JP2018506531A5 - - Google Patents

Download PDF

Info

Publication number
JP2018506531A5
JP2018506531A5 JP2017540605A JP2017540605A JP2018506531A5 JP 2018506531 A5 JP2018506531 A5 JP 2018506531A5 JP 2017540605 A JP2017540605 A JP 2017540605A JP 2017540605 A JP2017540605 A JP 2017540605A JP 2018506531 A5 JP2018506531 A5 JP 2018506531A5
Authority
JP
Japan
Prior art keywords
ring
oxadiazolyl
compound
optionally substituted
triazolyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2017540605A
Other languages
English (en)
Japanese (ja)
Other versions
JP2018506531A (ja
JP6835727B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2016/016709 external-priority patent/WO2016127025A1/en
Publication of JP2018506531A publication Critical patent/JP2018506531A/ja
Publication of JP2018506531A5 publication Critical patent/JP2018506531A5/ja
Application granted granted Critical
Publication of JP6835727B2 publication Critical patent/JP6835727B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2017540605A 2015-02-05 2016-02-05 Irak1/4阻害剤としての大環状化合物及びその使用 Expired - Fee Related JP6835727B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562112374P 2015-02-05 2015-02-05
US62/112,374 2015-02-05
PCT/US2016/016709 WO2016127025A1 (en) 2015-02-05 2016-02-05 Macrocyclic compounds as irak1/4 inhibitors and uses thereof

Publications (3)

Publication Number Publication Date
JP2018506531A JP2018506531A (ja) 2018-03-08
JP2018506531A5 true JP2018506531A5 (https=) 2019-03-14
JP6835727B2 JP6835727B2 (ja) 2021-02-24

Family

ID=55436167

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017540605A Expired - Fee Related JP6835727B2 (ja) 2015-02-05 2016-02-05 Irak1/4阻害剤としての大環状化合物及びその使用

Country Status (15)

Country Link
US (2) US9708324B2 (https=)
EP (1) EP3253764B1 (https=)
JP (1) JP6835727B2 (https=)
KR (1) KR20170109546A (https=)
CN (1) CN107849055B (https=)
AU (1) AU2016215185B2 (https=)
BR (1) BR112017013677B1 (https=)
CA (1) CA2970534C (https=)
ES (1) ES2886577T3 (https=)
IL (1) IL253520B (https=)
MX (1) MX383363B (https=)
NZ (1) NZ732538A (https=)
RU (1) RU2730016C2 (https=)
SG (1) SG11201704628VA (https=)
WO (1) WO2016127025A1 (https=)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2015371251B2 (en) 2014-12-23 2020-06-11 Dana-Farber Cancer Institute, Inc. Inhibitors of cyclin-dependent kinase 7 (CDK7)
HK1246645A1 (zh) 2015-03-27 2018-09-14 达纳-法伯癌症研究所股份有限公司 细胞周期蛋白依赖性激酶的抑制剂
TWI794171B (zh) 2016-05-11 2023-03-01 美商滬亞生物國際有限公司 Hdac抑制劑與pd-l1抑制劑之組合治療
TWI808055B (zh) 2016-05-11 2023-07-11 美商滬亞生物國際有限公司 Hdac 抑制劑與 pd-1 抑制劑之組合治療
US11542261B2 (en) 2016-08-17 2023-01-03 Children's Hospital Medical Center Substituted Imidazo[1,2-a]-pyridines as IRAK 1/4 and FLT3 inhibitors
US11254667B2 (en) 2016-08-17 2022-02-22 Children's Hospital Medical Center Substituted imidazo[1,2-A]pyridines as IRAK 1/4 and flt3 inhibitors
TW202340194A (zh) 2017-02-16 2023-10-16 美商基利科學股份有限公司 吡咯并[1,2-b]嗒𠯤衍生物
WO2019111218A1 (en) 2017-12-08 2019-06-13 Cadila Healthcare Limited Novel heterocyclic compounds as irak4 inhibitors
US12187701B2 (en) 2018-06-25 2025-01-07 Dana-Farber Cancer Institute, Inc. Taire family kinase inhibitors and uses thereof
TWI842978B (zh) 2018-07-13 2024-05-21 美商基利科學股份有限公司 衍生物
US12109193B2 (en) 2018-07-31 2024-10-08 Loxo Oncology Inc. Spray-dried dispersions, formulations, and polymorphs of (s)-5-amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoropropan-2-yl)-1H-pyrazole-4-carboxamide
JP7660063B2 (ja) 2018-12-28 2025-04-10 ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド サイクリン依存性キナーゼ7のインヒビターおよびそれらの使用
JP7530380B2 (ja) * 2019-03-28 2024-08-07 ルピン・リミテッド Stingアゴニストとしての大環状化合物
CN111603471B (zh) * 2020-06-24 2021-07-09 山东省科学院生物研究所 一种邻二氮杂环化合物在制备抑制tlr4受体的药物中的用途
US20230295146A1 (en) * 2020-07-24 2023-09-21 The University Of Rochester Inhibitors of interleukin-1 receptor-associated kinases 1 and 4
PL4223368T3 (pl) * 2020-09-30 2025-08-11 Asahi Kasei Pharma Corporation Makrocykliczne związki zawierające piperydynę i chinolinę lub chinoksalinę jako inhibitory irak-4 do leczenia stanów zapalnych
US20260034112A1 (en) * 2022-08-01 2026-02-05 Children's Hospital Medical Center Multi-cyclic irak1 and irak4 inhibiting compounds and uses thereof

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2008520670A (ja) * 2004-11-17 2008-06-19 メルク エンド カムパニー インコーポレーテッド アルツハイマー病の治療のための大環状第三アミンβ−セクレターゼ阻害剤
MY169441A (en) * 2004-12-08 2019-04-11 Janssen Pharmaceutica Nv 2,4, (4,6) pyrimidine derivatives
US8933066B2 (en) * 2011-04-14 2015-01-13 Bristol-Myers Squibb Company Compounds for the treatment of hepatitis C
WO2014058691A1 (en) 2012-10-08 2014-04-17 Merck Sharp & Dohme Corp. Inhibitors of irak4 activity
LT2953952T (lt) * 2013-02-07 2017-08-25 Merck Patent Gmbh Makrocikliniai piridazinono dariniai
EP2970334B1 (en) * 2013-03-15 2018-05-23 Biogen MA Inc. Macrocyclic compounds as irak4 inhibitors for the treatment of inflammatory diseases

Similar Documents

Publication Publication Date Title
JP2018506531A5 (https=)
RU2017130762A (ru) Макроциклические соединения в качестве irak1/4 ингибиторов и их применение
JP2008543956A5 (https=)
JP2018505166A5 (https=)
RU2018114017A (ru) Гетероарильные соединения в качестве ингибиторов irak и их применение
Stephenson et al. Structural relationship and desolvation behavior of cromolyn, cefazolin and fenoprofen sodium hydrates
JP2006528602A5 (https=)
CN103951634B (zh) 一种依帕司他结晶盐水合物和羟基哌啶共晶物及其制备方法和应用
CN105085533A (zh) 7-环戊基-2-(5-哌嗪-1-基-吡啶-2-基氨基)-7h-吡咯并[2,3-d]嘧啶-6-羧酸二甲酰胺单琥珀酸盐的新晶型
Eder et al. Ammonium Metatungstate,(NH4) 6 [H2W12O40]: crystallization and thermal behavior of various hydrous species
CN108794370A (zh) 一种拉罗替尼中间体的制备方法
AU2005308060A1 (en) (S)-(-)-1-(4-fluoroisoquinolin-5-yl)sulfonyl-2-methyl-1,4-homopiperazine hydrochloride dihydrate
CN115315418A (zh) 大麻二酚前药及其药物组合物和应用
Chen et al. Experimental and theoretical investigation on the correlation between aqueous precursors structure and crystalline phases of zirconia
He et al. In situ formation and solid-state oxidation of a triselenane NSeN-pincer MOF
CN110776420A (zh) 一种卡巴匹林钙的合成工艺
CN110143951B (zh) 一种盐酸帕唑帕尼原料药三聚体杂质的合成方法
ES2878083T3 (es) Método para purificar P1,P4-di(uridina 5'-)tetrafosfato
WO2020053198A1 (en) Improved method for the manufacture of 3-[(1s)-1-imidazo[1,2-a]pyridin-6-ylethyl]-5-(1-methylpyrazol-4-yl)triazolo[4,5-b]pyrazine and polymorphic forms thereof
CN103524490A (zh) 一种制备无定形埃索美拉唑镁盐的结晶方法
CN103923011A (zh) 一种塞来西布的合成方法
Rekis et al. Structure and stability of racemic and enantiopure pimobendan monohydrates: on the phenomenon of unusually high stability
CN103772486B (zh) 一种阿加曲班新晶型及其制备方法
CN107235973A (zh) 具有药物活性的哌啶酮链接邻氟苯‑钙配合物的制备方法
CN114957206A (zh) 伊马替尼共晶及其制备方法