BE2011C028I2 - Macrocyclic analogs and methods of their use and preparation - Google Patents

Macrocyclic analogs and methods of their use and preparation

Info

Publication number
BE2011C028I2
BE2011C028I2 BE2011C028C BE2011C028C BE2011C028I2 BE 2011C028 I2 BE2011C028 I2 BE 2011C028I2 BE 2011C028 C BE2011C028 C BE 2011C028C BE 2011C028 C BE2011C028 C BE 2011C028C BE 2011C028 I2 BE2011C028 I2 BE 2011C028I2
Authority
BE
Belgium
Prior art keywords
preparation
methods
macrocyclic analogs
analogs
macrocyclic
Prior art date
Application number
BE2011C028C
Other languages
English (en)
Original Assignee
Eisai R&D Man Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22219026&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=BE2011C028(I2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Eisai R&D Man Co Ltd filed Critical Eisai R&D Man Co Ltd
Publication of BE2011C028I2 publication Critical patent/BE2011C028I2/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/22Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains four or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Medicinal Preparation (AREA)
  • Steroid Compounds (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Peptides Or Proteins (AREA)
  • Saccharide Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
BE2011C028C 1998-06-17 2011-09-02 Macrocyclic analogs and methods of their use and preparation BE2011C028I2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US8968298P 1998-06-17 1998-06-17
PCT/US1999/013677 WO1999065894A1 (fr) 1998-06-17 1999-06-16 Analogues macrocycliques, leurs procedes d'utilisation et de preparation
EP99928746A EP1087960B1 (fr) 1998-06-17 1999-06-16 Analogues macrocycliques, leurs procedes d'utilisation et de preparation

Publications (1)

Publication Number Publication Date
BE2011C028I2 true BE2011C028I2 (en) 2018-08-24

Family

ID=22219026

Family Applications (1)

Application Number Title Priority Date Filing Date
BE2011C028C BE2011C028I2 (en) 1998-06-17 2011-09-02 Macrocyclic analogs and methods of their use and preparation

Country Status (22)

Country Link
US (4) US6214865B1 (fr)
EP (4) EP2277873B1 (fr)
JP (1) JP4454151B2 (fr)
KR (1) KR100798600B1 (fr)
CN (1) CN1216051C (fr)
AT (1) ATE502932T1 (fr)
AU (1) AU762998B2 (fr)
BE (1) BE2011C028I2 (fr)
BR (1) BRPI9911326B8 (fr)
CA (3) CA2632433C (fr)
CY (2) CY1111516T1 (fr)
DE (2) DE69943296D1 (fr)
DK (1) DK1087960T3 (fr)
FR (1) FR11C0038I2 (fr)
HU (1) HU227912B1 (fr)
IL (1) IL139960A0 (fr)
LU (1) LU91854I2 (fr)
NO (5) NO328280B1 (fr)
NZ (1) NZ508597A (fr)
PT (1) PT1087960E (fr)
WO (1) WO1999065894A1 (fr)
ZA (1) ZA200007159B (fr)

Families Citing this family (99)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL139960A0 (en) 1998-06-17 2002-02-10 Eisai Co Ltd Macrocylic analogs and methods of their use and preparation
US8097648B2 (en) * 1998-06-17 2012-01-17 Eisai R&D Management Co., Ltd. Methods and compositions for use in treating cancer
US6653341B1 (en) 1998-06-17 2003-11-25 Eisai Co., Ltd. Methods and compositions for use in treating cancer
DE10037310A1 (de) 2000-07-28 2002-02-07 Asta Medica Ag Neue Indolderivate und deren Verwendung als Arzneimittel
EP1531846A4 (fr) * 2002-02-27 2006-04-19 Us Gov Health & Human Serv Conjugues de ligand, adaptateur et agent cytotoxique, compositions associees et procedes d'utilisation relatifs
US7192972B2 (en) 2002-03-22 2007-03-20 Eisai Co., Ltd. Hemiasterlin derivatives and uses thereof
US20050075395A1 (en) * 2003-05-28 2005-04-07 Gary Gordon Continuous dosing regimen
CA2526385C (fr) * 2003-05-29 2008-07-22 Abbott Laboratories Schema posologique d'administration en continu
US20070196418A1 (en) * 2003-07-29 2007-08-23 Michael Lewis Drug delivery methods and devices
CN101899026B (zh) 2004-06-03 2016-08-03 卫材R&D管理有限公司 用于制备软海绵素b的类似物的中间体
CN109180615A (zh) * 2004-06-03 2019-01-11 卫材R&D管理有限公司 用于制备软海绵素b的类似物的中间体
US20060045846A1 (en) * 2004-08-30 2006-03-02 Horstmann Thomas E Reagents and methods for labeling terminal olefins
WO2006076100A2 (fr) * 2004-12-09 2006-07-20 Eisai Co. Ltd. Criblage de l'isotype tubuline en therapie du cancer faisant appel aux analogues de l'halichondrine b
BRPI0817909B1 (pt) * 2007-10-03 2022-06-21 Eisai R&D Management Co., Ltd Métodos de obtenção e de preparação de uma composição diastereomericamente pura, compostos, e método para produzir os referidos compostos
JP6001857B2 (ja) * 2008-04-04 2016-10-05 エーザイ・アール・アンド・ディー・マネジメント株式会社 ハリコンドリンb類似体
SI2415470T1 (sl) 2009-03-30 2016-12-30 Eisai R&D Management Co., Ltd. Liposomski sestavek
JP5622719B2 (ja) 2009-03-30 2014-11-12 エーザイ・アール・アンド・ディー・マネジメント株式会社 リポソーム組成物の製造方法
RU2476216C1 (ru) * 2009-03-30 2013-02-27 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Липосомальная композиция
WO2010119890A1 (fr) * 2009-04-14 2010-10-21 日産化学工業株式会社 Procédé de fabrication d'un composé tétrahydropyrane et d'un intermédiaire de celui-ci
TH121482A (th) 2009-08-19 2013-02-28 นางสาวปัณณพัฒน์ เหลืองธาตุทอง องค์ประกอบทางเภสัชกรรมที่ประกอบด้วยอนุพันธ์ของควิโนลีน
BR112012018232B8 (pt) 2010-01-26 2023-01-10 Eisai R&D Man Co Ltd Compostos derivados de furo [3,2-b] pirano úteis na síntese de análogos de halicondrina b e métodos de sintetização de er-80402 e de eribulina
ES2731653T3 (es) 2011-03-18 2019-11-18 Eisai R&D Man Co Ltd Métodos y usos para predecir la respuesta a la eribulina
WO2012147900A1 (fr) 2011-04-28 2012-11-01 Eisai R&D Management Co., Ltd. Procédé en microréacteurs pour synthèse d'analogue d'halichondrine b
EP3444363B1 (fr) 2011-06-03 2020-11-25 Eisai R&D Management Co., Ltd. Biomarqueurs pour la prédiction et l'estimation de la sensibilité de sujets atteints d'un cancer de la thyroïde et du rein vis-à-vis de composés lenvatinib
EP2785687B1 (fr) 2011-11-30 2019-02-20 Sandoz AG Procédé de préparation de (3r)-2,4-di-groupe partant-3-méthylbut-1-ène
EP2791123B1 (fr) 2011-12-16 2018-07-18 Sandoz AG Procédé de préparation de dérivés de 3-((2s,5s)-4-méthylène-5- (3-oxopropyl)tétrahydrofuran-2-yl)propanol et d'intermédiaires utiles à leur préparation
AU2012363334B2 (en) * 2011-12-29 2017-02-02 Alphora Research Inc. 2-((2s,3s,4r,5r)-5-((s)-3-amino-2-hydroxyprop-1-yl)-4-methoxy-3-(phenylsulfonylmethyl) tetrahydrofuran-2-yl)acetaldehyde derivatives and process for their preparation
CN104334562A (zh) * 2012-03-30 2015-02-04 阿方拉研究股份有限公司 用于制备软海绵素b的大环c1-酮类似物的合成方法及其中有用的中间体
WO2014087230A1 (fr) 2012-12-04 2014-06-12 Eisai R&D Management Co., Ltd. Utilisation d'éribuline dans le traitement de cancer du sein
WO2014183211A1 (fr) 2013-05-15 2014-11-20 Alphora Research Inc. Dérivés de 3-((2s,5s)-4-méthylène-5-(3-oxopropyl)tétrahydrofuran-2-yl)propanol, leur préparation et intermédiaires utiles correspondants
ES2705698T3 (es) 2013-06-26 2019-03-26 Eisai R&D Man Co Ltd Terapia de combinación para el tratamiento del cáncer que comprende eribulina y lenvatinib
AU2014286880B2 (en) * 2013-07-03 2017-12-14 Sandoz Ag Synthetic process for preparation of macrocyclic C1-keto analogs of Halichondrin B and intermediates useful therein including intermediates containing -SO2-(p-TOLYL) groups
CN103483352A (zh) * 2013-10-18 2014-01-01 李友香 抗肿瘤的药用原料药
HUE049387T2 (hu) 2013-11-04 2020-09-28 Eisai R&D Man Co Ltd A halichondrin B analógjainak szintézisében hasznos makrociklizációs reakciók és köztitermékek
SG10201805024YA (en) 2013-12-06 2018-07-30 Eisai R&D Man Co Ltd Methods useful in the synthesis of halichondrin b analogs
CN104860978A (zh) * 2014-02-20 2015-08-26 正大天晴药业集团股份有限公司 软海绵素b类似物的合成中间体
TW201617326A (zh) * 2014-03-06 2016-05-16 Alphora研發股份有限公司 (s)-1-((2r,3r,4s,5s)-5-烯丙-3-甲氧-4-(對甲苯磺醯甲基)四氫呋喃-2-基)-3-氨基丙-2-醇之結晶衍生物
KR20170039096A (ko) * 2014-05-28 2017-04-10 에자이 알앤드디 매니지먼트 가부시키가이샤 암의 치료에 있어서 에리불린의 용도
US10556910B2 (en) * 2014-06-30 2020-02-11 President And Fellows Of Harvard College Synthesis of halichondrin analogs and uses thereof
KR20230043234A (ko) 2014-08-28 2023-03-30 에자이 알앤드디 매니지먼트 가부시키가이샤 고순도의 퀴놀린 유도체 및 이를 제조하는 방법
WO2016038624A1 (fr) 2014-09-09 2016-03-17 Cipla Limited Procédé de préparation d'analogues de cétone macrocyclique de l'halichondrine b ou ses sels pharmaceutiquement acceptables et ses intermédiaires
CN105713031B (zh) * 2014-12-05 2021-05-07 正大天晴药业集团股份有限公司 一种用于制备艾日布林的中间体及其制备方法
LT3263106T (lt) 2015-02-25 2024-01-10 Eisai R&D Management Co., Ltd. Chinolino darinių kartumo sumažinimo būdas
JP6951248B2 (ja) * 2015-03-04 2021-10-20 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. がんを治療するための、pd−1アンタゴニスト及びエリブリンの組合せ
KR102662228B1 (ko) 2015-03-04 2024-05-02 머크 샤프 앤드 돔 코포레이션 암을 치료하기 위한 pd-1 길항제 및 vegfr/fgfr/ret 티로신 키나제 억제제의 조합
US10344038B2 (en) 2015-04-30 2019-07-09 President And Fellows Of Harvard College Chromium-mediated coupling and application to the synthesis of halichondrins
MX380284B (es) * 2015-05-07 2025-03-12 Eisai R&D Man Co Ltd Reacciones de macrociclización e intermediarios y otros fragmentos útiles en la síntesis de macrólidos de halicondrina.
US10597401B2 (en) 2015-05-08 2020-03-24 Albany Molecular Research, Inc. Methods and intermediates for the preparation of omacetaxine and cephalotaxine derivatives thereof
MX373231B (es) 2015-06-16 2020-05-08 Eisai R&D Man Co Ltd Agente anticancerigeno.
CA2994925C (fr) 2015-08-20 2023-08-29 Eisai R&D Management Co., Ltd. Agent therapeutique pour tumeur
US10676481B2 (en) 2016-02-12 2020-06-09 Eisai R&D Management Co., Ltd. Intermediates in the synthesis of eribulin and related methods of synthesis
EP3449921B1 (fr) 2016-04-28 2023-05-31 Eisai R&D Management Co., Ltd. Eribulin pour l' inhibition de croissance tumorale
EP3464297B1 (fr) 2016-05-26 2023-10-25 Dr. Reddy's Laboratories Ltd. Procédé de préparation d'éribuline et de ses intermédiaires
SG11201811671XA (en) 2016-06-30 2019-01-30 Eisai R&D Man Co Ltd Prins reaction and intermediates useful in the synthesis of halichondrin macrolides and analogs thereof
JP2019530706A (ja) 2016-10-14 2019-10-24 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. 尿路上皮がんを治療するための、pd−1アンタゴニスト及びエリブリンの組合せ
JP6978758B2 (ja) 2016-11-11 2021-12-08 プレジデント アンド フェローズ オブ ハーバード カレッジ パラジウム媒介ケトール化
WO2018096478A2 (fr) 2016-11-23 2018-05-31 Dr. Reddy’S Laboratories Limited Procédé de préparation d'éribuline et de ses intermédiaires
KR101880939B1 (ko) 2017-01-02 2018-08-17 연성정밀화학(주) 에리불린 메실산염의 제조 중간체 및 그의 제조방법
CN110139866B (zh) * 2017-01-02 2022-05-17 研成精密化学株式会社 用于制备甲磺酸艾日布林的中间体以及制备其的方法
KR101991710B1 (ko) 2017-12-14 2019-06-21 연성정밀화학(주) 에리불린 메실산염의 제조 중간체 및 그의 제조방법
CN108341828B (zh) * 2017-01-24 2021-04-06 江苏恒瑞医药股份有限公司 用于制备艾日布林的方法及其中间体
CN108341738B (zh) * 2017-01-24 2022-10-21 江苏恒瑞医药股份有限公司 用于制备艾日布林的方法及其中间体
US12303505B2 (en) 2017-02-08 2025-05-20 Eisai R&D Management Co., Ltd. Tumor-treating pharmaceutical composition
JP7168580B2 (ja) 2017-04-05 2022-11-09 プレジデント アンド フェローズ オブ ハーバード カレッジ 大環状化合物およびその使用
US9938288B1 (en) 2017-04-05 2018-04-10 President And Fellows Of Harvard College Macrocyclic compound and uses thereof
BR112019023064A2 (pt) 2017-05-16 2020-06-09 Eisai R&D Man Co Ltd tratamento de carcinoma hepatocelular
IL295588B2 (en) 2017-07-06 2024-03-01 Harvard College Synthesis of halichondrins
US11498892B2 (en) 2017-07-06 2022-11-15 President And Fellows Of Harvard College Fe/Cu-mediated ketone synthesis
US20190046513A1 (en) 2017-08-10 2019-02-14 Huya Bioscience International, Llc Combination therapies of hdac inhibitors and tubulin inhibitors
CN109694379B (zh) * 2017-10-24 2020-09-11 江苏恒瑞医药股份有限公司 用于制备艾日布林的中间体及其制备方法
JP6967811B2 (ja) * 2017-11-09 2021-11-17 ヨンスン ファイン ケミカル カンパニー,リミテッド エリブリンメシル酸塩の製造中間体及びその製造方法
ES2974243T3 (es) 2017-11-15 2024-06-26 Harvard College Compuestos macrocíclicos y usos de los mismos
WO2019097073A1 (fr) 2017-11-20 2019-05-23 Basilea Pharmaceutica International AG Associations pharmaceutiques destinées à être utilisées dans le traitement du cancer
WO2019102490A1 (fr) 2017-11-21 2019-05-31 Natco Pharma Limited Préparation d'intermédiaires d'éribuline
KR20250057138A (ko) 2018-01-03 2025-04-28 에자이 알앤드디 매니지먼트 가부시키가이샤 할리콘드린 마크롤리드 및 그의 유사체의 합성에 유용한 프린스 반응 및 화합물
WO2019211877A1 (fr) 2018-05-03 2019-11-07 Cipla Limited Procédé de préparation d'analogues cétoniques macrocycliques de halichondrine b
WO2020008382A1 (fr) * 2018-07-04 2020-01-09 Dr. Reddy’S Laboratories Limited Procédé de préparation d'éribuline et de ses intermédiaires
EP3823973A4 (fr) * 2018-07-20 2022-09-21 Dr. Reddy's Laboratories Limited Procédé de purification pour la préparation d'éribuline et de ses intermédiaires
US20210340156A1 (en) * 2018-10-09 2021-11-04 Dr. Reddy's Laboratories Limited Process for preparation of eribulin and intermediates thereof
US12522611B2 (en) * 2018-11-28 2026-01-13 Natco Pharma Limited Process for the preparation of high pure Eribulin and its Mesylate salt
WO2020132636A1 (fr) 2018-12-20 2020-06-25 Auransa Inc. Analogues de la pentamidine et utilisations associées
US11447499B2 (en) 2019-06-14 2022-09-20 Rk Pharma Inc. Process for the preparation of eribulin mesylate intermediate
JP7574232B2 (ja) 2019-06-21 2024-10-28 カウンスィル オブ サイエンティフィック アンド インダストリアル リサーチ ホモプロパルギルアルコールを調製するための化学酵素的プロセス
US11083705B2 (en) 2019-07-26 2021-08-10 Eisai R&D Management Co., Ltd. Pharmaceutical composition for treating tumor
US12036204B2 (en) 2019-07-26 2024-07-16 Eisai R&D Management Co., Ltd. Pharmaceutical composition for treating tumor
JP7657213B2 (ja) 2019-11-07 2025-04-04 エーザイ・アール・アンド・ディー・マネジメント株式会社 抗メソテリンエリブリン抗体-薬物コンジュゲート及び使用方法
CN113135876B (zh) * 2020-01-16 2024-05-17 南通诺泰生物医药技术有限公司 艾日布林及其中间体的制备方法
AU2021210079A1 (en) * 2020-01-22 2022-08-25 Jiangsu Hengrui Medicine Co., Ltd. Drug conjugate of Eribulin derivative, preparation method therefor and application thereof in medicine
KR102377262B1 (ko) 2020-05-11 2022-03-22 연성정밀화학(주) 결정성 에리불린 염
IL279168B (en) 2020-12-02 2022-04-01 Finetech Pharmaceutical Ltd A process for the preparation of eribulin
CN113354659B (zh) 2021-06-08 2022-04-08 江苏慧聚药业股份有限公司 甲磺酸艾日布林的合成
CA3225975A1 (fr) * 2021-07-22 2023-01-26 Shanghai Senhui Medicine Co., Ltd. Conjugue de medicament de derive d'eribuline
WO2023212746A2 (fr) * 2022-04-30 2023-11-02 William Marsh Rice University Stratégie unifiée pour la synthèse totale d'un analogue d'éribuline et de macrolactame d'halichondrine b
KR20250133788A (ko) * 2023-01-17 2025-09-08 시스트이뮨, 인코포레이티드 에리불린 약물 접합체
TW202513596A (zh) 2023-06-09 2025-04-01 大陸商徠特康(蘇州)生物製藥有限公司 抗her2抗體、抗體-藥物偶聯物及其藥物組合物、藥盒、製備方法和用途
CN118834221B (zh) * 2023-08-08 2025-10-21 浙江星月药物科技有限公司 一种软海绵素b类似物
WO2025081063A2 (fr) 2023-10-13 2025-04-17 Eisai R&D Management Co., Ltd. Métabolites à base de conjugués anticorps-médicaments
WO2025106586A1 (fr) * 2023-11-13 2025-05-22 Luxvitae Therapeutics Inc. Composés cétoniques macrocycliques et leurs applications
WO2025228172A1 (fr) * 2024-04-28 2025-11-06 上海拓济医药有限责任公司 Dérivé d'éribuline, conjugué anticorps-médicament de celui-ci et utilisation médicale associée

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5338865A (en) * 1992-03-12 1994-08-16 President And Fellows Of Harvard College Synthesis of halichondrin B and norhalichondrin B
US5436238A (en) 1992-03-12 1995-07-25 President And Fellows Of Harvard College Halichondrins and related compounds
GB9206244D0 (en) * 1992-03-23 1992-05-06 Pharma Mar Sa Cytotoxic compound from a marine sponge
US5426194A (en) * 1993-01-19 1995-06-20 Arizona Board Of Regents, A Body Corporate Acting On Behalf Of Arizona State University Isolation and structure of Halistatin 1
IL139960A0 (en) 1998-06-17 2002-02-10 Eisai Co Ltd Macrocylic analogs and methods of their use and preparation
US6653341B1 (en) * 1998-06-17 2003-11-25 Eisai Co., Ltd. Methods and compositions for use in treating cancer
CN101899026B (zh) 2004-06-03 2016-08-03 卫材R&D管理有限公司 用于制备软海绵素b的类似物的中间体
BRPI0817909B1 (pt) * 2007-10-03 2022-06-21 Eisai R&D Management Co., Ltd Métodos de obtenção e de preparação de uma composição diastereomericamente pura, compostos, e método para produzir os referidos compostos
JP5134686B2 (ja) * 2007-11-16 2013-01-30 エーザイ・アール・アンド・ディー・マネジメント株式会社 ハリコンドリンbアナログ合成のための新規な中間体及び前記中間体に用いるための新規な脱スルホニル化反応
JP6001857B2 (ja) 2008-04-04 2016-10-05 エーザイ・アール・アンド・ディー・マネジメント株式会社 ハリコンドリンb類似体
BR112012018232B8 (pt) * 2010-01-26 2023-01-10 Eisai R&D Man Co Ltd Compostos derivados de furo [3,2-b] pirano úteis na síntese de análogos de halicondrina b e métodos de sintetização de er-80402 e de eribulina

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PT1087960E (pt) 2011-06-17
ATE502932T1 (de) 2011-04-15
EP1087960B1 (fr) 2011-03-23
CA2335300A1 (fr) 1999-12-23
NO2011018I1 (no) 2011-09-26
ZA200007159B (en) 2001-12-04
JP2002518384A (ja) 2002-06-25
KR20010083050A (ko) 2001-08-31
NO331183B1 (no) 2011-10-24
EP2272840B1 (fr) 2012-08-22
NO20093217L (no) 2001-02-15
CN1312804A (zh) 2001-09-12
HK1035534A1 (en) 2001-11-30
US6469182B1 (en) 2002-10-22
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KR100798600B1 (ko) 2008-01-28
US20110172446A1 (en) 2011-07-14
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EP1087960A1 (fr) 2001-04-04
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NO2022019I1 (no) 2022-06-03
BR9911326A (pt) 2001-04-03
US6365759B1 (en) 2002-04-02
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JP4454151B2 (ja) 2010-04-21
EP2277873A1 (fr) 2011-01-26
CY2011010I1 (el) 2014-04-09
US6214865B1 (en) 2001-04-10
EP2272839B1 (fr) 2012-08-22
FR11C0038I1 (fr) 2011-10-14
CA2755266A1 (fr) 1999-12-23
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EP2272839A1 (fr) 2011-01-12
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