JP2012522840A5 - - Google Patents

Download PDF

Info

Publication number
JP2012522840A5
JP2012522840A5 JP2012504771A JP2012504771A JP2012522840A5 JP 2012522840 A5 JP2012522840 A5 JP 2012522840A5 JP 2012504771 A JP2012504771 A JP 2012504771A JP 2012504771 A JP2012504771 A JP 2012504771A JP 2012522840 A5 JP2012522840 A5 JP 2012522840A5
Authority
JP
Japan
Prior art keywords
ester
pharmaceutically acceptable
acceptable salt
alkenyl
alkyl ester
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
JP2012504771A
Other languages
English (en)
Japanese (ja)
Other versions
JP5687687B2 (ja
JP2012522840A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2010/030073 external-priority patent/WO2010118006A1/en
Publication of JP2012522840A publication Critical patent/JP2012522840A/ja
Publication of JP2012522840A5 publication Critical patent/JP2012522840A5/ja
Application granted granted Critical
Publication of JP5687687B2 publication Critical patent/JP5687687B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2012504771A 2009-04-06 2010-04-06 癌を治療するための(2’−デオキシ−リボフラノシル)−1,3,4,7−テトラヒドロ−(1,3)ジアゼピン−2−オン誘導体 Active JP5687687B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US16711209P 2009-04-06 2009-04-06
US61/167,112 2009-04-06
PCT/US2010/030073 WO2010118006A1 (en) 2009-04-06 2010-04-06 (2 ' -deoxy-ribofuranosyl) -1,3,4, 7-tetrahydro- (1,3) iazepin-2-0ne derivatives for treating cancer

Publications (3)

Publication Number Publication Date
JP2012522840A JP2012522840A (ja) 2012-09-27
JP2012522840A5 true JP2012522840A5 (enExample) 2013-05-23
JP5687687B2 JP5687687B2 (ja) 2015-03-18

Family

ID=42126083

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2012504771A Active JP5687687B2 (ja) 2009-04-06 2010-04-06 癌を治療するための(2’−デオキシ−リボフラノシル)−1,3,4,7−テトラヒドロ−(1,3)ジアゼピン−2−オン誘導体

Country Status (10)

Country Link
US (1) US8324180B2 (enExample)
EP (1) EP2417146B1 (enExample)
JP (1) JP5687687B2 (enExample)
AR (1) AR076262A1 (enExample)
AU (2) AU2010234637B2 (enExample)
CA (1) CA2757743C (enExample)
ES (1) ES2593088T3 (enExample)
JO (1) JO3197B1 (enExample)
TW (1) TWI477508B (enExample)
WO (1) WO2010118006A1 (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO2778B1 (en) 2007-10-16 2014-03-15 ايساي انك Certain Compounds, Compositions and Methods
US8609631B2 (en) 2009-04-06 2013-12-17 Eisai Inc. Compositions and methods for treating cancer
EP2416781B1 (en) * 2009-04-06 2017-03-08 Otsuka Pharmaceutical Co., Ltd. Combination of cytidine-based antineoplastic drugs with cytidine deaminase inhibitor and use thereof in the treatment of cancer
UY32546A (es) * 2009-04-06 2010-10-29 Eisai Inc Composiciones y metodos para tratar cancer
ES2956840T3 (es) * 2013-08-19 2023-12-29 Taris Biomedical Llc Dispositivos de administración de fármacos de múltiples unidades

Family Cites Families (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4017606A (en) * 1973-10-04 1977-04-12 The Upjohn Company Organic compounds and process
US4275057A (en) * 1980-01-28 1981-06-23 The United States Of America As Represented By The Department Of Health, Education And Welfare Seven-membered ring compounds as inhibitors of cytidine deaminase
US4526988A (en) 1983-03-10 1985-07-02 Eli Lilly And Company Difluoro antivirals and intermediate therefor
EP0160079B1 (en) * 1983-10-26 1990-01-31 GREER, Sheldon B. Method and materials for sensitizing neoplastic tissue to radiation
DE3587500T2 (de) * 1984-12-04 1993-12-16 Lilly Co Eli Tumorbehandlung bei Säugetieren.
US5223608A (en) * 1987-08-28 1993-06-29 Eli Lilly And Company Process for and intermediates of 2',2'-difluoronucleosides
US4965374A (en) * 1987-08-28 1990-10-23 Eli Lilly And Company Process for and intermediates of 2',2'-difluoronucleosides
US5968914A (en) * 1987-10-28 1999-10-19 Pro-Neuron, Inc. Treatment of chemotherapeutic agent and antiviral agent toxicity with acylated pyrimidine nucleosides
WO1992018517A1 (en) 1991-04-17 1992-10-29 Yale University Method of treating or preventing hepatitis b virus
FR2682112B1 (fr) * 1991-10-08 1993-12-10 Commissariat A Energie Atomique Procede de synthese d'acide ribonucleique (arn) utilisant un nouveau reactif de deprotection.
US5371210A (en) * 1992-06-22 1994-12-06 Eli Lilly And Company Stereoselective fusion glycosylation process for preparing 2'-deoxy-2',2'-difluoronucleosides and 2'-deoxy-2'-fluoronucleosides
US5821357A (en) * 1992-06-22 1998-10-13 Eli Lilly And Company Stereoselective glycosylation process for preparing 2'-deoxy-2',2'-difluoropurine and triazole nucleosides
US5594124A (en) * 1992-06-22 1997-01-14 Eli Lilly And Company Stereoselective glycosylation process for preparing 2'-Deoxy-2',2'-difluoropyrimidine nucleosides and 2'-deoxy-2'-fluoropyrimidine nucleosides and intermediates thereof
US5426183A (en) * 1992-06-22 1995-06-20 Eli Lilly And Company Catalytic stereoselective glycosylation process for preparing 2'-deoxy-2',2'-difluoronucleosides and 2'-deoxy-2'-fluoronucleosides
US5606048A (en) * 1992-06-22 1997-02-25 Eli Lilly And Company Stereoselective glycosylation process for preparing 2'-Deoxy-2', 2'-difluoronucleosides and 2'-deoxy-2'-fluoronucleosides
EP0641352B1 (en) * 1993-02-23 1997-06-04 City Of Hope 4-ethoxy 5-fluoro 2'deoxyuridine
AU6081294A (en) 1993-05-14 1994-12-12 Pro-Neuron, Inc. Treatment of chemotherapeutic agent and antiviral agent toxicity with acylated pyrimidine nucleosides
GB9311252D0 (en) 1993-06-01 1993-07-21 Hafslund Nycomed As Cell growth regualtors
US5637688A (en) * 1994-12-13 1997-06-10 Eli Lilly And Company Process for preparing 1-(2'-deoxy-2'-difluoro-d-ribofuranosyl)-4-aminopyrimidin-2-one hydrochloride
US5521294A (en) * 1995-01-18 1996-05-28 Eli Lilly And Company 2,2-difluoro-3-carbamoyl ribose sulfonate compounds and process for the preparation of beta nucleosides
US6001994A (en) 1995-12-13 1999-12-14 Eli Lilly And Company Process for making gemcitabine hydrochloride
US5760208A (en) * 1996-08-14 1998-06-02 The Board Of Governors For Higher Education, State Of Rhode Island And Providence Plantations Process to prepare pyrimidine nucleosides
TW466112B (en) 1998-04-14 2001-12-01 Lilly Co Eli Novel use of 2'-deoxy-2',2'-difluorocytidine for immunosuppressive therapy and pharmaceutical composition comprising the same
PT1115391E (pt) 1998-09-25 2003-02-28 Warner Lambert Co Quimioterapia do cancro com acetildinalina em combinacao com gemcitabina capecitabina ou cisplatina
US6933287B1 (en) * 1999-03-01 2005-08-23 Sheldon B. Greer Dramatic simplification of a method to treat neoplastic disease by radiation
ES2273672T3 (es) 1999-03-01 2007-05-16 Halogenetics, Inc. Uso de composiciones que comprenden cldc como radiosensibilizadores en el tratamiento de enfermedades neoplasticas.
US6462191B1 (en) 2000-07-13 2002-10-08 Air Products And Chemicals, Inc. Synthesis of 2-deoxy-2-fluoro-arabinose derivatives
CN102241720B (zh) * 2000-11-29 2014-01-29 三井化学株式会社 L-核酸衍生物及其合成方法
US7141576B2 (en) * 2001-01-16 2006-11-28 Smithkline Beecham (Cork) Limited Cancer treatment method
EP2322534A1 (en) 2001-05-18 2011-05-18 Rakesh Kumar Antiviral nucleosides
AU2003278904A1 (en) 2002-09-24 2004-04-19 Kornis Pharmaceuticals, Incorporated 1, 3, 5-triazines for treatment of viral diseases
WO2005115410A2 (en) 2004-05-06 2005-12-08 University Of Rochester Context dependent inhibitors of cytidine deaminases and uses thereof
US20060014949A1 (en) 2004-07-13 2006-01-19 Supergen Inc. Compositions and formulations of decitabine polymorphs and methods of use thereof
CN101076536A (zh) 2004-07-30 2007-11-21 药华医药股份有限公司 β-核苷的立体选择性合成
US20060173174A1 (en) 2004-12-08 2006-08-03 Anne-Ruth Born Difluoronucleosides and process for preparation thereof
US20080080163A1 (en) 2006-09-29 2008-04-03 Grote Industries, Inc. Illuminated devices utilizing light active sheet material with integrated light emitting diode (LED), methods of producing illuminated devices, and kits therefor
WO2008085611A2 (en) * 2006-11-27 2008-07-17 University Of Miami Designer theraphy of pancreatic tumors
WO2009021551A1 (en) 2007-08-13 2009-02-19 Universite De La Mediterranee A method for assessing the risk of toxicity in a chemotherapy
JO2778B1 (en) * 2007-10-16 2014-03-15 ايساي انك Certain Compounds, Compositions and Methods
WO2010047698A1 (en) 2008-10-22 2010-04-29 University Of Alabama At Birmingham Activation-induced cytidine deaminase inhibitor suppression of autoimmune diseases
UY32546A (es) * 2009-04-06 2010-10-29 Eisai Inc Composiciones y metodos para tratar cancer
EP2416781B1 (en) * 2009-04-06 2017-03-08 Otsuka Pharmaceutical Co., Ltd. Combination of cytidine-based antineoplastic drugs with cytidine deaminase inhibitor and use thereof in the treatment of cancer

Similar Documents

Publication Publication Date Title
JP2011518833A5 (enExample)
JP2010536766A5 (enExample)
JP2013032389A5 (enExample)
JP2011105738A5 (enExample)
JP2012092103A5 (enExample)
JP2010501534A5 (enExample)
JP2013532130A5 (enExample)
JP2009535462A5 (enExample)
JP2014500861A5 (enExample)
EP4328223A3 (en) Substituted diaminocarboxamide and diaminocarbonitrile pyrimidines, compositions thereof, and methods of treatment therewith
JP2009149903A5 (enExample)
JP2016510323A5 (enExample)
JP2013507423A5 (enExample)
JP2013528182A5 (enExample)
JP2009545527A5 (enExample)
JP2007522220A5 (enExample)
JP2007269812A5 (enExample)
EA201201377A1 (ru) Определенные аминопиридазины, композиции на их основе и способы их использования
JP2011527299A5 (enExample)
JP2013505929A5 (enExample)
JP2013515822A5 (enExample)
EP2682387A3 (en) C7-fluoro substituted tetracycline compounds
JP2013515006A5 (enExample)
JP2007302689A5 (enExample)
JP2010530373A5 (enExample)