JP2005506298A5 - - Google Patents

Download PDF

Info

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
Authority
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Withdrawn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)
Other versions
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Withdrawn legal-status Critical Current

Links

JP2002576907A 2001-03-29 2002-03-28 Ｅｇ５阻害剤を用いる増殖性疾患の治療方法 Withdrawn JP2005506298A (ja)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JP2002576907A Withdrawn JP2005506298A (ja) 2001-03-29 2002-03-28 Ｅｇ５阻害剤を用いる増殖性疾患の治療方法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
SI1847534T1 (sl) * 2001-12-11 2011-10-28 Kyowa Hakko Kirin Co Ltd Tiadiazolinski derivati za zdravljenje raka
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
US20070276017A1 (en) * 2003-06-10 2007-11-29 Chikara Murakata Thiadiazoline Derivative
US7166603B2 (en) 2003-07-23 2007-01-23 Bristol-Myers Squibb Co. Dihydropyrimidone inhibitors of calcium channel function
WO2005007124A2 (en) 2003-07-23 2005-01-27 Bristol-Myers Squibb Company Substituted dihydropyrimidine 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
EP1761515B1 (de) * 2003-12-20 2008-11-05 MERCK PATENT GmbH 2-(hetero-)aryl substituierte tetrahydrochinolinderivate
TW200600785A (en) * 2004-03-23 2006-01-01 Oncotherapy Science Inc Method for diagnosing non-small cell lung cancer
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
US20100152206A1 (en) * 2005-01-07 2010-06-17 Ralph Mazitschek Bicyclic Dihydropyrimidines and Uses Thereof
US20080262049A1 (en) * 2005-03-22 2008-10-23 Kyowa Hakko Kogyo Co., Ltd. Therapeutic Agent for Hematopoietic Tumor
KR20070113300A (ko) * 2005-03-22 2007-11-28 교와 핫꼬 고교 가부시끼가이샤 고형종양 치료제
JPWO2006137490A1 (ja) * 2005-06-24 2009-01-22 協和発酵キリン株式会社 再狭窄治療剤
DE102006002065B4 (de) * 2006-01-16 2007-11-29 Infineon Technologies Austria Ag Kompensationsbauelement mit reduziertem und einstellbarem Einschaltwiderstand
JP5385125B2 (ja) 2006-03-22 2014-01-08 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ ＭＤＭ２とｐ５３の間の相互作用の阻害剤
US8629118B2 (en) * 2008-05-30 2014-01-14 Dana-Farber Cancer Institute, Inc. Methods of treating a meiotic kinesin associated disease
AU2011256866B2 (en) 2010-05-20 2014-05-22 Astrazeneca Ab New process for the preparation of aryl substituted olefinic amines
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

Similar Documents

Publication Publication Date Title
JP2005506298A5 (enExample)
JP2004519469A5 (enExample)
JP2004531544A5 (enExample)
JP2007520440A5 (enExample)
RU2003119153A (ru) Орто-, мета-замещенные бис-арильные соединения, способ их получения, их применение в качестве медикаментов, а также содержащие их фармацевтические композиции
NO20072515L (no) 2-amido-4-fenyltnazolderivater, fremstilling og terapeutsik anvendelse derav
JP2004535436A5 (enExample)
JP2006151984A5 (enExample)
DE60316686D1 (de) Bisarylsulfonamid-derivate und ihre verwendung für krebs therapie
RU2007101685A (ru) Модуляторы никотиновых ацетилхолиновых рецепторов альфа 7 и их терапевтические применения
JP2012505879A5 (enExample)
JP2004516314A5 (enExample)
RU2005114021A (ru) Производные имидазола и их применение в качестве периферически-селективных ингибиторов дофамин-бета-гидролазы
JP2005511699A5 (enExample)
JP2008505157A5 (enExample)
RU2008126245A (ru) Комбинация ингибитора асне и антагониста 5-нт для лечения когнитивной дисфункции
JP2008506714A5 (enExample)
JP2005526024A5 (enExample)
ES2373561T3 (es) Uso de derivados de 1,4-bis(3-aminoalquil)piperazina en el tratamiento de enfermedades neurodegenerativas.
AR040126A1 (es) Compuesto de fenilsulfonilo, composicion farmaceutica que lo comprende y su uso para la elaboracion de un medicamento
JP2004534781A5 (enExample)
RU2002130247A (ru) Производные оксадиазола, обладающие противоопухолевым действием
JP2005505583A5 (enExample)
RU2010116779A (ru) Производное амида индазолакриловой кислоты
RU2009149518A (ru) Триазоло[1, 5-а]хинолины в качестве лигандов рецептора аденозина а3