JP2015508086A5 - - Google Patents

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Publication number
JP2015508086A5
JP2015508086A5 JP2014558028A JP2014558028A JP2015508086A5 JP 2015508086 A5 JP2015508086 A5 JP 2015508086A5 JP 2014558028 A JP2014558028 A JP 2014558028A JP 2014558028 A JP2014558028 A JP 2014558028A JP 2015508086 A5 JP2015508086 A5 JP 2015508086A5
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Japan
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disease
cancer
prevention
treatment
medicament
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JP2014558028A
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Japanese (ja)
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JP2015508086A (ja
JP6479476B2 (ja
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Priority claimed from PCT/EP2013/000189 external-priority patent/WO2013124026A1/en
Publication of JP2015508086A publication Critical patent/JP2015508086A/ja
Publication of JP2015508086A5 publication Critical patent/JP2015508086A5/ja
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Publication of JP6479476B2 publication Critical patent/JP6479476B2/ja
Expired - Fee Related legal-status Critical Current
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JP2014558028A 2012-02-21 2013-01-22 SykチロシンキナーゼインヒビターおよびGCN2セリンキナーゼインヒビターとしての8−置換2−アミノー[1,2,4]トリアゾロ[1,5−A]ピラジン類 Expired - Fee Related JP6479476B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP12001153 2012-02-21
EP12001153.1 2012-02-21
PCT/EP2013/000189 WO2013124026A1 (en) 2012-02-21 2013-01-22 8 - substituted 2 -amino - [1,2,4] triazolo [1, 5 -a] pyrazines as syk tryrosine kinase inhibitors and gcn2 serin kinase inhibitors

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2017173002A Division JP2018039805A (ja) 2012-02-21 2017-09-08 SykチロシンキナーゼインヒビターおよびGCN2セリンキナーゼインヒビターとしての8−置換2−アミノー[1,2,4]トリアゾロ[1,5−A]ピラジン類

Publications (3)

Publication Number Publication Date
JP2015508086A JP2015508086A (ja) 2015-03-16
JP2015508086A5 true JP2015508086A5 (enExample) 2016-03-17
JP6479476B2 JP6479476B2 (ja) 2019-03-06

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ID=47598786

Family Applications (2)

Application Number Title Priority Date Filing Date
JP2014558028A Expired - Fee Related JP6479476B2 (ja) 2012-02-21 2013-01-22 SykチロシンキナーゼインヒビターおよびGCN2セリンキナーゼインヒビターとしての8−置換2−アミノー[1,2,4]トリアゾロ[1,5−A]ピラジン類
JP2017173002A Withdrawn JP2018039805A (ja) 2012-02-21 2017-09-08 SykチロシンキナーゼインヒビターおよびGCN2セリンキナーゼインヒビターとしての8−置換2−アミノー[1,2,4]トリアゾロ[1,5−A]ピラジン類

Family Applications After (1)

Application Number Title Priority Date Filing Date
JP2017173002A Withdrawn JP2018039805A (ja) 2012-02-21 2017-09-08 SykチロシンキナーゼインヒビターおよびGCN2セリンキナーゼインヒビターとしての8−置換2−アミノー[1,2,4]トリアゾロ[1,5−A]ピラジン類

Country Status (11)

Country Link
US (1) US9120804B2 (enExample)
EP (1) EP2817310B1 (enExample)
JP (2) JP6479476B2 (enExample)
CN (1) CN104114557B (enExample)
AR (1) AR090104A1 (enExample)
AU (1) AU2013224421B2 (enExample)
CA (1) CA2863723C (enExample)
ES (1) ES2674451T3 (enExample)
IL (1) IL233982A (enExample)
TW (1) TW201339165A (enExample)
WO (1) WO2013124026A1 (enExample)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104114557B (zh) * 2012-02-21 2017-10-24 默克专利股份公司 作为syk酪氨酸激酶抑制剂和gcn2丝氨酸激酶抑制剂的8‑取代2‑氨基‑[1,2,4]三唑并[1,5‑a]吡嗪
NO2699580T3 (enExample) 2014-01-24 2018-02-24
BR112017007164A2 (pt) * 2014-10-06 2017-12-19 A Anton Mark implantes de mama cobertos com politetrafluoroetileno expandido para minimizar reação capsular e infecção enquanto reduzindo palpabilidade
JP6948345B2 (ja) * 2016-04-29 2021-10-13 イオメット ファーマ リミテッド インドールアミン2,3−ジオキシゲナーゼ及び/又はトリプトファン−2,3−ジオキシゲナーゼの阻害薬としての新規置換イミダゾピリジン化合物
CN114989205A (zh) 2016-12-22 2022-09-02 卡里塞拉生物科学股份公司 用于抑制精氨酸酶活性的组合物和方法
GB201709456D0 (en) * 2017-06-14 2017-07-26 Ucb Biopharma Sprl Therapeutic agents
JP7229257B2 (ja) 2018-01-29 2023-02-28 メルク パテント ゲーエムベーハー Gcn2阻害剤およびその使用
BR112020015396A2 (pt) 2018-01-29 2020-12-08 Merck Patent Gmbh Inididores de gcn2 e usos dos mesmos
CA3089240A1 (en) * 2018-02-07 2019-08-15 Insmed Incorporated Certain (2s)-n-[(1s)-1-cyano-2-phenylethyl]-1,4-oxazepane-2-carboxamides for treating anca associated vasculitides
HUE070049T2 (hu) 2018-03-01 2025-05-28 Astrazeneca Ab (2S)-{(1S)-1-ciano-2-[4-(3-metil-2-oxo-2,3-dihidro-1,3-benzoxazol-5-il)fenil]etil} -1,4-oxazepán-2-karboxamidot tartalmazó gyógyászati készítmények
JP7220204B2 (ja) * 2018-03-27 2023-02-09 本田技研工業株式会社 フッ化物イオン二次電池用正極活物質、当該活物質を用いた正極、およびフッ化物イオン二次電池、並びに当該活物質の製造方法
EP3781156A4 (en) 2018-04-16 2022-05-18 C4 Therapeutics, Inc. SPIROCYCLIC COMPOUNDS
EP3556760A1 (en) * 2018-04-19 2019-10-23 F. Hoffmann-La Roche AG Spiro compounds
EP3578561A1 (en) * 2018-06-04 2019-12-11 F. Hoffmann-La Roche AG Spiro compounds
WO2020018547A1 (en) 2018-07-17 2020-01-23 Insmed Incorporated Certain (2s)-n-[(1s)-1-cyano-2-phenylethyl]-1,4-oxazepane-2-carboxamides for treating lupus nephritis
EA202192575A1 (ru) 2019-03-21 2022-01-14 Онксео Соединения dbait в сочетании с ингибиторами киназ для лечения рака
CN114761006A (zh) 2019-11-08 2022-07-15 Inserm(法国国家健康医学研究院) 对激酶抑制剂产生耐药性的癌症的治疗方法
WO2021148581A1 (en) 2020-01-22 2021-07-29 Onxeo Novel dbait molecule and its use
CN113929678B (zh) * 2020-07-14 2025-09-30 武汉朗来科技发展有限公司 一种rock抑制剂及其制备方法和用途
WO2022238816A1 (en) * 2021-05-14 2022-11-17 Bm Pharma Consulting Pty. Ltd Bicyclic heterocyclic compounds for prophylaxis and treatment of viral infections
AU2022299051B2 (en) * 2021-06-23 2025-03-13 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
KR102659126B1 (ko) * 2022-03-24 2024-04-19 충남대학교산학협력단 항결핵 약학조성물
JP2026503035A (ja) 2023-01-06 2026-01-27 インスメッド インコーポレイテッド 新規な可逆性dpp1阻害剤及びその用途

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
DE69720965T2 (de) 1996-02-13 2004-02-05 Astrazeneca Ab Chinazolinderivate und deren verwendung als vegf hemmer
NZ331191A (en) 1996-03-05 2000-03-27 Zeneca Ltd 4-anilinoquinazoline derivatives and pharmaceutical compositions thereof
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
AU2001258628A1 (en) 2000-05-31 2001-12-11 Astrazeneca Ab Indole derivatives with vascular damaging activity
MXPA02012905A (es) 2000-07-07 2004-07-30 Angiogene Pharm Ltd Derivados de colquinol como agentes de dano vascular..
MXPA02012903A (es) 2000-07-07 2004-07-30 Angiogene Pharm Ltd Derivados de colquinol como inhibidores de angiogenesis.
US7834024B2 (en) 2007-03-26 2010-11-16 Rigel Pharmaceuticals, Inc. Compositions and methods for inhibition of the JAK pathway
SG165655A1 (en) 2008-04-16 2010-11-29 Portola Pharm Inc 2, 6-diamino- pyrimidin- 5-yl-carboxamides as syk or JAK kinases inhibitors
CN102131389A (zh) 2008-06-20 2011-07-20 健泰科生物技术公司 三唑并吡啶jak抑制剂化合物和方法
WO2010010184A1 (en) * 2008-07-25 2010-01-28 Galapagos Nv [1, 2, 4] triazolo [1, 5-a] pyridines as jak inhibitors
TWI453207B (zh) 2008-09-08 2014-09-21 Signal Pharm Llc 胺基三唑并吡啶,其組合物及使用其之治療方法
EP2438066A2 (en) * 2009-06-05 2012-04-11 Cephalon, Inc. PREPARATION AND USES OF 1,2,4-TRIAZOLO [1,5a]PYRIDINE DERIVATIVES
ES2519565T3 (es) 2009-07-15 2014-11-07 Janssen Pharmaceuticals Inc. Derivados de triazol e imidazol sustituidos como moduladores de gamma secretasa
EP2523949B1 (en) 2010-01-15 2014-08-20 Janssen Pharmaceuticals Inc. Novel substituted triazole derivatives as gamma secretase modulators
US20110190269A1 (en) * 2010-02-01 2011-08-04 Karlheinz Baumann Gamma secretase modulators
US8486967B2 (en) * 2010-02-17 2013-07-16 Hoffmann-La Roche Inc. Heteroaryl substituted piperidines
JP4940370B2 (ja) * 2010-06-29 2012-05-30 キヤノン株式会社 電子写真感光体、プロセスカートリッジおよび電子写真装置
EA201300282A1 (ru) * 2010-08-27 2013-08-30 Мерк Патент Гмбх Производные триазолопиразина
CN104114557B (zh) * 2012-02-21 2017-10-24 默克专利股份公司 作为syk酪氨酸激酶抑制剂和gcn2丝氨酸激酶抑制剂的8‑取代2‑氨基‑[1,2,4]三唑并[1,5‑a]吡嗪

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