JP2017538734A5 - - Google Patents

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Publication number
JP2017538734A5
JP2017538734A5 JP2017532819A JP2017532819A JP2017538734A5 JP 2017538734 A5 JP2017538734 A5 JP 2017538734A5 JP 2017532819 A JP2017532819 A JP 2017532819A JP 2017532819 A JP2017532819 A JP 2017532819A JP 2017538734 A5 JP2017538734 A5 JP 2017538734A5
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JP
Japan
Prior art keywords
alkyl
substituents
substituted
hydrogen
halo
Prior art date
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JP2017532819A
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English (en)
Japanese (ja)
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JP6568588B2 (ja
JP2017538734A (ja
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Application filed filed Critical
Priority claimed from PCT/EP2015/080604 external-priority patent/WO2016097347A1/en
Publication of JP2017538734A publication Critical patent/JP2017538734A/ja
Publication of JP2017538734A5 publication Critical patent/JP2017538734A5/ja
Application granted granted Critical
Publication of JP6568588B2 publication Critical patent/JP6568588B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2017532819A 2014-12-19 2015-12-18 PI3Kβ阻害剤としてのイミダゾピリダジン誘導体 Expired - Fee Related JP6568588B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP14199322 2014-12-19
EP14199322.0 2014-12-19
PCT/EP2015/080604 WO2016097347A1 (en) 2014-12-19 2015-12-18 IMIDAZOPYRIDAZINE DERIVATIVES AS ΡΙ3Κβ INHIBITORS

Publications (3)

Publication Number Publication Date
JP2017538734A JP2017538734A (ja) 2017-12-28
JP2017538734A5 true JP2017538734A5 (enExample) 2018-11-08
JP6568588B2 JP6568588B2 (ja) 2019-08-28

Family

ID=52134002

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017532819A Expired - Fee Related JP6568588B2 (ja) 2014-12-19 2015-12-18 PI3Kβ阻害剤としてのイミダゾピリダジン誘導体

Country Status (26)

Country Link
US (1) US10087187B2 (enExample)
EP (1) EP3233862B1 (enExample)
JP (1) JP6568588B2 (enExample)
KR (1) KR20170095239A (enExample)
CN (1) CN107108634B (enExample)
AU (1) AU2015366190B2 (enExample)
BR (1) BR112017012930A2 (enExample)
CA (1) CA2967551A1 (enExample)
CY (1) CY1122381T1 (enExample)
DK (1) DK3233862T3 (enExample)
EA (1) EA029789B1 (enExample)
ES (1) ES2761051T3 (enExample)
HR (1) HRP20191550T1 (enExample)
HU (1) HUE045220T2 (enExample)
IL (1) IL252866B (enExample)
LT (1) LT3233862T (enExample)
MA (1) MA41174B1 (enExample)
MD (1) MD3233862T2 (enExample)
ME (1) ME03517B (enExample)
MX (1) MX2017008074A (enExample)
PL (1) PL3233862T3 (enExample)
PT (1) PT3233862T (enExample)
RS (1) RS59301B1 (enExample)
SI (1) SI3233862T1 (enExample)
SM (1) SMT201900509T1 (enExample)
WO (1) WO2016097347A1 (enExample)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102630111B1 (ko) 2015-10-09 2024-01-25 얀센 파마슈티카 엔브이 PI3Kβ 저해제로서의 퀴녹살린 및 피리도피라진 유도체
DK3472160T3 (da) 2016-06-16 2021-05-10 Janssen Pharmaceutica Nv Bicykliske pyridin-, pyrazin- og pyrimidinderivater som pi3k-beta-inhibitorer
AU2018246321B2 (en) 2017-03-29 2021-07-29 Janssen Pharmaceutica Nv Quinoxaline and pyridopyrazine derivatives as PI3K-beta inhibitors
US12281119B2 (en) 2019-02-07 2025-04-22 Beigene, Ltd. Imidazo[2,1-f][1,2,4]triazin-4-amine derivatives as TLR7 agonist
CN110128505A (zh) * 2019-05-21 2019-08-16 梯尔希(南京)药物研发有限公司 一种戈舍瑞林杂质的合成方法

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20070078136A1 (en) 2005-09-22 2007-04-05 Bristol-Myers Squibb Company Fused heterocyclic compounds useful as kinase modulators
US8217177B2 (en) 2006-07-14 2012-07-10 Amgen Inc. Fused heterocyclic derivatives and methods of use
PE20121506A1 (es) 2006-07-14 2012-11-26 Amgen Inc Compuestos triazolopiridinas como inhibidores de c-met
WO2008014219A2 (en) 2006-07-24 2008-01-31 Smithkline Beecham Corporation Thiozolidinedione derivatives as p13 kinase inhibitors
EP2063962A2 (en) 2006-09-07 2009-06-03 Biogen Idec MA Inc. Irak modulators for treating an inflammatory condition, cell proliferative disorder, immune disorder
EA200901488A1 (ru) * 2007-05-09 2010-04-30 Новартис Аг Замещенные имидазолопиридазины, как ингибиторы липидкиназы
US20110046127A1 (en) 2007-11-08 2011-02-24 Paolo Pevarello Imidazopyridazines for Use as Protein Kinase Inhibitors
WO2009106577A1 (en) * 2008-02-28 2009-09-03 Novartis Ag Imidazo [1,2-b] pyridazine derivatives for the treatment of c-met tyrosine kinase mediated disease
WO2010007099A1 (en) 2008-07-15 2010-01-21 Cellzome Limited 2-aminoimidazo[1,2-b]pyridazine derivatives as pi3k inhibitors
ES2709108T3 (es) 2009-08-17 2019-04-15 Intellikine Llc Compuestos heterocíclicos y usos de los mismos
DE102009049679A1 (de) * 2009-10-19 2011-04-21 Merck Patent Gmbh Pyrazolopyrimidinderivate
WO2011058109A1 (en) 2009-11-12 2011-05-19 Ucb Pharma S.A. Fused bicyclic pyrrole and imidazole derivatives as kinase inhibitors
UY33304A (es) 2010-04-02 2011-10-31 Amgen Inc Compuestos heterocíclicos y sus usos
SI2624696T1 (sl) 2010-10-06 2017-04-26 Glaxosmithkline Llc Corporation Service Company Benzimidazolni derivati kot inhibitorji pi3-kinaze
EP2678016B1 (en) 2011-02-23 2016-08-10 Intellikine, LLC Heterocyclic compounds and uses thereof
WO2013028263A1 (en) 2011-08-24 2013-02-28 Glaxosmithkline Llc Pyrazolopyrimidine derivatives as pi3 kinase inhibitors
US8906910B2 (en) * 2011-12-20 2014-12-09 Glaxosmithkline Llc Imidazopyridine derivatives as PI3 kinase
US8778937B2 (en) 2011-12-20 2014-07-15 Glaxosmithkline Llc Benzimidazole boronic acid derivatives as PI3 kinase inhibitors
TWI574962B (zh) * 2012-11-14 2017-03-21 加拓科學公司 作爲pi3激酶調節劑的芳雜環化合物及其使用方法和用途
GB201321734D0 (en) * 2013-12-09 2014-01-22 Ucb Pharma Sa Therapeutic Agents

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