JP2014521735A5 - - Google Patents

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Publication number
JP2014521735A5
JP2014521735A5 JP2014525437A JP2014525437A JP2014521735A5 JP 2014521735 A5 JP2014521735 A5 JP 2014521735A5 JP 2014525437 A JP2014525437 A JP 2014525437A JP 2014525437 A JP2014525437 A JP 2014525437A JP 2014521735 A5 JP2014521735 A5 JP 2014521735A5
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Japan
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compound
pharmaceutically acceptable
acceptable salt
condition
disease
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JP2014525437A
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Japanese (ja)
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JP6059723B2 (ja
JP2014521735A (ja
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Priority claimed from GBGB1114103.3A external-priority patent/GB201114103D0/en
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Expired - Fee Related legal-status Critical Current
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JP2014525437A 2011-08-17 2012-08-15 4−(8−メトキシ−1−((1−メトキシプロパン−2−イル)−2−(テトラヒドロ−2H−ピラン−4−イル)−1H−イミダゾ[4,5−c]キノリン−7−イル)−3,5−ジメチルイソオキサゾールおよびブロモドメイン阻害剤としてのその使用 Expired - Fee Related JP6059723B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB1114103.3 2011-08-17
GBGB1114103.3A GB201114103D0 (en) 2011-08-17 2011-08-17 Novel compounds
PCT/EP2012/065918 WO2013024104A1 (en) 2011-08-17 2012-08-15 4-(8-methoxy-1-((1-methoxypropan-2-yl)-2-(tetrahydro-2h-pyran-4-yl)-1 h-imidazo[4,5-c]quinolin-7-yl)-3,5-dimethylisoxazole and its use as bromodomain inhibitor

Publications (3)

Publication Number Publication Date
JP2014521735A JP2014521735A (ja) 2014-08-28
JP2014521735A5 true JP2014521735A5 (enExample) 2015-09-10
JP6059723B2 JP6059723B2 (ja) 2017-01-11

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JP2014525437A Expired - Fee Related JP6059723B2 (ja) 2011-08-17 2012-08-15 4−(8−メトキシ−1−((1−メトキシプロパン−2−イル)−2−(テトラヒドロ−2H−ピラン−4−イル)−1H−イミダゾ[4,5−c]キノリン−7−イル)−3,5−ジメチルイソオキサゾールおよびブロモドメイン阻害剤としてのその使用

Country Status (38)

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US (4) US9067936B2 (enExample)
EP (2) EP3150601A1 (enExample)
JP (1) JP6059723B2 (enExample)
KR (1) KR20140064878A (enExample)
CN (1) CN103889984B (enExample)
AR (1) AR087545A1 (enExample)
AU (1) AU2012296914B2 (enExample)
BR (1) BR112014003681A8 (enExample)
CA (1) CA2843537A1 (enExample)
CL (1) CL2014000365A1 (enExample)
CO (1) CO6862151A2 (enExample)
CR (1) CR20140076A (enExample)
CY (1) CY1118370T1 (enExample)
DK (1) DK2744809T3 (enExample)
DO (1) DOP2014000031A (enExample)
EA (1) EA023374B1 (enExample)
ES (1) ES2609857T3 (enExample)
GB (1) GB201114103D0 (enExample)
HR (1) HRP20161674T1 (enExample)
HU (1) HUE030106T2 (enExample)
IL (1) IL230489A (enExample)
IN (1) IN2014CN00568A (enExample)
JO (1) JO3187B1 (enExample)
LT (1) LT2744809T (enExample)
ME (1) ME02589B (enExample)
MX (1) MX350597B (enExample)
MY (1) MY170729A (enExample)
PE (1) PE20141406A1 (enExample)
PH (1) PH12014500379A1 (enExample)
PL (1) PL2744809T3 (enExample)
PT (1) PT2744809T (enExample)
RS (1) RS55560B1 (enExample)
SI (1) SI2744809T1 (enExample)
SM (2) SMT201700005T1 (enExample)
TW (1) TWI558704B (enExample)
UA (1) UA110838C2 (enExample)
UY (1) UY34264A (enExample)
WO (1) WO2013024104A1 (enExample)

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EP2970312B1 (en) 2013-03-11 2017-11-15 The Regents of The University of Michigan Bet bromodomain inhibitors and therapeutic methods using the same
BR112015022861A8 (pt) 2013-03-11 2019-11-26 Abbvie Inc inibidores de bromodomínio
MX366703B (es) * 2013-03-15 2019-07-22 Incyte Holdings Corp Heterociclos tricíclicos como inhibidores de la proteína bet.
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WO2015004533A2 (en) 2013-06-21 2015-01-15 Zenith Epigenetics Corp. Novel substituted bicyclic compounds as bromodomain inhibitors
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WO2015006193A1 (en) 2013-07-08 2015-01-15 Incyte Corporation Tricyclic heterocycles as bet protein inhibitors
WO2015015318A2 (en) 2013-07-31 2015-02-05 Zenith Epigenetics Corp. Novel quinazolinones as bromodomain inhibitors
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WO2015081203A1 (en) 2013-11-26 2015-06-04 Incyte Corporation Bicyclic heterocycles as bet protein inhibitors
US9315501B2 (en) 2013-11-26 2016-04-19 Incyte Corporation Bicyclic heterocycles as BET protein inhibitors
US9309246B2 (en) 2013-12-19 2016-04-12 Incyte Corporation Tricyclic heterocycles as BET protein inhibitors
US9580430B2 (en) 2014-02-28 2017-02-28 The Regents Of The University Of Michigan 9H-pyrimido[4,5-B]indoles and related analogs as BET bromodomain inhibitors
UA119870C2 (uk) 2014-04-23 2019-08-27 Інсайт Корпорейшн 1H-ПІРОЛО[2,3-c]ПІРИДИН-7(6H)-ОНИ ТА ПІРАЗОЛО[3,4-c]ПІРИДИН-7(6H)-ОНИ ЯК ІНГІБІТОРИ БІЛКІВ BET
CN106687463B (zh) 2014-06-20 2019-04-09 星座制药公司 一种乙酰胺类化合物的晶型
ES2855225T3 (es) 2014-09-15 2021-09-23 Incyte Corp Heterociclos tricíclicos para su uso como inhibidores de proteínas BET
US10710992B2 (en) 2014-12-01 2020-07-14 Zenith Epigenetics Ltd. Substituted pyridinones as bromodomain inhibitors
EP3227280B1 (en) 2014-12-01 2019-04-24 Zenith Epigenetics Ltd. Substituted pyridines as bromodomain inhibitors
JP2017537946A (ja) 2014-12-11 2017-12-21 ゼニス・エピジェネティクス・リミテッドZenith Epigenetics Ltd. ブロモドメイン阻害剤としての置換複素環
HK1245247A1 (zh) 2014-12-17 2018-08-24 恒翼生物医药科技(上海)有限公司 溴结构域的抑制剂
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WO2016138332A1 (en) 2015-02-27 2016-09-01 The Regents Of The University Of Michigan 9h-pyrimido [4,5-b] indoles as bet bromodomain inhibitors
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JP2018527340A (ja) 2015-08-11 2018-09-20 ネオメド インスティテュートNeomed Institute アリール置換ジヒドロキノリノン、その調製及び医薬品としてのその使用
CA2994478C (en) 2015-08-12 2023-10-03 Neomed Institute Substituted benzimidazoles, their preparation and their use as pharmaceuticals
US10501459B2 (en) 2015-10-21 2019-12-10 Neomed Institute Substituted imidazo[1,2-a]pyridines as bromodomain inhibitors
TW201722966A (zh) 2015-10-29 2017-07-01 英塞特公司 Bet蛋白質抑制劑之非晶固體形式
WO2017127930A1 (en) 2016-01-28 2017-08-03 Neomed Institute Substituted [1,2,4]triazolo[4,3-a]pyridines, their preparation and their use as pharmaceuticals
ES2882066T3 (es) 2016-02-15 2021-12-01 Univ Michigan Regents 1,4-oxazepinas fusionadas y análogos relacionados como inhibidores de bromodominio BET
AU2017246453A1 (en) 2016-04-06 2018-11-08 The Regents Of The University Of Michigan Monofunctional intermediates for ligand-dependent target protein degradation
CN113788818A (zh) 2016-04-06 2021-12-14 密执安大学评议会 Mdm2蛋白质降解剂
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CN110062759B (zh) 2016-09-13 2022-05-24 密执安大学评议会 作为bet蛋白降解剂的稠合的1,4-氧氮杂䓬
US10975093B2 (en) 2016-09-13 2021-04-13 The Regents Of The University Of Michigan Fused 1,4-diazepines as BET protein degraders
WO2018144789A1 (en) 2017-02-03 2018-08-09 The Regents Of The University Of Michigan Fused 1,4-diazepines as bet bromodomain inhibitors
WO2019055444A1 (en) 2017-09-13 2019-03-21 The Regents Of The University Of Michigan DEGRADATION AGENTS OF BROMODOMAIN BET PROTEIN WITH CLEAR BINDERS
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