JP2017527590A5 - - Google Patents

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Publication number
JP2017527590A5
JP2017527590A5 JP2017514411A JP2017514411A JP2017527590A5 JP 2017527590 A5 JP2017527590 A5 JP 2017527590A5 JP 2017514411 A JP2017514411 A JP 2017514411A JP 2017514411 A JP2017514411 A JP 2017514411A JP 2017527590 A5 JP2017527590 A5 JP 2017527590A5
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JP
Japan
Prior art keywords
pharmaceutically acceptable
acceptable salt
compound
aryl
alkyl
Prior art date
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Granted
Application number
JP2017514411A
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English (en)
Japanese (ja)
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JP2017527590A (ja
JP6660060B2 (ja
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Publication date
Application filed filed Critical
Priority claimed from PCT/US2015/050289 external-priority patent/WO2016044342A1/en
Publication of JP2017527590A publication Critical patent/JP2017527590A/ja
Publication of JP2017527590A5 publication Critical patent/JP2017527590A5/ja
Application granted granted Critical
Publication of JP6660060B2 publication Critical patent/JP6660060B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2017514411A 2014-09-16 2015-09-15 ヒストンデメチラーゼ阻害剤 Expired - Fee Related JP6660060B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201462051268P 2014-09-16 2014-09-16
US62/051,268 2014-09-16
PCT/US2015/050289 WO2016044342A1 (en) 2014-09-16 2015-09-15 Histone demethylase inhibitors

Publications (3)

Publication Number Publication Date
JP2017527590A JP2017527590A (ja) 2017-09-21
JP2017527590A5 true JP2017527590A5 (enExample) 2018-10-25
JP6660060B2 JP6660060B2 (ja) 2020-03-04

Family

ID=55533770

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017514411A Expired - Fee Related JP6660060B2 (ja) 2014-09-16 2015-09-15 ヒストンデメチラーゼ阻害剤

Country Status (17)

Country Link
US (2) US9676770B2 (enExample)
EP (1) EP3193881B1 (enExample)
JP (1) JP6660060B2 (enExample)
KR (1) KR20170048590A (enExample)
CN (1) CN107073006A (enExample)
AU (1) AU2015317904A1 (enExample)
BR (1) BR112017005128A2 (enExample)
CA (1) CA2961525A1 (enExample)
CL (1) CL2017000643A1 (enExample)
CO (1) CO2017002772A2 (enExample)
EA (1) EA201790502A1 (enExample)
EC (1) ECSP17020172A (enExample)
ES (1) ES2911292T3 (enExample)
IL (1) IL251103A0 (enExample)
MX (1) MX2017003464A (enExample)
SG (1) SG11201702108PA (enExample)
WO (1) WO2016044342A1 (enExample)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2731773T3 (es) 2013-03-14 2019-11-19 Celgene Quanticel Res Inc Inhibidores de la histona desmetilasa
US9896436B2 (en) 2014-09-16 2018-02-20 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
US9676770B2 (en) * 2014-09-16 2017-06-13 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
US9586949B2 (en) 2015-02-09 2017-03-07 Incyte Corporation Aza-heteroaryl compounds as PI3K-gamma inhibitors
TWI744256B (zh) 2015-11-06 2021-11-01 美商英塞特公司 作為PI3K-γ抑制劑之雜環化合物
AR107293A1 (es) * 2016-01-05 2018-04-18 Incyte Corp COMPUESTOS DE PIRIDINA Y PIRIDIMINA COMO INHIBIDORES DE PI3K-g
EP3436445B1 (en) * 2016-03-15 2023-09-06 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
US10150754B2 (en) 2016-04-19 2018-12-11 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
US10138248B2 (en) 2016-06-24 2018-11-27 Incyte Corporation Substituted imidazo[2,1-f][1,2,4]triazines, substituted imidazo[1,2-a]pyridines, substituted imidazo[1,2-b]pyridazines and substituted imidazo[1,2-a]pyrazines as PI3K-γ inhibitors
CN111542526B (zh) 2017-10-18 2024-01-09 因赛特公司 作为PI3K-γ抑制剂的由叔羟基取代的缩合咪唑衍生物
CR20250050A (es) 2018-09-05 2025-03-19 Incyte Corp Formas cristalinas de un inhibidor de fosfoinositida 3–quinasa (pi3k) (divisional 2021-0165)
CN111116571B (zh) * 2019-12-27 2022-07-12 吉首大学 含恶唑及三唑双杂环的化合物及其制备与应用方法

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1058549A4 (en) 1998-12-23 2003-11-12 Bristol Myers Squibb Pharma Co FACTOR Xa OR THROMBIN INHIBITORS
CA2427284A1 (en) 2000-10-26 2002-05-30 Tularik Inc. Antiinflammation agents
GB0217780D0 (en) * 2002-07-31 2002-09-11 Glaxo Group Ltd Compounds
US20040127733A1 (en) 2002-10-31 2004-07-01 Boehringer Ingelheim Pharma Gmbh & Co. Kg New beta-agonists, processes for preparing them and their use as pharmaceutical compositions
DE102004021779A1 (de) 2004-04-30 2005-11-24 Boehringer Ingelheim Pharma Gmbh & Co. Kg Neue Beta-Agonisten, Verfahren zu deren Herstellung und deren Verwendung als Arzneimittel
WO2007071653A1 (en) 2005-12-19 2007-06-28 Boehringer Ingelheim International Gmbh Use of aminoalcohol derivatives for the treatment of overactive bladder
JP2010540649A (ja) 2007-10-03 2010-12-24 バーテックス ファーマシューティカルズ インコーポレイテッド c−METタンパク質の阻害剤
DE102009019962A1 (de) 2009-05-05 2010-11-11 Merck Patent Gmbh 3-([1,2,3]Triazol-4-yl)-pyrrolo[2,3-b]pyridinderivate
EP2676958B1 (en) 2009-11-10 2015-07-01 Pfizer Inc. N1-Pyrazolospiroketone acetyl-CoA carboxylase inhibitors
WO2011088181A1 (en) 2010-01-13 2011-07-21 Tempero Pharmaceuticals, Inc. Compounds and methods
EP3763367A1 (en) 2012-12-06 2021-01-13 Celgene Quanticel Research, Inc. Pyridine-pyrazole derivatives as histone demethylase inhibitors
ES2731773T3 (es) 2013-03-14 2019-11-19 Celgene Quanticel Res Inc Inhibidores de la histona desmetilasa
US9695167B2 (en) 2014-07-10 2017-07-04 Incyte Corporation Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors
US9896436B2 (en) * 2014-09-16 2018-02-20 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
US9676770B2 (en) 2014-09-16 2017-06-13 Celgene Quanticel Research, Inc. Histone demethylase inhibitors

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