JP2008546706A5 - - Google Patents

Download PDF

Info

Publication number
JP2008546706A5
JP2008546706A5 JP2008517095A JP2008517095A JP2008546706A5 JP 2008546706 A5 JP2008546706 A5 JP 2008546706A5 JP 2008517095 A JP2008517095 A JP 2008517095A JP 2008517095 A JP2008517095 A JP 2008517095A JP 2008546706 A5 JP2008546706 A5 JP 2008546706A5
Authority
JP
Japan
Prior art keywords
trimethoxy
methoxy
group
composition
phenyl
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
JP2008517095A
Other languages
English (en)
Japanese (ja)
Other versions
JP5354775B2 (ja
JP2008546706A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2006/023251 external-priority patent/WO2006138427A2/en
Publication of JP2008546706A publication Critical patent/JP2008546706A/ja
Publication of JP2008546706A5 publication Critical patent/JP2008546706A5/ja
Application granted granted Critical
Publication of JP5354775B2 publication Critical patent/JP5354775B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2008517095A 2005-06-14 2006-06-14 チューブリン結合活性を有するコンブレタスタチンアナログ Expired - Fee Related JP5354775B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US69068905P 2005-06-14 2005-06-14
US60/690,689 2005-06-14
PCT/US2006/023251 WO2006138427A2 (en) 2005-06-14 2006-06-14 Combretastatin analogs with tubulin binding activity

Publications (3)

Publication Number Publication Date
JP2008546706A JP2008546706A (ja) 2008-12-25
JP2008546706A5 true JP2008546706A5 (enExample) 2009-11-26
JP5354775B2 JP5354775B2 (ja) 2013-11-27

Family

ID=37076178

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008517095A Expired - Fee Related JP5354775B2 (ja) 2005-06-14 2006-06-14 チューブリン結合活性を有するコンブレタスタチンアナログ

Country Status (6)

Country Link
US (2) US7429681B2 (enExample)
EP (1) EP1896391B1 (enExample)
JP (1) JP5354775B2 (enExample)
CA (1) CA2611712C (enExample)
ES (1) ES2551086T3 (enExample)
WO (1) WO2006138427A2 (enExample)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2048126A1 (de) * 2007-10-11 2009-04-15 Bayer Schering Pharma AG Benzocycloheptanderivate als selektiv wirksame Estrogene
US20090264382A1 (en) 2007-11-21 2009-10-22 David Chaplin Methods for Treating Hematopoietic Neoplasms
WO2010132498A1 (en) * 2009-05-11 2010-11-18 Oxigene, Inc. Vascular disrupting agents for treatment of polypoidal choroidal vasculopathy
EP2470177B1 (en) 2009-08-27 2015-07-15 Bionomics Limited Combination therapy for treating proliferative diseases
WO2013026942A1 (en) 2011-08-25 2013-02-28 The Provost, Fellows, Foundation Scholars, And The Other Members Of Board, Of The College Of The Holy And Undivided Trinity Of Queen Elizabeth, Near Dublin Tubulin binding agents
AU2013204313C1 (en) 2012-06-01 2016-04-07 Bionomics Limited Combination Therapy
CN104817519B (zh) * 2015-05-11 2016-11-16 中国药科大学 一类ca-4的衍生物、其制法及其医药用途
US11419934B2 (en) 2015-08-18 2022-08-23 Oncotelic Therapeutics, Inc. Use of VDAS to enhance immunomodulating therapies against tumors
WO2017066668A1 (en) * 2015-10-15 2017-04-20 Baylor University Drug-linker conjugate pharmaceutical compositions
AU2017221083B2 (en) * 2016-02-15 2021-06-24 Sanofi 6,7-dihydro-5H-benzo[7]annulene derivatives as estrogen receptor modulators
US20180002355A1 (en) * 2016-07-01 2018-01-04 Baylor University Benzocyclooctene-based and indene-based anticancer agents
SG11201903908PA (en) 2016-11-17 2019-05-30 Sanofi Sa Novel substituted n-(3-fluoropropyl)-pyrrolidine compounds, processes for their preparation and therapeutic uses thereof
EP3434272A1 (en) 2017-07-25 2019-01-30 Sanofi Combination comprising palbociclib and 6-(2,4-dichlorophenyl)-5-[4-[(3s)-1-(3-fluoropropyl)pyrrolidin-3-yl]oxyphenyl]-8,9-dihydro-7h-benzo[7]annulene-2-carboxylic acid
WO2020037209A1 (en) * 2018-08-17 2020-02-20 Baylor University Benzosuberene analogues and related compounds with activity as anticancer agents
ES2923412T3 (es) 2018-09-07 2022-09-27 Sanofi Sa Sales de 6-(2,4-diclorofenil)-5-[4-[(3S)-1-(3-fluoropropil)pirrolidin-3-il]oxifenil]-8,9-dihidro-7H-benzo[7]anuleno-2-carboxilato de metilo y proceso de preparación de las mismas
JP7680438B2 (ja) 2019-10-01 2025-05-20 サノフイ 新規の置換6,7-ジヒドロ-5h-ベンゾ[7]アンヌレン化合物、その製造方法およびその治療的使用
BR112022009705A2 (pt) 2019-12-09 2022-08-09 Sanofi Sa Forma cristalina anidra de um derivado de ácido 7h-benzo[7]anuleno-2-carboxílico, seus usos e processos de preparação, forma sólida, medicamento e composição farmacêutica
TW202146007A (zh) 2020-02-27 2021-12-16 法商賽諾菲公司 包含阿培利司(alpelisib)與6-(2,4-二氯苯基)-5-[4-[(3s)-1-(3-氟丙基)吡咯啶-3-基]氧苯基]-8,9-二氫-7h-苯并[7]輪烯-2-羧酸之組合
US12595230B2 (en) 2020-10-19 2026-04-07 Sanofi Substituted 6,7-dihydro-5H-benzo[7]annulene compounds and their derivatives, processes for their preparation and therapeutic uses thereof
AU2021366223A1 (en) 2020-10-19 2023-06-22 Sanofi Substituted 6,7-dihydro-5h-benzo[7]annulene compounds and their derivatives, processes for their preparation and therapeutic uses thereof

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2447099A (en) * 1944-08-23 1948-08-17 Hoffmann La Roche 2-phenylindene derivatives and process for the manufacture of same
US2493730A (en) * 1946-10-23 1950-01-03 Hoffmann La Roche 2-(p-oxyphenyl)-3-isopropyl-6-oxyindanes
US3859358A (en) * 1967-12-20 1975-01-07 Standard Oil Co Ohio Process for the oxidation of olefins to unsaturated aldehydes
US3813430A (en) * 1970-10-26 1974-05-28 Sterling Drug Inc 1-aryl-2-alkyl or-alkenyl-3,4-dihydronaphthalenes
US3859356A (en) 1972-07-24 1975-01-07 Sandoz Ag Benzylidene substituted bicyclic and tricyclic compounds
FR2320734A1 (fr) 1975-08-14 1977-03-11 Roussel Uclaf Nouveaux derives de l'aminomethyl benzocycloheptene et leurs sels, procede de preparation et application a titre de medicaments de ces produits
EP0298466A3 (en) * 1987-07-10 1990-10-24 F. Hoffmann-La Roche Ag Substituted alkene carboxylic acid amides and derivatives
US4927838A (en) 1987-07-10 1990-05-22 Hoffman-La Roche Inc. Pyridine compounds which are useful in treating a disease state characterized by an excess of platelet activating factors
WO1993011258A1 (fr) 1991-11-29 1993-06-10 Bioxytech Procede de dosage de l'activite sod utilisant un compose autoxydable, necessaire pour sa mise en ×uvre, composes autoxydables et leur preparation
JPH06256244A (ja) * 1993-03-01 1994-09-13 Sankyo Co Ltd インデンストロール誘導体
US5561122A (en) 1994-12-22 1996-10-01 Arizona Board Of Regents Acting On Behalf Of Arizona State University Combretastatin A-4 prodrug
US5811421A (en) 1995-07-31 1998-09-22 Eli Lilly And Company Naphthyl and dihydronaphthyl intermediates, compounds, compositions, and methods
US5886025A (en) 1997-03-06 1999-03-23 Baylor University Anti-mitotic agents which inhibit tubulin polymerization
US6162930A (en) 1998-03-06 2000-12-19 Baylor University Anti-mitotic agents which inhibit tubulin polymerization
US7001926B2 (en) * 2000-03-10 2006-02-21 Oxigene, Inc. Tubulin binding agents and corresponding prodrug constructs
WO2000048606A1 (en) 1999-02-18 2000-08-24 Oxigene, Inc. Compositions and methods for use in targeting vascular destruction
WO2001019794A2 (en) 1999-09-17 2001-03-22 Baylor University Indole-containing and combretastatin-related anti-mitotic and anti-tubulin polymerization agents
US7091240B2 (en) * 2000-03-10 2006-08-15 Oxigene, Inc. Tubulin binding ligands and corresponding prodrug constructs
JP2004505888A (ja) * 2000-03-10 2004-02-26 ベイラー・ユニバーシテイ チューブリン結合リガンドおよび対応するプロドラッグ構造
US6670344B2 (en) 2000-09-14 2003-12-30 Bristol-Myers Squibb Company Combretastatin A-4 phosphate prodrug mono- and di-organic amine salts, mono- and di- amino acid salts, and mono- and di-amino acid ester salts
AUPR283801A0 (en) * 2001-02-01 2001-03-01 Australian National University, The Chemical compounds and methods
CA2445922A1 (en) * 2001-05-10 2002-11-21 Merck & Co., Inc. Estrogen receptor modulators
US7011926B2 (en) * 2001-10-11 2006-03-14 Taiwan Semiconductor Manufacturing Co., Ltd. Gap forming pattern fracturing method for forming optical proximity corrected masking layer
US6919324B2 (en) * 2001-10-26 2005-07-19 Oxigene, Inc. Functionalized stilbene derivatives as improved vascular targeting agents
CA2512000C (en) * 2002-12-26 2011-08-09 Eisai Co., Ltd. Selective estrogen receptor modulator
WO2005003100A2 (en) * 2003-07-03 2005-01-13 Myriad Genetics, Inc. 4-arylamino-quinazolines as activators of caspases and inducers of apoptosis

Similar Documents

Publication Publication Date Title
JP2019537570A5 (enExample)
Cai Small molecule vascular disrupting agents: potential new drugs for cancer treatment
JP2019519503A5 (enExample)
JP2004536879A5 (enExample)
JP2013505945A5 (enExample)
US10377759B2 (en) Brk inhibitory compound
KR20210075992A (ko) Sting 작동 화합물
JP2013505946A5 (enExample)
JP2014534200A5 (enExample)
JPH026473A (ja) 置換フラボノイド化合物、それらの塩、製法およびこれらを含有する医薬
BRPI0820518A2 (pt) compostos, composição farmacêutica e métodos de quimiossensibilização de células cancerígenas e de tratamento de mamífero com câncer
JP2020506951A5 (enExample)
JP2009526761A5 (enExample)
JP2013505947A5 (enExample)
JP2012502964A5 (enExample)
JP2008526756A (ja) 抗腫瘍化合物、癌の治療方法および製剤学的組成物
JP2014505696A5 (enExample)
JP2013534922A5 (enExample)
JP2003528096A5 (enExample)
JP2012525329A5 (enExample)
KR102775891B1 (ko) 신경 내분비 종양의 치료에서 이중 표적화를 위한 조성물 및 방법
AU2010286334A1 (en) Combination therapy for treating proliferative diseases
JP2014510080A5 (enExample)
JP2018520147A (ja) 医薬共結晶組成物及びその用途
ES2742078T3 (es) Piridonas bicíclicas novedosas como moduladores de gamma-secretasa