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
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
JP2017514411A
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English (en)
Japanese (ja)
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JP6660060B2 (ja
JP2017527590A (ja
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Publication date
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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
Active 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 Active 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 (pt-PT) 2018-10-25
JP6660060B2 JP6660060B2 (ja) 2020-03-04

Family

ID=55533770

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2017514411A Active 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 (pt-PT)
EP (1) EP3193881B1 (pt-PT)
JP (1) JP6660060B2 (pt-PT)
KR (1) KR20170048590A (pt-PT)
CN (1) CN107073006A (pt-PT)
AU (1) AU2015317904A1 (pt-PT)
BR (1) BR112017005128A2 (pt-PT)
CA (1) CA2961525A1 (pt-PT)
CL (1) CL2017000643A1 (pt-PT)
CO (1) CO2017002772A2 (pt-PT)
EA (1) EA201790502A1 (pt-PT)
EC (1) ECSP17020172A (pt-PT)
ES (1) ES2911292T3 (pt-PT)
IL (1) IL251103A0 (pt-PT)
MX (1) MX2017003464A (pt-PT)
SG (1) SG11201702108PA (pt-PT)
WO (1) WO2016044342A1 (pt-PT)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9527829B2 (en) 2013-03-14 2016-12-27 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
US9896436B2 (en) 2014-09-16 2018-02-20 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
CN107073006A (zh) * 2014-09-16 2017-08-18 赛尔基因昆蒂赛尔研究公司 组蛋白脱甲基酶抑制剂
US9586949B2 (en) 2015-02-09 2017-03-07 Incyte Corporation Aza-heteroaryl compounds as PI3K-gamma inhibitors
EP4086259A1 (en) 2015-11-06 2022-11-09 Incyte Corporation Heterocyclic compounds as pi3k-gamma inhibitors
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
WO2017223414A1 (en) 2016-06-24 2017-12-28 Incyte Corporation HETEROCYCLIC COMPOUNDS AS PI3K-γ INHIBITORS
PT3697789T (pt) 2017-10-18 2021-12-31 Incyte Corp Derivados de imidazol condensados substituídos por grupos hidróxi terciários como inibidores de pi3kgama
HRP20240252T1 (hr) 2018-09-05 2024-05-24 Incyte Corporation Kristalni oblici inhibitora fosfoinozitid 3 kinaze (pi3k)
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
WO2000039102A1 (en) 1998-12-23 2000-07-06 Du Pont Pharmaceuticals Company THROMBIN OR FACTOR Xa 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
CA2632444A1 (en) 2005-12-19 2007-06-28 Boehringer Ingelheim International Gmbh Use of aminoalcohol derivatives for the treatment of overactive bladder
EP2205589B1 (en) 2007-10-03 2011-03-23 Vertex Pharmaceuticals Incorporated C-met protein kinase inhibitors
DE102009019962A1 (de) 2009-05-05 2010-11-11 Merck Patent Gmbh 3-([1,2,3]Triazol-4-yl)-pyrrolo[2,3-b]pyridinderivate
JP5114610B1 (ja) 2009-11-10 2013-01-09 ファイザー・インク N1−ピラゾロスピロケトンアセチル−CoAカルボキシラーゼ阻害薬
EP2533783B8 (en) 2010-01-13 2015-12-16 Tempero Pharmaceuticals, Inc. COMPOUNDS AND METHODS for the inhibition of HDAC
MX2015007205A (es) * 2012-12-06 2016-03-31 Quanticel Pharmaceuticals Inc Inhibidores de la desmetilasa de histona.
US9527829B2 (en) 2013-03-14 2016-12-27 Celgene Quanticel Research, Inc. Histone demethylase inhibitors
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
CN107073006A (zh) 2014-09-16 2017-08-18 赛尔基因昆蒂赛尔研究公司 组蛋白脱甲基酶抑制剂

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