JP2012518598A5 - - Google Patents

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Publication number
JP2012518598A5
JP2012518598A5 JP2011535742A JP2011535742A JP2012518598A5 JP 2012518598 A5 JP2012518598 A5 JP 2012518598A5 JP 2011535742 A JP2011535742 A JP 2011535742A JP 2011535742 A JP2011535742 A JP 2011535742A JP 2012518598 A5 JP2012518598 A5 JP 2012518598A5
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JP
Japan
Prior art keywords
group
pyrimido
anticancer
alkyl group
substituted
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.)
Pending
Application number
JP2011535742A
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English (en)
Japanese (ja)
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JP2012518598A (ja
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Publication date
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Priority to JP2011535742A priority Critical patent/JP2012518598A/ja
Priority claimed from PCT/JP2010/052910 external-priority patent/WO2010098367A1/en
Publication of JP2012518598A publication Critical patent/JP2012518598A/ja
Publication of JP2012518598A5 publication Critical patent/JP2012518598A5/ja
Pending legal-status Critical Current

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JP2011535742A 2009-02-25 2010-02-18 ピリミドピリミドインダゾール誘導体 Pending JP2012518598A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2011535742A JP2012518598A (ja) 2009-02-25 2010-02-18 ピリミドピリミドインダゾール誘導体

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP2009042873 2009-02-25
JP2009042873 2009-02-25
PCT/JP2010/052910 WO2010098367A1 (en) 2009-02-25 2010-02-18 Pyrimidopyrimidoindazole derivative
JP2011535742A JP2012518598A (ja) 2009-02-25 2010-02-18 ピリミドピリミドインダゾール誘導体

Publications (2)

Publication Number Publication Date
JP2012518598A JP2012518598A (ja) 2012-08-16
JP2012518598A5 true JP2012518598A5 (enExample) 2013-04-04

Family

ID=42665571

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011535742A Pending JP2012518598A (ja) 2009-02-25 2010-02-18 ピリミドピリミドインダゾール誘導体

Country Status (6)

Country Link
US (1) US8288396B2 (enExample)
EP (1) EP2401281A4 (enExample)
JP (1) JP2012518598A (enExample)
AU (1) AU2010218781A1 (enExample)
CA (1) CA2750716A1 (enExample)
WO (1) WO2010098367A1 (enExample)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
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RU2017127088A (ru) 2010-11-16 2019-02-04 Эррэй Биофарма Инк. Комбинация ингибиторов чекпойнт-киназы 1 и ингибиторов киназы wee 1
JP6313312B2 (ja) 2012-10-02 2018-04-18 バイエル・クロップサイエンス・アクチェンゲゼルシャフト 農薬としての複素環化合物
FR3030513B1 (fr) * 2014-12-19 2016-12-23 Oreal Derives de benzoxazine cationiques et utilisation en coloration capillaire.
DE102015012050A1 (de) * 2015-09-15 2017-03-16 Merck Patent Gmbh Verbindungen als ASIC-Inhibitoren und deren Verwendungen
AU2018243667A1 (en) 2017-03-31 2019-10-17 Seagen Inc. Combinations of Chk1- and Wee1 - inhibitors
AR111419A1 (es) 2017-04-27 2019-07-10 Novartis Ag Compuestos fusionados de indazol piridona como antivirales
US11234977B2 (en) 2017-12-20 2022-02-01 Novartis Ag Fused tricyclic pyrazolo-dihydropyrazinyl-pyridone compounds as antivirals
CN109912606B (zh) * 2019-04-16 2021-05-04 新乡医学院 一种嘧啶并吲唑类化合物的合成方法
CA3145344A1 (en) 2019-06-28 2020-12-30 Shanghai Pharmaceuticals Holding Co., Ltd. Pyrazolopyrimidine compound, preparation method for same and applications thereof
CN112142748B (zh) 2019-06-28 2023-07-04 上海医药集团股份有限公司 一种吡唑酮并嘧啶类化合物、其制备方法及应用

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Publication number Priority date Publication date Assignee Title
JPS6019790A (ja) 1983-07-14 1985-01-31 Yakult Honsha Co Ltd 新規なカンプトテシン誘導体
US5223608A (en) 1987-08-28 1993-06-29 Eli Lilly And Company Process for and intermediates of 2',2'-difluoronucleosides
ATE186461T1 (de) 1990-09-28 1999-11-15 Smithkline Beecham Corp Verfahren zur herstellung wasserlöslicher camptothecinanaloge, sowie die verbindungen 10- hydroxy-11-c(1-6)-alkoxycamptothecin
US5162532A (en) 1990-12-20 1992-11-10 North Carolina State University Intermediates and method of making camptothecin and camptothecin analogs
US5243050A (en) 1990-12-20 1993-09-07 North Carolina State University Alkylpyridone DE ring intermediates useful for the manufacture of camptothecin and camptothecin analogs
US5200524A (en) 1990-12-20 1993-04-06 North Carolina State University Camptothecin intermediates and method of making same
US5191082A (en) 1990-12-20 1993-03-02 North Carolina State University Camptothecin intermediate and method of making camptothecin intermediates
US5247089A (en) 1990-12-20 1993-09-21 North Carolina State University Method of making intermediates useful for the manufacture of camptothecin and camptothecin analogs
ATE348110T1 (de) 1992-10-28 2007-01-15 Genentech Inc Hvegf rezeptor als vegf antagonist
JP3025602B2 (ja) 1993-05-21 2000-03-27 デビオファーム エス.アー. 光学的に高純度なシス−オキザラート(トランス−l−1,2−シクロヘキサンジアミン)白金(II)錯体の製造方法
GB9508538D0 (en) 1995-04-27 1995-06-14 Zeneca Ltd Quinazoline derivatives
EP0831880A4 (en) 1995-06-07 2004-12-01 Imclone Systems Inc ANTIBODIES AND FRAGMENTS OF ANTIBODIES INHIBITING TUMOR GROWTH
JP3154399B2 (ja) 1996-07-04 2001-04-09 デビオファーム エス.アー. 白金化合物の製造方法
CN1138778C (zh) * 1998-05-26 2004-02-18 沃尼尔·朗伯公司 用作细胞增殖抑制剂的二环嘧啶及二环3,4-二氢嘧啶化合物及用途
US20040044012A1 (en) 1998-05-26 2004-03-04 Dobrusin Ellen Myra Bicyclic pyrimidines and bicyclic 3,4-dihydropyrimidines as inhibitors of cellular proliferation
CA2483496A1 (en) 2002-04-26 2003-11-06 Warner-Lambert Company Llc Inhibitors of checkpoint kinases (wee1 and chk1)
US7094798B1 (en) * 2002-04-26 2006-08-22 Pfizer Inc Inhibitors of checkpoint kinases (Wee1 and Chk1)
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AR060635A1 (es) * 2006-04-27 2008-07-02 Banyu Pharma Co Ltd Derivados de 1,2-dihidro-3h-pirazolo[3,4-d]pirimidin-3-ona, composiciones farmaceuticas que los comprenden y su uso en el tratamiento del cancer
CA2689429C (en) * 2007-06-15 2012-08-21 Banyu Pharmaceutical Co., Ltd. Bicycloaniline derivatives

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