AR045738A1 - Derivados de bencimidazol n3 alquilados como inhibidores de mek - Google Patents

Derivados de bencimidazol n3 alquilados como inhibidores de mek

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AR045738A1
AR045738A1 ARP040103103A ARP040103103A AR045738A1 AR 045738 A1 AR045738 A1 AR 045738A1 AR P040103103 A ARP040103103 A AR P040103103A AR P040103103 A ARP040103103 A AR P040103103A AR 045738 A1 AR045738 A1 AR 045738A1
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aryl
heteroaryl
heterocyclyl
nr3r4
alkyl
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Eli M Wallace
Joseph Lyssikatos
Allison L Marlow
T Brian Hurley
Kevin Koch
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Array Biopharma Inc
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    • C07F9/6503Five-membered rings
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Abstract

Una prodroga de fosfato o aminoácido de un compuesto (1H-benzoimidazol-5-il) (fenil 4-sustituido)-amina alquilada que tiene la fórmula (1) y sales farmacéuticamente aceptables, prodrogas y solvatos de ellos, en donde: ------- es un enlace opcional, siempre que uno y sólo un N del anillo tenga enlace doble; R1, R9 y R10 ase seleccionan independientemente de H, halógeno, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, -OR3, -C(O)R3, -C(O)OR3, NR4C(O)OR6, -OC(O)R3, - NR4SO2R6, -SO2NR3R4, -NR4C(O)R3, -C(O)NR3R4, -NR5C(O)NR3R4, -NR5C(NCN)NR3R4, -NR3R4, alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-10, cicloalquilalquilo C3-10, -S(O)j(alquilo C1-6), -S(O)j(CR4R5)m-arilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, heterociclilo, heterociclilalquilo, -O(CR4R5)m-arilo, -NR4(CR4R5)m-arilo, -O(CR4R5)m-heteroarilo, -NR4(CR4R5)m-heteroarilo, -O(CR4R5)m-heterociclilo o -NR4(CR4R5)m-heterociclilo, donde cada porción de alquilo, alquenilo, alquinilo, cicloalquilo, arilo, heteroarilo y heterociclilo se sustituye optativamente con uno a cinco grupos que se seleccionan independientemente de oxo, halógeno, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, - NR4SO2R6, -SO2NR3R4, -C(O)R3, -C(O)OR3, -OC(O)R3, -NR4C(O)OR6, -NR4C(O)R3, -C(O)NR3R4, -NR3R4, -NR5C(O)NR3R4, -NR5C(NCN)NR3R4, -OR3, arilo, heteroarilo, arilalquilo, heteroarilalquilo, heterociclilo, y heterociclilalquilo; R3 se selecciona de H, trifluorometilo, alquilo C1-10, alquenilo, C2-10, alquinilo C2-10, cicloalquilo C3-10, cicloalquilalquilo C3-10, arilo, arilalquilo, heteroarilo, heteroarilalquilo, heterociclilo, heterociclilalquilo, donde cada porción de alquilo, alquenilo, alquinilo, cicloalquilo, arilo, heteroarilo y heterociclilo se sustituye optativamente con uno a cinco grupos que se seleccionan independientemente de oxo, halógeno, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, fosfato, residuo de aminoácido, polipéptido, hemisuccinato, ésteres de fosfato, dimetilaminoacetato, fosforilmetiloxicarbonilo, fosfonamida, -NR´SO2R""´, -SO2NR´R", -C(O)R´, -C(O)OR´, -OC(O)R´, -NR´C(O)OR"", -NR´C(O)R", -C(O)NR´R", -SR´, -S(O)R"", -SO2R"", - NR´R", -NR´C(O)NR"R"´, -NR¨C(NCN)NR"R"¨, -OR´, arilo, heteroarilo, arilalquilo, heteroarilalquilo, heterociclilo y heterociclilalquilo, o R3 y R4 junto con el átomo al cual están unidos forman un anillo carbocíclico, de heteroarilo o heterociclilo de 4 a 10 miembros, cada uno de los cuales se sustituye optativamente con uno a tres grupos que se seleccionan independientemente de halógeno, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, -NR´SO2R"", -SO2NR´R", -C(O)R´, - C(O)OR´, -OC(O)R´, -NR´C(O)OR"", -NR´C(O)R", -C(O)NR´R", - SO2R"", -NR´R", -NR´C(O)NR"R"´, -NR´C(NCN)NR"R"´, -OR´, arilo, heteroarilo, arilalquilo, heteroarilalquilo, heterociclilo, y heterociclilalquilo; R´, R" y R"´se seleccionan independientemente de H, alquilo inferior, alquenilo inferior, arilo y arilalquilo; R"" se selecciona de alquilo inferior, alquenilo inferior, arilo y arilalquilo; o dos cualquiera de R´, R", R"´o R"" junto con el átomo al cual están unidos, forman un anillo carbocíclico, de heteroarilo o heterocíclico de 4 a 10 miembros, cada uno de los cuales se sustituye optativamente con uno a tres grupos que se seleccionan independientemente de halógeno, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, arilo, heteroarilo, arilalquilo, heteroarilalquilo, heterociclilo, y heterociclilalquilo; R4 y R5 representan independientemente H o alquilo C1-6, o R4 y R5 junto con el átomo al cual están unidos forman un anillo carbocíclico de heteroarilo o heterocíclico de 4 a 10 miembros, cada uno de los cuales se sustituye optativamente con uno a tres grupos que se seleccionan independientemente de halógeno, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, -NR´SO2R"", -SO2NR´R", -C(O)R´, -C(O)OR´, -OC(O)R´, -NR´C(O)OR"", -NR´C(O)R", -C(O)NR´R", - SO2R"", -NR´R", -NR´C(O)NR"R"´, -NR´C(NCN)NR"R"´, -OR´, arilo, heteroarilo, arilalquilo, heteroarilalquilo, heterociclilo, y heterociclilalquilo; R6 se selecciona de trifluorometilo, alquilo C1-10, cicloalquilo C3-10, arilo, arilalquilo, heteroarilo, heteroarilalquilo, heterociclilo, heterociclilalquilo, en donde cada porción de alquilo, cicloalquilo, arilo, heteroarilo y heterociclilo se sustituye optativamente con uno a tres grupos oxo, halógeno, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, -NR´SO2R"", -SO2NR´R", -C(O)R´, -C(O)OR´, -OC(O)R´, -NR´C(O)OR"", -NR´C(O)R", -C(O)NR´R", - SO2R"", - NR´R", -NR´C(O)NR"R"´, -NR´C(NCN)NR"R"´, -OR´, arilo, heteroarilo, arilalquilo, heteroarilalquilo, heterociclilo, y heterociclilalquilo; R7 se selecciona, de alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-10, cicloalquilalquilo C3- 10, arilo, arilalquilo, heteroarilo, heteroarilalquilo, heterociclilo, heterociclilalquilo, donde cada porción de alquilo, alquenilo, alquinilo, cicloalquilo, arilo, heteroarilo y heterociclilo se sustituye optativamente con uno a cinco grupos que se seleccionan independientemente de oxo, halógeno, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, -NR4SO2R6, -SO2NR3R4, -C(O)R3, -C(O)OR3, -OC(O)R3, -NR4C(O)OR6, -NR4C(O)R3, -C(O)NR3R4, -SO2R6, -NR3R4, -NR5C(O)NR3R4, - NR5C(NCN)NR3R4, -OR3, arilo, heteroarilo, arilalquilo, heteroarilalquilo, heterociclilo, y heterociclilalquilo; W se selecciona de heteroarilo, heterociclilo, -C(O)R3, -C(O)NR3R4, -C(O)NR4OR3, -C(O)R4OR3, -C(O)(cicloalquilo C3-10), -C(O)(alquilo C1- 10), -C(O)(arilo), -C(O)(heteroarilo) y -C(O)(heterociclilo), cada uno de los cuales se sustituye optativamente con 1-5 grupos que se seleccionan de: -NR3R4, -OR3, -R2, alquilo C1-10, alquenilo C2-10, y alquinilo C2-10, cada uno de los cuales se sustituye optativamente con 1 o 2 grupos que se seleccionan independientemente de --NR3R4 y -OR3; R8 se selecciona de H, -SCF3, -Cl. -Br, -F, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, -OR3, -C(O)R3, -C(O)OR3, - NR4C(O)OR6, -OC(O)R3, -NR4SO2R6, -SO2NR3R4, -NR4C(O)R3, -C(O)NR3R4, -NR5C(O)NR3R4, -NR3R4, alquilo C1-10, alquenilo C2-10, alquinilo C2-10, cicloalquilo C3-10, cicloalquilalquilo C3-10, S(O)j(alquilo C1-6), -S(O)j(CR4R5)m-arilo, arilo, arilalquilo, heteroarilo, heteroarilalquilo, heterociclilo, heterociclilalquilo, -O(CR4R5)m-arilo, -NR4(CR4R5)m-arilo, -O(CR4R5)m-heteroarilo, -NR4(CR4R5)m-heteroarilo, -O(CR4R5)m-heterociclilo o -NR4(CR4R5)m-heterociclilo, donde cada porción de alquilo, alquenilo, alquinilo, cicloalquilo, arilo, heteroarilo y heterociclilo se sustituye optativamente con uno a cinco grupos que se seleccionan independientemente de oxo, halógeno, ciano, nitro, trifluorometilo, difluorometoxi, trifluorometoxi, azido, - NR4SO2R6, SO2NE3R4, -C(O)R3, -C(O)OR3, -OC(O)R3, -NR4C(O)OR6, -NR4C(O)R3, -C(O)NR3R4, -NR3R4, -NR5C(O)NR3R4, -NR5C(NCN)NR3R4, -OR3, arilo, heteroarilo, arilalquilo, heteroarilalquilo, heterociclilo, y heterociclilalquilo; m es 0, 1, 2, 3, 4º 5; y j es 1 o 2. Composición que comprende dicho compuesto y un portador farmacéuticamente aceptable. Uso de dicho compuesto para fabricar la composición farmacéutica útil para inhibir la actividad de MEK es un mamífero que lo necesita. Uso de dicho compuesto para fabricar una composición farmacéutica para el tratamiento de un trastorno hiperproliferativo en un mamífero que lo necesita mediante la administración de una cantidad eficaz para tratar ese trastorno.
ARP040103103A 2003-08-29 2004-08-27 Derivados de bencimidazol n3 alquilados como inhibidores de mek AR045738A1 (es)

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EP (1) EP1663210B1 (es)
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Families Citing this family (72)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL401637A1 (pl) 2002-03-13 2013-05-27 Array Biopharma Inc. N3 alkilowane pochodne benzimidazolu jako inhibitory MEK
CA2532067C (en) * 2003-07-24 2010-12-21 Stephen Douglas Barrett N-methyle-substituted benzamidazoles
US7144907B2 (en) * 2003-09-03 2006-12-05 Array Biopharma Inc. Heterocyclic inhibitors of MEK and methods of use thereof
US7538120B2 (en) * 2003-09-03 2009-05-26 Array Biopharma Inc. Method of treating inflammatory diseases
US7517994B2 (en) * 2003-11-19 2009-04-14 Array Biopharma Inc. Heterocyclic inhibitors of MEK and methods of use thereof
WO2005051302A2 (en) * 2003-11-19 2005-06-09 Array Biopharma Inc. Bicyclic inhibitors of mek and methods of use thereof
US7732616B2 (en) * 2003-11-19 2010-06-08 Array Biopharma Inc. Dihydropyridine and dihydropyridazine derivatives as inhibitors of MEK and methods of use thereof
WO2005051304A2 (en) * 2003-11-21 2005-06-09 Array Biopharma Inc. Akt protein kinase inhibitors
KR20080019236A (ko) * 2005-05-18 2008-03-03 어레이 바이오파마 인크. Mek의 헤테로시클릭 억제제 및 그의 사용 방법
NZ567140A (en) * 2005-10-07 2011-09-30 Exelixis Inc Azetidines as MEK inhibitors for the treatment of proliferative diseases
EP1971601B1 (en) 2005-11-15 2009-10-21 Array Biopharma Inc. N4-phenyl-quinazoline-4 -amine derivatives and related compounds as erbb type i receptor tyrosine kinase inhibitors for the treatment of hyperproliferative diseases
WO2007071951A1 (en) * 2005-12-21 2007-06-28 Astrazeneca Ab Tosylate salt of 6- (4-br0m0-2-chl0r0phenylamin0) -7-fluoro-n- (2-hydroxyethoxy) -3-methyl-3h-benzimi dazole- 5 - carboxamide , mek inhibitor useful in the treatment of cancer
TWI405756B (zh) * 2005-12-21 2013-08-21 Array Biopharma Inc 新穎硫酸氫鹽
GB0601962D0 (en) 2006-01-31 2006-03-15 Ucb Sa Therapeutic agents
ATE493418T1 (de) 2006-07-06 2011-01-15 Array Biopharma Inc Dihydrofuropyrimidine als akt- proteinkinaseinhibitoren
BRPI0713555A2 (pt) 2006-07-06 2012-03-20 Array Biopharma, Inc. ciclopenta [d] pirimidinas como inibidores de akt protéina cinase
SI2054418T1 (sl) 2006-07-06 2012-02-29 Array Biopharma Inc Dihidrotieno pirimidini kot AKT protein kinazni inhibitorji
US8063050B2 (en) * 2006-07-06 2011-11-22 Array Biopharma Inc. Hydroxylated and methoxylated pyrimidyl cyclopentanes as AKT protein kinase inhibitors
WO2008016123A1 (fr) * 2006-08-03 2008-02-07 Takeda Pharmaceutical Company Limited INHIBITEUR DE LA GSK-3β
EP2099796B1 (en) * 2006-11-30 2011-06-01 Genentech, Inc. Aza-indolyl compounds and methods of use
US7999006B2 (en) * 2006-12-14 2011-08-16 Exelixis, Inc. Methods of using MEK inhibitors
US8846683B2 (en) 2007-07-05 2014-09-30 Array Biopharma, Inc. Pyrimidyl cyclopentanes as Akt protein kinase inhibitors
US9409886B2 (en) 2007-07-05 2016-08-09 Array Biopharma Inc. Pyrimidyl cyclopentanes as AKT protein kinase inhibitors
CN101918373B (zh) * 2007-07-05 2013-06-05 阵列生物制药公司 作为akt蛋白激酶抑制剂的嘧啶基环戊烷
KR20150089099A (ko) 2007-07-05 2015-08-04 어레이 바이오파마 인크. Akt 단백질 키나제 억제제로서의 피리미딜 시클로펜탄
GB0714384D0 (en) 2007-07-23 2007-09-05 Ucb Pharma Sa theraputic agents
AU2008288556A1 (en) * 2007-08-16 2009-02-19 F. Hoffmann-La Roche Ag Substituted hydantoins
ES2456966T3 (es) 2007-11-12 2014-04-24 Takeda Pharmaceutical Company Limited Inhibidores de MAPK/ERK cinasa
WO2009074827A2 (en) * 2007-12-12 2009-06-18 Astrazeneca Ab Combination comprising a mek inhibitor and an aurora kinase inhibitor 188
CA2707650A1 (en) 2007-12-20 2009-07-02 F. Hoffmann-La Roche Ag Substituted hydantoins as mek kinase inhibitors
JP5346345B2 (ja) * 2008-01-09 2013-11-20 アレイ バイオファーマ、インコーポレイテッド Aktタンパク質キナーゼ阻害剤としての水酸化されたピリミジルシクロペンタン類
WO2009089453A1 (en) * 2008-01-09 2009-07-16 Array Biopharma Inc. Hydroxylated pyrimidyl cyclopentane as akt protein kinase inhibitor
WO2009093008A1 (en) 2008-01-21 2009-07-30 Ucb Pharma S.A. Thieno-pyridine derivatives as mek inhibitors
GB0811304D0 (en) 2008-06-19 2008-07-30 Ucb Pharma Sa Therapeutic agents
WO2010006225A1 (en) * 2008-07-11 2010-01-14 Novartis Ag Combination of (a) a phosphoinositide 3-kinase inhibitor and (b) a modulator of ras/raf/mek pathway
JP5746630B2 (ja) 2008-11-10 2015-07-08 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH 置換スルホンアミドフェノキシベンズアミド
WO2011054620A1 (en) * 2009-10-12 2011-05-12 F. Hoffmann-La Roche Ag Combinations of a pi3k inhibitor and a mek inhibitor
CA2777304A1 (en) 2009-10-21 2011-04-28 Marion Hitchcock Substituted benzosulphonamides
EP2491014A1 (en) 2009-10-21 2012-08-29 Bayer Pharma Aktiengesellschaft Substituted halophenoxybenzamide derivatives
WO2011047795A1 (en) 2009-10-21 2011-04-28 Bayer Schering Pharma Aktiengesellschaft Substituted benzosulphonamides
CN103221043B (zh) 2010-08-05 2016-04-06 卡斯西部储备大学 用于治疗神经元连接发育障碍的erk抑制剂
HUE033209T2 (hu) 2010-10-06 2017-11-28 Glaxosmithkline Llc PI3 kináz inhibitor hatású benzimidazol-származékok
US9045429B2 (en) 2010-10-29 2015-06-02 Bayer Intellectual Property Gmbh Substituted phenoxypyridines
CN102020651B (zh) 2010-11-02 2012-07-18 北京赛林泰医药技术有限公司 6-芳基氨基吡啶酮甲酰胺mek抑制剂
PL2655375T3 (pl) 2010-12-23 2015-05-29 Sanofi Sa Pochodne pirymidynonu, ich wytwarzanie i ich farmaceutyczne zastosowanie
EP2694073B1 (en) 2011-04-01 2018-08-08 Genentech, Inc. Combinations of akt and mek inhibitors for treating cancer
CN107233343A (zh) 2011-04-01 2017-10-10 基因泰克公司 Akt抑制剂化合物和化疗剂的组合以及使用方法
ES2597052T3 (es) 2011-05-25 2017-01-13 Université Paris Descartes Inhibidores de ERK para su uso en el tratamiento de atrofia muscular espinal
CN103764144B (zh) * 2011-08-31 2016-07-20 诺华股份有限公司 Pi3k抑制剂与mek抑制剂的协同组合
CN103204822B (zh) 2012-01-17 2014-12-03 上海科州药物研发有限公司 作为蛋白激酶抑制剂的苯并噁唑化合物及其制备方法和用途
EP2834237B1 (en) 2012-03-14 2018-06-06 Lupin Limited Heterocyclyl compounds as mek inhibitors
AR091876A1 (es) * 2012-07-26 2015-03-04 Novartis Ag Combinaciones farmaceuticas para el tratamiento de enfermedades proliferativas
SI2909188T1 (en) 2012-10-12 2018-07-31 Exelixis, Inc. A novel process for the manufacture of compounds for use in the treatment of cancer
ES2772498T3 (es) 2012-10-19 2020-07-07 Array Biopharma Inc Preparación de un inhibidor mek y formulación que comprende el mismo
WO2014097125A1 (en) * 2012-12-20 2014-06-26 Novartis Ag Pharmaceutical combination comprising binimetinib
MA38522A1 (fr) 2013-03-21 2017-10-31 Novartis Ag Thérapie de combinaison comprenant un inhibiteur de b-raf et un second inhibiteur.
EP3043822A1 (en) 2013-09-11 2016-07-20 The J. David Gladstone Institutes, A Testamentary Trust Established under The Will of J. David Gladstone Compositions for preparing cardiomyocytes
WO2016009306A1 (en) 2014-07-15 2016-01-21 Lupin Limited Heterocyclyl compounds as mek inhibitors
CN105384754B (zh) * 2014-09-02 2018-04-20 上海科州药物研发有限公司 作为蛋白激酶抑制剂的杂环类化合物及其制备方法和用途
WO2016035008A1 (en) 2014-09-04 2016-03-10 Lupin Limited Pyridopyrimidine derivatives as mek inhibitors
CN105566225A (zh) * 2015-02-16 2016-05-11 苏州晶云药物科技有限公司 一种口服丝裂原活化蛋白激酶抑制剂的晶型及其制备方法
WO2017033113A1 (en) 2015-08-21 2017-03-02 Acerta Pharma B.V. Therapeutic combinations of a mek inhibitor and a btk inhibitor
CN109890386B (zh) * 2016-06-03 2022-05-24 阵列生物制药公司 药物组合
CN109438362B (zh) * 2017-11-14 2020-07-21 深圳市塔吉瑞生物医药有限公司 一种取代的苯并咪唑化合物及包含该化合物的组合物
TW202038957A (zh) 2018-12-21 2020-11-01 日商第一三共股份有限公司 抗體-藥物結合物與激酶抑制劑之組合
US11447482B1 (en) 2019-02-14 2022-09-20 KUDA Therapeutics, Inc. Imidazopyridine and oxazolopyridine derivatives and analogs thereof, methods of preparation thereof, methods of HIF-2A pathway inhibition, and induction of ferroptosis
JP2022526713A (ja) 2019-03-21 2022-05-26 オンクセオ がんの処置のための、キナーゼ阻害剤と組み合わせたDbait分子
CN114761006A (zh) 2019-11-08 2022-07-15 Inserm(法国国家健康医学研究院) 对激酶抑制剂产生耐药性的癌症的治疗方法
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
CN115322105A (zh) * 2021-05-11 2022-11-11 江苏润安制药有限公司 一种合成艾拉莫德关键中间体的方法
WO2022262699A1 (zh) * 2021-06-17 2022-12-22 深圳市塔吉瑞生物医药有限公司 取代的苯并咪唑类化合物及包含该化合物的组合物及其用途
AU2022306297A1 (en) 2021-07-09 2024-02-08 Plexium, Inc. Aryl compounds and pharmaceutical compositions that modulate ikzf2

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0710654A4 (en) * 1993-07-23 1996-08-28 Green Cross Corp TRIAZOLE DERIVATIVE AND ITS PHARMACEUTICAL USE
US5525625A (en) 1995-01-24 1996-06-11 Warner-Lambert Company 2-(2-Amino-3-methoxyphenyl)-4-oxo-4H-[1]benzopyran for treating proliferative disorders
UA73073C2 (uk) 1997-04-03 2005-06-15 Уайт Холдінгз Корпорейшн Заміщені 3-ціанохіноліни, спосіб їх одержання та фармацевтична композиція
US6821963B2 (en) 1997-07-01 2004-11-23 Warner-Lambert Company 4-Bromo or 4-iodo phenylamino benzhydroxamic acid derivatives and their use as MEK inhibitors
US6310060B1 (en) * 1998-06-24 2001-10-30 Warner-Lambert Company 2-(4-bromo or 4-iodo phenylamino) benzoic acid derivatives and their use as MEK inhibitors
NZ501277A (en) 1997-07-01 2002-12-20 Warner Lambert Co -2(4-bromo or 4-iodo phenylamino) benzoic acid derivatives and their use as MEK inhibitors
US6506798B1 (en) 1997-07-01 2003-01-14 Warner-Lambert Company 4-Arylamino, 4-aryloxy, and 4-arylthio diarylamines and derivatives thereof as selective MEK inhibitors
PT993439E (pt) 1997-07-01 2004-12-31 Warner Lambert Co Derivados de acido 4-bromo ou 4-iodofenilaminobenzidroxamico e sua utilizacao como inibidores de mek
WO2000040237A1 (en) 1999-01-07 2000-07-13 Warner-Lambert Company Antiviral method using mek inhibitors
US6696440B1 (en) * 1999-01-07 2004-02-24 Warner-Lambert Company Treatment of asthma with MEK inhibitors
OA11819A (en) * 1999-01-13 2005-08-17 Warner Lambert Co 1-Heterocycle substituted diarylamines.
EP1144385B1 (en) 1999-01-13 2005-08-17 Warner-Lambert Company Llc Benzoheterocycles and their use as mek inhibitors
EP1150950A2 (en) 1999-01-13 2001-11-07 Warner-Lambert Company Anthranilic acid derivatives
EP1144371B1 (en) * 1999-01-13 2005-11-09 Warner-Lambert Company Llc Benzenesulphonamide derivatives and their use as mek inhibitors
CA2349467A1 (en) * 1999-01-13 2000-07-20 Warner-Lambert Company Sulphohydroxamic acids and sulphohydroxamates and their use as mek inhibitors
CA2348236A1 (en) 1999-01-13 2000-07-20 Stephen Douglas Barrett 4-arylamino, 4-aryloxy, and 4-arylthio diarylamines and derivatives thereof as selective mek inhibitors
GB9910577D0 (en) 1999-05-08 1999-07-07 Zeneca Ltd Chemical compounds
US7030119B1 (en) * 1999-07-16 2006-04-18 Warner-Lambert Company Method for treating chronic pain using MEK inhibitors
CA2378381A1 (en) 1999-07-16 2001-01-25 Warner-Lambert Company Method for treating chronic pain using mek inhibitors
CA2377092A1 (en) 1999-07-16 2001-01-25 Warner-Lambert Company Method for treating chronic pain using mek inhibitors
NZ515567A (en) 1999-07-16 2004-03-26 Warner Lambert Co Method for treating chronic pain using MEK inhibitors
HUP0202381A3 (en) 1999-07-16 2004-12-28 Warner Lambert Co Method for treating chronic pain using mek inhibitors
CA2403017A1 (en) 2000-03-15 2001-09-20 Warner-Lambert Company 5-amide substituted diarylamines as mex inhibitors
EP1339702A1 (en) * 2000-03-15 2003-09-03 Warner-Lambert Company 5-amide substituted diarylamines as mek inhibitors
EE05450B1 (et) 2000-07-19 2011-08-15 Warner-Lambert Company 4-jodofenlaminobenshdroksaamhapete oksgeenitud estrid, nende kristallvormid ja farmatseutilised kompositsioonid ning kasutamine
AP2001002249A0 (en) 2000-08-25 2001-09-30 Warner Lambert Co Process for making N-ARYL-ANTHRANILIC acids and their derivatives.
EP1337524A1 (en) 2000-11-02 2003-08-27 AstraZeneca AB Substituted quinolines as antitumor agents
US20040039208A1 (en) * 2001-07-20 2004-02-26 Chen Michael Huai Gu Process for making n-aryl-anthranilic acids and their derivatives
MXPA04008894A (es) * 2002-03-13 2005-06-20 Array Biopharma Inc Derivados de bencimidazol n3 alquilados como inhibidores de mek.
PL401637A1 (pl) * 2002-03-13 2013-05-27 Array Biopharma Inc. N3 alkilowane pochodne benzimidazolu jako inhibitory MEK
CA2532067C (en) * 2003-07-24 2010-12-21 Stephen Douglas Barrett N-methyle-substituted benzamidazoles

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