JP2005506298A5 - - Google Patents

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Publication number
JP2005506298A5
JP2005506298A5 JP2002576907A JP2002576907A JP2005506298A5 JP 2005506298 A5 JP2005506298 A5 JP 2005506298A5 JP 2002576907 A JP2002576907 A JP 2002576907A JP 2002576907 A JP2002576907 A JP 2002576907A JP 2005506298 A5 JP2005506298 A5 JP 2005506298A5
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JP
Japan
Prior art keywords
alkyl
composition
group
arylalkyl
heteroarylalkyl
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.)
Withdrawn
Application number
JP2002576907A
Other languages
English (en)
Japanese (ja)
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JP2005506298A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2002/009817 external-priority patent/WO2002078639A2/en
Publication of JP2005506298A publication Critical patent/JP2005506298A/ja
Publication of JP2005506298A5 publication Critical patent/JP2005506298A5/ja
Withdrawn legal-status Critical Current

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JP2002576907A 2001-03-29 2002-03-28 Ｅｇ５阻害剤を用いる増殖性疾患の治療方法 Withdrawn JP2005506298A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US27995601P 2001-03-29 2001-03-29
US28036601P 2001-03-30 2001-03-30
PCT/US2002/009817 WO2002078639A2 (en) 2001-03-29 2002-03-28 A method of treating proliferative diseases using eg5 inhibitors

Publications (2)

Publication Number Publication Date
JP2005506298A JP2005506298A (ja) 2005-03-03
JP2005506298A5 true JP2005506298A5 (enExample) 2005-12-22

Family

ID=26959985

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002576907A Withdrawn JP2005506298A (ja) 2001-03-29 2002-03-28 Ｅｇ５阻害剤を用いる増殖性疾患の治療方法

Country Status (7)

Country Link
US (1) US20020165240A1 (enExample)
EP (1) EP1372657A4 (enExample)
JP (1) JP2005506298A (enExample)
CA (1) CA2442455A1 (enExample)
IL (1) IL158083A0 (enExample)
MX (1) MXPA03008691A (enExample)
WO (1) WO2002078639A2 (enExample)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040009156A1 (en) * 2001-10-12 2004-01-15 Christoph Reinhard Antisense therapy using oligonucleotides that target human kinesin genes for treatment of cancer
ATE480527T1 (de) * 2001-12-11 2010-09-15 Kyowa Hakko Kirin Co Ltd Thiadiazolinderivate zur krebsbehandlung
US7199107B2 (en) * 2002-05-23 2007-04-03 Isis Pharmaceuticals, Inc. Antisense modulation of kinesin-like 1 expression
KR101096948B1 (ko) 2003-04-18 2011-12-20 후지필름 홀딩스 가부시끼가이샤 Ｍ기 키네신 저해제
CA2528433A1 (en) * 2003-06-10 2004-12-23 Kyowa Hakko Kogyo Co., Ltd. Thiadiazoline derivative
WO2005007124A2 (en) 2003-07-23 2005-01-27 Bristol-Myers Squibb Company Substituted dihydropyrimidine inhibitors of calcium channel function
US7166603B2 (en) 2003-07-23 2007-01-23 Bristol-Myers Squibb Co. Dihydropyrimidone inhibitors of calcium channel function
US20050100508A1 (en) * 2003-11-12 2005-05-12 Nichols M. J. Methods for identifying drug combinations for the treatment of proliferative diseases
US20050158320A1 (en) * 2003-11-12 2005-07-21 Nichols M. J. Combinations for the treatment of proliferative diseases
US7662581B1 (en) 2003-12-18 2010-02-16 Novartis Vaccines And Diagnostics, Inc. Eg5 co-crystals
DK1761515T3 (da) * 2003-12-20 2009-02-16 Merck Patent Gmbh 2-(hetero-)aryl-substituerede tetrahydroquinolinderivater
EP2343384A3 (en) * 2004-03-23 2012-01-04 Oncotherapy Science, Inc. Method for diagnosing non-small cell lung cancer
DE102004021637A1 (de) * 2004-05-03 2005-12-01 Merck Patent Gmbh Dihydrobenzothiophene
CN101027309B (zh) 2004-08-18 2010-10-27 阿斯利康(瑞典)有限公司 所选择的稠合嘧啶酮的对映体和在治疗和预防癌症中的用途
WO2006074293A2 (en) * 2005-01-07 2006-07-13 President And Fellows Of Harvard College Bicyclic dihydropyrimidines as eg5 inhibitors
CN101193878A (zh) * 2005-03-22 2008-06-04 协和发酵工业株式会社 实体肿瘤治疗剂
CN101193877A (zh) * 2005-03-22 2008-06-04 协和发酵工业株式会社 造血系统肿瘤治疗剂
WO2006137490A1 (ja) * 2005-06-24 2006-12-28 Kyowa Hakko Kogyo Co., Ltd. 再狭窄治療剤
DE102006002065B4 (de) * 2006-01-16 2007-11-29 Infineon Technologies Austria Ag Kompensationsbauelement mit reduziertem und einstellbarem Einschaltwiderstand
WO2007107543A1 (en) 2006-03-22 2007-09-27 Janssen Pharmaceutica N.V. Inhibitors of the interaction between mdm2 and p53
MX2010012931A (es) 2008-05-30 2011-02-24 Dana Farber Cancer Inst Inc Metodos para tratar una enfermedad asociada con quinesina meiotica.
BR112012029326A2 (pt) 2010-05-20 2017-08-08 Astrazeneca Ab processo para a preparação de animais olefínicas substituídas por arila
RU2427373C1 (ru) * 2010-11-08 2011-08-27 Виктор Вениаминович Тец Средство для индукции эндогенного интерферона
CN113135859B (zh) * 2021-04-26 2022-08-26 安徽省庆云医药股份有限公司 一种绿色合成瑞舒伐他汀钙中间体的方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2658804A1 (de) * 1976-12-24 1978-07-06 Bayer Ag Kreislaufbeeinflussende mittel
EP0330470A3 (en) * 1988-02-24 1992-01-02 Ajinomoto Co., Inc. 1,4-dihydropyridine derivatives useful against tumour cells
US5536724A (en) * 1992-03-03 1996-07-16 Sri International Antiinflammatory and antineoplastic 5-deazaaminopterins and 5,10-dideazaaminopterins
US5767131A (en) * 1993-04-05 1998-06-16 Synaptic Pharmaceutical Corporation Dihydropyridines and new uses thereof

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