SI2307409T1 - Pirolopiridini kot kinazni inhibitorji - Google Patents

Pirolopiridini kot kinazni inhibitorji

Info

Publication number
SI2307409T1
SI2307409T1 SI200931284T SI200931284T SI2307409T1 SI 2307409 T1 SI2307409 T1 SI 2307409T1 SI 200931284 T SI200931284 T SI 200931284T SI 200931284 T SI200931284 T SI 200931284T SI 2307409 T1 SI2307409 T1 SI 2307409T1
Authority
SI
Slovenia
Prior art keywords
pyrrolopyridines
kinase inhibitors
kinase
inhibitors
Prior art date
Application number
SI200931284T
Other languages
English (en)
Slovenian (sl)
Inventor
Huerou Yvan Le
James F. Blake
Indrani W. Gunwardana
Peter J. Mohr
Eli M. Wallace
Bin Wang
Mark Chicarelli
Michael Lyon
Original Assignee
Array Biopharma, Inc.
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40810786&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SI2307409(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Array Biopharma, Inc. filed Critical Array Biopharma, Inc.
Publication of SI2307409T1 publication Critical patent/SI2307409T1/sl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (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)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Pain & Pain Management (AREA)
  • Cardiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Oncology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Psychiatry (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
SI200931284T 2008-05-13 2009-05-13 Pirolopiridini kot kinazni inhibitorji SI2307409T1 (sl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US5292608P 2008-05-13 2008-05-13
PCT/US2009/043691 WO2009140320A1 (en) 2008-05-13 2009-05-13 Pyrrolopyridines as kinase inhibitors
EP09747404.3A EP2307409B1 (en) 2008-05-13 2009-05-13 Pyrrolopyridines as kinase inhibitors

Publications (1)

Publication Number Publication Date
SI2307409T1 true SI2307409T1 (sl) 2015-11-30

Family

ID=40810786

Family Applications (1)

Application Number Title Priority Date Filing Date
SI200931284T SI2307409T1 (sl) 2008-05-13 2009-05-13 Pirolopiridini kot kinazni inhibitorji

Country Status (30)

Country Link
US (6) US8178131B2 (cg-RX-API-DMAC7.html)
EP (2) EP2307409B1 (cg-RX-API-DMAC7.html)
JP (2) JP5703212B2 (cg-RX-API-DMAC7.html)
KR (2) KR101643426B1 (cg-RX-API-DMAC7.html)
CN (3) CN102089307B (cg-RX-API-DMAC7.html)
AR (1) AR071717A1 (cg-RX-API-DMAC7.html)
AU (1) AU2009246402B2 (cg-RX-API-DMAC7.html)
BR (1) BRPI0913580B8 (cg-RX-API-DMAC7.html)
CA (1) CA2724262C (cg-RX-API-DMAC7.html)
CL (1) CL2009001152A1 (cg-RX-API-DMAC7.html)
CO (1) CO6321244A2 (cg-RX-API-DMAC7.html)
CR (1) CR11803A (cg-RX-API-DMAC7.html)
CY (1) CY1116692T1 (cg-RX-API-DMAC7.html)
DK (1) DK2307409T3 (cg-RX-API-DMAC7.html)
ES (1) ES2552643T3 (cg-RX-API-DMAC7.html)
HK (1) HK1219950A1 (cg-RX-API-DMAC7.html)
HR (1) HRP20151018T1 (cg-RX-API-DMAC7.html)
HU (1) HUE026160T2 (cg-RX-API-DMAC7.html)
IL (1) IL209258A (cg-RX-API-DMAC7.html)
MX (1) MX2010012449A (cg-RX-API-DMAC7.html)
NZ (1) NZ589318A (cg-RX-API-DMAC7.html)
PH (1) PH12013501779B1 (cg-RX-API-DMAC7.html)
PL (1) PL2307409T3 (cg-RX-API-DMAC7.html)
PT (1) PT2307409E (cg-RX-API-DMAC7.html)
RS (1) RS54358B1 (cg-RX-API-DMAC7.html)
RU (1) RU2517194C2 (cg-RX-API-DMAC7.html)
SI (1) SI2307409T1 (cg-RX-API-DMAC7.html)
TW (2) TWI458727B (cg-RX-API-DMAC7.html)
UA (1) UA111933C2 (cg-RX-API-DMAC7.html)
WO (1) WO2009140320A1 (cg-RX-API-DMAC7.html)

Families Citing this family (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101959887B (zh) 2008-01-08 2013-07-31 阵列生物制药公司 作为激酶抑制剂的吡咯并吡啶
US8372842B2 (en) 2008-01-09 2013-02-12 Array Biopharma Inc. Pyrazolopyridines as kinase inhibitors
JP2009256298A (ja) * 2008-03-26 2009-11-05 Sumitomo Chemical Co Ltd ピペリジン−3−イルカーバメート化合物の光学分割方法およびその中間体
CL2009001152A1 (es) 2008-05-13 2009-10-16 Array Biopharma Inc Compuestos derivados de n-(4-(cicloalquilo nitrogenado-1-il)-1h-pirrolo[2,3-b]piridin-3-il)amida, inhibidores de cinasa; proceso de preparacion; composicion farmaceutica; y su uso para el tratamiento de una enfermedad proliferativa.
BRPI1013920A2 (pt) * 2009-04-11 2016-04-05 Array Biopharma Inc inibidores de ponto de checagem de quinase 1 para potencializar agentes de danificação de dna
US8481557B2 (en) * 2009-04-11 2013-07-09 Array Biopharma Inc. Method of treatment using checkpoint kinase 1 inhibitors
TWI466885B (zh) 2009-07-31 2015-01-01 Japan Tobacco Inc 含氮螺環化合物及其醫藥用途
EP2485589A4 (en) * 2009-09-04 2013-02-06 Biogen Idec Inc HETEROARYL-BTK INHIBITORS
CN103119045B (zh) 2010-08-20 2016-02-17 和记黄埔医药(上海)有限公司 吡咯并嘧啶化合物及其用途
TW201304778A (zh) 2010-11-16 2013-02-01 Array Biopharma Inc 檢查點激酶1抑制劑及wee1激酶抑制劑之組合
UA111075C2 (uk) 2011-02-25 2016-03-25 Еррей Біофарма Інк. Триазолопіридинові сполуки як інгібітори кінази рім
WO2012148775A1 (en) 2011-04-29 2012-11-01 Amgen Inc. Bicyclic pyridazine compounds as pim inhibitors
GB201201566D0 (en) 2012-01-30 2012-03-14 Vernalis R&D Ltd New chemical compounds
KR102096679B1 (ko) 2012-04-23 2020-04-02 제넨테크, 인크. 화합물의 제조를 위한 중간체 및 방법
CA2938626A1 (en) 2013-07-26 2015-01-29 John Rothman Compositions to improve the therapeutic benefit of bisantrene
WO2015027090A1 (en) * 2013-08-22 2015-02-26 Genentech, Inc. Intermediates and processes for preparing compounds
JP6463758B2 (ja) * 2013-08-22 2019-02-06 ジェネンテック, インコーポレイテッド 化合物の調製方法
CN105722838B (zh) * 2013-09-25 2017-10-24 沃泰克斯药物股份有限公司 磷脂酰肌醇3‑激酶‑γ的选择性抑制剂
KR102359214B1 (ko) 2014-04-04 2022-02-07 델 마 파마슈티컬스 폐의 비소세포 암종 및 난소암을 치료하기 위한 디안하이드로갈락티톨 및 이의 유사체 또는 유도체
US9580416B2 (en) 2014-07-02 2017-02-28 Pharmacyclics Llc Inhibitors of Bruton's tyrosine kinase
MA41599A (fr) * 2015-02-26 2018-01-02 Array Biopharma Inc Formes cristallines d'un composé pyrrolopyridine
WO2017003090A1 (ko) 2015-06-30 2017-01-05 서울바이오시스 주식회사 Uv led가 적용된 포충기
KR20250133463A (ko) 2015-11-04 2025-09-05 메르크 파텐트 게엠베하 Btk 억제 활성을 갖는 피리미딘 및 피리딘 화합물을 사용하여 암 치료하는 방법
JP2018538330A (ja) * 2015-12-22 2018-12-27 ヴァイティー ファーマシューティカルズ,インコーポレイテッド menin−MLL相互作用の阻害剤
PL3468966T3 (pl) 2016-06-10 2021-04-06 Vitae Pharmaceuticals, Llc Inhibitory interakcji menina-mll
EP3461480A1 (en) 2017-09-27 2019-04-03 Onxeo Combination of a dna damage response cell cycle checkpoint inhibitors and belinostat for treating cancer
CN112839648B (zh) 2018-06-07 2025-04-04 达萨玛治疗公司 Sarm1抑制剂
TWI873098B (zh) * 2018-07-03 2025-02-21 瑞士商諾華製藥公司 用於治療與sting活性相關之病症的化合物及組合物
CN109053526A (zh) * 2018-08-13 2018-12-21 南通大学 一种(3r,4s)-4-甲基吡咯烷-3-基氨基甲酸叔丁酯盐酸盐的化学合成方法
CN108912032A (zh) * 2018-08-13 2018-11-30 南通大学 一种(3s,4r)-4-甲基吡咯烷-3-基氨基甲醇叔丁酯盐酸盐的化学合成方法
US12083114B2 (en) 2018-12-19 2024-09-10 Disarm Therapeutics, Inc. Inhibitors of SARM1 in combination with neuro-protective agents
TW202043198A (zh) 2019-01-17 2020-12-01 美商Ifm Due有限公司 用於治療與sting活性相關之病況的化合物及組合物
EP4182310A1 (en) 2020-07-15 2023-05-24 IFM Due, Inc. Compounds and compositions for treating conditions associated with sting activity
JP2024502474A (ja) 2021-01-08 2024-01-19 アイエフエム デュー インコーポレイテッド Sting活性に関連する状態を治療するための、尿素を有するヘテロ二環式化合物または類似体およびその組成物
IL308476A (en) 2021-05-14 2024-01-01 Syndax Pharmaceuticals Inc Inhibitors of the menin-mil interaction
CN119798252A (zh) * 2023-10-09 2025-04-11 中国石油化工股份有限公司 一种制备n邻位-酰基取代的含氮杂环化合物及其缩胺合铁(ii)配合物的方法

Family Cites Families (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU689809B2 (en) 1993-10-14 1998-04-09 Abbott Laboratories Quinolizinone type compounds
US5543523A (en) 1994-11-15 1996-08-06 Regents Of The University Of Minnesota Method and intermediates for the synthesis of korupensamines
WO2001058869A2 (en) 2000-02-11 2001-08-16 Bristol-Myers Squibb Company Cannabinoid receptor modulators, their processes of preparation, and use of cannabinoid receptor modulators in treating respiratory and non-respiratory diseases
WO2001079198A1 (en) 2000-04-18 2001-10-25 Agouron Pharmaceuticals, Inc. Pyrazoles for inhibiting protein kinase
US7115741B2 (en) 2001-09-06 2006-10-03 Levy Daniel E 4-thieno[2,3-D]pyrimidin-4-YL piperazine compounds
WO2003028724A1 (en) 2001-10-04 2003-04-10 Smithkline Beecham Corporation Chk1 kinase inhibitors
US6797825B2 (en) * 2001-12-13 2004-09-28 Abbott Laboratories Protein kinase inhibitors
TWI329112B (en) 2002-07-19 2010-08-21 Bristol Myers Squibb Co Novel inhibitors of kinases
CA2494785A1 (en) 2002-08-07 2004-02-19 Mitsubishi Pharma Corporation Dihydropyrazolopyridine compounds
US20050256157A1 (en) * 2002-08-23 2005-11-17 Chiron Corporation Combination therapy with CHK1 inhibitors
US8580782B2 (en) 2002-09-04 2013-11-12 Merck Sharp & Dohme Corp. Substituted pyrazolo[1,5-a]pyrimidines as cyclin dependent kinase inhibitors
AR042667A1 (es) 2002-12-26 2005-06-29 Taisho Pharmaceutical Co Ltd Derivados de pirrolopirimidina y pirrolopiridina sustituidos con un grupo amino ciclico
US20070149560A1 (en) 2003-03-14 2007-06-28 Astrazeneca Ab Novel fused triazolones and the uses thereof
GB0308208D0 (en) * 2003-04-09 2003-05-14 Glaxo Group Ltd Chemical compounds
GB0330043D0 (en) * 2003-12-24 2004-01-28 Pharmacia Italia Spa Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions comprising them
GB0330042D0 (en) * 2003-12-24 2004-01-28 Pharmacia Italia Spa Pyrrolo [2,3-b] pyridine derivatives active as kinase inhibitors process for their preparation and pharmaceutical compositions them
MXPA06011328A (es) * 2004-04-02 2006-12-15 Vertex Pharma Azaindoles utiles como inhibidotes de roca y otras proteinas cinasas.
AU2005244745B2 (en) * 2004-04-13 2012-05-03 Synta Pharmaceuticals Corp. Disalt inhibitors of IL-12 production
GB0409080D0 (en) 2004-04-23 2004-05-26 Biofocus Discovery Ltd Compounds which interact with protein kinases
JP2007161585A (ja) 2004-06-25 2007-06-28 Taisho Pharmaceut Co Ltd 環状アミノ基で置換されているピロロピリミジン及びピロロピリジン誘導体
UY29177A1 (es) 2004-10-25 2006-05-31 Astex Therapeutics Ltd Derivados sustituidos de purina, purinona y deazapurina, composiciones que los contienen métodos para su preparación y sus usos
GB0501999D0 (en) 2005-02-01 2005-03-09 Sentinel Oncology Ltd Pharmaceutical compounds
MX2007012448A (es) 2005-04-06 2007-10-19 Astrazeneca Ab Heterociclos sustituidos y su uso como inhibidores de chk1, pdk1 y pak.
CA2609126A1 (en) * 2005-05-20 2006-11-30 Vertex Pharmaceuticals Incorporated Pyrrolopyridines useful as inhibitors of protein kinase
JP5220414B2 (ja) * 2005-08-30 2013-06-26 旭化成ファーマ株式会社 スルホンアミド化合物
CN101321760A (zh) 2005-10-06 2008-12-10 先灵公司 作为蛋白激酶抑制剂的吡唑并嘧啶
EP1942900B1 (en) * 2005-10-06 2015-06-03 Merck Sharp & Dohme Corp. Use of pyrazolo [1,5-a] pyrimidine derivatives for inhibiting kinases methods for inhibiting protein kinases
SI2455382T1 (sl) 2005-12-13 2017-03-31 Incyte Holdings Corporation S heteroarilom substituirani pirolo(2,3b)piridini in pirolo(2,3-b)pirimidini kot zaviralci janus kinaze
TW200738709A (en) 2006-01-19 2007-10-16 Osi Pharm Inc Fused heterobicyclic kinase inhibitors
DE102006005179A1 (de) 2006-02-06 2007-08-09 Merck Patent Gmbh Aminoindazolderivate
DE102006005180A1 (de) 2006-02-06 2007-08-09 Merck Patent Gmbh Indazol-heteroaryl-derivate
US20090082370A1 (en) 2006-04-25 2009-03-26 Neil Thomas Thompson Pharmaceutical Combinations of PK Inhibitors and Other Active Agents
WO2007125315A2 (en) 2006-04-25 2007-11-08 Astex Therapeutics Limited Pharmaceutical compounds
EP3719018B1 (en) 2006-04-25 2025-08-27 Astex Therapeutics Ltd Purine and deazapurine derivatives as pharmaceutical compounds
WO2008012635A2 (en) * 2006-07-26 2008-01-31 Pfizer Products Inc. Amine derivatives useful as anticancer agents
WO2008075007A1 (en) 2006-12-21 2008-06-26 Cancer Research Technology Limited Morpholino-substituted bicycloheteroaryl compounds and their use as anti cancer agents
WO2008106692A1 (en) 2007-03-01 2008-09-04 Novartis Vaccines And Diagnostics, Inc. Pim kinase inhibitors and methods of their use
WO2009004329A1 (en) 2007-07-02 2009-01-08 Cancer Research Technology Limited 9h-pyrimido[4,5-b]indoles, 9h-pyrido[4',3':4,5]pyrrolo[2,3-d]pyridines, and 9h-1,3,6,9-tetraaza-fluorenes as chk1 kinase function inhibitors
EP2217611B1 (en) 2007-11-07 2013-07-31 Merck Sharp & Dohme Corp. Novel modulators of cell cycle checkpoints and their use in combination with checkpoint kinase inhibitors
CN101959887B (zh) * 2008-01-08 2013-07-31 阵列生物制药公司 作为激酶抑制剂的吡咯并吡啶
US8372842B2 (en) * 2008-01-09 2013-02-12 Array Biopharma Inc. Pyrazolopyridines as kinase inhibitors
CL2009001152A1 (es) * 2008-05-13 2009-10-16 Array Biopharma Inc Compuestos derivados de n-(4-(cicloalquilo nitrogenado-1-il)-1h-pirrolo[2,3-b]piridin-3-il)amida, inhibidores de cinasa; proceso de preparacion; composicion farmaceutica; y su uso para el tratamiento de una enfermedad proliferativa.
US8481557B2 (en) * 2009-04-11 2013-07-09 Array Biopharma Inc. Method of treatment using checkpoint kinase 1 inhibitors
US20140221370A1 (en) 2010-07-09 2014-08-07 Array Biopharma Inc. Pyrrolopyridines as kinase inhibitors
TW201304778A (zh) 2010-11-16 2013-02-01 Array Biopharma Inc 檢查點激酶1抑制劑及wee1激酶抑制劑之組合

Also Published As

Publication number Publication date
JP2015098482A (ja) 2015-05-28
AU2009246402A1 (en) 2009-11-19
MX2010012449A (es) 2011-05-25
NZ589318A (en) 2011-06-30
US20140100369A1 (en) 2014-04-10
BRPI0913580B8 (pt) 2021-05-25
TWI554512B (zh) 2016-10-21
CA2724262A1 (en) 2009-11-19
PL2307409T3 (pl) 2016-01-29
US20110070317A1 (en) 2011-03-24
BRPI0913580A2 (pt) 2015-10-20
UA111933C2 (uk) 2016-07-11
CY1116692T1 (el) 2017-03-15
EP2307409B1 (en) 2015-08-12
EP2990407A1 (en) 2016-03-02
HK1219950A1 (en) 2017-04-21
HRP20151018T1 (hr) 2015-10-23
US20140243520A1 (en) 2014-08-28
RS54358B1 (sr) 2016-04-28
WO2009140320A1 (en) 2009-11-19
IL209258A0 (en) 2011-01-31
PH12013501779B1 (en) 2019-02-13
ES2552643T3 (es) 2015-12-01
KR20110008102A (ko) 2011-01-25
HUE026160T2 (en) 2016-05-30
TW201529573A (zh) 2015-08-01
CN109942575A (zh) 2019-06-28
CN104926810A (zh) 2015-09-23
CN104926810B (zh) 2019-02-19
US20150322061A1 (en) 2015-11-12
CR11803A (es) 2011-02-11
DK2307409T3 (en) 2015-09-21
EP2307409A1 (en) 2011-04-13
US9969727B2 (en) 2018-05-15
PH12013501779A1 (en) 2014-08-27
US8178131B2 (en) 2012-05-15
TWI458727B (zh) 2014-11-01
EP2990407B1 (en) 2019-10-16
CN102089307A (zh) 2011-06-08
US8758830B2 (en) 2014-06-24
AR071717A1 (es) 2010-07-07
CN102089307B (zh) 2015-07-01
US8545897B2 (en) 2013-10-01
US8981085B2 (en) 2015-03-17
CO6321244A2 (es) 2011-09-20
RU2517194C2 (ru) 2014-05-27
US9365568B2 (en) 2016-06-14
JP5703212B2 (ja) 2015-04-15
PT2307409E (pt) 2015-11-04
HK1152035A1 (en) 2012-02-17
CL2009001152A1 (es) 2009-10-16
KR20140093266A (ko) 2014-07-25
IL209258A (en) 2017-01-31
US20130045286A1 (en) 2013-02-21
TW201002707A (en) 2010-01-16
RU2010150786A (ru) 2012-06-20
KR101657856B1 (ko) 2016-09-19
AU2009246402B2 (en) 2013-05-23
JP2011520896A (ja) 2011-07-21
CA2724262C (en) 2017-08-15
US20160368916A1 (en) 2016-12-22
KR101643426B1 (ko) 2016-07-27
BRPI0913580B1 (pt) 2020-03-10

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