TNSN97208A1 - Prevention de la perte et restauration de la masse osseuse par certains agonistes des prostaglandines - Google Patents

Prevention de la perte et restauration de la masse osseuse par certains agonistes des prostaglandines

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Publication number
TNSN97208A1
TNSN97208A1 TNTNSN97208A TNSN97208A TNSN97208A1 TN SN97208 A1 TNSN97208 A1 TN SN97208A1 TN TNSN97208 A TNTNSN97208 A TN TNSN97208A TN SN97208 A TNSN97208 A TN SN97208A TN SN97208 A1 TNSN97208 A1 TN SN97208A1
Authority
TN
Tunisia
Prior art keywords
restoration
prevention
loss
bone mass
prostaglandin agonists
Prior art date
Application number
TNTNSN97208A
Other languages
English (en)
Inventor
O'keefe Cameron Kimberly
Zhu Ke Hua
Allen Lefker Bruce
Louis Rosati Robert
Duane Thompson David
Original Assignee
Pfizer
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer filed Critical Pfizer
Publication of TNSN97208A1 publication Critical patent/TNSN97208A1/fr

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    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
    • C07D207/2632-Pyrrolidones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms
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    • 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
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
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    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
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    • C07C235/34Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
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Abstract

L'INVENTION CONCERNE UN COMPOSE DE FORMULE I ............DANS LAQUELLE B REPRESENTE N OU UN GROUPE -C(H) ET A, M, Q, ET Z REPRESENTENT DIVERS RADICAUX ET K REPRESENTE UNE LIAISON OU UN RADICAL ELLE CONCERNE EGALEMENT UNE COMPOSITION PHARMACEUTIQUE LE CONTENANT ET DES KITS RENFERMANT UNE TELLE COMPOSITION. APPLICATION : UTILISATION POUR LE TRAITEMENT D'AFFECTIONS DES TISSUS OSSEUX COMPRENANT L'OSTEOPOROSE.
TNTNSN97208A 1996-12-20 1997-12-17 Prevention de la perte et restauration de la masse osseuse par certains agonistes des prostaglandines TNSN97208A1 (fr)

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Families Citing this family (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5552412A (en) * 1995-01-09 1996-09-03 Pfizer Inc 5-substitued-6-cyclic-5,6,7,8-tetrahydronaphthalen2-ol compounds which are useful for treating osteoporosis
IL130333A0 (en) 1996-12-20 2000-06-01 Pfizer Prevention and treatment of skeletal disorder with EP2 receptor subtype selective prostaglandin E2 agonists
UA59384C2 (uk) * 1996-12-20 2003-09-15 Пфайзер, Інк. Похідні сульфонамідів та амідів як агоністи простагландину, фармацевтична композиція та способи лікування на їх основі
UA67754C2 (uk) 1997-10-10 2004-07-15 Пфайзер, Інк. Агоністи простагландину, фармацевтична композиція на їх основі (варіанти), спосіб нарощення та збереження кісткової маси у хребетних та спосіб лікування (варіанти)
EP1000619A3 (fr) 1998-06-23 2002-07-24 Pfizer Products Inc. Méthode de traitement du glaucome
CN1329586A (zh) * 1998-12-11 2002-01-02 日产化学工业株式会社 对氯苯基丙醇衍生物的制备方法
MXPA01008955A (es) 1999-03-05 2002-04-24 Procter & Gamble Analogos de prostaglandinas selectivas de fp no saturadas de c16.
IL139941A0 (en) * 1999-12-02 2002-02-10 Pfizer Prod Inc Use of prostaglandin agonists to treat erectile dysfunction or impotence
ATE327751T1 (de) 2000-01-31 2006-06-15 Pfizer Prod Inc Verwendung von aktivatoren des prostaglandinrezeptores 4 zur behandlung von akuter oder chronischer niereninsuffizienz
US6911476B2 (en) * 2000-03-13 2005-06-28 Eli Lilly And Company Sulfonamide derivatives
US20020013294A1 (en) 2000-03-31 2002-01-31 Delong Mitchell Anthony Cosmetic and pharmaceutical compositions and methods using 2-decarboxy-2-phosphinico derivatives
US20020172693A1 (en) 2000-03-31 2002-11-21 Delong Michell Anthony Compositions and methods for treating hair loss using non-naturally occurring prostaglandins
EP1149583A3 (fr) * 2000-04-13 2001-11-14 Pfizer Products Inc. Combinaison des antagonistes de la facteur de la liberation de la corticotropin et des secrétagogues de l hormone de croissance
US6472372B1 (en) 2000-12-06 2002-10-29 Ortho-Mcneil Pharmaceuticals, Inc. 6-O-Carbamoyl ketolide antibacterials
CA2372450A1 (fr) * 2001-05-10 2001-09-19 Pharmaceutical Partners Of Canada Inc. Preparation injectable liquide de pamidronate disodique
EP1430068A1 (fr) 2001-09-17 2004-06-23 Ortho-Mcneil Pharmaceutical, Inc. Agents antimicrobiens 6-o-carbamate-11,12-lacto-cetolide
EP1448182A1 (fr) * 2001-11-30 2004-08-25 Pfizer Products Inc. Compositions pharmaceutiques et methodes d'administration d'agonistes selectifs de recepteur ep2
HUP0402135A3 (en) 2001-11-30 2008-04-28 Pfizer Controlled release implant forming polymeric compositions of bone growth promoting compounds and process for their preparation
WO2003048140A1 (fr) 2001-12-03 2003-06-12 Japan Tobacco Inc. Compose azole et utilisation medicinale de celui-ci
PL370714A1 (en) 2001-12-05 2005-05-30 Ortho-Mcneil Pharmaceutical, Inc. 6-o-acyl ketolide derivatives of erythromycine useful as antibacterials
WO2003053923A2 (fr) * 2001-12-20 2003-07-03 Applied Research Systems Ars Holding N.V. Derives de pyrrolidine utilises en tant que modulateurs de la prostaglandine
JP4754820B2 (ja) * 2002-06-10 2011-08-24 メルク セローノ ソシエテ アノニム プロスタグランジン作動薬としてのγラクタムおよびその使用
JP2006021998A (ja) * 2002-07-18 2006-01-26 Ono Pharmaceut Co Ltd Ep2アゴニストを有効成分とする月経困難症治療剤
US6986884B2 (en) * 2002-09-04 2006-01-17 Rosenberg E William Composition and method for treating soft nails
HUE029417T2 (en) 2002-10-10 2017-02-28 Ono Pharmaceutical Co Microspheres containing ONO-1301
EP1661580B1 (fr) 2003-07-25 2014-01-08 Ono Pharmaceutical Co., Ltd. Remede destine a traiter des maladies liees au cartilage
EP1659918B1 (fr) 2003-08-08 2009-01-14 Amgen Fremont Inc. Anticorps diriges vers l'hormone parathyroide et leurs utilisations
US7318925B2 (en) * 2003-08-08 2008-01-15 Amgen Fremont, Inc. Methods of use for antibodies against parathyroid hormone
WO2005027931A1 (fr) * 2003-09-19 2005-03-31 Pfizer Products Inc. Compositions pharmaceutiques et methodes de traitement consistant en des associations d'un derive de la 2-alkylidene-19-nor-vitamine d et d'un agoniste selectif de ep2 ou ep4
US20050203086A1 (en) * 2004-03-04 2005-09-15 Pfizer Inc. Methods of treatment using an EP2 selective receptor agonist
JP2008503561A (ja) * 2004-06-21 2008-02-07 ファルマシア・アンド・アップジョン・カンパニー・エルエルシー 骨芽細胞機能を刺激するためのpyk2阻害薬
US7183310B2 (en) * 2004-08-10 2007-02-27 Allergan, Inc. Cyclopentane heptan(ene)oic acid, 2-heteroarylalkenyl derivatives as therapeutic agents
US7906552B2 (en) 2004-08-10 2011-03-15 Allergan, Inc. Cyclopentane heptan(ENE)OIC acid, 2-heteroarylalkenyl derivatives as therapeutic agents
US7662837B2 (en) 2004-10-22 2010-02-16 Janssen Pharmaceutica N.V. Inhibitors of c-fms kinase
WO2006043655A1 (fr) 2004-10-22 2006-04-27 Ono Pharmaceutical Co., Ltd. Préparation thérapeutique pour inhalation
US7645755B2 (en) 2004-10-22 2010-01-12 Janssen Pharmaceutical N.V. Inhibitors of c-fms kinase
ATE455760T1 (de) 2004-12-06 2010-02-15 Merck Serono Sa Pyrrolidin-2-on-derivate zur verwendung als dp1- rezeptoragonisten
NZ563863A (en) 2005-06-03 2011-02-25 Ono Pharmaceutical Co Agent for regeneration and/or protection of nerves
US20060281788A1 (en) 2005-06-10 2006-12-14 Baumann Christian A Synergistic modulation of flt3 kinase using a flt3 inhibitor and a farnesyl transferase inhibitor
US7915316B2 (en) * 2005-08-22 2011-03-29 Allergan, Inc Sulfonamides
UA93085C2 (en) 2006-04-20 2011-01-10 Янссен Фармацевтика Н.В. Inhibitors of c-fms kinase
EP2021335B1 (fr) 2006-04-20 2011-05-25 Janssen Pharmaceutica N.V. Composés hétérocycliques inhibiteurs de c-fms kinase
US8697716B2 (en) 2006-04-20 2014-04-15 Janssen Pharmaceutica Nv Method of inhibiting C-KIT kinase
JP4583500B2 (ja) 2006-07-28 2010-11-17 ファイザー・プロダクツ・インク Ep2作動薬
GB0711463D0 (en) * 2007-06-14 2007-07-25 Opal Drug Discovery Ltd Trimethylsilylbeneylsulphamates as treatments for diseases of bone loss
JO3240B1 (ar) 2007-10-17 2018-03-08 Janssen Pharmaceutica Nv c-fms مثبطات كيناز
DK2264009T3 (en) 2008-03-12 2019-04-15 Ube Industries PYRIDYLAMINE ACEDIC ACID COMPOUND
SI2415763T1 (sl) 2009-03-30 2016-05-31 Ube Industries, Ltd. Farmacevtski sestavek za zdravljenje ali preprečevanje glavkoma
WO2010116270A1 (fr) 2009-04-10 2010-10-14 Pfizer Inc. Agonistes de ep2/4
CA2785668A1 (fr) 2009-12-25 2011-06-30 Ube Industries, Ltd. Compose d'aminopyridine
US9090584B2 (en) 2010-01-26 2015-07-28 Allergan, Inc. Therapeutic agents for treatment of ocular hypertension
US8772541B2 (en) * 2011-12-15 2014-07-08 University of Pittsburgh—of the Commonwealth System of Higher Education Cannabinoid receptor 2 (CB2) inverse agonists and therapeutic potential for multiple myeloma and osteoporosis bone diseases
JP6359537B2 (ja) 2012-08-07 2018-07-18 ヤンセン ファーマシューティカ エヌ.ベー. 複素環エステル誘導体の調製プロセス
JOP20180012A1 (ar) 2012-08-07 2019-01-30 Janssen Pharmaceutica Nv عملية السلفنة باستخدام نونافلوروبوتانيسولفونيل فلوريد
WO2014069401A1 (fr) 2012-10-29 2014-05-08 株式会社カルディオ Agent thérapeutique spécifique de maladie pulmonaire
CN105308023A (zh) 2013-03-28 2016-02-03 宇部兴产株式会社 取代联芳基化合物
JP6449166B2 (ja) 2013-10-15 2019-01-09 小野薬品工業株式会社 薬剤溶出性ステントグラフト
KR102006862B1 (ko) * 2019-01-07 2019-08-02 주식회사 하이센스바이오 신규한 펩타이드
CN114805120A (zh) * 2022-05-23 2022-07-29 江苏瑞达环保科技有限公司 一种间氰甲基苯甲酸甲酯的合成工艺

Family Cites Families (74)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE51251C (de) W. LANGENBRUCH in Düren, Rheinl., Kölnstr. 68 b Sicherheitslampe für Bergwerke
DE512251C (de) 1930-01-24 1930-11-07 Koch & Sterzel Akt Ges Verfahren zum Einstellen der Kapazitaet eines auf Induktionswirkung beruhenden elektrischen Apparates, insbesondere Stromwandlers
FR897566A (fr) * 1942-08-28 1945-03-26 Bopp & Reuther Gmbh Machine à rotors
US3442890A (en) 1965-06-15 1969-05-06 Mead Johnson & Co Substituted 3-benzazocin-16-ones
CH549555A (de) 1969-04-02 1974-06-14 Byk Gulden Lomberg Chem Fab Verfahren zur herstellung von cylierten anilinocarbonsaeuren oder deren salze.
DE1917006B2 (de) 1969-04-02 1971-09-23 Siemens AG, 1000 Berlin u. 8000 München Elektrooptischer regelkreis zum regeln der lichtpunktinten sitaet einer kathodenstrahlroehre
US3780095A (en) 1970-04-08 1973-12-18 Byk Gulden Lomberg Chem Fab Acylated anilino-carboxylic acids and their salts
US4066692A (en) 1972-10-30 1978-01-03 Merck & Co., Inc. 11,12-secoprostaglandins
US4092356A (en) 1972-10-30 1978-05-30 Merck & Co., Inc. 11,12-Secoprostaglandins
US4055597A (en) 1973-01-26 1977-10-25 Merck & Co., Inc. 10-Aza-11,12-secoprostaglandins
US3987091A (en) 1973-04-12 1976-10-19 Merck & Co., Inc. 11,12-secoprostaglandins
US4033996A (en) * 1973-04-25 1977-07-05 Merck & Co., Inc. 8-Aza-9-oxo(and dioxo)-thia-11,12-secoprostaglandins
US4091107A (en) 1973-04-25 1978-05-23 Merck & Co., Inc. 8-Aza-9-oxo(and dioxo)-thia-11,12-secoprostaglandins
US3894065A (en) 1973-04-27 1975-07-08 Merck & Co Inc Aryl-oxo-alkanoic acids
JPS5019756A (fr) 1973-06-25 1975-03-01
US3989749A (en) 1973-10-17 1976-11-02 Merck & Co., Inc. 11,12-Secoprostaglandins
US3991087A (en) 1973-12-13 1976-11-09 Merck & Co., Inc. 8-Halo-11,12-secoprostaglandins
SE7414770L (fr) * 1973-12-13 1975-06-16 Merck & Co Inc
US4020177A (en) 1974-08-30 1977-04-26 Merck & Co., Inc. Substituted phenoxy-tridecanoic acids
DK366475A (da) 1974-08-30 1976-03-01 Merck & Co Inc Fremgangsmade til fremstilling af aryloxy- eller arylthioholdige secoprostaglandiner
US4055596A (en) * 1974-09-13 1977-10-25 Merck & Co., Inc. 11,12-Seco-prostaglandins
US3991106A (en) 1974-09-13 1976-11-09 Merck & Co., Inc. 16-Ethers of 8-aza-9-dioxothia-11,12-seco-prostaglandins
US4210749A (en) 1974-11-12 1980-07-01 Pennwalt Corporation Substituted 1,2,4,5-tetrahydro-3H,3 benzazepines
GB1479158A (en) 1974-12-18 1977-07-06 Basford A Furniture
US4018802A (en) 1975-04-09 1977-04-19 Merck & Co., Inc. 9-Thia- and oxothia- and 9-dioxothia-11,12-seco-prostaglandins and processes
US4097504A (en) 1975-04-23 1978-06-27 Merck & Co., Inc. 11,12-Secoprostaglandins
US4150235A (en) 1976-12-17 1979-04-17 Merck & Co., Inc. Interphenylene 11,12-secoprostaglandins
US4175203A (en) 1976-12-17 1979-11-20 Merck & Co., Inc. Interphenylene 11,12-secoprostaglandins
US4087435A (en) 1977-02-17 1978-05-02 Merck & Co., Inc. 8-Aza-9-dioxothiaprostanoic acids
US4112236A (en) 1977-04-04 1978-09-05 Merck & Co., Inc. Interphenylene 8-aza-9-dioxothia-11,12-secoprostaglandins
AT368358B (de) 1977-12-24 1982-10-11 Fisons Ltd Schaedlingsbekaempfungs- und pflanzenwachstumsregulierungsmittel
GB2012170B (en) * 1977-12-24 1982-09-02 Fisons Ltd Pesticidal and platn growth regulant compounds and composiions
US4243678A (en) 1977-12-30 1981-01-06 Byk Gulden Lomberg Chemische Fabrik Gmbh Acylhydrocarbylaminoalkanoic acids, compositions and uses
DK373383A (da) 1982-08-20 1984-02-21 Midit Fremgangsmaade til fremstilling af omega-aminosyrederivater
US4803197A (en) 1987-01-12 1989-02-07 Ciba-Geigy Corporation 2,1-benzothiazepine-2,2-dioxide-5-carboxylic acid derivatives
DE3719046A1 (de) 1987-06-06 1988-12-15 Basf Ag Verwendung von salzen von sulfonamidcarbonsaeuren als korrosionsinhibitoren in waessrigen systemen
DE3829455A1 (de) 1988-08-31 1990-03-15 Boehringer Mannheim Gmbh Sulfonamidoalkyl-cyclohexan-verbindungen, verfahren zu ihrer herstellung sowie arzneimittel
US5084466A (en) 1989-01-31 1992-01-28 Hoffmann-La Roche Inc. Novel carboxamide pyridine compounds which have useful pharmaceutical utility
US5081152A (en) 1989-07-05 1992-01-14 Kotobuki Seiyaku Co., Ltd. Azulene derivatives as thromboxane a2 and prostaglandin endoperoxide receptor antagonist
EP0505467A1 (fr) 1989-12-16 1992-09-30 Astra Pharmaceuticals Limited Derives pharmacologiquement actifs de carboxylates d'amides
ES2036926B1 (es) 1991-08-08 1994-01-16 Uriach & Cia Sa J "procedimiento para la obtencion de derivados de la (2-alquil-3-piridil)metilpiperazina".
US6743929B1 (en) * 1992-08-25 2004-06-01 G. D. Searle & Co. Sulfonylalkanoylamino hydroxyethylamino sulfonamides useful as retroviral protease inhibitors
US5352708A (en) 1992-09-21 1994-10-04 Allergan, Inc. Non-acidic cyclopentane heptanoic acid, 2-cycloalkyl or arylalkyl derivatives as therapeutic agents
DE69326321T2 (de) 1992-10-15 2000-01-13 Zaidan Hojin Biseibutsu Neues aminosäurederivat
US5332730A (en) 1992-10-16 1994-07-26 Allergan, Inc. Azido derivatives of cyclopentane heptanoic or heptenoic acid
US5578593A (en) 1992-12-11 1996-11-26 Merck & Co., Inc. Spiro piperidines and homologs promote release of growth hormone
PL176993B1 (pl) 1992-12-11 1999-08-31 Merck & Co Inc Nowe związki spiropiperydynowe oraz sposób ich wytwarzania
TW383306B (en) 1992-12-22 2000-03-01 Lilly Co Eli New use of 2-phenyl-3-aroylbenzothiophenes in lowering serum cholesterol
US5455258A (en) 1993-01-06 1995-10-03 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamic acids
US5605814A (en) 1993-08-31 1997-02-25 Merck Frosst Canada Inc. DNA encoding human prostaglandin receptor EP2
EP0739204A4 (fr) 1993-11-09 2000-03-15 Merck & Co Inc Piperidines, pyrrolidines et hexahydro-1h-azepines favorisant la liberation de l'hormone de croissance
JPH09505601A (ja) 1993-11-24 1997-06-03 メルク エンド カンパニー インコーポレーテッド インドリル基含有化合物類および成長ホルモン放出を促進するためのそれらの使用
JPH07334432A (ja) * 1994-06-07 1995-12-22 Hitachi Ltd メモリ制御回路
US5777112A (en) 1994-06-13 1998-07-07 Merck & Co., Inc Piperazine compounds promote release of growth hormone
AU5772296A (en) 1995-05-19 1996-11-29 Chiroscience Limited 3,4-disubstituted-phenylsulphonamides and their therapeutic use
JPH11510697A (ja) 1995-08-08 1999-09-21 トーマス ジェファソン ユニバーシティー 組換え体c−プロテイナーゼ、ならびにそのプロセス、方法および使用
JP3843145B2 (ja) * 1995-12-25 2006-11-08 株式会社ルネサステクノロジ 同期型半導体記憶装置
DE19603033A1 (de) 1996-01-19 1997-07-24 Schering Ag Perfluoralkylhaltige Metallkomplexe, Verfahren zu deren Herstellung und ihre Verwendung in der NMR-Diagnostik
TR199801419T2 (xx) * 1996-01-23 1998-10-21 Shionogi & Co.Ltd. S�lfone amino asit t�revleri ve ayn� i�erikte metaloproteinez �nleyicileri.
CA2242416C (fr) 1996-01-23 2006-03-21 Shionogi & Co., Ltd. Derives d'acides amines sulfones et inhibiteurs de metalloproteinases contenant ces derives
US5658897A (en) 1996-04-08 1997-08-19 Allergan Cyclopentane(ene) heptanoic or cyclopentane(ene) heptenoic acid, 2-hydrocarbyl phosphinyloxyalkyl or phosphonamidoalkyl as therapeutic agents
KR20000049047A (ko) * 1996-10-11 2000-07-25 로즈 암스트롱, 크리스틴 에이. 트러트웨인 술폰아미드 인터루킨-1β 전환 효소 억제제
UA59384C2 (uk) 1996-12-20 2003-09-15 Пфайзер, Інк. Похідні сульфонамідів та амідів як агоністи простагландину, фармацевтична композиція та способи лікування на їх основі
IL130333A0 (en) 1996-12-20 2000-06-01 Pfizer Prevention and treatment of skeletal disorder with EP2 receptor subtype selective prostaglandin E2 agonists
RU2203272C2 (ru) * 1997-02-21 2003-04-27 Байер Акциенгезелльшафт Замещенные бициклические соединения, исходные и промежуточные продукты для их получения и фармацевтическая композиция на их основе
TW378330B (en) * 1997-06-03 2000-01-01 Fujitsu Ltd Semiconductor memory device
US5910923A (en) * 1997-10-23 1999-06-08 Texas Instruments Incorporated Memory access circuits for test time reduction
US6436989B1 (en) * 1997-12-24 2002-08-20 Vertex Pharmaceuticals, Incorporated Prodrugs of aspartyl protease inhibitors
EP1000619A3 (fr) 1998-06-23 2002-07-24 Pfizer Products Inc. Méthode de traitement du glaucome
US6436914B1 (en) * 1998-06-30 2002-08-20 Bristol-Myers Squibb Company 2-hydroxy-3—(4-hydroxy-3-sulfonamidophenyl)—propylamines useful as beta 3 adrenergic agonists
US6069829A (en) * 1998-09-29 2000-05-30 Texas Instruments Incorporated Internal clock multiplication for test time reduction
US6246619B1 (en) * 2000-02-07 2001-06-12 Vanguard International Semiconductor Corp. Self-refresh test time reduction scheme
NZ521620A (en) * 2000-05-19 2004-08-27 Lilly Co Eli Sulfonamide derivatives their use as pharmaceuticals and preparation method thereof
US6822001B2 (en) * 2000-11-03 2004-11-23 Tularik Inc. Combination therapy using pentafluorobenzenesulfonamides and antineoplastic agents

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AU721260B2 (en) 2000-06-29
EP0946501A1 (fr) 1999-10-06
DK0946501T3 (da) 2006-10-02
DE69736007D1 (de) 2006-07-06
JP3679418B2 (ja) 2005-08-03
BG64893B1 (bg) 2006-08-31
AP1041A (en) 2002-02-01
KR100311566B1 (ko) 2001-11-03
DZ2375A1 (fr) 2002-12-28
CO4910163A1 (es) 2000-04-24
TR199901366T2 (xx) 1999-09-21
MA24425A1 (fr) 1998-07-01
ATE327976T1 (de) 2006-06-15
HRP970696A2 (en) 1998-10-31
PE47499A1 (es) 1999-05-13
PL192670B1 (pl) 2006-11-30
YU32799A (sh) 2002-06-19
UA59384C2 (uk) 2003-09-15
EA199900474A1 (ru) 2000-02-28
HN1997000161A (es) 1998-10-22
US6649657B2 (en) 2003-11-18
PL334343A1 (en) 2000-02-28
PT946501E (pt) 2006-10-31
AP9701166A0 (en) 1998-01-31
EA200200806A1 (ru) 2003-02-27
WO1998028264A1 (fr) 1998-07-02
SI0946501T1 (sl) 2006-10-31
SA97180721A (ar) 2005-12-03
TWI242560B (en) 2005-11-01
PA8443001A1 (es) 2000-05-24
GT199700141A (es) 1999-06-22
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SA97180721B1 (ar) 2006-04-22
HRP970696B1 (en) 2007-07-31
JP4067105B2 (ja) 2008-03-26
US6998423B2 (en) 2006-02-14
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US20020016368A1 (en) 2002-02-07
US6288120B1 (en) 2001-09-11
HUP0000739A2 (hu) 2000-09-28
ES2267133T3 (es) 2007-03-01
NO992996L (no) 1999-08-18
CA2275479A1 (fr) 1998-07-02
JP2000514827A (ja) 2000-11-07
DE69736007T2 (de) 2006-12-28
JP2005068154A (ja) 2005-03-17
EA005161B1 (ru) 2004-12-30
TW541310B (en) 2003-07-11
IS5055A (is) 1999-05-21
CA2275479C (fr) 2007-05-08
AR010843A1 (es) 2000-07-12
EA003529B1 (ru) 2003-06-26
HUP0000739A3 (en) 2001-02-28
CZ300107B6 (cs) 2009-02-11
KR20000057684A (ko) 2000-09-25
US20030105092A1 (en) 2003-06-05
EP0946501B1 (fr) 2006-05-31
UY24816A1 (es) 2000-09-29
OA11065A (en) 2002-11-15
CZ223399A3 (cs) 2000-08-16
MY141384A (en) 2010-04-30
US20040176461A1 (en) 2004-09-09
NO992996D0 (no) 1999-06-18
SA05260205B1 (ar) 2008-05-27
SK78299A3 (en) 2000-10-09
ZA9711437B (en) 1999-06-21
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IL130306A (en) 2008-12-29
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AU4720097A (en) 1998-07-17
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