JP2020514360A5 - - Google Patents

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Publication number
JP2020514360A5
JP2020514360A5 JP2019550652A JP2019550652A JP2020514360A5 JP 2020514360 A5 JP2020514360 A5 JP 2020514360A5 JP 2019550652 A JP2019550652 A JP 2019550652A JP 2019550652 A JP2019550652 A JP 2019550652A JP 2020514360 A5 JP2020514360 A5 JP 2020514360A5
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JP
Japan
Prior art keywords
crystal
peaks
disease
powder
ray diffraction
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Pending
Application number
JP2019550652A
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English (en)
Japanese (ja)
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JP2020514360A (ja
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Priority claimed from PCT/US2018/022543 external-priority patent/WO2018170199A1/en
Publication of JP2020514360A publication Critical patent/JP2020514360A/ja
Publication of JP2020514360A5 publication Critical patent/JP2020514360A5/ja
Priority to JP2022172305A priority Critical patent/JP2023017840A/ja
Pending legal-status Critical Current

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JP2019550652A 2017-03-16 2018-03-15 Mk2阻害剤の形態および組成物 Pending JP2020514360A (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2022172305A JP2023017840A (ja) 2017-03-16 2022-10-27 Mk2阻害剤の形態および組成物

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201762472015P 2017-03-16 2017-03-16
US62/472,015 2017-03-16
PCT/US2018/022543 WO2018170199A1 (en) 2017-03-16 2018-03-15 Forms and compositions of a mk2 inhibitor

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2022172305A Division JP2023017840A (ja) 2017-03-16 2022-10-27 Mk2阻害剤の形態および組成物

Publications (2)

Publication Number Publication Date
JP2020514360A JP2020514360A (ja) 2020-05-21
JP2020514360A5 true JP2020514360A5 (enExample) 2021-04-22

Family

ID=63522534

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2019550652A Pending JP2020514360A (ja) 2017-03-16 2018-03-15 Mk2阻害剤の形態および組成物
JP2022172305A Pending JP2023017840A (ja) 2017-03-16 2022-10-27 Mk2阻害剤の形態および組成物

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2022172305A Pending JP2023017840A (ja) 2017-03-16 2022-10-27 Mk2阻害剤の形態および組成物

Country Status (8)

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US (2) US10882867B2 (enExample)
EP (1) EP3595658A4 (enExample)
JP (2) JP2020514360A (enExample)
CN (1) CN110678178B (enExample)
AU (1) AU2018236286B2 (enExample)
CA (1) CA3054823A1 (enExample)
MX (1) MX393600B (enExample)
WO (1) WO2018170199A1 (enExample)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG10201902326XA (en) 2014-09-17 2019-04-29 Celgene Car Llc Mk2 inhibitors and uses thereof
US11124525B2 (en) 2017-03-16 2021-09-21 Celgene Car Llc Heteroaryl compounds useful as MK2 inhibitors
CA3054826A1 (en) 2017-03-16 2018-09-20 Celgene Car Llc Mk2 inhibitors, synthesis thereof, and intermediates thereto
CN110678178B (zh) 2017-03-16 2023-10-03 百时美施贵宝公司 Mk2抑制剂的形式和组合物
JP2020514361A (ja) * 2017-03-16 2020-05-21 セルジーン シーエーアール エルエルシー 9,10,11,12−テトラヒドロ−8h−[1,4]ジアゼピノ[5’,6’:4,5]チエノ[3,2−f]キノリン−8−オン化合物およびその使用
JP2020511468A (ja) 2017-03-16 2020-04-16 セルジーン シーエーアール エルエルシー Mk2阻害剤の重水素化アナログおよびその使用
WO2020236636A1 (en) * 2019-05-17 2020-11-26 Celgene Car Llc Methods of treating a mk2-mediated disorder
EP4284805A1 (en) 2021-02-01 2023-12-06 Celgene Corporation Mk2 inhibitors, the synthesis thereof, and intermediates thereto
AU2023207395A1 (en) 2022-01-14 2024-07-11 Jiangsu Hansoh Pharmaceutical Group Co., Ltd. Pyridine-containing polycyclic derivative, and preparation method therefor and use thereof

Family Cites Families (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997038705A1 (en) * 1996-04-12 1997-10-23 Bristol-Myers Squibb Company N-formyl hydroxylamine containing compounds useful as ace inhibitors and/or nep inhibitors
AU2003301226A1 (en) 2002-12-20 2004-07-22 Pharmacia Corp Acyclic pyrazole compounds for the inhibition of mitogen activated protein kinase-activated protein kinase-2
WO2005105814A1 (en) 2004-04-28 2005-11-10 Incyte Corporation Tetracyclic inhibitors of janus kinases
US7790712B2 (en) * 2005-03-17 2010-09-07 Boehringer Ingelheim Pharmaceutical, Inc. Substituted [1,4]diazepino[1,2-A]indoles and azepino[1,2-A]indoles as anti-cytokine inhibitors
CN101360750A (zh) * 2005-11-23 2009-02-04 英特芒尼公司 应激活化蛋白激酶系统的调节方法
CN101687869A (zh) 2007-07-16 2010-03-31 诺瓦提斯公司 作为mk2抑制剂的四环内酰胺衍生物
US9126978B2 (en) * 2009-11-17 2015-09-08 The Regents Of The University Of Michigan 1,4-benzodiazepine-2,5-diones and related compounds with therapeutic properties
WO2011153553A2 (en) 2010-06-04 2011-12-08 The Regents Of The University Of California Methods and compositions for kinase inhibition
CN102464639A (zh) * 2010-11-16 2012-05-23 北京京卫信康医药科技发展有限公司 麦考酚酸钠的新晶型及其制备方法
SG194216A1 (en) * 2011-04-21 2013-11-29 Origenis Gmbh Heterocyclic compounds as kinase inhibitors
EP2872144A4 (en) 2012-07-11 2015-12-02 Nimbus Iris Inc IRAQ INHIBITOR AND USES THEREOF
KR20150133172A (ko) * 2013-03-15 2015-11-27 셀진 아빌로믹스 리서치, 인코포레이티드 Mk2 억제제 및 이의 용도
WO2014210319A2 (en) * 2013-06-26 2014-12-31 The Trustees Of Columbia University In The City Of New York Inhibitors of plasmodium falciparum equilibrative nucleoside transporter type 1 as anti-parasitic compounds
WO2016032882A1 (en) * 2014-08-25 2016-03-03 Stc.Unm Inhibition of mk2 in the treatment of cancer
SG10201902326XA (en) * 2014-09-17 2019-04-29 Celgene Car Llc Mk2 inhibitors and uses thereof
MX2017008994A (es) 2015-01-08 2018-09-18 Moerae Matrix Inc Formulacion de peptidos inhibidores mk2.
JP2020511468A (ja) 2017-03-16 2020-04-16 セルジーン シーエーアール エルエルシー Mk2阻害剤の重水素化アナログおよびその使用
JP2020514361A (ja) 2017-03-16 2020-05-21 セルジーン シーエーアール エルエルシー 9,10,11,12−テトラヒドロ−8h−[1,4]ジアゼピノ[5’,6’:4,5]チエノ[3,2−f]キノリン−8−オン化合物およびその使用
CN110678178B (zh) 2017-03-16 2023-10-03 百时美施贵宝公司 Mk2抑制剂的形式和组合物
CA3054826A1 (en) 2017-03-16 2018-09-20 Celgene Car Llc Mk2 inhibitors, synthesis thereof, and intermediates thereto
US11124525B2 (en) 2017-03-16 2021-09-21 Celgene Car Llc Heteroaryl compounds useful as MK2 inhibitors
WO2020236636A1 (en) 2019-05-17 2020-11-26 Celgene Car Llc Methods of treating a mk2-mediated disorder
KR20230044446A (ko) 2020-07-24 2023-04-04 브리스톨-마이어스 스큅 컴퍼니 급성 호흡기 장애의 치료 방법
EP4284805A1 (en) 2021-02-01 2023-12-06 Celgene Corporation Mk2 inhibitors, the synthesis thereof, and intermediates thereto

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