JP2010529088A5 - - Google Patents

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Publication number
JP2010529088A5
JP2010529088A5 JP2010510815A JP2010510815A JP2010529088A5 JP 2010529088 A5 JP2010529088 A5 JP 2010529088A5 JP 2010510815 A JP2010510815 A JP 2010510815A JP 2010510815 A JP2010510815 A JP 2010510815A JP 2010529088 A5 JP2010529088 A5 JP 2010529088A5
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JP
Japan
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compounds
drug
isotope
labeled compounds
isotopes
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JP2010510815A
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English (en)
Japanese (ja)
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JP5574957B2 (ja
JP2010529088A (ja
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Priority claimed from PCT/EP2008/057058 external-priority patent/WO2008148867A2/en
Publication of JP2010529088A publication Critical patent/JP2010529088A/ja
Publication of JP2010529088A5 publication Critical patent/JP2010529088A5/ja
Application granted granted Critical
Publication of JP5574957B2 publication Critical patent/JP5574957B2/ja
Expired - Fee Related legal-status Critical Current
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JP2010510815A 2007-06-08 2008-06-06 Janusキナーゼのチロシンキナーゼ活性の阻害剤としてのキノキサリン誘導体 Expired - Fee Related JP5574957B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
EP07109880.0 2007-06-08
EP07109880 2007-06-08
EP07150266 2007-12-20
EP07150266.0 2007-12-20
PCT/EP2008/057058 WO2008148867A2 (en) 2007-06-08 2008-06-06 Quinoxaline derivatives as inhibitors of the tyrosine kinase activity of janus kinases

Publications (3)

Publication Number Publication Date
JP2010529088A JP2010529088A (ja) 2010-08-26
JP2010529088A5 true JP2010529088A5 (cg-RX-API-DMAC7.html) 2012-07-05
JP5574957B2 JP5574957B2 (ja) 2014-08-20

Family

ID=39720643

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010510815A Expired - Fee Related JP5574957B2 (ja) 2007-06-08 2008-06-06 Janusキナーゼのチロシンキナーゼ活性の阻害剤としてのキノキサリン誘導体

Country Status (17)

Country Link
US (1) US8193189B2 (cg-RX-API-DMAC7.html)
EP (1) EP2155201B1 (cg-RX-API-DMAC7.html)
JP (1) JP5574957B2 (cg-RX-API-DMAC7.html)
KR (1) KR20100020465A (cg-RX-API-DMAC7.html)
CN (1) CN101678020B (cg-RX-API-DMAC7.html)
AR (1) AR066879A1 (cg-RX-API-DMAC7.html)
AU (1) AU2008258486B2 (cg-RX-API-DMAC7.html)
BR (1) BRPI0812893A2 (cg-RX-API-DMAC7.html)
CA (1) CA2690288A1 (cg-RX-API-DMAC7.html)
CL (1) CL2008001659A1 (cg-RX-API-DMAC7.html)
EA (1) EA200901608A1 (cg-RX-API-DMAC7.html)
ES (1) ES2392570T3 (cg-RX-API-DMAC7.html)
MX (1) MX2009013218A (cg-RX-API-DMAC7.html)
PA (1) PA8783501A1 (cg-RX-API-DMAC7.html)
TW (1) TW200904814A (cg-RX-API-DMAC7.html)
UY (1) UY31126A1 (cg-RX-API-DMAC7.html)
WO (1) WO2008148867A2 (cg-RX-API-DMAC7.html)

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US8349828B2 (en) 2008-02-20 2013-01-08 Actelion Pharmaceuticals Ltd. Azatricyclic antibiotic compounds
JP5351254B2 (ja) 2008-05-23 2013-11-27 ノバルティス アーゲー キノキサリン−およびキノリン−カルボキシアミド誘導体
EP2298731A4 (en) * 2008-06-25 2011-09-21 Takeda Pharmaceutical AMIDE COMPOUND
AR073774A1 (es) 2008-10-07 2010-12-01 Actelion Pharmaceuticals Ltd Compuestos antibioticos oxazolidinona triciclicos
CA2752150A1 (en) 2009-02-11 2010-08-19 Reaction Biology Corp. Selective kinase inhibitors
US20140128392A1 (en) 2009-03-19 2014-05-08 Bioenergenix Heterocyclic compounds for the inhibition of pask
HUE024874T2 (en) * 2009-09-03 2016-02-29 Bioenergenix Heterocyclic compounds for the inhibition of pask
AU2011234644B2 (en) 2010-03-30 2014-07-17 Novartis Ag PKC inhibitors for the treatment of B-cell lymphoma having chronic active B-cell-receptor signalling
GB201007286D0 (en) 2010-04-30 2010-06-16 Astex Therapeutics Ltd New compounds
GB201020179D0 (en) 2010-11-29 2011-01-12 Astex Therapeutics Ltd New compounds
US9073902B2 (en) * 2011-01-05 2015-07-07 Bioenergenix, Llc Substituted quinoxaline carboxylic acid compounds for the inhibition of PASK
US8263298B1 (en) 2011-02-24 2012-09-11 Xerox Corporation Electrically tunable and stable imaging members
EP2727920B1 (en) 2011-07-29 2016-11-02 FUJIFILM Corporation 1,5-naphthyridine derivative or salt thereof
GB201118656D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
GB201118652D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
GB201118675D0 (en) 2011-10-28 2011-12-14 Astex Therapeutics Ltd New compounds
GB201118654D0 (en) 2011-10-28 2011-12-07 Astex Therapeutics Ltd New compounds
JP2014533294A (ja) 2011-11-15 2014-12-11 ノバルティス アーゲー ホスホイノシチド3−キナーゼ阻害剤およびヤヌスキナーゼ2−シグナル伝達兼転写活性化因子5経路の調節剤の組合せ
GB201209609D0 (en) 2012-05-30 2012-07-11 Astex Therapeutics Ltd New compounds
GB201209613D0 (en) 2012-05-30 2012-07-11 Astex Therapeutics Ltd New compounds
WO2014013014A1 (en) 2012-07-18 2014-01-23 Fundació Privada Centre De Regulació Genòmica (Crg) Jak inhibitors for activation of epidermal stem cell populations
GB201307577D0 (en) 2013-04-26 2013-06-12 Astex Therapeutics Ltd New compounds
US9776997B2 (en) 2013-06-04 2017-10-03 Bayer Pharma Aktiengesellschaft 3-aryl-substituted imidazo[1,2-A]pyridines and their use
CN105873914B (zh) * 2013-10-23 2018-10-19 拜耳作物科学股份公司 作为害虫防治剂的取代的喹喔啉衍生物
CA2939793A1 (en) 2014-02-19 2015-08-27 Bayer Pharma Aktiengesellschaft 3-(pyrimidine-2-yl)imidazo[1,2-a]pyridines
HUE053653T2 (hu) 2014-03-26 2021-07-28 Astex Therapeutics Ltd FGFR inhibitor és IGF1R inhibitor kombinációi
JO3512B1 (ar) 2014-03-26 2020-07-05 Astex Therapeutics Ltd مشتقات كينوكسالين مفيدة كمعدلات لإنزيم fgfr كيناز
RU2715236C2 (ru) 2014-03-26 2020-02-26 Астекс Терапьютикс Лтд Комбинации
EP3227287B1 (de) 2014-12-02 2019-08-07 Bayer Pharma Aktiengesellschaft Heteroaryl-substituierte imidazo[1,2-a]pyridine und ihre verwendung
JOP20200201A1 (ar) 2015-02-10 2017-06-16 Astex Therapeutics Ltd تركيبات صيدلانية تشتمل على n-(3.5- ثنائي ميثوكسي فينيل)-n'-(1-ميثيل إيثيل)-n-[3-(ميثيل-1h-بيرازول-4-يل) كينوكسالين-6-يل]إيثان-1.2-ثنائي الأمين
US10478494B2 (en) 2015-04-03 2019-11-19 Astex Therapeutics Ltd FGFR/PD-1 combination therapy for the treatment of cancer
CN108137514A (zh) * 2015-07-30 2018-06-08 百时美施贵宝公司 芳基取代的二环杂芳基化合物
US11542247B2 (en) 2015-09-23 2023-01-03 Janssen Pharmaceutica Nv Bi-heteroaryl substitute 1,4-benzodiazepines and uses thereof for the treatment of cancer
JP6898919B2 (ja) 2015-09-23 2021-07-07 ヤンセン ファーマシューティカ エヌ.ベー. 新規化合物
US10045981B2 (en) 2015-11-24 2018-08-14 Jakpharm, Llc Selective kinase inhibitors
AU2017222417B2 (en) * 2016-02-24 2020-07-09 Pfizer Inc. Pyrazolo[1,5-a]pyrazin-4-yl derivatives as JAK-inhibitors
WO2018041989A1 (en) 2016-09-02 2018-03-08 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods for diagnosing and treating refractory celiac disease type 2
AU2019358074A1 (en) 2018-10-10 2021-05-06 Albert Einstein College Of Medicine Benzoxazole and related compounds useful as chaperone-mediated autophagy modulators
CN113710661B (zh) * 2019-04-02 2022-11-22 上海睿跃生物科技有限公司 治疗癌症的化合物和方法
US20220177978A1 (en) 2019-04-02 2022-06-09 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods of predicting and preventing cancer in patients having premalignant lesions
EP3955920A1 (en) 2019-04-16 2022-02-23 Institut National de la Santé et de la Recherche Médicale (INSERM) Use of jak inhibitors for the treatment of painful conditions involving nav1.7 channels
TWI865563B (zh) 2019-07-30 2024-12-11 德商拜耳動物保健有限公司 新穎異喹啉衍生物
CN110698418B (zh) * 2019-09-11 2022-07-01 广西师范大学 一种3-芳胺基喹喔啉-2-甲酰胺类衍生物及其制备方法和应用
AU2020356575A1 (en) 2019-09-27 2022-04-14 Disc Medicine, Inc. Methods for treating myelofibrosis and related conditions
CN110981819B (zh) * 2019-12-24 2022-07-01 广西师范大学 一种喹喔啉类信号通路抑制剂及其制备方法和应用
EP4149548A4 (en) 2020-05-13 2024-05-08 Disc Medicine, Inc. ANTI-HEMOJUVELIN ANTIBODIES (HJV) FOR THE TREATMENT OF MYELOFIBROSIS
WO2023222565A1 (en) 2022-05-16 2023-11-23 Institut National de la Santé et de la Recherche Médicale Methods for assessing the exhaustion of hematopoietic stems cells induced by chronic inflammation
CN115385863A (zh) * 2022-08-17 2022-11-25 河南师范大学 一种3-(二乙氧基甲基)-1-烷基-2(1h)-喹喔啉酮衍生物的合成方法

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DE4321030A1 (de) * 1993-06-24 1995-01-05 Bayer Ag 4-bicyclisch substituierte Dihydropyridine, Verfahren zu ihrer Herstellung und ihre Verwendung in Arzneimittel
SE9800836D0 (sv) * 1998-03-13 1998-03-13 Astra Ab New Compounds
JP4361276B2 (ja) * 2001-04-10 2009-11-11 メルク エンド カムパニー インコーポレーテッド Akt活性の阻害物質
CA2548172A1 (en) * 2003-12-04 2005-06-23 Vertex Pharmaceuticals Incorporated Quinoxalines useful as inhibitors of protein kinases
NZ608667A (en) * 2005-10-07 2014-08-29 Exelixis Inc N-(3-amino-quinoxalin-2-yl)-sulfonamide derivatives and their use as phosphatidylinositol 3-kinase inhibitors

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