JP2013539765A5 - - Google Patents

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Publication number
JP2013539765A5
JP2013539765A5 JP2013532985A JP2013532985A JP2013539765A5 JP 2013539765 A5 JP2013539765 A5 JP 2013539765A5 JP 2013532985 A JP2013532985 A JP 2013532985A JP 2013532985 A JP2013532985 A JP 2013532985A JP 2013539765 A5 JP2013539765 A5 JP 2013539765A5
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JP
Japan
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alkyl
cycloalkyl
heterocyclyl
heteroaryl
mmol
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JP2013532985A
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English (en)
Japanese (ja)
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JP2013539765A (ja
JP6023062B2 (ja
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Priority claimed from PCT/US2011/055428 external-priority patent/WO2012048259A2/en
Publication of JP2013539765A publication Critical patent/JP2013539765A/ja
Publication of JP2013539765A5 publication Critical patent/JP2013539765A5/ja
Application granted granted Critical
Publication of JP6023062B2 publication Critical patent/JP6023062B2/ja
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JP2013532985A 2010-10-08 2011-10-07 置換ピリダジンカルボキサミド化合物 Active JP6023062B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US39142310P 2010-10-08 2010-10-08
US61/391,423 2010-10-08
PCT/US2011/055428 WO2012048259A2 (en) 2010-10-08 2011-10-07 Substituted pyridazine carboxamide compounds

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2016124463A Division JP6235078B2 (ja) 2010-10-08 2016-06-23 置換ピリダジンカルボキサミド化合物

Publications (3)

Publication Number Publication Date
JP2013539765A JP2013539765A (ja) 2013-10-28
JP2013539765A5 true JP2013539765A5 (cg-RX-API-DMAC7.html) 2016-09-01
JP6023062B2 JP6023062B2 (ja) 2016-11-09

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ID=45928473

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2013532985A Active JP6023062B2 (ja) 2010-10-08 2011-10-07 置換ピリダジンカルボキサミド化合物
JP2016124463A Active JP6235078B2 (ja) 2010-10-08 2016-06-23 置換ピリダジンカルボキサミド化合物

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2016124463A Active JP6235078B2 (ja) 2010-10-08 2016-06-23 置換ピリダジンカルボキサミド化合物

Country Status (12)

Country Link
US (3) US9126947B2 (cg-RX-API-DMAC7.html)
EP (1) EP2625176B1 (cg-RX-API-DMAC7.html)
JP (2) JP6023062B2 (cg-RX-API-DMAC7.html)
KR (1) KR101886812B1 (cg-RX-API-DMAC7.html)
CN (1) CN103298806B (cg-RX-API-DMAC7.html)
AU (1) AU2011311814B2 (cg-RX-API-DMAC7.html)
BR (1) BR112013008523B1 (cg-RX-API-DMAC7.html)
CA (1) CA2813607C (cg-RX-API-DMAC7.html)
EA (1) EA024809B1 (cg-RX-API-DMAC7.html)
ES (1) ES2610226T3 (cg-RX-API-DMAC7.html)
PL (1) PL2625176T3 (cg-RX-API-DMAC7.html)
WO (1) WO2012048259A2 (cg-RX-API-DMAC7.html)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013522347A (ja) * 2010-03-23 2013-06-13 ビーエーエスエフ ソシエタス・ヨーロピア 無脊椎有害生物を防除するためのピリダジン化合物
AU2011311814B2 (en) * 2010-10-08 2016-12-22 Xcovery Holdings, Inc. Substituted pyridazine carboxamide compounds
JP6013029B2 (ja) * 2012-05-25 2016-10-25 千葉県 抗癌剤
RU2550346C2 (ru) * 2013-09-26 2015-05-10 Общество с ограниченной ответственностью "Отечественные Фармацевтические Технологии" ООО"ФармТех" Новые химические соединения (варианты) и их применение для лечения онкологических заболеваний
CN105085550B (zh) * 2014-05-21 2017-05-24 海门慧聚药业有限公司 一类alk激酶抑制剂及其制备方法
RU2015110071A (ru) * 2015-03-23 2016-10-10 Общество с ограниченной ответственностью "Отечественные Фармацевтические Технологии" ООО "ФармТех" Применение новых химических соединений (варианты) в качестве ингибиторов nuak1 киназы для лечения онкологических заболеваний
TWI646094B (zh) * 2016-06-01 2019-01-01 大陸商貝達藥業股份有限公司 Crystal form of inhibitory protein kinase active compound and application thereof
RU2631430C1 (ru) * 2016-10-26 2017-09-22 Общество С Ограниченной Ответственностью "Отечественные Фармацевтические Технологии" НОВЫЙ СПОСОБ СИНТЕЗА ПРОИЗВОДНЫХ ТЕТРАГИДРОПИРАЗИНО[2,3-c]ПИРИДАЗИНА
JP7367908B2 (ja) * 2018-04-09 2023-10-24 上海科技大学 標的タンパク質分解化合物、その抗腫瘍応用、その中間体および中間体の応用
WO2022031636A1 (en) 2020-08-03 2022-02-10 Teva Pharmaceuticals International Gmbh Solid state forms of ensartinib and ensartinib salts
US20240342169A1 (en) * 2021-08-10 2024-10-17 Betta Pharmaceuticals Co., Ltd Use of ensartinib or salt thereof in treatment of disease carrying met 14 exon skipping mutation
CN116082110B (zh) * 2023-01-09 2024-04-12 北京肿瘤医院(北京大学肿瘤医院) 一种11c标记靶向间变性淋巴瘤激酶alk突变分子探针及应用

Family Cites Families (14)

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Publication number Priority date Publication date Assignee Title
US4369172A (en) 1981-12-18 1983-01-18 Forest Laboratories Inc. Prolonged release therapeutic compositions based on hydroxypropylmethylcellulose
EP0188040B1 (en) 1985-01-11 1991-08-14 Abbott Laboratories Limited Slow release solid preparation
JP2773959B2 (ja) 1990-07-10 1998-07-09 信越化学工業株式会社 大腸内放出性固形製剤
UA73092C2 (uk) 1998-07-17 2005-06-15 Брістол-Майерс Сквібб Компані Таблетка з ентеросолюбільним покриттям і спосіб її приготування
ATE292961T1 (de) 1998-07-28 2005-04-15 Tanabe Seiyaku Co Zur wirkstoffabgabe an zielorten im darm fähige zubereitung
US6461631B1 (en) 1999-11-16 2002-10-08 Atrix Laboratories, Inc. Biodegradable polymer composition
US6800663B2 (en) 2002-10-18 2004-10-05 Alkermes Controlled Therapeutics Inc. Ii, Crosslinked hydrogel copolymers
CN103265477B (zh) 2003-02-26 2017-01-11 苏根公司 作为蛋白激酶抑制剂的氨基杂芳基化合物
JP2008510792A (ja) * 2004-08-26 2008-04-10 ファイザー・インク タンパク質チロシンキナーゼ阻害剤としてのアミノヘテロアリール化合物
ES2355923T3 (es) 2004-08-26 2011-04-01 Pfizer, Inc. Compuestos de aminoheteroarilo sustituidos con pirazol como inhibidores de proteina quinasa.
ES2531002T3 (es) 2007-01-19 2015-03-09 Xcovery Inc Compuestos inhibidores de quinasa
MX2010014171A (es) * 2008-06-19 2011-07-04 Xcovery Holding Co Llc Compuestos de piridazin-carboxamida sustituida como compuestos inhibidores de cinasa.
EP2625173A4 (en) * 2010-10-08 2014-03-26 Xcovery Holding Co Llc SUBSTITUTED PYRIDAZINE CARBOXAMIDE COMPOUNDS AS KINASE INHIBITORY COMPOUNDS
AU2011311814B2 (en) * 2010-10-08 2016-12-22 Xcovery Holdings, Inc. Substituted pyridazine carboxamide compounds

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