JP2011515462A - 置換されたピリミジン、及びトリアジン、並びに癌療法におけるこれらの使用 - Google Patents

置換されたピリミジン、及びトリアジン、並びに癌療法におけるこれらの使用 Download PDF

Info

Publication number
JP2011515462A
JP2011515462A JP2011501736A JP2011501736A JP2011515462A JP 2011515462 A JP2011515462 A JP 2011515462A JP 2011501736 A JP2011501736 A JP 2011501736A JP 2011501736 A JP2011501736 A JP 2011501736A JP 2011515462 A JP2011515462 A JP 2011515462A
Authority
JP
Japan
Prior art keywords
difluoromethyl
morpholinyl
triazin
methoxy
chloroacetyl
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.)
Abandoned
Application number
JP2011501736A
Other languages
English (en)
Japanese (ja)
Other versions
JP2011515462A5 (enExample
Inventor
ウイルリアム レウカストレ ゴルドン
ロビン シェプヘルド ペテル
チャウスサデ クライレ
アレクアンデル デンンイ ウイルリアム
アクラトイヤ ガマゲ スワルナラトハ
Original Assignee
アウククランド ウニセルビセス リミテッド
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by アウククランド ウニセルビセス リミテッド filed Critical アウククランド ウニセルビセス リミテッド
Publication of JP2011515462A publication Critical patent/JP2011515462A/ja
Publication of JP2011515462A5 publication Critical patent/JP2011515462A5/ja
Abandoned legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/16Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
    • C07D251/18Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicinal Preparation (AREA)
JP2011501736A 2008-03-27 2009-03-26 置換されたピリミジン、及びトリアジン、並びに癌療法におけるこれらの使用 Abandoned JP2011515462A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US4006408P 2008-03-27 2008-03-27
US61/040,064 2008-03-27
PCT/NZ2009/000038 WO2009120094A2 (en) 2008-03-27 2009-03-26 Substituted pyrimidines and triazines and their use in cancer therapy

Publications (2)

Publication Number Publication Date
JP2011515462A true JP2011515462A (ja) 2011-05-19
JP2011515462A5 JP2011515462A5 (enExample) 2012-05-17

Family

ID=40810252

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011501736A Abandoned JP2011515462A (ja) 2008-03-27 2009-03-26 置換されたピリミジン、及びトリアジン、並びに癌療法におけるこれらの使用

Country Status (4)

Country Link
US (1) US20110053907A1 (enExample)
EP (1) EP2276750A2 (enExample)
JP (1) JP2011515462A (enExample)
WO (1) WO2009120094A2 (enExample)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012521983A (ja) * 2009-03-27 2012-09-20 パトフワイ トヘラペウトイクス インコーポレイテッド ピリミジニル及び1,3,5−トリアジニルベンゾイミダゾールスルホンアミド及びガンの療法におけるその使用
JP2013525419A (ja) * 2010-04-30 2013-06-20 ユニバーシティ・オブ・バーゼル 抗増殖性障害の処置における使用のためのpi3k阻害剤としてのピペラジノトリアジン
JP2016516702A (ja) * 2013-03-13 2016-06-09 ザ リージェンツ オブ ザ ユニバーシティー オブ ミシガン Mek/pi3k二重阻害剤および該阻害剤を使用する治療方法

Families Citing this family (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008128088A1 (en) 2007-04-13 2008-10-23 The Regents Of The University Of Michigan Systems and methods for tissue imaging
EP2282672A4 (en) * 2008-02-29 2013-03-20 Univ Michigan SYSTEMS AND METHOD FOR ILLUSTRATING TISSUE CHANGES
US20120165309A1 (en) * 2009-02-12 2012-06-28 Astellas Pharma Inc. Hetero ring derivative
MX2011009796A (es) 2009-03-20 2011-12-14 Amgen Inc Inhibidores de la cinasa pi3.
WO2010110686A1 (en) * 2009-03-27 2010-09-30 Pathway Therapeutics Limited Pyrimidinyl and 1,3,5 triazinyl benzimidazoles and their use in cancer therapy
UY32582A (es) 2009-04-28 2010-11-30 Amgen Inc Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero
TW201105662A (en) 2009-07-07 2011-02-16 Pathway Therapeutics Ltd Pyrimidinyl and 1,3,5-triazinyl benzimidazoles and their use in cancer therapy
CA2775942A1 (en) * 2009-09-29 2011-04-07 Xcovery Holding Company Llc Pi3k (delta) selective inhibitors
WO2011049625A1 (en) 2009-10-20 2011-04-28 Mansour Samadpour Method for aflatoxin screening of products
JP5889795B2 (ja) 2009-11-05 2016-03-22 ライゼン・ファーマシューティカルズ・エスアー 新規キナーゼモジュレーター
EP2604601B1 (en) * 2010-08-10 2016-02-24 Astellas Pharma Inc. Hetero ring compound
WO2012044641A1 (en) 2010-09-29 2012-04-05 Pathway Therapeutics Inc. 1,3,5-triazinyl benzimidazole sulfonamides and their use in cancer therapy
CZ305457B6 (cs) 2011-02-28 2015-09-30 Ústav organické chemie a biochemie, Akademie věd ČR v. v. i. Pyrimidinové sloučeniny inhibující tvorbu oxidu dusnatého a prostaglandinu E2, způsob výroby a použití
AU2012236834B2 (en) 2011-03-28 2015-12-10 Mei Pharma, Inc (alpha- substituted aralkylamino and heteroarylalkylamino) pyrimidinyl and 1,3,5 -triazinyl benzimidazoles, pharmaceutical compositions containing them, and these compounds for use in treating proliferative diseases
PH12013502240B1 (en) 2011-05-04 2018-06-27 Rhizen Pharmaceuticals Sa Novel compounds as modulators of protein kinase
US9773311B2 (en) 2011-06-29 2017-09-26 The Regents Of The University Of Michigan Tissue phasic classification mapping system and method
JP6026544B2 (ja) 2011-09-27 2016-11-16 ノバルティス アーゲー 変異体idhの阻害剤としての3−ピリミジン−4−イル−オキサゾリジン−2−オン類
CA2851082A1 (en) * 2011-10-06 2013-04-11 Merck Sharp & Dohme Corp. 1,3-substituted azetidine pde10 inhibitors
WO2013078370A1 (en) 2011-11-23 2013-05-30 The Regents Of The University Of Michigan Voxel-based approach for disease detection and evolution
PL2790705T3 (pl) 2011-12-15 2018-06-29 Novartis Ag Zastosowanie inhibitorów czynności lub funkcji PI3K
UY34632A (es) 2012-02-24 2013-05-31 Novartis Ag Compuestos de oxazolidin- 2- ona y usos de los mismos
US9851426B2 (en) 2012-05-04 2017-12-26 The Regents Of The University Of Michigan Error analysis and correction of MRI ADC measurements for gradient nonlinearity
KR102216606B1 (ko) 2012-07-04 2021-02-17 리젠 파마슈티컬스 소시에떼 아노님 선택적 pi3k 델타 억제제
WO2014055647A1 (en) * 2012-10-03 2014-04-10 Mei Pharma, Inc. (sulfinyl and sulfonyl benzimidazolyl) pyrimidines and triazines, pharmaceutical compositions thereof, and their use for treating proliferative diseases
US9296733B2 (en) 2012-11-12 2016-03-29 Novartis Ag Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases
GEP201706699B (en) 2013-03-14 2017-07-10 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
CA3026149A1 (en) 2016-06-02 2017-12-07 Cadent Therapeutics, Inc. Potassium channel modulators
US10650512B2 (en) 2016-06-14 2020-05-12 The Regents Of The University Of Michigan Systems and methods for topographical characterization of medical image data
JP2019519593A (ja) 2016-07-06 2019-07-11 ザ・リージェンツ・オブ・ザ・ユニバーシティ・オブ・ミシガンThe Regents Of The University Of Michigan MEK/PI3K及びmTOR/MEK/PI3K生物学的経路の多官能性阻害剤、並びに同多官能性阻害剤を用いた治療方法
BR112019014814B1 (pt) 2017-01-23 2024-03-12 Novartis Ag Compostos, composições farmacêuticas dos mesmos e seus usos no tratamento de doenças associadas à disfunção de canais iônicos de potássio
CN117860758A (zh) 2017-05-23 2024-04-12 梅制药公司 联合疗法
US11311624B2 (en) 2017-08-11 2022-04-26 The Regents Of The University Of Michigan Inhibitors of MEK/PI3K, JAK/MEK, JAK/PI3K/mTOR and MEK/PI3K/mTOR biological pathways and methods for improving lymphatic uptake, bioavailability, and solubility of therapeutic compounds
MX2020001727A (es) 2017-08-14 2020-03-20 Mei Pharma Inc Terapia de combinacion.
WO2019119206A1 (en) * 2017-12-18 2019-06-27 Merck Sharp & Dohme Corp. Purine inhibitors of human phosphatidylinositol 3-kinase delta
CA3116339A1 (en) 2018-10-22 2020-04-30 Cadent Therapeutics, Inc. Crystalline forms of potassium channel modulators
CN113004246B (zh) * 2021-02-22 2022-02-01 广西医科大学 1,3,5-三嗪-2-胺-4,6取代衍生物或其药学上可接受的盐和用途
EP4320110A1 (en) * 2021-04-09 2024-02-14 Universität Basel Triazine derivative as covalent inhibitors of pi3k
CN117751127A (zh) * 2021-08-20 2024-03-22 南京大美生物制药有限公司 一种五元含氮杂环并杂芳基类衍生物及其用途

Family Cites Families (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1222049B (it) * 1987-07-16 1990-08-31 Ciba Geygi Spa Composti piperidin triazinici utilizzabili come stabilizzanti per polimeri sintetici
US5244948A (en) * 1988-06-30 1993-09-14 Ciba-Geigy Corporation Process for the stabilization of polyolefins
US5306495A (en) * 1988-08-04 1994-04-26 Ciba-Geigy Corporation Compounds containing substituted piperidine groups for use as stabilizers for organic materials
IT1237126B (it) * 1989-11-07 1993-05-18 Ciba Geigy Spa Stabilizzanti polimerici contenenti gruppi amminici impediti e gruppi idrossilamminici
US5258138A (en) * 1990-07-20 1993-11-02 Ciba-Geigy Corporation Process for stabilizing ethylenically unsaturated compounds and stabilized monomer compositions
TW224983B (enExample) * 1991-08-28 1994-06-11 Hoechst Ag
AU665238B2 (en) * 1992-02-28 1995-12-21 Zenyaku Kogyo Kabushiki Kaisha S-triazine derivative and remedy for estrogen-dependent diseases containing the same as active ingredient
HU209678B (en) * 1992-06-09 1994-10-28 Richter Gedeon Vegyeszet Process for producing biologically active eburnamenin-14-carbonyl-amino derivatives and pharmaceutical compositions containing them
IT1263993B (it) * 1993-04-05 1996-09-06 Ciba Geigy Spa Composti piperidin-triazinici atti all'impiego come stabilizzanti per materiali organici
IT1270975B (it) * 1993-06-03 1997-05-26 Ciba Geigy Spa Composti piperidin-triazinici atti all'impiego come stabilizzanti allaluce, al calore e alla ossidazione per materiali organici
ATE180283T1 (de) * 1994-01-19 1999-06-15 Ciba Geigy Ag Stabilisieren von leder gegen thermische und photochemische zersetzung
EP0707035B1 (de) * 1994-10-12 1999-01-13 Ciba SC Holding AG HALS-Phosphorinane als Stabilisatoren
EP0711804A3 (de) * 1994-11-14 1999-09-22 Ciba SC Holding AG Kryptolichtschutzmittel
DE19522137A1 (de) * 1995-06-19 1997-01-02 Hoechst Schering Agrevo Gmbh 2-Amino-1,3,5-triazine, Verfahren zu deren Herstellung und deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren
JP3512911B2 (ja) * 1995-07-11 2004-03-31 富士写真フイルム株式会社 紫外線吸収剤前駆体化合物、それを含有する感光性樹脂組成物及び画像形成方法
US6046304A (en) * 1995-12-04 2000-04-04 Ciba Specialty Chemicals Corporation Block oligomers containing 2,2,6,6-tetramethyl-4-piperidyl groups as stabilizers for organic materials
US6432947B1 (en) * 1997-02-19 2002-08-13 Berlex Laboratories, Inc. N-heterocyclic derivatives as NOS inhibitors
DE69821633T2 (de) * 1997-07-24 2004-12-16 Zenyaku Kogyo K.K. Heterozyklische verbindungen und antitumormittel, das diese als aktiven wirkstoff enthält
JPH11174638A (ja) * 1997-12-08 1999-07-02 Konica Corp ハロゲン化銀カラー写真感光材料
US6150362A (en) * 1997-12-12 2000-11-21 Henkin; Jack Triazine angiogenesis inhibitors
US5990208A (en) * 1997-12-15 1999-11-23 Ciba Specialty Chemicals Corporation Stabilization of polycarbonate/ABS blends with mixtures of hindered amines and UV absorbers
CA2359678A1 (en) * 1999-01-13 2000-07-20 Miles Hacker Use of s-triazines for treating apicomplexan parasitic infections
ATE361917T1 (de) * 1999-04-22 2007-06-15 Lundbeck & Co As H Selektive npy(y5)-antagonisten
KR100551853B1 (ko) * 2000-07-19 2006-02-13 에프. 호프만-라 로슈 아게 피리미딘 유도체
US6465645B1 (en) * 2001-04-17 2002-10-15 Ciba Specialty Chemicals Corporation Long chain hindered amines and compositions stabilized therewith
PT1389617E (pt) * 2001-04-27 2007-04-30 Zenyaku Kogyo Kk Composto heterocíclico e agente antitumoral contendo o mesmo como igrediente activo
AU2003275630B2 (en) * 2002-10-25 2010-02-18 Zenyaku Kogyo Kabushiki Kaisha Heterocyclic compounds and antitumor agent comprising the same as effective component
WO2005028467A1 (en) * 2003-09-15 2005-03-31 Anadys Pharmaceuticals, Inc. Antibacterial 3,5-diaminopiperidine-substitute aromatic and heteroaromatic compounds
ES2400056T3 (es) * 2004-03-31 2013-04-05 Zenyaku Kogyo Kabushikikaisha Compuesto heterocíclico y agente anti tumores malignos que comprende el mismo como componente eficaz
EP1824490A4 (en) * 2004-12-13 2008-06-04 Neurogen Corp PIPERAZINYL-PYRIDINE ANALOGS
CA2590586A1 (en) * 2004-12-13 2006-07-06 Neurogen Corporation Substituted biaryl analogues
GB0503962D0 (en) * 2005-02-25 2005-04-06 Kudos Pharm Ltd Compounds
TWI381841B (zh) * 2005-03-11 2013-01-11 Zenyaku Kogyo Kk An immunosuppressive agent and an antitumor agent containing a heterocyclic compound as an active ingredient
ES2401192T3 (es) * 2005-09-30 2013-04-17 Vertex Pharmceuticals Incorporated Deazapurinas útiles como inhibidores de janus cinasas
JO2660B1 (en) * 2006-01-20 2012-06-17 نوفارتيس ايه جي Pi-3 inhibitors and methods of use
US20070244110A1 (en) * 2006-04-14 2007-10-18 Zenyaku Kogyo Kabushiki Kaisha Treatment of prostate cancer, melanoma or hepatic cancer
WO2007127175A2 (en) * 2006-04-26 2007-11-08 F. Hoffmann-La Roche Ag Pharmaceutical compounds
WO2008032072A1 (en) * 2006-09-14 2008-03-20 Astrazeneca Ab 2-benzimidaz0lyl-6-m0rph0lin0-4-piperidin-4-ylpyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
US20090325954A1 (en) * 2006-09-14 2009-12-31 Sam Butterworth 2-benzimidazolyl-6-morpholino-4-phenylpyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
JP2010503649A (ja) * 2006-09-14 2010-02-04 アストラゼネカ アクチボラグ ピリミジン誘導体
WO2008032028A1 (en) * 2006-09-14 2008-03-20 Astrazeneca Ab 2 -benzimidazolyl- 6 -morpholino-4- (azetidine, pyrrolidine, piperidine or azepine) pyrimidine derivatives as pi3k and mtor inhibitors for the treatment of proliferative disorders
WO2008072850A1 (en) * 2006-12-11 2008-06-19 Amorepacific Corporation Triazine derivatives having inhibitory activity against acetyl-coa carboxylase
EA201001017A1 (ru) * 2008-01-15 2011-02-28 ВАЙЕТ ЭлЭлСи 3h-[1,2,3]триазоло[4,5-d]пиримидиновые соединения, их применение в качестве ингибиторов киназы mtor и киназы pi3 и их синтезы
US20090192176A1 (en) * 2008-01-30 2009-07-30 Wyeth 1H-PYRAZOLO[3,4-D]PYRIMIDINE, PURINE, 7H-PURIN-8(9H)-ONE, 3H-[1,2,3]TRIAZOLO[4,5-D]PYRIMIDINE, AND THIENO[3,2-D]PYRIMIDINE COMPOUNDS, THEIR USE AS mTOR KINASE AND PI3 KINASE INHIBITORS, AND THEIR SYNTHESES

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012521983A (ja) * 2009-03-27 2012-09-20 パトフワイ トヘラペウトイクス インコーポレイテッド ピリミジニル及び1,3,5−トリアジニルベンゾイミダゾールスルホンアミド及びガンの療法におけるその使用
US9108980B2 (en) 2009-03-27 2015-08-18 Vetdc, Inc. Pyrimidinyl and 1,3,5-triazinyl benzimidazole sulfonamides and their use in cancer therapy
JP2013525419A (ja) * 2010-04-30 2013-06-20 ユニバーシティ・オブ・バーゼル 抗増殖性障害の処置における使用のためのpi3k阻害剤としてのピペラジノトリアジン
JP2016516702A (ja) * 2013-03-13 2016-06-09 ザ リージェンツ オブ ザ ユニバーシティー オブ ミシガン Mek/pi3k二重阻害剤および該阻害剤を使用する治療方法

Also Published As

Publication number Publication date
WO2009120094A3 (en) 2010-01-28
EP2276750A2 (en) 2011-01-26
US20110053907A1 (en) 2011-03-03
WO2009120094A2 (en) 2009-10-01

Similar Documents

Publication Publication Date Title
JP2011515462A (ja) 置換されたピリミジン、及びトリアジン、並びに癌療法におけるこれらの使用
JP5766177B2 (ja) ピリミジニル及び1,3,5−トリアジニルベンゾイミダゾールスルホンアミド及びガンの療法におけるその使用
US11787788B2 (en) Benzimidazole derivatives, and pharmaceutical compositions and methods of use thereof
DK3072890T3 (en) Pyrimidinyl and 1,3,5-triazinylbenzimidazoles and their use in cancer therapy
JP6042406B2 (ja) (α−置換アラルキルアミノ及びヘテロアリールアルキルアミノ)ピリミジニル及び1,3,5−トリアジニルベンズイミダゾール、それらを含む医薬組成物、並びに増殖性疾患の治療で使用するためのこれらの化合物
US10590108B2 (en) Benzimidazoles for use in the treatment of cancer and inflammatory diseases
KR102409739B1 (ko) 암 치료용의 erbb 티로신 키나제 억제제로서의 벤즈이미다졸 유도체
TW201629019A (zh) 3,5-二胺基吡唑激酶抑制劑
HK1228387B (en) Pyrimidinyl and 1,3,5-triazinyl benzimidazoles and their use in cancer therapy
HK1228387A1 (en) Pyrimidinyl and 1,3,5-triazinyl benzimidazoles and their use in cancer therapy

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20120323

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20120323

A762 Written abandonment of application

Free format text: JAPANESE INTERMEDIATE CODE: A762

Effective date: 20120702