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
Prior art keywords
alkyl
cycloalkyl
heterocyclyl
heteroaryl
mmol
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JP2013532985A
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English (en)
Japanese (ja)
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JP6023062B2 (ja
JP2013539765A (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 (enExample) 2016-09-01
JP6023062B2 JP6023062B2 (ja) 2016-11-09

Family

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 (enExample)
EP (1) EP2625176B1 (enExample)
JP (2) JP6023062B2 (enExample)
KR (1) KR101886812B1 (enExample)
CN (1) CN103298806B (enExample)
AU (1) AU2011311814B2 (enExample)
BR (1) BR112013008523B1 (enExample)
CA (1) CA2813607C (enExample)
EA (1) EA024809B1 (enExample)
ES (1) ES2610226T3 (enExample)
PL (1) PL2625176T3 (enExample)
WO (1) WO2012048259A2 (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102812018A (zh) * 2010-03-23 2012-12-05 巴斯夫欧洲公司 用于防治无脊椎动物害虫的哒嗪化合物
PL2625176T3 (pl) * 2010-10-08 2017-08-31 Xcovery Holding Company Llc Podstawione związki 6-amino-pirydazyn-3-ylo-karboksyamidu jako modulatory kinazy białkowej
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
EP3778590A4 (en) 2018-04-09 2021-12-22 ShanghaiTech University ANTI PROTEIN DEGRADATION COMPOUND, ANTITUMOR APPLICATION, INTERMEDIATE THEREOF, AND INTERMEDIATE USE
CN112321566B (zh) 2019-08-05 2022-06-10 上海科技大学 Egfr蛋白降解剂及其抗肿瘤应用
WO2022031636A1 (en) 2020-08-03 2022-02-10 Teva Pharmaceuticals International Gmbh Solid state forms of ensartinib and ensartinib salts
WO2023016321A1 (zh) * 2021-08-10 2023-02-16 贝达药业股份有限公司 恩沙替尼或其盐在治疗携带met 14外显子跳跃突变的疾病中的用途
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)

* Cited by examiner, † Cited by third party
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
DE3583799D1 (de) 1985-01-11 1991-09-19 Abbott Lab Ltd Feste zubereitung mit langsamer freisetzung.
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
EP1101490B1 (en) 1998-07-28 2005-04-13 Tanabe Seiyaku Co., Ltd. Preparation capable of releasing drug at target site in intestine
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
GEP20084341B (en) 2003-02-26 2008-03-25 Sugen Inc Aminoheteroaryl compounds as protein kinase inhibitors
WO2006021886A1 (en) * 2004-08-26 2006-03-02 Pfizer Inc. Aminoheteroaryl compounds as protein tyrosine kinase inhibitors
NZ552946A (en) 2004-08-26 2010-09-30 Pfizer Pyrazole-substituted aminoheteroaryl compounds as protein kinase inhibitors
CA2675755C (en) * 2007-01-19 2015-10-06 Xcovery, Inc. Pyridine and pyridazine derivatives as kinase inhibitors
BRPI0914305B8 (pt) * 2008-06-19 2021-05-25 Xcovery Holding Co Llc compostos de piridazina carboxamida substituída como compostos inibidores da quinase, uso dos compostos e uso de uma composição compreendendo os compostos
PL2625176T3 (pl) * 2010-10-08 2017-08-31 Xcovery Holding Company Llc Podstawione związki 6-amino-pirydazyn-3-ylo-karboksyamidu jako modulatory kinazy białkowej
CN103298803A (zh) * 2010-10-08 2013-09-11 艾科睿控股公司 作为激酶抑制剂化合物的取代的哒嗪羧酰胺化合物

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