KR101432316B1 - 증식성 장애의 치료를 위한 단백질 키나제 plk1 억제제로서의 4,5-디히드로-[1,2,4]트리아졸로[4,3-f]프테리딘 - Google Patents

증식성 장애의 치료를 위한 단백질 키나제 plk1 억제제로서의 4,5-디히드로-[1,2,4]트리아졸로[4,3-f]프테리딘 Download PDF

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KR101432316B1
KR101432316B1 KR1020087027593A KR20087027593A KR101432316B1 KR 101432316 B1 KR101432316 B1 KR 101432316B1 KR 1020087027593 A KR1020087027593 A KR 1020087027593A KR 20087027593 A KR20087027593 A KR 20087027593A KR 101432316 B1 KR101432316 B1 KR 101432316B1
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aliphatic
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KR20080109919A (ko
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쟝-다미엥 샤리에
데이비드 카이
로날드 네그텔
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버텍스 파마슈티칼스 인코포레이티드
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    • 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
    • C07D487/12Heterocyclic 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 three hetero rings
    • C07D487/14Ortho-condensed systems
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    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/12Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
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    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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KR1020087027593A 2006-04-12 2007-04-12 증식성 장애의 치료를 위한 단백질 키나제 plk1 억제제로서의 4,5-디히드로-[1,2,4]트리아졸로[4,3-f]프테리딘 Expired - Fee Related KR101432316B1 (ko)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US79132706P 2006-04-12 2006-04-12
US60/791,327 2006-04-12
US83872006P 2006-08-18 2006-08-18
US60/838,720 2006-08-18
PCT/US2007/009006 WO2007120752A2 (en) 2006-04-12 2007-04-12 4, 5-dihydro- [1, 2, 4] triazolo [4, 3-f] pteridines as protein kinase plk1 inhibitors for the treatment of proliferative disorders

Publications (2)

Publication Number Publication Date
KR20080109919A KR20080109919A (ko) 2008-12-17
KR101432316B1 true KR101432316B1 (ko) 2014-08-29

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KR1020087027593A Expired - Fee Related KR101432316B1 (ko) 2006-04-12 2007-04-12 증식성 장애의 치료를 위한 단백질 키나제 plk1 억제제로서의 4,5-디히드로-[1,2,4]트리아졸로[4,3-f]프테리딘

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US (3) US7763629B2 (https=)
EP (1) EP2010542B1 (https=)
JP (1) JP5313875B2 (https=)
KR (1) KR101432316B1 (https=)
AR (1) AR060432A1 (https=)
AT (1) ATE542823T1 (https=)
AU (1) AU2007238690B2 (https=)
CA (1) CA2649324A1 (https=)
ES (1) ES2381212T3 (https=)
IL (1) IL194699A (https=)
MX (1) MX2008013110A (https=)
NO (1) NO20084747L (https=)
NZ (1) NZ571969A (https=)
RU (1) RU2441006C2 (https=)
TW (1) TW200808805A (https=)
WO (1) WO2007120752A2 (https=)

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CA2695753A1 (en) * 2007-08-15 2009-02-19 Vertex Pharmaceuticals Incorporated Compounds useful as protein kinases inhibitors
BRPI0821209A2 (pt) 2007-12-19 2019-09-24 Amgen Inc composto, composição farmacêutica, métodos de tratar câncer, para reduzir o tamanho de tumor, para tratar distúrbios, e para reduzir metástase em um tumor.
US8389533B2 (en) 2008-04-07 2013-03-05 Amgen Inc. Gem-disubstituted and spirocyclic amino pyridines/pyrimidines as cell cycle inhibitors
WO2010008459A1 (en) * 2008-06-23 2010-01-21 Vertex Pharmaceuticals Incorporated Protein kinase inhibitors
MX2011000026A (es) * 2008-06-23 2011-02-24 Vertex Pharma Inhibidores de proteina cinasas.
CA2773827A1 (en) * 2009-09-25 2011-03-31 Vertex Pharmaceuticals Incorporated Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors
SG179206A1 (en) 2009-09-25 2012-04-27 Vertex Pharma Methods for preparing pyrimidine derivatives useful as protein kinase inhibitors
US8541418B2 (en) 2009-12-23 2013-09-24 Elan Pharmaceutical, Inc. Inhibitors of polo-like kinase
JP5850321B2 (ja) * 2010-02-10 2016-02-03 公立大学法人横浜市立大学 神経選択的転写抑制因子NRSFに特異的に結合するmSin3Bに結合する化合物の利用
US8933070B2 (en) 2010-07-02 2015-01-13 University Health Network Methods of targeting PTEN mutant diseases and compositions therefor
US20120115848A1 (en) 2010-10-08 2012-05-10 Elan Pharmaceuticals, Inc. Inhibitors of Polo-Like Kinase
TW201307347A (zh) 2010-11-01 2013-02-16 Arqule Inc 經取代苯並-咪唑並-吡啶並-二氮呯化合物
CN103703000B (zh) 2011-03-23 2015-11-25 安姆根有限公司 Cdk4/6和flt3的稠合三环双重抑制剂
MD4300C1 (ro) * 2012-12-28 2015-03-31 Государственный Университет Молд0 Inhibitor al proliferării celulelor HepG2 în cancerul hepatic în bază de cloro-[2-fenil(piridin-2-il)metanon-4-(3-metoxifenil)tiosemicarbazono]nichel
US9840503B2 (en) 2015-05-11 2017-12-12 Incyte Corporation Heterocyclic compounds and uses thereof
WO2017027717A1 (en) 2015-08-12 2017-02-16 Incyte Corporation Bicyclic fused pyrimidine compounds as tam inhibitors
US10053465B2 (en) 2015-08-26 2018-08-21 Incyte Corporation Pyrrolopyrimidine derivatives as TAM inhibitors
MD3436461T2 (ro) 2016-03-28 2024-05-31 Incyte Corp Compuși pirolotriazină ca inhibitori TAM
SI3687996T1 (sl) 2017-09-27 2022-04-29 Incyte Corporation Soli pirolotriazinskih derivatov, ki so uporabne kot zaviralci TAM
MD3813800T2 (ro) 2018-06-29 2025-10-31 Incyte Corp Formulări de inhibitor al AXL/MER
CN109734809A (zh) * 2019-02-27 2019-05-10 南方科技大学 治疗性的人Plk1蛋白单克隆抗体及其制备方法
EP4114401A1 (en) 2020-03-06 2023-01-11 Incyte Corporation Combination therapy comprising axl/mer and pd-1/pd-l1 inhibitors
JP7545622B2 (ja) 2021-02-08 2024-09-05 江蘇星盛新輝医薬有限公司 5,6-ジドヒロチエノ[3,4-h]キナゾリン系化合物
EP4157849A4 (en) * 2021-08-10 2024-12-11 Uppthera, Inc. NOVEL PLK1 DEGRADATION-INDUCING COMPOUND

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WO2002076985A1 (en) 2001-03-23 2002-10-03 Smithkline Beecham Corporation Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases
WO2004030635A2 (en) 2002-10-03 2004-04-15 Targegen, Inc. Vasculostatic agents and methods of use thereof
WO2005123736A1 (de) 2004-06-21 2005-12-29 Boehringer Ingelheim International Gmbh Neue 2-benzylaminodihydropteridinone, verfahren zu deren herstellung und deren verwendung als arzneimittel

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EP2010542A2 (en) 2009-01-07
IL194699A (en) 2014-07-31
EP2010542B1 (en) 2012-01-25
US8067417B2 (en) 2011-11-29
NZ571969A (en) 2011-10-28
RU2008144584A (ru) 2010-05-20
TW200808805A (en) 2008-02-16
US8524902B2 (en) 2013-09-03
ES2381212T3 (es) 2012-05-24
AU2007238690A1 (en) 2007-10-25
AR060432A1 (es) 2008-06-18
IL194699A0 (en) 2009-08-03
NO20084747L (no) 2008-11-25
WO2007120752A3 (en) 2008-05-08
US20120277425A1 (en) 2012-11-01
KR20080109919A (ko) 2008-12-17
JP2009536155A (ja) 2009-10-08
RU2441006C2 (ru) 2012-01-27
US20110021519A1 (en) 2011-01-27
CA2649324A1 (en) 2007-10-25
WO2007120752A2 (en) 2007-10-25
AU2007238690B2 (en) 2013-05-02
MX2008013110A (es) 2009-03-06
US7763629B2 (en) 2010-07-27
HK1134486A1 (en) 2010-04-30
US20090062292A1 (en) 2009-03-05
JP5313875B2 (ja) 2013-10-09
ATE542823T1 (de) 2012-02-15

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