JP2007536224A5 - - Google Patents

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Publication number
JP2007536224A5
JP2007536224A5 JP2007511366A JP2007511366A JP2007536224A5 JP 2007536224 A5 JP2007536224 A5 JP 2007536224A5 JP 2007511366 A JP2007511366 A JP 2007511366A JP 2007511366 A JP2007511366 A JP 2007511366A JP 2007536224 A5 JP2007536224 A5 JP 2007536224A5
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JP
Japan
Prior art keywords
optionally substituted
alkyl
aryl
compound
pharmaceutically acceptable
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JP2007511366A
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English (en)
Japanese (ja)
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JP2007536224A (ja
JP4604086B2 (ja
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Priority claimed from PCT/US2005/010187 external-priority patent/WO2005112932A2/en
Publication of JP2007536224A publication Critical patent/JP2007536224A/ja
Publication of JP2007536224A5 publication Critical patent/JP2007536224A5/ja
Application granted granted Critical
Publication of JP4604086B2 publication Critical patent/JP4604086B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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JP2007511366A 2004-05-07 2005-03-25 Rafモジュレーターおよびその使用方法 Expired - Fee Related JP4604086B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US56900904P 2004-05-07 2004-05-07
PCT/US2005/010187 WO2005112932A2 (en) 2004-05-07 2005-03-25 Raf modulators and methods of use

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2009235794A Division JP2010006840A (ja) 2004-05-07 2009-10-09 Rafモジュレーターおよびその使用方法

Publications (3)

Publication Number Publication Date
JP2007536224A JP2007536224A (ja) 2007-12-13
JP2007536224A5 true JP2007536224A5 (enExample) 2009-08-27
JP4604086B2 JP4604086B2 (ja) 2010-12-22

Family

ID=35428836

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2007511366A Expired - Fee Related JP4604086B2 (ja) 2004-05-07 2005-03-25 Rafモジュレーターおよびその使用方法
JP2009235794A Withdrawn JP2010006840A (ja) 2004-05-07 2009-10-09 Rafモジュレーターおよびその使用方法

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2009235794A Withdrawn JP2010006840A (ja) 2004-05-07 2009-10-09 Rafモジュレーターおよびその使用方法

Country Status (6)

Country Link
US (2) US7846959B2 (enExample)
EP (1) EP1751124A4 (enExample)
JP (2) JP4604086B2 (enExample)
AU (1) AU2005244736B2 (enExample)
CA (1) CA2565200C (enExample)
WO (1) WO2005112932A2 (enExample)

Families Citing this family (43)

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GB0419481D0 (en) * 2004-09-02 2004-10-06 Cancer Rec Tech Ltd Isoindolin-1-one derivatives
RU2452469C2 (ru) * 2006-07-21 2012-06-10 Новартис Аг Составы бензимидазолилпиридилэфиров
PE20090370A1 (es) 2007-06-05 2009-04-30 Takeda Pharmaceutical Derivados de heterociclo fusionado como inhibidores de quinasa
WO2009017838A2 (en) * 2007-08-01 2009-02-05 Exelixis, Inc. Combinations of jak-2 inhibitors and other agents
WO2009025358A1 (ja) 2007-08-23 2009-02-26 Takeda Pharmaceutical Company Limited 複素環化合物およびその用途
JP5350247B2 (ja) 2007-08-29 2013-11-27 武田薬品工業株式会社 複素環化合物およびその用途
JP5579619B2 (ja) 2008-12-01 2014-08-27 武田薬品工業株式会社 複素環化合物およびその用途
JO3101B1 (ar) 2008-12-02 2017-09-20 Takeda Pharmaceuticals Co مشتقات بنزوثيازول كعوامل مضادة للسرطان
WO2010093808A1 (en) * 2009-02-11 2010-08-19 Reaction Biology Corp. Selective kinase inhibitors
US20100222381A1 (en) 2009-02-27 2010-09-02 Hariprasad Vankayalapati Cyclopentathiophene/cyclohexathiophene DNA methyltransferase inhibitors
AR082453A1 (es) 2010-04-21 2012-12-12 Novartis Ag Compuestos de furopiridina, composiciones farmaceuticas que los contienen y usos de los mismos
PT2624696T (pt) 2010-10-06 2017-03-21 Glaxosmithkline Llc Derivados de benzimidazole como inibidores da cinase pi3
US9408885B2 (en) 2011-12-01 2016-08-09 Vib Vzw Combinations of therapeutic agents for treating melanoma
JP5965499B2 (ja) * 2012-12-25 2016-08-03 日本曹達株式会社 ハロゲン化アニリンおよびその製造方法
EP2842614A1 (en) * 2013-08-30 2015-03-04 Biotage AB Sample preparation method for analysis of acrylamide
BR112016011024B1 (pt) 2013-11-18 2020-09-01 Forma Therapeutics, Inc Composto, composição farmacêutica, e, usos dos mesmos
WO2015074081A1 (en) 2013-11-18 2015-05-21 Bair Kenneth W Benzopiperazine compositions as bet bromodomain inhibitors
EP3134443B1 (en) * 2014-04-23 2019-10-30 Sun Chemical Corporation Led photoinitiators
US10562886B2 (en) 2015-05-21 2020-02-18 The Regents Of The University Of California Anti-cancer compounds
WO2017091681A1 (en) 2015-11-24 2017-06-01 Aclaris Therapeutics, Inc. Selective kinase inhibitors
EP3889139B1 (en) 2015-11-30 2025-03-19 The Children's Medical Center Corporation Compounds for treating proliferative diseases
US11072600B2 (en) 2016-06-24 2021-07-27 The Regents Of The University Of California Phthalazine derivatives as inhibitors of PARP1, PARP2, and/or tubulin useful for the treatment of cancer
EP3579872A1 (en) 2017-02-10 2019-12-18 INSERM (Institut National de la Santé et de la Recherche Médicale) Methods and pharmaceutical compositions for the treatment of cancers associated with activation of the mapk pathway
CA3086765A1 (en) 2017-12-28 2019-07-04 Tract Pharmaceuticals, Inc. Stem cell culture systems for columnar epithelial stem cells, and uses related thereto
HUE066783T2 (hu) 2018-04-18 2024-09-28 Constellation Pharmaceuticals Inc Metil módosító enzimek modulátorai, ezek készítményei és alkalmazásuk
WO2019226491A1 (en) 2018-05-21 2019-11-28 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
RS65335B1 (sr) 2018-10-05 2024-04-30 Annapurna Bio Inc Jedinjenja i kompozicije za lečenje stanja povezanih sa aktivnošću receptora apj
EP3876939A4 (en) 2018-11-07 2022-08-10 Dana-Farber Cancer Institute, Inc. Benzothiazole derivatives and 7-aza-benzothiazole derivatives as janus kinase 2 inhibitors and uses thereof
PH12022552056A1 (en) 2020-02-07 2024-02-12 Gasherbrum Bio Inc Heterocyclic glp-1 agonists
BR112022022409A2 (pt) 2020-05-06 2023-02-07 Ajax Therapeutics Inc 6-heteroarilóxi benzimidazóis e azabenzimidazóis como inibidores de jak2
WO2021257863A1 (en) 2020-06-19 2021-12-23 Incyte Corporation Pyrrolotriazine compounds as jak2 v617f inhibitors
US11691971B2 (en) 2020-06-19 2023-07-04 Incyte Corporation Naphthyridinone compounds as JAK2 V617F inhibitors
IL299612A (en) 2020-07-02 2023-03-01 Incyte Corp Tricyclic urea compounds as JAK2 V617F inhibitors
US11767323B2 (en) 2020-07-02 2023-09-26 Incyte Corporation Tricyclic pyridone compounds as JAK2 V617F inhibitors
US11661422B2 (en) 2020-08-27 2023-05-30 Incyte Corporation Tricyclic urea compounds as JAK2 V617F inhibitors
WO2022140231A1 (en) 2020-12-21 2022-06-30 Incyte Corporation Deazaguaine compounds as jak2 v617f inhibitors
EP4267574B1 (en) 2020-12-23 2025-04-23 Ajax Therapeutics, Inc. 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors
US11958861B2 (en) 2021-02-25 2024-04-16 Incyte Corporation Spirocyclic lactams as JAK2 V617F inhibitors
CN113045479B (zh) * 2021-03-29 2022-05-24 南京工业大学 一种可见光促进3-羟基异吲哚-1-酮类化合物的合成方法
US11970494B2 (en) 2021-11-09 2024-04-30 Ajax Therapeutics, Inc. 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors
WO2023086320A1 (en) 2021-11-09 2023-05-19 Ajax Therapeutics, Inc. Forms and compositions of inhibitors of jak2
EP4493558A1 (en) 2022-03-17 2025-01-22 Incyte Corporation Tricyclic urea compounds as jak2 v617f inhibitors
CN120957993A (zh) 2023-02-16 2025-11-14 加舒布鲁姆生物公司 杂环glp-1激动剂

Family Cites Families (2)

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Publication number Priority date Publication date Assignee Title
EP1534862A4 (en) * 2002-08-07 2007-10-10 Exelixis Inc RABGGT MODULATORS AND METHODS OF USE THEREOF
WO2004103974A1 (ja) * 2003-05-23 2004-12-02 Japan Tobacco Inc. 置換2-オキソキノリン化合物およびその医薬用途

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