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Withdrawn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
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English (en)
Japanese (ja)
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JP2005506298A (ja
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Publication date
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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Withdrawn legal-status Critical Current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JP2002576907A 2001-03-29 2002-03-28 Eg5阻害剤を用いる増殖性疾患の治療方法 Withdrawn JP2005506298A (ja)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 (cg-RX-API-DMAC7.html) 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JP2002576907A Withdrawn JP2005506298A (ja) 2001-03-29 2002-03-28 Eg5阻害剤を用いる増殖性疾患の治療方法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 (cg-RX-API-DMAC7.html)
EP (1) EP1372657A4 (cg-RX-API-DMAC7.html)
JP (1) JP2005506298A (cg-RX-API-DMAC7.html)
CA (1) CA2442455A1 (cg-RX-API-DMAC7.html)
IL (1) IL158083A0 (cg-RX-API-DMAC7.html)
MX (1) MXPA03008691A (cg-RX-API-DMAC7.html)
WO (1) WO2002078639A2 (cg-RX-API-DMAC7.html)

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
DK1847534T3 (da) * 2001-12-11 2011-08-29 Kyowa Hakko Kirin Co Ltd Thiadiazolin-derivater til behandling af kræft
US7199107B2 (en) 2002-05-23 2007-04-03 Isis Pharmaceuticals, Inc. Antisense modulation of kinesin-like 1 expression
CN1774428B (zh) * 2003-04-18 2010-06-16 协和发酵麒麟株式会社 M期驱动蛋白抑制剂
JPWO2004111024A1 (ja) * 2003-06-10 2006-07-20 協和醗酵工業株式会社 チアジアゾリン誘導体
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
US20050158320A1 (en) * 2003-11-12 2005-07-21 Nichols M. J. Combinations for the treatment of proliferative diseases
US20050100508A1 (en) * 2003-11-12 2005-05-12 Nichols M. J. Methods for identifying drug combinations for the treatment of proliferative diseases
US7662581B1 (en) 2003-12-18 2010-02-16 Novartis Vaccines And Diagnostics, Inc. Eg5 co-crystals
ES2315727T3 (es) * 2003-12-20 2009-04-01 Merck Patent Gmbh Derivados de tetrahidroquinolina 2-(hetero-)aril-substituidos.
ES2360073T3 (es) * 2004-03-23 2011-05-31 Oncotherapy Science, Inc. Método para diagnosticar cáncer de pulmón de células no pequeñas.
DE102004021637A1 (de) * 2004-05-03 2005-12-01 Merck Patent Gmbh Dihydrobenzothiophene
BRPI0514390A (pt) 2004-08-18 2008-06-10 Astrazeneca Ab enanciÈmero de um composto ou um sal farmacêuticamente aceitável ou um éster hidrolisável in vivo do mesmo, uso do mesmo, métodos para o tratamento de cáncer, para produzir um efeito inibidor de eg5 em um animal de sangue quente e para tratar doenças, e, composição farmacêutica
WO2006074293A2 (en) * 2005-01-07 2006-07-13 President And Fellows Of Harvard College Bicyclic dihydropyrimidines as eg5 inhibitors
JPWO2006101103A1 (ja) * 2005-03-22 2008-09-04 協和醗酵工業株式会社 造血器腫瘍治療剤
EP1867640A4 (en) * 2005-03-22 2010-07-14 Kyowa Hakko Kirin Co Ltd MEANS FOR TREATING SOLID TUMORS
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
KR20110022000A (ko) 2008-05-30 2011-03-04 다나-파버 캔서 인스티튜트 인크. 감수분열 키네신-연관된 질환의 치료 방법
JP2013528601A (ja) 2010-05-20 2013-07-11 アストラゼネカ・アクチエボラーグ アリール置換オレフィン系アミンの新規な製造方法
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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