JP2011516426A5 - - Google Patents

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Publication number
JP2011516426A5
JP2011516426A5 JP2011502126A JP2011502126A JP2011516426A5 JP 2011516426 A5 JP2011516426 A5 JP 2011516426A5 JP 2011502126 A JP2011502126 A JP 2011502126A JP 2011502126 A JP2011502126 A JP 2011502126A JP 2011516426 A5 JP2011516426 A5 JP 2011516426A5
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JP
Japan
Prior art keywords
cancer
deuterium
hydrogen
compound
compound according
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
JP2011502126A
Other languages
English (en)
Japanese (ja)
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JP2011516426A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2009/038701 external-priority patent/WO2009121042A1/en
Publication of JP2011516426A publication Critical patent/JP2011516426A/ja
Publication of JP2011516426A5 publication Critical patent/JP2011516426A5/ja
Pending legal-status Critical Current

Links

JP2011502126A 2008-03-28 2009-03-27 キナゾリン誘導体および治療方法 Pending JP2011516426A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US4064708P 2008-03-28 2008-03-28
US61/040,647 2008-03-28
US15754909P 2009-03-04 2009-03-04
US61/157,549 2009-03-04
PCT/US2009/038701 WO2009121042A1 (en) 2008-03-28 2009-03-27 Quinazoline derivatives and methods of treatment

Publications (2)

Publication Number Publication Date
JP2011516426A JP2011516426A (ja) 2011-05-26
JP2011516426A5 true JP2011516426A5 (cg-RX-API-DMAC7.html) 2012-05-24

Family

ID=40638034

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011502126A Pending JP2011516426A (ja) 2008-03-28 2009-03-27 キナゾリン誘導体および治療方法

Country Status (5)

Country Link
US (1) US20090269354A1 (cg-RX-API-DMAC7.html)
JP (1) JP2011516426A (cg-RX-API-DMAC7.html)
KR (1) KR20110005828A (cg-RX-API-DMAC7.html)
CN (1) CN102083801A (cg-RX-API-DMAC7.html)
WO (1) WO2009121042A1 (cg-RX-API-DMAC7.html)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20110053968A1 (en) 2009-06-09 2011-03-03 Auspex Pharmaceuticals, Inc. Aminopyrimidine inhibitors of tyrosine kinase
US20110195066A1 (en) * 2010-02-05 2011-08-11 Auspex Pharmaceuticals, Inc. Quinoline inhibitors of tyrosine kinase
CN102946880A (zh) * 2010-04-23 2013-02-27 尼基制药公司 治疗胰腺癌的方法
US9145390B2 (en) 2011-03-03 2015-09-29 Concert Pharmaceuticals, Inc. Derivatives of pyrazole-substituted amino-heteroaryl compounds
WO2014028914A1 (en) * 2012-08-17 2014-02-20 Beta Pharma, Inc. Deuterated icotinib derivatives
US9192609B2 (en) 2013-04-17 2015-11-24 Hedgepath Pharmaceuticals, Inc. Treatment and prognostic monitoring of proliferation disorders using hedgehog pathway inhibitors
CN103536925B (zh) * 2013-10-28 2015-07-01 中国医学科学院基础医学研究所 强心苷化合物在非小细胞肺癌治疗中的应用
CN106188072A (zh) * 2015-05-07 2016-12-07 刘文沛 氘代4-[(3-乙炔苯基)氨基]-6,7-苯-12冠-4-喹唑啉衍生物以及包含该衍生物的药物组合物
JP2022515256A (ja) * 2018-12-25 2022-02-17 ソル - ゲル テクノロジーズ リミテッド Egfr阻害剤を含む組成物による皮膚障害の治療

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL259609A (cg-RX-API-DMAC7.html) * 1959-12-31
US6221335B1 (en) * 1994-03-25 2001-04-24 Isotechnika, Inc. Method of using deuterated calcium channel blockers
ATE446955T1 (de) * 1995-03-30 2009-11-15 Pfizer Prod Inc Chinazolinone derivate
US5747498A (en) * 1996-05-28 1998-05-05 Pfizer Inc. Alkynyl and azido-substituted 4-anilinoquinazolines
US6440710B1 (en) * 1998-12-10 2002-08-27 The Scripps Research Institute Antibody-catalyzed deuteration, tritiation, dedeuteration or detritiation of carbonyl compounds
YU13200A (sh) * 1999-03-31 2002-10-18 Pfizer Products Inc. Postupci i intermedijeri za dobijanje anti-kancernih jedinjenja
UA74803C2 (uk) * 1999-11-11 2006-02-15 Осі Фармасьютікалз, Інк. Стійкий поліморф гідрохлориду n-(3-етинілфеніл)-6,7-біс(2-метоксіетокси)-4-хіназолінаміну, спосіб його одержання (варіанти) та фармацевтичне застосування
DK1104760T3 (da) * 1999-12-03 2003-06-30 Pfizer Prod Inc Sulfamoylheteroarylpyrazolforbindelser som anti-inflammatoriske/analgetiske midler
CZ20031903A3 (cs) * 2001-01-31 2004-07-14 Pfizer Products Inc. Amidové deriváty thiazolyl-, oxazolyl-, pyrrolyl- a imidazolyl karboxylových kyselin užitečné jako inhibitory isozymů PDE4
TW200413273A (en) * 2002-11-15 2004-08-01 Wako Pure Chem Ind Ltd Heavy hydrogenation method of heterocyclic rings
RU2006146625A (ru) * 2004-06-03 2008-07-20 Ф.Хоффманн-Ля Рош Аг (Ch) Лечение иринотеканом (срт-11) и ингибитором рецептора эпидермального фактора роста (egfr)
CN101309917B (zh) * 2005-10-06 2013-09-11 奥斯拜客斯制药有限公司 具有增强治疗性质的胃h+,k+-atp酶氘代抑制剂
US7750168B2 (en) * 2006-02-10 2010-07-06 Sigma-Aldrich Co. Stabilized deuteroborane-tetrahydrofuran complex
CA2661223A1 (en) * 2006-08-22 2008-02-28 Concert Pharmaceuticals Inc. 4-aminoquinazoline derivatives and methods of use thereof
WO2008030382A1 (en) * 2006-09-05 2008-03-13 Schering Corporation Pharmaceutical combinations for lipid management and in the treatment of atherosclerosis and hepatic steatosis
US8343950B2 (en) * 2006-12-15 2013-01-01 Concert Pharmaceuticals, Inc. Quinazoline derivatives and methods of treatment
US20090076042A1 (en) * 2007-09-15 2009-03-19 Protia, Llc Deuterium-enriched erlotinib

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