JP2013531013A5 - - Google Patents

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Publication number
JP2013531013A5
JP2013531013A5 JP2013518686A JP2013518686A JP2013531013A5 JP 2013531013 A5 JP2013531013 A5 JP 2013531013A5 JP 2013518686 A JP2013518686 A JP 2013518686A JP 2013518686 A JP2013518686 A JP 2013518686A JP 2013531013 A5 JP2013531013 A5 JP 2013531013A5
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Japan
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salt
compound according
disease
compound
pharmaceutical composition
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JP2013518686A
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Japanese (ja)
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JP5739527B2 (ja
JP2013531013A (ja
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Priority claimed from PCT/US2011/042508 external-priority patent/WO2012006203A1/en
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Publication of JP2013531013A5 publication Critical patent/JP2013531013A5/ja
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JP2013518686A 2010-07-07 2011-06-30 RhoキナーゼインヒビターとしてのN−環式−3−(環状カルボニルアミノメチル)ベンズアミド誘導体 Active JP5739527B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US36203210P 2010-07-07 2010-07-07
US61/362,032 2010-07-07
PCT/US2011/042508 WO2012006203A1 (en) 2010-07-07 2011-06-30 N-cyclyl-3 - (cyclylcarbonylaminomethyl) benzamide derivatives as rho kinase inhibitors

Publications (3)

Publication Number Publication Date
JP2013531013A JP2013531013A (ja) 2013-08-01
JP2013531013A5 true JP2013531013A5 (cg-RX-API-DMAC7.html) 2014-08-14
JP5739527B2 JP5739527B2 (ja) 2015-06-24

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JP2013518686A Active JP5739527B2 (ja) 2010-07-07 2011-06-30 RhoキナーゼインヒビターとしてのN−環式−3−(環状カルボニルアミノメチル)ベンズアミド誘導体

Country Status (4)

Country Link
US (1) US8697911B2 (cg-RX-API-DMAC7.html)
EP (1) EP2590950B1 (cg-RX-API-DMAC7.html)
JP (1) JP5739527B2 (cg-RX-API-DMAC7.html)
WO (1) WO2012006203A1 (cg-RX-API-DMAC7.html)

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US8697911B2 (en) 2010-07-07 2014-04-15 Boehringer Ingelheim International Gmbh Rho kinase inhibitors
US9079880B2 (en) 2010-07-07 2015-07-14 Boehringer Ingelheim International Gmbh Rho kinase inhibitors
US9000154B2 (en) 2010-10-19 2015-04-07 Boehringer Ingelheim International Gmbh Rho kinase inhibitors
CN103420917B (zh) * 2012-05-18 2015-08-19 国药一心制药有限公司 含稠环结构的苯甲酰胺类化合物及其作为抗肿瘤药物应用
JP6284490B2 (ja) * 2012-12-28 2018-02-28 株式会社新日本科学 イミダゾピリジン誘導体を有効成分として含むoct3活性阻害剤又はoct3検出剤
TW201444798A (zh) 2013-02-28 2014-12-01 必治妥美雅史谷比公司 作爲強效rock1及rock2抑制劑之苯基吡唑衍生物
JP6423372B2 (ja) 2013-02-28 2018-11-14 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company 強力なrock1およびrock2阻害剤としてのフェニルピラゾール誘導体
EP3027616B1 (en) 2013-07-30 2018-01-10 Boehringer Ingelheim International GmbH Azaindole compounds as modulators of rorc
EP3294871A1 (en) 2015-05-12 2018-03-21 Platod Combination of pharmacological and microfluidic features for improved platelets production
JP2018515623A (ja) 2015-05-18 2018-06-14 トランスレイショナル・ドラッグ・ディベロップメント・エルエルシー キナーゼ阻害剤としての複素環式化合物
US10738007B2 (en) 2016-10-24 2020-08-11 Translation Drug Development, LLC Amide compounds as kinase inhibitors, compositions and methods of treatment
CN110099906B (zh) * 2016-10-24 2022-07-26 转化药物开发有限责任公司 作为激酶抑制剂的酰胺化合物
JP2020502066A (ja) 2016-11-21 2020-01-23 トランスレイショナル・ドラッグ・ディベロップメント・エルエルシー キナーゼ阻害剤としての複素環式化合物
WO2018108156A1 (zh) * 2016-12-16 2018-06-21 成都先导药物开发有限公司 Rock抑制剂及其应用
DK3684767T3 (da) 2017-09-22 2024-07-15 Jubilant Epipad LLC Heterocykliske forbindelser som pad-inhibitorer
US11261184B2 (en) 2017-10-02 2022-03-01 Boehringer Ingelheim International Gmbh [1,6]naphthyridine compounds and derivatives as CDK8/CDK19 inhibitors
AU2018352142B2 (en) 2017-10-18 2022-08-25 Jubilant Epipad LLC Imidazo-pyridine compounds as PAD inhibitors
CN111386265A (zh) 2017-11-06 2020-07-07 朱比连特普罗德尔有限责任公司 作为pd1/pd-l1活化的抑制剂的嘧啶衍生物
SMT202400203T1 (it) 2017-11-24 2024-07-09 Jubilant Episcribe Llc Composti eterociclici come inibitori di prmt5
CA3093527A1 (en) 2018-03-13 2019-09-19 Jubilant Prodel LLC Bicyclic compounds as inhibitors of pd1/pd-l1 interaction/activation
JP7490569B2 (ja) * 2018-04-24 2024-05-27 トランスレイショナル・ドラッグ・ディベロップメント・エルエルシー キナーゼ阻害剤としてのアミド化合物、組成物および処置方法
CN109678815B (zh) * 2019-01-09 2022-11-29 中国药科大学 N-苄基苯甲酰胺类衍生物及其制备方法与制药用途
US20250074904A1 (en) * 2021-11-17 2025-03-06 The University Of North Carolina At Chapel Hill Nsd2-targeted checmical degraderts and compositions and methods of use thereof
CN116284045A (zh) * 2023-05-18 2023-06-23 西南交通大学 一种手性吲哚单元取代的四氢异喹啉化合物及其合成方法
WO2025242921A1 (en) * 2024-05-23 2025-11-27 Storm Therapeutics Limited Processes for the preparation of inhibitory compounds

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