxidase inhibitors
JPH09149797A (ja) 1995-11-30 1997-06-10 Internatl Reagents Corp 酵素、抗原又は抗体の定量方法及び酵素活性測定用の基質
EE9800172A (et) 1995-12-06 1998-12-15 Astra Pharmaceuticals Limited Ühendid
FR2744720B1 (fr) 1996-02-09 1998-04-10 Rhone Poulenc Chimie Procede d'hydroxylation de composes phenoliques
FR2745285B1 (fr) 1996-02-28 1998-04-10 Rhone Poulenc Chimie Nouveau catalyseur de c-alkylation d'un compose aromatique et son utilisation
FR2745287B1 (fr) 1996-02-28 1998-04-10 Rhone Poulenc Chimie Nouvelle composition catalytique et sa mise en oeuvre dans un procede d'acylation d'un compose aromatique
GB9605945D0 (en) 1996-03-21 1996-05-22 Smithkline Beecham Plc Novel compounds
GB9606370D0 (en) 1996-03-26 1996-06-05 Dormer Tools Sheffield Ltd Improvements in or relating to twist drills
EP0889892A1 (en) 1996-03-27 1999-01-13 Smithkline Beecham Plc Azaspiro derivatives
GB9606396D0 (en) 1996-03-27 1996-06-05 Smithkline Beecham Plc Novel compounds
GB9607219D0 (en) 1996-04-04 1996-06-12 Smithkline Beecham Plc Novel compounds
WO1997048786A1 (de) 1996-06-19 1997-12-24 Call Hans Peter Mehrkomponentensystem zur verwendung mit waschaktiven substanzen
PT920312E (pt) 1996-07-08 2005-04-29 Galderma Res & Dev Derivados de adamantilo indutores de apoptose e sua utilizacao como agentes anticancerigenos
US6462064B1 (en) 1996-07-08 2002-10-08 Galderma Research & Development S.N.C. Apoptosis inducing adamantyl derivatives and their usage as anti-cancer agents, especially for cervical cancers and dysplasias
AU729320B2 (en) 1996-07-31 2001-02-01 Shionogi & Co., Ltd. Novel para-terphenyl compounds
DE19631131A1 (de) 1996-08-01 1998-02-05 Consortium Elektrochem Ind Mehrkomponentensystem zum Verändern, Abbau oder Bleichen von Lignin, ligninhaltigen Materialien oder ähnlichen Stoffen sowie Verfahren zu seiner Anwendung
JP3202607B2 (ja) * 1996-08-01 2001-08-27 帝人株式会社 ２−（４−アルコキシ−３−シアノフェニル）チアゾール誘導体の製造法
FR2752165B1 (fr) * 1996-08-12 1998-10-09 Intertechnique Sa Equipement de protection respiratoire a mise en place rapide
US5668182A (en) 1996-08-19 1997-09-16 Virginia Commonwealth University Method of calming or sedating an animal with a hydroxy benzaldehyde compound
WO1998016504A2 (en) 1996-10-11 1998-04-23 Warner-Lambert Company SULFONAMIDE SUBSTITUTED ASPARTIC ACID INTERLEUKIN-1β CONVERTING ENZYME INHIBITORS
FR2754533B1 (fr) 1996-10-14 1998-11-27 Rhodia Chimie Sa Procede de preparation selective d'un acide 2-hydroxybenzoique et d'un 4-hydroxybenzaldehyde et derives
FR2756278B1 (fr) 1996-11-22 1998-12-31 Rhodia Chimie Sa Procede de preparation d'un 4-hydroxybenzaldehyde et derives
FR2756279B1 (fr) 1996-11-27 1999-01-22 Rhodia Chimie Sa Procede d'acylation d'un compose aromatique
US6005009A (en) 1997-03-19 1999-12-21 Duke University Method of inhibiting fibrosis with pyridoxal benzoyl hydrazone and analogs thereof
FR2761687B1 (fr) * 1997-04-08 2000-09-15 Centre Nat Rech Scient Derives de quinoleines, possedant notamment des proprietes antivirales, leurs preparations et leurs applications biologiques
JP2001526648A (ja) 1997-04-22 2001-12-18 コセンシス・インコーポレイテッド 炭素環及びヘテロ環で置換されたセミカルバゾン及びチオセミカルバゾン、及びその使用
US6288276B1 (en) 1997-05-21 2001-09-11 Henkel Kommanditgeselschaft Auf Aktien Salicylaldoximes and method of preparation
US6013841A (en) 1997-07-17 2000-01-11 Dakota Gasification Company Method for the conversion of 3- and 4-methylcatechol to benzaldehyde
FR2768729A1 (fr) 1997-09-19 1999-03-26 Rhodia Chimie Sa Procede d'acylation d'un compose aromatique et complexes catalytiques
FR2768728B1 (fr) 1997-09-19 1999-12-03 Rhodia Chimie Sa Procede d'acylation d'un compose aromatique
US6174656B1 (en) 1997-09-30 2001-01-16 Fuji Photo Film Co., Ltd. Silver halide photographic light-sensitive material, aromatic aldehyde derivative compound, and image-forming method
US6124507A (en) 1997-12-10 2000-09-26 Union Carbide Chemicals & Plastics Technology Corporation Electron donors
ES2281146T3 (es) 1997-12-19 2007-09-16 MERCK & CO., INC. Ariltiazolidindionas utiles como compuestos terapeuticos.
EP0938025A1 (en) 1998-02-20 1999-08-25 Fuji Photo Film Co., Ltd. Heat developable color photographic light-sensitive material
US6528529B1 (en) 1998-03-31 2003-03-04 Acadia Pharmaceuticals Inc. Compounds with activity on muscarinic receptors
US6340685B1 (en) 1998-05-22 2002-01-22 Scios, Inc. Compounds and methods to treat cardiac failure and other disorders
CA2335497A1 (en) 1998-06-25 1999-12-29 Merck & Co., Inc. Carbapenem antibacterial compounds, compositions containing such compounds and methods of treatment
HUP0102693A3 (en) 1998-06-26 2002-12-28 Pfizer Prod Inc Improved process for preparing schiff base adducts of amines with o-hydroxy aldehydes and compositions of matter based thereon
US6307087B1 (en) 1998-07-10 2001-10-23 Massachusetts Institute Of Technology Ligands for metals and improved metal-catalyzed processes based thereon
CA2336691C (en) 1998-07-10 2009-02-10 Massachusetts Institute Of Technology Ligands for metals and metal-catalyzed processes
JP2000026438A (ja) 1998-07-14 2000-01-25 Fujimoto Brothers:Kk 新規な２−（ｎ−シアノイミノ）チアゾリジン−４− オン誘導体
CN1325380A (zh) 1998-09-11 2001-12-05 味之素株式会社 苯衍生物和它们的药物用途
US6521641B1 (en) 1998-10-08 2003-02-18 Allergan, Inc. Male anti-fertility agents
WO2000019990A2 (en) 1998-10-08 2000-04-13 Allergan Sales, Inc. Rar antagonists as male anti-fertility agents
DE19846514A1 (de) 1998-10-09 2000-04-20 Bayer Ag Neue Heterocyclyl-methyl-substituierte Pyrazole
WO2000042026A1 (en) 1999-01-15 2000-07-20 Novo Nordisk A/S Non-peptide glp-1 agonists
AUPP873799A0 (en) 1999-02-17 1999-03-11 Fujisawa Pharmaceutical Co., Ltd. Pyridine compounds
US6548529B1 (en) 1999-04-05 2003-04-15 Bristol-Myers Squibb Company Heterocyclic containing biphenyl aP2 inhibitors and method
IT1306129B1 (it) 1999-04-13 2001-05-30 Sigma Tau Ind Farmaceuti Esteri della l-carnitina o di alcanoil l-carnitine utilizzabili comelipidi cationici per l'immissione intracellulare di composti
US6251927B1 (en) 1999-04-20 2001-06-26 Medinox, Inc. Methods for treatment of sickle cell anemia
EP1053989B1 (en) 1999-05-20 2007-07-25 Ciba SC Holding AG Hydroxydiphenyl ether compounds
AU5852300A (en) 1999-07-15 2001-02-05 Sumitomo Pharmaceuticals Company, Limited Heteroaromatic ring compounds
WO2001007031A1 (en) 1999-07-26 2001-02-01 Shionogi & Co., Ltd. Benzene derivatives and immunopotentiating compositions or drug-sensitivity restoring agents containing the same
WO2001014314A1 (en) 1999-08-20 2001-03-01 Nippon Kayaku Kabushiki Kaisha Benzene derivatives having aromatic substituents and processes for the preparation thereof
CA2384511A1 (en) 1999-08-24 2001-03-01 Virginia Commonwealth University Substituted chiral allosteric hemoglobin modifiers
CA2383347A1 (en) 1999-08-31 2001-03-08 Maxia Pharmaceuticals, Inc. Benzylidene-thiazolidinediones and analogues and their use in the treatment of diabetes
DE19942700C1 (de) 1999-09-07 2001-04-05 Consortium Elektrochem Ind Verfahren zur Herstellung cyclischer N-Hydroxydicarboximide
HUP0203448A3 (en) 1999-10-13 2005-07-28 Pfizer Prod Inc Biaryl ether derivatives useful as monoamine reuptake inhibitors and pharmaceutical compositions containing them
JP4285723B2 (ja) 1999-11-12 2009-06-24 株式会社フジモト・コーポレーション 新規な２−（ｎ−シアノイミノ）チアゾリジン−４−オン誘導体
JP2001215669A (ja) 1999-11-25 2001-08-10 Fuji Photo Film Co Ltd 熱現像カラー感光材料
US6329129B1 (en) 1999-11-25 2001-12-11 Fuji Photo Film Co., Ltd. Heat-developable color light-sensitive material
KR20010074549A (ko) 2000-01-25 2001-08-04 고사이 아끼오 키랄 구리 착물, 이의 제조 방법 및 이를 이용한 비대칭합성
AU2001230565A1 (en) 2000-02-04 2001-08-14 Nihon Nohyaku Co. Ltd. Perfluoroisopropylbenzene derivatives
SE0000540D0 (sv) 2000-02-18 2000-02-18 Astrazeneca Ab New compounds
JP2001316294A (ja) 2000-03-14 2001-11-13 Pfizer Prod Inc ｏ−バニリンおよびｏ−バニリン／テトラメチルクロマニルカルボン酸化合物の組み合わせの使用法
WO2001074762A2 (en) * 2000-04-03 2001-10-11 Phycogen, Inc. Arylsulfates and their use as enhancers or inhibitors of bioadhesion to surfaces
WO2001083451A1 (en) 2000-04-28 2001-11-08 Asahi Kasei Kabushiki Kaisha Novel bicyclic compounds
WO2003024441A1 (en) 2001-09-14 2003-03-27 Shionogi & Co., Ltd. Novel use of tricyclic compound
JP2001335476A (ja) 2000-05-29 2001-12-04 Shionogi & Co Ltd 三環化合物の新規用途
TWI275589B (en) 2000-06-22 2007-03-11 Dow Agrosciences Llc 2-(3,5-disubstituted-4-pyridyl)-4-(thienyl, thiazolyl or arylphenyl)-1,3-oxazoline compounds
AU2001279294A1 (en) 2000-07-06 2002-01-21 Neurogen Corporation Melanin concentrating hormone receptor ligands
DE10038639A1 (de) 2000-07-28 2002-02-21 Schering Ag Nichtsteroidale Entzündungshemmer
EP1178036A1 (en) 2000-08-04 2002-02-06 Aventis Cropscience S.A. Fungicidal phenylimidate derivatives
GB0019359D0 (en) 2000-08-07 2000-09-27 Melacure Therapeutics Ab Novel guanidines
DE10040051A1 (de) 2000-08-11 2002-02-21 Basf Ag Derivate des 4-(Trifluormethyl)-phenols sowie Derivate des 4-(Trifluormethylphenyl)-2-(tetrahydropyranyl)ethers und Verfahren zu ihre Herstellung
DE10046272A1 (de) 2000-09-19 2002-03-28 Merck Patent Gmbh Aminoheterocyclen (Faktor Xa Inhibitoren 14)
DE10047109A1 (de) 2000-09-22 2002-04-11 Bayer Ag Verfahren zur Herstellung von DELTA·1·-Pyrrolinen
DE10047111A1 (de) 2000-09-22 2002-04-11 Bayer Ag Verfahren zur Herstellung von DELTA·1·-Pyrrolinen
CA2357833C (en) 2000-10-04 2005-11-15 Warner-Lambert Company Treatment of pulmonary hypertension using vasopressin antagonist
EP1339458B1 (en) 2000-11-22 2007-08-15 Novartis AG Combination comprising an agent decreasing vegf activity and an agent decreasing egf activity
AU2002223966A1 (en) 2000-12-20 2002-07-01 Warner Lambert Company Non-halogenated naphthol compounds and antimicrobial compositions containing the same
JP2002275165A (ja) 2001-01-12 2002-09-25 Sumitomo Pharmaceut Co Ltd トリアゾール誘導体
US20040147557A1 (en) 2001-01-15 2004-07-29 Anne Bouillot Aryl piperidine derivatives as inducers of ldl-receptor expression
DE10102341A1 (de) 2001-01-19 2002-08-08 Ralf Steffens Profilkontur einer Schraubenspindelpumpe
WO2002070464A2 (en) * 2001-01-22 2002-09-12 Arpida Ag Hydrazones and their therapeutic use
MXPA01013326A (es) 2001-02-14 2002-08-26 Warner Lambert Co Bifenil sulfonamidas utiles como inhibisdores de metaloproteinasa de matriz.
US20030022923A1 (en) 2001-03-01 2003-01-30 Medinox, Inc. Methods for treatment of sickle cell anemia
AU2002254171A2 (en) 2001-03-08 2002-09-24 Incyte San Diego, Inc. RXR activating molecules
US6936590B2 (en) 2001-03-13 2005-08-30 Bristol Myers Squibb Company C-aryl glucoside SGLT2 inhibitors and method
US7250521B2 (en) 2001-04-09 2007-07-31 Bayer Cropscience Aktiengesellschaft Method for production of Δ1-pyrrolines
US7326700B2 (en) 2001-04-12 2008-02-05 Wyeth Cyclohexenyl phenyl carboxamides tocolytic oxytocin receptor antagonists
US7109193B2 (en) 2001-04-12 2006-09-19 Wyeth Tricyclic diazepines tocolytic oxytocin receptor antagonists
ATE460163T1 (de) 2001-04-12 2010-03-15 Pharmacopeia Llc Arly und diaryl piperidinderivate verwendbar als mch-hemmer
US6900200B2 (en) 2001-04-12 2005-05-31 Wyeth Tricyclic hydroxy carboxamides and derivatives thereof tocolytic oxytocin receptor antagonists
US20020193403A1 (en) 2001-05-03 2002-12-19 Allergan Sales, Inc. Methods of treating hyperlipidemia
AU2002310187A1 (en) 2001-05-30 2002-12-09 Lg Biomedical Institute Inhibitors of protein kinase for the treatment of disease
SI1404653T1 (sl) 2001-06-28 2008-12-31 Pfizer Prod Inc S triamidom substituirani indoli, benzofurani in benzotiofeni kot zaviralci mikrosomske prenašalnebeljakovine za trigliceride (MTP) in/ali izločanja apolipoproteina B (APO B)
GB0119172D0 (en) 2001-08-06 2001-09-26 Melacure Therapeutics Ab Phenyl pyrrole derivatives
US6605620B1 (en) 2001-08-30 2003-08-12 Kowa Co., Ltd. Cyclic amine compounds and pharmaceutical composition containing the same
US6867221B2 (en) 2001-08-30 2005-03-15 Kowa Co., Ltd. Cyclic amine compounds and pharmaceutical composition containing the same
WO2003026587A2 (en) 2001-09-26 2003-04-03 Bristol-Myers Squibb Company Compounds useful for treating hepatitus c virus
CA2462860A1 (en) 2001-10-05 2003-04-17 Wyeth Stereospecific process for the synthesis of 2-yl chroman derivatives
DE10150335A1 (de) 2001-10-15 2003-04-24 Degussa Neue chirale Liganden und deren Übergangsmetallkomplexe sowie deren katalytische Anwendung
JP4581321B2 (ja) 2001-10-23 2010-11-17 住友化学株式会社 不飽和有機化合物誘導体の製造方法
US20060287337A1 (en) 2001-11-09 2006-12-21 Proteologics, Inc. Trans-golgi network-associated processes, methods and compositions related thereto
US8246969B2 (en) 2001-11-16 2012-08-21 Skinmedica, Inc. Compositions containing aromatic aldehydes and their use in treatments
EP1569912B1 (en) 2002-12-03 2015-04-29 Pharmacyclics, Inc. 2-(2-hydroxybiphenyl-3-yl)-1h-benzoimidazole-5-carboxamidine derivatives as factor viia inhibitors
US20030157154A1 (en) 2002-01-04 2003-08-21 Bryan Fuller Compositions containing hydroxy aromatic aldehydes and their use in treatments
US6835745B2 (en) 2002-01-15 2004-12-28 Wyeth Phenyl substituted thiophenes as estrogenic agents
JP2003229174A (ja) * 2002-01-31 2003-08-15 Sanyo Electric Co Ltd フィルム状外装体を用いた非水電解質二次電池
AR038377A1 (es) 2002-02-08 2005-01-12 Merck & Co Inc Derivados de n-bifenil-aminocicloalcancarboxamida (con sustitucion con metilo)
WO2003065789A2 (en) 2002-02-08 2003-08-14 Merck & Co., Inc. N-biphenylmethyl aminocycloalkanecarboxamide derivatives
US7078421B2 (en) 2002-03-20 2006-07-18 Metabolex, Inc. Substituted phenylacetic acids
WO2003086403A1 (en) 2002-04-08 2003-10-23 Merck & Co., Inc. Inhibitors of akt activity
WO2003086394A1 (en) 2002-04-08 2003-10-23 Merck & Co., Inc. Inhibitors of akt activity
MY134200A (en) 2002-04-12 2007-11-30 Kowa Co Method for treating cancer
DE10216368A1 (de) 2002-04-12 2003-10-16 Henkel Kgaa Arylsulfatase-Inhibitoren in Deodorantien und Antitranspirantien
US20030229149A1 (en) 2002-05-28 2003-12-11 Werner Baschong Anti-inflammatory agents
GB0216252D0 (en) 2002-07-12 2002-08-21 Glaxo Group Ltd Compounds
GB0216224D0 (en) 2002-07-12 2002-08-21 Glaxo Group Ltd Compounds
GB0216233D0 (en) 2002-07-12 2002-08-21 Glaxo Group Ltd Compounds
US20040034064A1 (en) 2002-08-06 2004-02-19 Kuduk Scott D. 2-(biarylalkyl)amino-3-(alkanoylamino)pyridine derivatives
US20040044041A1 (en) 2002-08-06 2004-03-04 Kuduk Scott D. 2-(Biarylalkyl)amino-3-(cyanoalkanoylamino)pyridine derivatives
US20040063761A1 (en) 2002-08-06 2004-04-01 Kuduk Scott D. 2-(biarylalkyl)amino-3-(fluoroalkanoylamino)pyridine derivatives
SE0202692D0 (sv) 2002-09-11 2002-09-11 Astrazeneca Ab Compounds
WO2004037816A1 (en) * 2002-10-28 2004-05-06 Chugai Seiyaku Kabushiki Kaisha Benzofuran compounds having antitumor activity
US7300639B2 (en) 2002-12-03 2007-11-27 Bristol-Myers Squibb Company Process for removing metals from liquids
US6894061B2 (en) 2002-12-04 2005-05-17 Wyeth Substituted dihydrophenanthridinesulfonamides
WO2004050030A2 (en) 2002-12-04 2004-06-17 Virginia Commonwealth University Anti-sickling agents
WO2004052859A1 (ja) 2002-12-06 2004-06-24 Kowa Co., Ltd. エリスロポエチン産生促進剤
DE10257357A1 (de) 2002-12-09 2004-06-24 Bayer Ag Fluorhaltige Benzaldehyde
WO2004056727A2 (en) 2002-12-19 2004-07-08 Atherogenics, Inc. Process of making chalcone derivatives
JP2006516979A (ja) * 2003-02-05 2006-07-13 ニューサウス イノベーションズ ピーティーワイ リミテッド 金属イオンキレート化剤およびその治療的使用
JP4331954B2 (ja) 2003-02-13 2009-09-16 株式会社リコー ユニット支持装置および画像形成装置
WO2004077885A2 (en) 2003-02-28 2004-09-10 Ciba Specialty Chemicals Holding Inc. Electroluminescent device
MY142651A (en) 2003-03-18 2010-12-15 Merck Sharp & Dohme Biaryl substituted triazoles as sodium channel blockers
CN1791580A (zh) 2003-03-24 2006-06-21 麦克公司 联芳基取代的6元杂环钠通道阻滞剂
EP1620089A4 (en) 2003-03-26 2008-12-24 Crc For Asthma Ltd Therapeutic and prophylactic compositions and their uses
CN1798738A (zh) 2003-04-03 2006-07-05 麦克公司 作为钠通道阻滞剂的联芳基取代吡唑
WO2004094379A2 (en) 2003-04-16 2004-11-04 Amgen Inc. 3-phenyl-4- (pyrimidin-2-yl) -6- (piperidin-4-yl) derivatives and related compounds as tnf-alpha and il-1 inhibitors for the treatment of inflammations
CA2522476A1 (en) 2003-04-18 2004-11-04 Merck & Co., Inc. Biaryl substituted thiazoles, oxazoles and imidazoles as sodium channel blockers
WO2004100998A2 (en) 2003-05-07 2004-11-25 General Electric Company Compositions and methods for non-invasive imaging of soluble beta-amyloid
US20040223912A1 (en) 2003-05-07 2004-11-11 Montalto Michael Christopher Compositions and methods for non-invasive imaging of soluble beta-amyloid
DK1638544T3 (da) 2003-05-07 2008-03-31 Univ Aberdeen Ketoner og reducerede ketoner som terapeutiske midler til behandling af knogletilstande
GB0312654D0 (en) 2003-06-03 2003-07-09 Glaxo Group Ltd Therapeutically useful compounds
FR2857010B1 (fr) 2003-07-01 2005-09-16 Servier Lab Nouveaux derives bicycliques alkyles, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
KR20060036091A (ko) 2003-07-15 2006-04-27 스미스클라인 비참 코포레이션 신규 화합물
BRPI0412805A (pt) 2003-07-23 2006-09-26 Synta Pharmaceuticals Corp método para modular canais de ìon de cálcio ativado por liberação de ìon de cálcio
KR100672273B1 (ko) 2003-07-25 2007-01-24 도요다 지도샤 가부시끼가이샤 가스 공급 장치
CA2535665A1 (en) 2003-08-14 2005-02-24 Asahi Kasei Pharma Corporation Substituted arylalkanoic acid derivative and use thereof
US20060226766A1 (en) 2003-09-05 2006-10-12 Thomas Schafer Electroluminescent device
GB0321538D0 (en) 2003-09-13 2003-10-15 Glaxo Group Ltd Therapeutically useful compounds
WO2005034953A1 (ja) 2003-10-10 2005-04-21 Kowa Co., Ltd. 血管新生抑制薬
US6990935B2 (en) 2003-10-27 2006-01-31 Borgwarner Inc. Pivoting lifter control system using spool valve and check valve to recirculate oil
EP1678149A2 (en) 2003-10-31 2006-07-12 Neurogen Corporation 4-amino(aza)quinoline derivatives as capsaicin receptor agonists
AR046698A1 (es) 2003-11-11 2005-12-21 Ishihara Sangyo Kaisha Derivado bifenilo o su sal, y pesticida que lo contienen como un ingrediente activo
ATE355617T1 (de) 2003-11-26 2006-03-15 Ciba Sc Holding Ag Elektrolumineszente bauelemente mit 2-(p- triphenyl)-3-phenyl-pyrazinderivaten
US7119208B2 (en) 2003-12-03 2006-10-10 Virginia Commonwealth University Anti-sickling agents
EP1704856A4 (en) 2003-12-26 2009-08-19 Kyowa Hakko Kirin Co Ltd PROTEIN INHIBITOR OF THE HSP90 FAMILY
US20050165025A1 (en) 2004-01-22 2005-07-28 Recordati Ireland Ltd. Combination therapy with 5HT 1A and 5HT 1B-receptor antagonists
US7501510B2 (en) 2004-03-26 2009-03-10 The University Of Hong Kong Thiourea compositions and uses thereof
FR2868417B1 (fr) 2004-04-02 2006-06-23 Rhodia Chimie Sa Procede de formation d'une liaison carbone-carbone
JP2006151946A (ja) 2004-04-30 2006-06-15 Konishi Kagaku Ind Co Ltd ジアリール誘導体の製造方法
GB0412874D0 (en) 2004-06-09 2004-07-14 Pfizer Ltd Novel pharmaceuticals
BRPI0512273A (pt) 2004-06-18 2008-02-19 Millennium Pharm Inc inibidores do fator xa
DOP2005000123A (es) 2004-07-02 2011-07-15 Merck Sharp & Dohme Inhibidores de cetp
DE102004035322A1 (de) 2004-07-21 2006-02-16 Universität des Saarlandes Selektive Hemmstoffe humaner Corticoidsynthasen
FR2874611B1 (fr) 2004-08-31 2006-11-17 Servier Lab Nouveaux derives d'imidazopyridine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
JP2008513364A (ja) * 2004-09-14 2008-05-01 ザ ジェネティクス カンパニー，インコーポレイテッド ヒドラゾン誘導体およびβ−セクレターゼインヒビターとしてのその使用
CA2585550A1 (en) 2004-10-28 2006-05-11 The Institutes For Pharmaceutical Discovery, Llc Substituted carboxylic acids
JP2006135153A (ja) 2004-11-08 2006-05-25 Canon Inc ビルドアッププリント配線基板および電子部品との接合構造
EP1824839A2 (en) 2004-12-13 2007-08-29 Neurogen Corporation Substituted biaryl analogues
WO2006074919A2 (de) 2005-01-12 2006-07-20 Curacyte Discovery Gmbh 3 -AMINO- 6-ARYL (BZW.6-HETEROARYL) -THIENO [2 , 3-B] PYRIDIN-2-CARBONSÄUREAMIDE, DIESE ENTHALTENDE PHARMAZEUTISCHE ZUBEREITUNGEN UND IHRE VERWENDUNG ALS INHIBITOREN DER TNFα-FREISETZUNG
JP3839454B2 (ja) 2005-02-07 2006-11-01 三菱電機株式会社 内燃機関の制御装置
US20090123563A1 (en) * 2005-02-07 2009-05-14 Novo Nordisk A/S Pharmaceutical Preparations Comprising Insulin, Zinc Ions and Zinc-Binding Ligand
PL1850669T3 (pl) 2005-02-11 2015-06-30 Bayer Cropscience Ltd Kompozycja grzybobójcza zawierająca pochodną pirydylometylobenzamidu oraz pochodną tiazolokarboksamidu
US20060194821A1 (en) * 2005-02-18 2006-08-31 The Brigham And Women's Hospital, Inc. Compounds inhibiting the aggregation of superoxide dismutase-1
US7691848B2 (en) 2005-03-02 2010-04-06 Wyeth Pyrrolobenzodiazepine arylcarboxamides and derivatives thereof as follicle-stimulating hormone receptor antagonists
DE102005009705A1 (de) 2005-03-03 2006-09-07 Universität des Saarlandes Selektive Hemmstoffe humaner Corticoidsynthasen
US8828429B2 (en) 2005-03-03 2014-09-09 Takeda Pharmaceutical Company Limited Release-control composition
US9271963B2 (en) 2005-03-03 2016-03-01 Universitat Des Saarlandes Selective inhibitors of human corticosteroid synthases
TW200702363A (en) 2005-04-05 2007-01-16 Sumitomo Chemical Co Crosslinked polymer electrolyte and method for producing the same
US7482027B2 (en) 2005-04-30 2009-01-27 Angiolab, Inc. Composition for the prevention or treatment of diseases associated with angiogenesis
WO2006122186A2 (en) 2005-05-10 2006-11-16 Microbia, Inc. 1,4-diphenyl-3-hydroxyalkyl-2-azetidinone derivatives for treating hypercholestrolemia
WO2006124780A2 (en) 2005-05-12 2006-11-23 Kalypsys, Inc. Ih-benzo [d] imidazole compounds as inhibitors of b-raf kinase
EP1879897A1 (en) 2005-05-12 2008-01-23 Wyeth a Corporation of the State of Delaware Pyrrolobenzodiazepines and heteroaryl, aryl and cycloalkylamino ketone derivatives as follicle stimulating hormone receptor -(fish-r) antagonists
CA2607882A1 (en) 2005-05-12 2006-11-23 Wyeth Pyrrolobenzodiazepines and heterocyclic carboxamide derivatives as follicle stimulating hormone receptor (fsh-r) antagonists
WO2006124897A2 (en) 2005-05-13 2006-11-23 Lexicon Genetics Incorporated Methods and compositions for improving cognition
BRPI0611439A2 (pt) 2005-05-13 2010-09-08 Lexicon Pharmaceuticals Inc compostos multicìclicos e métodos para uso dos mesmos
US7705002B2 (en) 2005-05-19 2010-04-27 Vertex Pharmaceuticals Incorporated Biaryls useful as modulators of ion channels
EP1893615A1 (en) 2005-06-09 2008-03-05 Wyeth a Corporation of the State of Delaware Pyrrolobenzodiazepine pyridine carboxamides and derivatives as follicle-stimulating hormone receptor antagonists
SG148192A1 (en) 2005-07-29 2008-12-31 Hoffmann La Roche Azabenzimidazole derivatives, their manufacture and use as anti-cancer agents
US7812025B2 (en) 2005-08-12 2010-10-12 Takeda Pharmaceutical Company Limited Brain/neuronal cell-protecting agent and therapeutic agent for sleep disorder
EP1922383A1 (en) 2005-08-26 2008-05-21 Koninklijke Philips Electronics N.V. Substrate material for handling and analysing samples
US20070054884A1 (en) 2005-08-31 2007-03-08 Emergent Product Development Gaithersburg Inc. 4-substituted 2-aryloxyphenol derivatives as antibacterial agents
WO2007031507A1 (en) 2005-09-13 2007-03-22 Bayer Cropscience Ag Fungicide composition comprising an arylamidine derivative and two known fungicide compounds
TW200800956A (en) 2005-09-13 2008-01-01 Palau Pharma Sa 2-Aminopyrimidine derivatives
JP2007084415A (ja) 2005-09-17 2007-04-05 Chikosha:Kk 木材チップを混入した軽量注入材。
WO2007034277A1 (en) 2005-09-19 2007-03-29 Pfizer Products Inc. Aryl substituted imidazo [4,5-c] pyridine compounds as c3a receptor antagonists
JP2007084454A (ja) 2005-09-20 2007-04-05 Fujifilm Corp スルホニウム化合物の製造方法
DE102005045132A1 (de) 2005-09-22 2007-03-29 Archimica Gmbh Verfahren zur Herstellung von 2-Arylcarbonylverbindungen, 2-Arylestern und 2-Arylnitrilen sowie ihrer heteroaromatischen Analoga
GB0519651D0 (en) 2005-09-27 2005-11-02 Univ Nottingham Ferrocenyl phosphite ligands for asymmetric catalysis and a method for their production
CN1958568B (zh) 2005-11-03 2011-04-13 中国科学院上海药物研究所 一类预防或治疗幽门螺杆菌感染化合物、其制法和用途
US8629147B2 (en) * 2005-11-03 2014-01-14 Chembridge Corporation Heterocyclic compounds useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders
US8017331B2 (en) 2005-11-04 2011-09-13 Mannkind Corporation IRE-1α substrates
JP2009516691A (ja) 2005-11-21 2009-04-23 タツプ・フアーマシユーテイカル・プロダクツ・インコーポレイテツド Ｑｔ間隔延長およびこれに伴う疾病の治療
EP1971584A2 (en) 2005-12-01 2008-09-24 University of Pittsburgh - Of the Commonwealth System of Higher Education Isotopically-labeled benzothiazole compounds as imaging agents for amyloidogenic proteins
US20110040115A1 (en) 2005-12-02 2011-02-17 Finorga Sas Intermediates and process for the preparation of aromatic derivatives of 1-adamantane
EP1993986B1 (en) 2005-12-02 2010-07-14 Finorga Sas Process for the preparation of aromatic derivatives of 1-adamantane
ATE516016T1 (de) 2005-12-05 2011-07-15 Merck Sharp & Dohme Selbstemulgierende formulierungen von cetp- hemmern
AR057218A1 (es) 2005-12-15 2007-11-21 Astra Ab Compuestos de oxazolidinona y su uso como pontenciadores del receptor metabotropico de glutamato
TWI403320B (zh) 2005-12-16 2013-08-01 Infinity Discovery Inc 用於抑制ｂｃｌ蛋白和結合夥伴間之交互作用的化合物及方法
NZ569327A (en) 2005-12-28 2011-09-30 Vertex Pharma 1-(benzo [d] [1,3] dioxol-5-yl) -n- (phenyl) cyclopropane- carboxamide derivatives and related compounds as modulators of ATP-binding cassette transporters for the treatment of cystic fibrosis
WO2007079186A2 (en) 2005-12-30 2007-07-12 Merck & Co., Inc. 1, 3-oxazolidin-2-one derivatives useful as cetp inhibitors
WO2007077457A2 (en) 2006-01-06 2007-07-12 The Royal Veterinary College Treatment of equine laminitis with 5-ht1b/ 1d antagonists
KR100814109B1 (ko) 2006-01-09 2008-03-14 한국생명공학연구원 로다닌 유도체, 이의 제조방법 및 이를 유효성분으로함유하는 약학적 조성물
GB0601031D0 (en) 2006-01-18 2006-03-01 Novartis Ag Organic compounds
WO2007092930A2 (en) 2006-02-08 2007-08-16 Regents Of The University Of California Method of treatment for mycobacterium tuberculosis
US8372861B2 (en) * 2006-02-27 2013-02-12 The Board Of Trustees Of The Leland Stanford Junior University Inhibitors of the unfolded protein response and methods for their use
EP1834642A3 (en) 2006-03-08 2007-10-03 National Institute of Immunology 2-thioxothiazolidin-4-one compounds and compositions as antimicrobial and antimalarial agents targeting enoyl-ACP reductase of type II fatty acid synthesis pathway and other cell growth pathways
CA2652109A1 (en) 2006-04-10 2007-10-18 Painceptor Pharma Corporation Compositions and methods for modulating gated ion channels
US20070249607A1 (en) 2006-04-17 2007-10-25 Bristol-Myers Squibb Company Nk-1 and serotonin transporter inhibitors
US20080064717A1 (en) 2006-05-19 2008-03-13 Rajesh Iyengar Inhibitors of diacylglycerol O-acyltransferase type 1 enzyme
WO2008002246A1 (en) 2006-06-28 2008-01-03 Astrazeneca Ab A pharmaceutical composition comprising an ikk2 inhibitor and a second active ingrdient.
CN101490037B (zh) 2006-07-11 2013-06-12 大熊制药株式会社 联芳基苯并咪唑衍生物以及包含该衍生物的药物组合物
US8329159B2 (en) 2006-08-11 2012-12-11 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7659270B2 (en) 2006-08-11 2010-02-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
US7759495B2 (en) 2006-08-11 2010-07-20 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2054056A4 (en) 2006-08-16 2010-08-25 J David Gladstone Inst A Testa SMALL MOLECULAR INHIBITORS OF KYNURENINE-3-MONOOXYGENASE
WO2008024963A1 (en) 2006-08-24 2008-02-28 Serenex, Inc. Benzene, pyridine, and pyridazine derivatives
US20080089845A1 (en) 2006-09-07 2008-04-17 N.V. Organon Methods for determining effective doses of fatty acid amide hydrolase inhibitors in vivo
WO2008037266A1 (en) 2006-09-25 2008-04-03 Universite Libre De Bruxelles Inhibitors of conventional protein kinase c isozymes and use thereof for treating inflammatory diseases
WO2008042892A2 (en) 2006-10-02 2008-04-10 N.V. Organon Fatty acid amide hydrolase inhibitors for energy metabolism disorders
CN103450077B (zh) 2007-06-08 2016-07-06 满康德股份有限公司 IRE-1α抑制剂
JP5127330B2 (ja) 2007-07-12 2013-01-23 日立造船株式会社 光電変換素子およびその製造方法
JP5127335B2 (ja) 2007-07-17 2013-01-23 三井造船株式会社 接続部の構造、バラ積み貨物荷役装置及び接続部の気密保持方法
JP2009149797A (ja) 2007-12-21 2009-07-09 Tohoku Carbon Kk 木炭粉含有塗料組成物及びその塗装方法
USD675543S1 (en) 2011-07-26 2013-02-05 Gizmode, LLC Moisture detection device
JP6135153B2 (ja) 2013-01-30 2017-05-31 井関農機株式会社 管理機

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