JP2012514044A5 - - Google Patents

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Publication number
JP2012514044A5
JP2012514044A5 JP2011544601A JP2011544601A JP2012514044A5 JP 2012514044 A5 JP2012514044 A5 JP 2012514044A5 JP 2011544601 A JP2011544601 A JP 2011544601A JP 2011544601 A JP2011544601 A JP 2011544601A JP 2012514044 A5 JP2012514044 A5 JP 2012514044A5
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JP
Japan
Prior art keywords
ring
nitrogen
sulfur
oxygen
independently selected
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JP2011544601A
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English (en)
Japanese (ja)
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JP2012514044A (ja
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Priority claimed from PCT/US2009/069795 external-priority patent/WO2010078408A1/en
Publication of JP2012514044A publication Critical patent/JP2012514044A/ja
Publication of JP2012514044A5 publication Critical patent/JP2012514044A5/ja
Withdrawn legal-status Critical Current

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JP2011544601A 2008-12-30 2009-12-30 Rafキナーゼ阻害剤として有用なヘテロアリール化合物 Withdrawn JP2012514044A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US14156108P 2008-12-30 2008-12-30
US61/141,561 2008-12-30
PCT/US2009/069795 WO2010078408A1 (en) 2008-12-30 2009-12-30 Heteroaryl compounds useful as raf kinase inhibitors

Publications (2)

Publication Number Publication Date
JP2012514044A JP2012514044A (ja) 2012-06-21
JP2012514044A5 true JP2012514044A5 (OSRAM) 2013-02-21

Family

ID=41719139

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011544601A Withdrawn JP2012514044A (ja) 2008-12-30 2009-12-30 Rafキナーゼ阻害剤として有用なヘテロアリール化合物

Country Status (9)

Country Link
US (1) US20120040951A1 (OSRAM)
EP (1) EP2379513A1 (OSRAM)
JP (1) JP2012514044A (OSRAM)
CN (1) CN102361859A (OSRAM)
AU (1) AU2009334997A1 (OSRAM)
CA (1) CA2748274A1 (OSRAM)
IL (1) IL213601A0 (OSRAM)
MX (1) MX2011006997A (OSRAM)
WO (1) WO2010078408A1 (OSRAM)

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CN101743242A (zh) 2007-06-29 2010-06-16 苏尼西斯制药有限公司 用作raf激酶抑制剂的杂环化合物
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US9085570B2 (en) * 2010-10-11 2015-07-21 The Board Of Trustees Of The Leland Stanford Junior University Substituted benzamides and their uses
CN102250065B (zh) * 2011-05-20 2015-05-13 浙江海正药业股份有限公司 取代的三嗪苯脲衍生物及其用途
EP2714667B1 (en) * 2011-05-27 2020-11-25 Laxman S. DESAI Aminooxazole inhibitors of cyclin dependent kinases
US9453003B2 (en) 2011-08-11 2016-09-27 Jikai Biosciences, Inc. Pyrimidine derivatives as PIM kinase inhibitors and preparation methods and use in medicinal manufacture thereof
CN102924446B (zh) * 2011-08-11 2015-08-26 上海吉铠医药科技有限公司 Pim激酶抑制剂及其制备方法与在制药中的应用
US9458151B2 (en) 2011-08-11 2016-10-04 Jikai Biosciences, Inc. Isothiazole derivatives as PIM kinase inhibitors and preparation methods and use in medicinal manufacture thereof
US9452995B2 (en) 2011-08-11 2016-09-27 Jikai Biosciences, Inc. Pyridine derivatives as PIM kinase inhibitors and preparation methods and use in medicinal manufacture thereof
US9408885B2 (en) 2011-12-01 2016-08-09 Vib Vzw Combinations of therapeutic agents for treating melanoma
AU2013245809A1 (en) 2012-04-12 2014-11-06 Auckland Uniservices Limited Substituted benzamides and their uses
JP6359537B2 (ja) * 2012-08-07 2018-07-18 ヤンセン ファーマシューティカ エヌ.ベー. 複素環エステル誘導体の調製プロセス
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GB201401886D0 (en) 2014-02-04 2014-03-19 Lytix Biopharma As Neurodegenerative therapies
CN105384738B (zh) * 2014-08-21 2017-08-29 上海科州药物研发有限公司 作为蛋白激酶抑制剂的杂环类化合物及其制备方法和用途
UY36294A (es) * 2014-09-12 2016-04-29 Novartis Ag Compuestos y composiciones como inhibidores de quinasa
BR112017011416A2 (pt) 2014-12-02 2018-02-27 Bayer Cropscience Ag compostos bicíclicos como agentes de controle de pragas
WO2017001660A1 (en) 2015-07-02 2017-01-05 Janssen Sciences Ireland Uc Antibacterial compounds
JP6810988B2 (ja) 2015-10-23 2021-01-13 ヴィフォール (インターナショナル) アクチェンゲゼルシャフトVifor (International) AG 新規なフェロポーチン阻害剤
EA039916B1 (ru) * 2015-10-23 2022-03-28 Вифор (Интернациональ) Аг Новые ингибиторы ферропортина
JP2019518046A (ja) 2016-06-16 2019-06-27 ヤンセン・サイエンシズ・アイルランド・アンリミテッド・カンパニー 抗菌薬としての複素環式化合物
US11471538B2 (en) 2017-02-10 2022-10-18 INSERM (Institut National de la Santéet de la Recherche Medicale) Methods and pharmaceutical compositions for the treatment of cancers associated with activation of the MAPK pathway
WO2018158280A1 (en) 2017-03-01 2018-09-07 Janssen Sciences Ireland Uc Combination therapy
WO2019005241A1 (en) * 2017-03-23 2019-01-03 Clavius Pharmaceuticals, Llc TRI-SUBSTITUTED IMIDAZOLES FOR INHIBITION OF TGF-BETA AND METHODS OF TREATMENT
JOP20180036A1 (ar) 2017-04-18 2019-01-30 Vifor Int Ag أملاح لمثبطات فروبورتين جديدة
EP3732285A1 (en) 2017-12-28 2020-11-04 Tract Pharmaceuticals, Inc. Stem cell culture systems for columnar epithelial stem cells, and uses related thereto
US12077548B2 (en) 2018-08-22 2024-09-03 Clavius Pharmaceuticals, LLC. Substituted imidazoles for the inhibition of TGF-β and methods of treatment
WO2020227020A1 (en) 2019-05-03 2020-11-12 Kinnate Biopharma Inc. Inhibitors of raf kinases
US11098031B1 (en) * 2019-10-24 2021-08-24 Kinnate Biopharma Inc. Inhibitors of RAF kinases
US11407737B2 (en) 2020-09-18 2022-08-09 Kinnate Biopharma Inc. Inhibitors of RAF kinases
US11377431B2 (en) 2020-10-12 2022-07-05 Kinnate Biopharma Inc. Inhibitors of RAF kinases
CN112535793B (zh) * 2020-11-19 2021-10-08 融冲(深圳)生物医疗科技有限责任公司 药物涂层球囊导管的制备方法与应用
CN117561057A (zh) 2021-04-23 2024-02-13 金耐特生物制药公司 用raf抑制剂治疗癌症
CN117143095A (zh) * 2023-08-03 2023-12-01 苏州汉德创宏生化科技有限公司 一种6-溴吡唑并[1,5-a]吡啶-3-羧酸及其制备方法
CN117567388B (zh) * 2023-11-14 2024-04-16 济南悟通生物科技有限公司 一种2-乙酰基-5-噻唑甲酸的合成方法
CN119241530A (zh) * 2024-09-20 2025-01-03 武汉九州钰民医药科技有限公司 一种Tovorafenib的药物合成工艺
CN119241529A (zh) * 2024-09-20 2025-01-03 武汉九州钰民医药科技有限公司 一种Tovorafenib的制备方法

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WO2004028526A1 (ja) * 2002-09-25 2004-04-08 Santen Pharmaceutical Co., Ltd. ベンズアミド誘導体を有効成分とするリウマチ治療剤
EP1828186A1 (en) * 2004-12-13 2007-09-05 Sunesis Pharmaceuticals, Inc. Pyrido pyrimidinones, dihydro pyrimido pyrimidinones and pteridinones useful as raf kinase inhibitors
CL2008001933A1 (es) * 2007-06-29 2009-09-25 Millennium Pharm Inc Compuestos derivados de pirimidina, inhibidores de la raf quinasa; compuestos intermediarios; procedimiento de preparacion; composicion farmaceutica; y su uso para tratar trastornos proliferativos, cardiacos, neurodegenerativos, inflamatorios, oseos, inmunologicos enfermedad viral, entre otros.
CN101743242A (zh) * 2007-06-29 2010-06-16 苏尼西斯制药有限公司 用作raf激酶抑制剂的杂环化合物

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