ES2396613T3 - Imidazopirazinas e imidazotriazinas sustituidas - Google Patents

Imidazopirazinas e imidazotriazinas sustituidas Download PDF

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Publication number
ES2396613T3
ES2396613T3 ES09751280T ES09751280T ES2396613T3 ES 2396613 T3 ES2396613 T3 ES 2396613T3 ES 09751280 T ES09751280 T ES 09751280T ES 09751280 T ES09751280 T ES 09751280T ES 2396613 T3 ES2396613 T3 ES 2396613T3
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Spain
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alkyl
independently selected
substituted
cr8r9
cyclic
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Andrew P. Crew
Meizhong Jin
Mridula Kadalbajoo
Andrew Kleinberg
Mark J. Mulvihill
Jing Wang
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OSI Pharmaceuticals LLC
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OSI Pharmaceuticals LLC
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Un compuesto de acuerdo con la Fórmula I: en la que: A es CH o N; Q1 es -X1-Y1-Z1; o Q1 es: X1 es cíclico5-10, que puede estar sustituido con uno o más grupos G1 seleccionados independientemente; Y1 se selecciona entre >C(R2)R3, >C(OR2)R3, >C>=O, >C>=C(R2)R3, >C>=NR2, >C>=NOR2, >NR2, >O, >S(O)m; Z1 se selecciona entre cíclico5-10 o alcoxi C1-6, cualquiera de los cuales puede estar sustituido con uno o más gruposG1 seleccionados independientemente; y en la que cuando Y es >O y R1 es ciclobutilo, al menos uno de X o Z está sustituido; cada caso de G1 seselecciona independientemente entre halo, -CN, -CF3, -OCF3, -NO2, alquilo C1-6, cíclico3-6alquilo C0-6, -OR4, -NR4R5, -C(O)R4, -C(O)NR4R5, -C(O)OR4 o -NR4C(O)R5 , cualquiera de los cuales puede estar sustituido con uno o más grupos G2 seleccionados independientemente; cada caso de G2 se selecciona independientemente entre halo, -CN, -OH, -NH2, -NO2, oxo, -CF3, -OCF3 o alquilo C1-6, cualquiera de los cuales puede estar sustituido con uno o más grupos seleccionados independientemente entrehalo, -CN, -OH, -NH2, alquilo C1-6 (en el que cualquiera de los siguientes puede estar parcial o totalmentehalogenado), -Oalquilo C1-6 o -N(alquil C1-6) alquilo C1-6; cada caso de G3 se selecciona independientemente entre halo, oxo, -CN, -CF3, -OCF3, alquilo C1-6, cíclico3-6alquiloC0-6, -OR8, -NR8R9, -C(O)R8, -C(O)NR8R9, -C(O)OR8, -NR8C(O)R9, -(CR8R9)nNR6R7, -(CR8R9)nOR6, -NR8C(O)OR9, -O(CR8R9)nNR6R7, -N(CR8R9)nOR6 o - (CR8R9)nNR6C(O)OR7, cualquiera de los cuales puede estar sustituido con unoo más sustituyentes G2 seleccionados independientemente R1 se selecciona entre -SR2, alquilo C1-6, 5,6-bicíclicoarilo, o cíclico3-6, cualquiera de los cuales puede estar sustituidocon uno o más grupos G3 seleccionados independientemente; cada caso de R2 y R3 se selecciona independientemente entre H, halo o -alquilo C1-6; cada caso de R4, R5, R6, R7, R8, R9 se selecciona independientemente entre H, alquilo C1-6 o cíclico3-6alquilo C0-6; enlos que cualquier par R4/R5, R6/R7, R8/R9, junto con el átomo al que está unido, puede formar un cíclico3-6 quepueden incluir uno o más heteroátomos seleccionados entre O, N(alquilo C0-3) o S(O)m; cada m se selecciona independientemente entre 0-2; y cada n se selecciona independientemente entre 0-4; o una sal farmacéuticamente aceptable del mismo.
ES09751280T 2008-05-19 2009-05-18 Imidazopirazinas e imidazotriazinas sustituidas Active ES2396613T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US5434508P 2008-05-19 2008-05-19
US54345P 2008-05-19
PCT/US2009/044325 WO2009143051A1 (en) 2008-05-19 2009-05-18 Substituted imidazopyr-and imidazotri-azines

Publications (1)

Publication Number Publication Date
ES2396613T3 true ES2396613T3 (es) 2013-02-22

Family

ID=40983400

Family Applications (1)

Application Number Title Priority Date Filing Date
ES09751280T Active ES2396613T3 (es) 2008-05-19 2009-05-18 Imidazopirazinas e imidazotriazinas sustituidas

Country Status (5)

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US (1) US8481733B2 (es)
EP (1) EP2283020B8 (es)
JP (1) JP2011520970A (es)
ES (1) ES2396613T3 (es)
WO (1) WO2009143051A1 (es)

Families Citing this family (42)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
HRP20090495T1 (hr) 2004-04-02 2009-10-31 Osi Pharmaceuticals Heterobiciklički inhibitori protein kinaze supstituirani 6,6-bicikličkim prstenom
JP2011510018A (ja) * 2008-01-18 2011-03-31 オーエスアイ・フアーマスーテイカルズ・インコーポレーテツド 癌治療のためのイミダゾピラジノール誘導体
CN102405214A (zh) 2009-04-20 2012-04-04 Osi药物有限责任公司 C-吡嗪-甲胺的制备
JP2012526138A (ja) * 2009-05-07 2012-10-25 オーエスアイ・ファーマシューティカルズ,エルエルシー 副腎皮質癌を治療するためのosi−906の使用
AP2013007070A0 (en) 2011-02-23 2013-08-31 Pfizer Imidazo[5,1-f][1,2,4] triazines for the treatment of neurological disorders
ES2570187T3 (es) 2011-07-13 2016-05-17 Basf Agro Bv Compuestos fungicidas de 2-[2-halogenoalquil-4-(fenoxi)-fenil]-1-[1,2,4]triazol-1-il-etanol sustituido
US9173402B2 (en) 2011-07-15 2015-11-03 Basf Se Fungicidal alkyl-substituted 2[2-chloro-4-(4-chioro-phenoxy)-phenyl]-1[1,2,4]triazol-1-yl-ethanol compounds
US9137996B2 (en) 2011-07-15 2015-09-22 Basf Se Fungicidal alkyl- and aryl-substituted 2[-2-chloro-4-(dihalo-phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds
AU2012296887A1 (en) 2011-08-15 2014-01-30 Basf Se Fungicidal substituted 1-{2-[2-halo-4-(4-halogen-phenoxy)-phenyl]-2-alkoxy-3-methyl-butyl}-1H-[1,2,4]triazole compounds
BR112014003412A2 (pt) 2011-08-15 2017-03-14 Basf Se compostos de fórmula i, processo, compostos de fórmula xii, viii e xi, composições agroquímicas, utilização e semente revestida
MX2014001669A (es) 2011-08-15 2014-05-27 Basf Se Compuestos de fungicidas de 1-{2-[2-halo-4-(4-halogen-fenoxi)-feni l]-2-alcoxi-2-alquinil/alquenil-etil}-1h-[1,2,4]triazol sustituidos.
CN103374001B (zh) * 2012-04-19 2015-10-28 山东轩竹医药科技有限公司 咪唑并三嗪类mTOR抑制剂
MX2015003874A (es) * 2012-09-26 2015-12-16 Univ California Modulacion de ire1.
BR112015014753B8 (pt) 2012-12-20 2020-03-03 Basf Agro Bv composições, uso de uma composição, método para o combate de fungos fitopatogênicos e uso dos componentes
BR112015016446B1 (pt) 2013-01-09 2019-10-29 Basf Agro Bv processo para preparar compostos de fórmula ii, solução aquosa e uso da solução aquosa
WO2014113942A1 (en) * 2013-01-23 2014-07-31 Merck Sharp & Dohme Corp. Btk inhibitors
BR112016000299B8 (pt) 2013-07-08 2021-04-20 Basf Agro Bv composições, uso de uma composição, método para o combate dos fungos fitopatogênicos e uso dos componentes
CA2922058A1 (en) * 2013-10-18 2015-04-23 Medivation Technologies, Inc. Heterocyclic compounds and methods of use
CA2833867A1 (en) * 2013-11-21 2015-05-21 Pharmascience Inc. Protein kinase inhibitors
AU2015281187B2 (en) 2014-06-25 2018-10-04 BASF Agro B.V. Pesticidal compositions
WO2016019237A2 (en) * 2014-07-31 2016-02-04 Pharmacyclics Llc Inhibitors of bruton's tyrosine kinase
UA120628C2 (uk) 2014-11-07 2020-01-10 Басф Се Пестицидні суміші
WO2016106624A1 (en) 2014-12-31 2016-07-07 Merck Sharp & Dohme Corp. Tertiary alcohol imidazopyrazine btk inhibitors
WO2016106652A1 (en) * 2014-12-31 2016-07-07 Merck Sharp & Dohme Corp. Biarylether imidazopyrazine btk inhibitors
WO2016106628A1 (en) * 2014-12-31 2016-07-07 Merck Sharp & Dohme Corp. Btk inhibitors
WO2016161571A1 (en) 2015-04-08 2016-10-13 Merck Sharp & Dohme Corp. Indazole and azaindazole btk inhibitors
PL3426637T3 (pl) * 2016-03-11 2022-05-30 Angel Pharmaceutical Co., Ltd. Związki i sposoby modulowania kinazy tyrozynowej brutona
US11241012B2 (en) 2016-03-16 2022-02-08 Basf Se Use of tetrazolinones for combating resistant phytopathogenic fungi on soybean
WO2017157920A1 (en) 2016-03-16 2017-09-21 Basf Se Use of tetrazolinones for combating resistant phytopathogenic fungi on fruits
EP3429357B1 (en) 2016-03-16 2025-09-17 Basf Se Use of a specific tetrazolinone for combating resistant phytopathogenic fungi on cereals
CN106831787B (zh) * 2017-01-20 2018-10-23 成都倍特药业有限公司 用作布鲁顿酪氨酸激酶抑制剂的化合物及其制备方法和应用
US11554118B2 (en) * 2017-03-22 2023-01-17 Xibin Liao Bruton's tyrosine kinase inhibitors
KR20200066301A (ko) * 2017-09-01 2020-06-09 옵티키라 엘엘씨 Ire1 억제를 위한 화합물 및 조성물
CN108191871B (zh) * 2018-01-02 2020-02-18 成都倍特药业有限公司 新型布鲁顿酪氨酸激酶抑制剂及其制备方法和应用
CN118955506A (zh) 2019-01-18 2024-11-15 杭州邦顺制药有限公司 布鲁顿酪氨酸激酶抑制剂
ES2961673T3 (es) * 2019-03-15 2024-03-13 Alterity Therapeutics Ltd Compuestos para y métodos para tratar enfermedades
MX2022008148A (es) * 2020-01-02 2022-07-21 Dizal Jiangsu Pharmaceutical Co Ltd Inhibidores de btk.
WO2021184154A1 (en) * 2020-03-16 2021-09-23 Flash Therapeutics, Llc Compounds for treating or inhibiting recurrence of acute myeloid leukemia
US11155547B1 (en) 2020-06-18 2021-10-26 Alterity Therapeutics Limited Compounds for and methods of treating diseases
CN113943294A (zh) * 2020-07-15 2022-01-18 成都海博为药业有限公司 一种作为btk抑制剂的化合物及其制备方法与用途
CN113861179A (zh) * 2021-10-22 2021-12-31 上海应用技术大学 一种新型flt3激酶抑制剂及其合成与应用
TW202502334A (zh) * 2023-05-25 2025-01-16 大陸商正大天晴藥業集團股份有限公司 含有醯胺取代的芳香環的化合物、其藥物組成物及用途

Family Cites Families (62)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5217999A (en) * 1987-12-24 1993-06-08 Yissum Research Development Company Of The Hebrew University Of Jerusalem Styryl compounds which inhibit EGF receptor protein tyrosine kinase
US5302606A (en) * 1990-04-16 1994-04-12 Rhone-Poulenc Rorer Pharmaceuticals Inc. Styryl-substituted pyridyl compounds which inhibit EGF receptor tyrosine kinase
US6645969B1 (en) * 1991-05-10 2003-11-11 Aventis Pharmaceuticals Inc. Aryl and heteroaryl quinazoline compounds which inhibit CSF-1R receptor tyrosine kinase
CA2108889A1 (en) * 1991-05-29 1992-11-30 Robert Lee Dow Tricyclic polyhydroxylic tyrosine kinase inhibitors
MX9304801A (es) * 1992-08-06 1997-06-28 Warner Lambert Co 2-toindoles (selenoidoles) disulfuros (seleniduros) relacinados, los cuales inhiben a las proteinas tirosina cinasas y los cuales tienen propiedades anti-tumorales.
GB9226855D0 (en) * 1992-12-23 1993-02-17 Erba Carlo Spa Vinylene-azaindole derivatives and process for their preparation
US20030108545A1 (en) * 1994-02-10 2003-06-12 Patricia Rockwell Combination methods of inhibiting tumor growth with a vascular endothelial growth factor receptor antagonist
GB9624482D0 (en) * 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
CH690773A5 (de) 1996-02-01 2001-01-15 Novartis Ag Pyrrolo(2,3-d)pyrimide und ihre Verwendung.
JP2000506880A (ja) * 1996-03-15 2000-06-06 ゼネカ・リミテッド シンノリン誘導体及びその使用
US6232299B1 (en) * 1996-05-01 2001-05-15 Eli Lilly And Company Use of protein kinase C inhibitors to enhance the clinical efficacy of oncolytic agents and radiation therapy
GB9707800D0 (en) * 1996-05-06 1997-06-04 Zeneca Ltd Chemical compounds
ZA200007412B (en) * 1998-05-15 2002-03-12 Imclone Systems Inc Treatment of human tumors with radiation and inhibitors of growth factor receptor tyrosine kinases.
US6713474B2 (en) * 1998-09-18 2004-03-30 Abbott Gmbh & Co. Kg Pyrrolopyrimidines as therapeutic agents
US6337338B1 (en) * 1998-12-15 2002-01-08 Telik, Inc. Heteroaryl-aryl ureas as IGF-1 receptor antagonists
EP2042194A3 (en) * 1999-05-14 2009-04-22 Imclone Systems, Inc. Treatment of refractory human tumors with epidermal growth factor receptor antagonists
US6982265B1 (en) * 1999-05-21 2006-01-03 Bristol Myers Squibb Company Pyrrolotriazine inhibitors of kinases
DK1202746T3 (da) 1999-08-12 2007-01-02 Wyeth Corp NSAID- og EGFR-kinaseinhibitorerholdigt præparat til behandling eller inhibering af colonpolypper og colorektal cancer
US7087613B2 (en) * 1999-11-11 2006-08-08 Osi Pharmaceuticals, Inc. Treating abnormal cell growth with a stable polymorph of N-(3-ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine hydrochloride
AU2000240570A1 (en) 2000-03-29 2001-10-08 Knoll Gesellschaft Mit Beschraenkter Haftung Pyrrolopyrimidines as tyrosine kinase inhibitors
GB0008368D0 (en) * 2000-04-06 2000-05-24 Astrazeneca Ab Combination product
GB0017635D0 (en) * 2000-07-18 2000-09-06 Pharmacia & Upjohn Spa Antitumor combined therapy
WO2002045653A2 (en) * 2000-12-08 2002-06-13 Uab Research Foundation Combination radiation therapy and chemotherapy in conjuction with administration of growth factor receptor antibody
KR20030068205A (ko) * 2001-01-09 2003-08-19 메르크 파텐트 게엠베하 수용체 타이로신 키나아제 저해제 및 혈관형성 저해제를사용하는 병용 요법
EP1363702A4 (en) * 2001-01-30 2007-08-22 Cytopia Pty Ltd PROCESS FOR INHIBITING KINASES
MXPA03008560A (es) * 2001-03-22 2004-06-30 Abbot Gmbh & Co Kg Pirazolopirimidinas como agentes terapeuticos.
KR20030083016A (ko) 2001-03-28 2003-10-23 브리스톨-마이어스스퀴브컴파니 신규 타이로신 카이나제 억제제
AU2002315306B2 (en) * 2001-05-08 2007-05-17 Merck Patent Gmbh Combination therapy using anti-EGFR antibodies and anti-hormonal agents
TWI238824B (en) * 2001-05-14 2005-09-01 Novartis Ag 4-amino-5-phenyl-7-cyclobutyl-pyrrolo[2,3-d]pyrimidine derivatives
SE0102168D0 (sv) * 2001-06-19 2001-06-19 Karolinska Innovations Ab New use and new compounds
EP1463742A4 (en) * 2001-06-21 2006-05-10 Ariad Pharma Inc NEW PYRAZOLO AND PYRROLO PYRIMIDINES AND THEIR USES
US7115617B2 (en) * 2001-08-22 2006-10-03 Amgen Inc. Amino-substituted pyrimidinyl derivatives and methods of use
US6939874B2 (en) * 2001-08-22 2005-09-06 Amgen Inc. Substituted pyrimidinyl derivatives and methods of use
GB0122560D0 (en) * 2001-09-19 2001-11-07 Aventis Pharma Ltd Chemical compounds
SE0104140D0 (sv) * 2001-12-07 2001-12-07 Astrazeneca Ab Novel Compounds
CA2470088A1 (en) * 2001-12-20 2003-07-03 Tularik Inc. Identification of an amplified gene and target for drug intervention
US20050215564A1 (en) * 2002-02-14 2005-09-29 Stiles Charles D Methods and compositions for treating hyperproliferative conditions
US20030199525A1 (en) 2002-03-21 2003-10-23 Hirst Gavin C. Kinase inhibitors
BR0309226A (pt) * 2002-04-16 2005-02-09 Astrazeneca Ab Métodos para a produção de um efeito de danificação vascular em um animal de sangue quente, e para o tratamento de um câncer envolvendo um tumor sólido em um animal de sangue quente, composição farmacêutica, kit, e, usos de zd6126 ou de um seu sal farmaceuticamente aceitável, e de zd1839 ou de um seu sal farmaceuticamente aceitável
DE10230604A1 (de) * 2002-07-08 2004-01-29 Bayer Ag Heterocyclisch substituierte Imidazotriazine
DE10230605A1 (de) * 2002-07-08 2004-01-29 Bayer Ag Substituierte Imidazotriazine
TW200501960A (en) * 2002-10-02 2005-01-16 Bristol Myers Squibb Co Synergistic kits and compositions for treating cancer
UA80171C2 (en) * 2002-12-19 2007-08-27 Pfizer Prod Inc Pyrrolopyrimidine derivatives
US7157460B2 (en) * 2003-02-20 2007-01-02 Sugen Inc. Use of 8-amino-aryl-substituted imidazopyrazines as kinase inhibitors
AP2005003390A0 (en) * 2003-03-12 2005-09-30 Pfizer Prod Inc Pyridyloxymethyl and benzisoxazole azabicyclic derivatives.
ES2372694T3 (es) * 2003-10-15 2012-01-25 OSI Pharmaceuticals, LLC Inhibidores de tirosina cinasa de imidazo[1,5-a]pirazina.
WO2005061519A1 (en) * 2003-12-19 2005-07-07 Takeda San Diego, Inc. Kinase inhibitors
HRP20090495T1 (hr) * 2004-04-02 2009-10-31 Osi Pharmaceuticals Heterobiciklički inhibitori protein kinaze supstituirani 6,6-bicikličkim prstenom
RU2006146612A (ru) * 2004-06-03 2008-07-20 Ф.Хоффманн-Ля Рош Аг (Ch) Лечение цисплатином и ингибитором рецептора эпидермального фактора роста (egfr)
MXPA06015237A (es) * 2004-06-29 2007-12-10 Amgen Inc Pirrolo[2-3-d]pirimidinas que modulan la actividad de ack1 y lck.
AR053090A1 (es) * 2004-07-20 2007-04-25 Osi Pharm Inc Imidazotriazinas como inhibidores de proteina quinasas y su uso para la preparacion de medicamentos
US7674907B2 (en) * 2004-07-23 2010-03-09 Amgen Inc. Furanopyridine derivatives and methods of use
DE202005016343U1 (de) * 2005-10-19 2007-02-22 Weidmüller Interface GmbH & Co. KG Elektrische Steckverbindung mit Schnellentriegelung
ES2436877T3 (es) * 2005-11-17 2014-01-07 OSI Pharmaceuticals, LLC Intermedios para la preparación de inhibidores de mTOR bicíclicos condensados
AR057960A1 (es) * 2005-12-02 2007-12-26 Osi Pharm Inc Inhibidores de proteina quinasa biciclicos
US8575164B2 (en) * 2005-12-19 2013-11-05 OSI Pharmaceuticals, LLC Combination cancer therapy
US20080299113A1 (en) * 2005-12-19 2008-12-04 Arnold Lee D Combined treatment with and composition of 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitor and anti-cancer agents
TW200801008A (en) * 2005-12-29 2008-01-01 Abbott Lab Protein kinase inhibitors
WO2007106503A2 (en) * 2006-03-13 2007-09-20 Osi Pharmaceuticals, Inc. Combined treatment with an egfr kinase inhibitor and an agent that sensitizes tumor cells to the effects of egfr kinase inhibitors
PL2526933T3 (pl) * 2006-09-22 2015-08-31 Pharmacyclics Llc Inhibitory kinazy tyrozynowej Brutona
WO2008076143A1 (en) 2006-12-18 2008-06-26 Osi Pharmaceuticals, Inc. Combination of igfr inhibitor and anti-cancer agent
TW200900070A (en) 2007-02-27 2009-01-01 Osi Pharm Inc Combination cancer therapy

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Publication number Publication date
JP2011520970A (ja) 2011-07-21
EP2283020B1 (en) 2012-10-31
EP2283020A1 (en) 2011-02-16
WO2009143051A1 (en) 2009-11-26
EP2283020B8 (en) 2012-12-12
US8481733B2 (en) 2013-07-09
US20090286768A1 (en) 2009-11-19

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