JP2004535362A5 - - Google Patents

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Publication number
JP2004535362A5
JP2004535362A5 JP2002557917A JP2002557917A JP2004535362A5 JP 2004535362 A5 JP2004535362 A5 JP 2004535362A5 JP 2002557917 A JP2002557917 A JP 2002557917A JP 2002557917 A JP2002557917 A JP 2002557917A JP 2004535362 A5 JP2004535362 A5 JP 2004535362A5
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JP
Japan
Prior art keywords
administration
powders
freeze
agents
dried
Prior art date
Legal status (The legal status 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 status listed.)
Granted
Application number
JP2002557917A
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English (en)
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JP2004535362A (ja
JP4180375B2 (ja
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Publication date
Priority claimed from DE10102322A external-priority patent/DE10102322A1/de
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Publication of JP2004535362A publication Critical patent/JP2004535362A/ja
Publication of JP2004535362A5 publication Critical patent/JP2004535362A5/ja
Application granted granted Critical
Publication of JP4180375B2 publication Critical patent/JP4180375B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Description

特に錠剤、ピル、被覆剤、カプセル剤、粉剤、顆粒剤、シロップ剤、ジュース、またはドロップは経口投与用に適切であり、座薬は直腸投与用に適切であり、更に溶液、好ましくは油性液または水溶液、更に懸濁液、乳液またはインプラントは、非経口投与に適切であり、軟膏、クリーム、または粉剤、もしくはスプレー式点鼻薬としての局所投与に適切である。新規化合物は凍結乾燥もでき、得られた凍結乾燥物を例えば、注射剤の調製に用いることができる。指摘した製剤は殺菌でき、および/または潤滑剤、保存剤、安定剤、および/または湿潤剤、乳化剤、浸透圧を修正する塩、緩衝剤、着色剤、および香味剤および/または複数の活性化合物、例えば1種または2種以上のビタミンなどの補助剤を含むこともできる。
JP2002557917A 2001-01-19 2001-12-05 フェニル誘導体 Expired - Fee Related JP4180375B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE10102322A DE10102322A1 (de) 2001-01-19 2001-01-19 Phenylderivate
PCT/EP2001/014296 WO2002057236A1 (en) 2001-01-19 2001-12-05 Phenyl derivatives

Publications (3)

Publication Number Publication Date
JP2004535362A JP2004535362A (ja) 2004-11-25
JP2004535362A5 true JP2004535362A5 (ja) 2006-02-09
JP4180375B2 JP4180375B2 (ja) 2008-11-12

Family

ID=7671098

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002557917A Expired - Fee Related JP4180375B2 (ja) 2001-01-19 2001-12-05 フェニル誘導体

Country Status (19)

Country Link
US (1) US7273867B2 (ja)
EP (1) EP1351938B1 (ja)
JP (1) JP4180375B2 (ja)
KR (1) KR20030072598A (ja)
CN (1) CN1518541A (ja)
AT (1) ATE359271T1 (ja)
AU (1) AU2002227993B2 (ja)
BR (1) BR0116804A (ja)
CA (1) CA2434937C (ja)
CZ (1) CZ20032151A3 (ja)
DE (2) DE10102322A1 (ja)
ES (1) ES2284718T3 (ja)
HU (1) HUP0500110A2 (ja)
MX (1) MXPA03006483A (ja)
PL (1) PL362834A1 (ja)
RU (1) RU2003124072A (ja)
SK (1) SK10142003A3 (ja)
WO (1) WO2002057236A1 (ja)
ZA (1) ZA200306419B (ja)

Families Citing this family (38)

* Cited by examiner, † Cited by third party
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DE10139060A1 (de) 2001-08-08 2003-02-20 Merck Patent Gmbh Phenylderivate
US7030141B2 (en) 2001-11-29 2006-04-18 Christopher Franklin Bigge Inhibitors of factor Xa and other serine proteases involved in the coagulation cascade
DE10204072A1 (de) * 2002-01-31 2003-08-14 Morphochem Ag Komb Chemie Neue Verbindungen, die Faktor Xa-Aktivität inhibieren
DE10214832A1 (de) * 2002-04-04 2003-10-16 Merck Patent Gmbh Phenylderivate 4
JP4567439B2 (ja) * 2002-04-27 2010-10-20 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング カルボン酸アミド
WO2004031145A2 (en) * 2002-10-02 2004-04-15 Bristol-Myers Squibb Company Lactam-containing diaminoalkyl, beta-aminoacids, alpha-aminoacids and derivatives thereof as factor xa inhibitors
DE10254336A1 (de) 2002-11-21 2004-06-03 Merck Patent Gmbh Carbonsäureamide
JP2006517589A (ja) * 2003-02-11 2006-07-27 ブリストル−マイヤーズ スクイブ カンパニー セリンプロテアーゼ・インヒビターとして有用なベンゼンアセトアミド化合物
DE10308907A1 (de) * 2003-02-28 2004-09-09 Merck Patent Gmbh Ethynylderivate
US7205318B2 (en) * 2003-03-18 2007-04-17 Bristol-Myers Squibb Company Lactam-containing cyclic diamines and derivatives as a factor Xa inhibitors
US7135469B2 (en) 2003-03-18 2006-11-14 Bristol Myers Squibb, Co. Linear chain substituted monocyclic and bicyclic derivatives as factor Xa inhibitors
AU2004226278B2 (en) * 2003-04-03 2010-07-29 Merck Patent Gmbh Pyrrolidino-1,2-dicarboxy-1-(phenylamide)-2-(4-(3-oxo-morpholino-4-yl)-phenylamide) derivatives and related compounds for use as inhibitors of coagulation factor Xa in the treatment of thrombo-embolic diseases
US7250415B2 (en) 2003-06-04 2007-07-31 Bristol-Myers Squibb Company 1,1-Disubstitutedcycloalkyl-, glycinamidyl-, sulfonyl-amidino-, and tetrahydropyrimidinyl-containing diaminoalkyl, β-aminoacids, α-aminoacids and derivatives thereof as factor Xa inhibitors
DE10336716A1 (de) 2003-08-11 2005-03-10 Merck Patent Gmbh Verfahren zur Herstellung von N-Aryl-morpholinonen
WO2005020921A2 (en) * 2003-08-29 2005-03-10 Exelixis, Inc. C-kit modulators and methods of use
US7371743B2 (en) 2004-02-28 2008-05-13 Boehringer Ingelheim International Gmbh Carboxylic acid amides, the preparation thereof and their use as medicaments
EP1571154A1 (en) * 2004-03-03 2005-09-07 Aventis Pharma Deutschland GmbH Beta-aminoacid-derivatives as factor Xa inhibitors
US7166738B2 (en) 2004-04-23 2007-01-23 Roche Palo Alto Llc Non-nucleoside reverse transcriptase inhibitors
US7625949B2 (en) 2004-04-23 2009-12-01 Roche Palo Alto Llc Methods for treating retroviral infections
US7511035B2 (en) 2005-01-25 2009-03-31 Glaxo Group Limited Antibacterial agents
EP1893583B1 (en) 2005-05-31 2012-04-04 Pfizer Inc. Substituted aryloxy-n-bicyclomethyl acetamide compounds as vr1 antagonists
EP1910298B1 (en) * 2005-06-24 2010-01-13 Brystol-Myers Squibb Company Phenylglycinamide and pyridylglycinamide derivatives useful as anticoagulants
CA2624102A1 (en) 2005-09-29 2007-04-12 Sanofi-Aventis Phenyl- and pyridinyl- 1, 2 , 4 - oxadiazolone derivatives, processes for their preparation and their use as pharmaceuticals
WO2007045573A1 (en) 2005-10-19 2007-04-26 F. Hoffmann-La Roche Ag Phenyl-acetamide nnrt inhibitors
EP1996541B1 (en) * 2006-03-09 2014-04-23 Bristol-Myers Squibb Company 2-(aryloxy)acetamide factor viia inhibitors useful as anticoagulants
WO2008076805A2 (en) * 2006-12-15 2008-06-26 Bristol-Myers Squibb Company Arylpropionamide, arylacrylamide, arylpropynamide, or arylmethylurea analogs as factor xia inhibitors
WO2009075874A1 (en) * 2007-12-13 2009-06-18 Amgen Inc. Gamma secretase modulators
JP2014523400A (ja) * 2011-04-20 2014-09-11 ビオタ サイエンティフィック マネジメント プティ リミテッド 芳香族アミド類およびそれらの使用
CA2929753A1 (en) 2013-11-08 2015-05-14 Bayer Pharma Aktiengesellschaft Substituted uracils and use thereof
CN105440020B (zh) * 2013-12-10 2018-12-18 常州大学 具有抗肿瘤活性的1,2,3-三唑类化合物及其制备方法
US10471023B2 (en) 2015-03-12 2019-11-12 British Columbia Cancer Agency Branch Bisphenol ether derivatives and methods for using the same
BR112018011562B1 (pt) * 2015-12-09 2023-05-02 F. Hoffmann-La Roche Ag Novos derivados de fenil
CN108558741B (zh) * 2017-12-27 2020-10-30 浙江天宇药业股份有限公司 一种阿哌沙班的中间体的合成方法
WO2019226991A1 (en) 2018-05-25 2019-11-28 Essa Pharma, Inc. Androgen receptor modulators and methods for their use
EP3867216A4 (en) 2018-10-18 2022-07-13 Essa Pharma, Inc. ANDROGEN RECEPTOR MODULATORS AND METHODS OF USE THEREOF
KR20230004498A (ko) 2020-04-17 2023-01-06 에싸 파마 아이엔씨. N-말단 도메인 안드로겐 수용체 억제제의 고형분 형태 및 이의 용도
CN112624930A (zh) * 2020-12-21 2021-04-09 上海如鲲新材料有限公司 一种2,2-双(4-氨基苯基)六氟丙烷的制备方法
US11596612B1 (en) 2022-03-08 2023-03-07 PTC Innovations, LLC Topical anesthetics

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US2361327A (en) * 1940-07-12 1944-10-24 Du Pont Aryloxy-alkacyl-arylenes
DE2926049A1 (de) * 1979-06-28 1981-01-08 Basf Ag M-anilidurethane und diese enthaltende herbizide
DE19743435A1 (de) 1997-10-01 1999-04-08 Merck Patent Gmbh Benzamidinderivate
JP2003500386A (ja) * 1999-05-24 2003-01-07 シーオーアール セラピューティクス インコーポレイテッド Xa因子阻害剤
DE10035144A1 (de) * 2000-07-19 2002-01-31 Merck Patent Gmbh Cyclische Aminosäurederivate

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