NZ630205A - Enhancer of zeste homolog 2 inhibitors - Google Patents

Enhancer of zeste homolog 2 inhibitors

Info

Publication number
NZ630205A
NZ630205A NZ630205A NZ63020514A NZ630205A NZ 630205 A NZ630205 A NZ 630205A NZ 630205 A NZ630205 A NZ 630205A NZ 63020514 A NZ63020514 A NZ 63020514A NZ 630205 A NZ630205 A NZ 630205A
Authority
NZ
New Zealand
Prior art keywords
enhancer
inhibitors
sarcoma
zeste homolog
tumor
Prior art date
Application number
NZ630205A
Other languages
English (en)
Inventor
Jiri Kasparec
Juan I Luengo
Neil W Johnson
William Henry Miller
Xinrong Tian
Joelle Lorraine Burgess
Dai-Shi Su
Jr Charles William Blackledge
Stuart Paul Romeril
Kenneth Allen Newlander
Mark Schulz
Steven David Knight
Iii Louis V Lafrance
Original Assignee
Glaxosmithkline Intellectual Property (No 2) Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Glaxosmithkline Intellectual Property (No 2) Ltd filed Critical Glaxosmithkline Intellectual Property (No 2) Ltd
Publication of NZ630205A publication Critical patent/NZ630205A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Epidemiology (AREA)
NZ630205A 2013-04-30 2014-04-25 Enhancer of zeste homolog 2 inhibitors NZ630205A (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201361817436P 2013-04-30 2013-04-30
US201361842038P 2013-07-02 2013-07-02
US201361907024P 2013-11-21 2013-11-21
US201461936460P 2014-02-06 2014-02-06
PCT/IB2014/061012 WO2014177982A1 (en) 2013-04-30 2014-04-25 Enhancer of zeste homolog 2 inhibitors

Publications (1)

Publication Number Publication Date
NZ630205A true NZ630205A (en) 2017-03-31

Family

ID=50877537

Family Applications (1)

Application Number Title Priority Date Filing Date
NZ630205A NZ630205A (en) 2013-04-30 2014-04-25 Enhancer of zeste homolog 2 inhibitors

Country Status (20)

Country Link
US (2) US9505745B2 (enExample)
EP (1) EP2991980B1 (enExample)
JP (1) JP6373973B2 (enExample)
KR (1) KR20160003115A (enExample)
CN (1) CN105308038B (enExample)
AU (1) AU2014261075B2 (enExample)
BR (1) BR112015027527A2 (enExample)
CA (1) CA2910873A1 (enExample)
CL (1) CL2015003200A1 (enExample)
DO (1) DOP2015000270A (enExample)
EA (1) EA030196B1 (enExample)
ES (1) ES2717680T3 (enExample)
HK (1) HK1214815A1 (enExample)
MX (1) MX2015015144A (enExample)
NZ (1) NZ630205A (enExample)
PE (1) PE20151981A1 (enExample)
PH (1) PH12015502414A1 (enExample)
SG (1) SG11201508203TA (enExample)
WO (1) WO2014177982A1 (enExample)
ZA (1) ZA201507398B (enExample)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2862289C (en) * 2012-02-10 2019-11-26 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
EP2908823B1 (en) 2012-10-15 2019-09-25 Epizyme, Inc. Methods of treating cancer
CA2910873A1 (en) * 2013-04-30 2014-11-06 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
AU2014288839B2 (en) 2013-07-10 2017-02-02 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of Zeste Homolog 2 inhibitors
WO2015118342A1 (en) 2014-02-06 2015-08-13 Heptares Therapeutics Limited Bicyclic aza compounds as muscarinic m1 receptor agonists.
WO2016066697A1 (en) * 2014-10-28 2016-05-06 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
TW201636344A (zh) * 2014-12-05 2016-10-16 美國禮來大藥廠 Ezh2抑制劑
UY36758A (es) * 2015-06-30 2016-12-30 Glaxosmithkline Ip No 2 Ltd Inhibidores del potenciador del homólogo zeste 2
EA201890567A1 (ru) 2015-08-24 2018-08-31 Эпизайм, Инк. Способ лечения рака
TW201718598A (zh) 2015-08-27 2017-06-01 美國禮來大藥廠 Ezh2抑制劑
EP3370725A4 (en) * 2015-11-06 2019-07-03 Epizyme, Inc. PEDIATRIC DOSAGE FOR THE TREATMENT OF CANCER WITH AN EZH2 INHIBITOR
KR20180081587A (ko) 2015-11-19 2018-07-16 지앙수 헨그루이 메디슨 컴퍼니 리미티드 벤조푸란 유도체, 이의 제조 방법 및 의학에서의 이의 용도
US10604531B2 (en) * 2016-05-05 2020-03-31 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
US20170337814A1 (en) * 2016-05-20 2017-11-23 Donald Edward Morgan Safety alerting drivers device and system
EA038701B1 (ru) 2016-09-07 2021-10-07 Хайхэ Биофарма Ко., Лтд. Пиридо пятичленное ароматическое циклическое соединение, способ его получения и применение
WO2018125983A1 (en) 2016-12-30 2018-07-05 Mitobridge, Inc. Oxopyridine derivatives useful as aminocarboxymuconate semialdehyde decarboxylase (acmsd) inhibitors
US10266542B2 (en) 2017-03-15 2019-04-23 Mirati Therapeutics, Inc. EZH2 inhibitors
HUE069170T2 (hu) 2018-01-31 2025-02-28 Mirati Therapeutics Inc PRC2-inhibitorok
WO2020011607A1 (en) 2018-07-09 2020-01-16 Fondation Asile Des Aveugles Inhibition of prc2 subunits to treat eye disorders
US12421228B2 (en) 2019-04-22 2025-09-23 Mirati Therapeutics, Inc. Naphthyridine derivatives as PRC2 inhibitors
BR112021024131A2 (pt) * 2019-05-31 2022-01-11 Haisco Pharmaceuticals Pte Ltd Derivado de anel inibidor de btk, método de preparação para o mesmo e aplicação farmacêutica do mesmo
KR20220027933A (ko) 2019-06-05 2022-03-08 미라티 테라퓨틱스, 인크. 암을 치료하기 위한 prc2 억제제로서의 이미다조[1,2-c]피리미딘 유도체
KR20220066892A (ko) 2019-08-22 2022-05-24 주노 쎄러퓨티크스 인코퍼레이티드 T 세포 요법 및 제스트 동족체 2의 인핸서 (ezh2) 억제제의 병용 요법 및 관련 방법
CN110964200A (zh) * 2019-12-19 2020-04-07 新纳奇材料科技江苏有限公司 一种基于聚硅氧烷馏出物的羟基封端聚硅氧烷的制备方法
CN114787143A (zh) * 2019-12-23 2022-07-22 四川海思科制药有限公司 Zeste增强子同源物2抑制剂及其用途
CN111233768B (zh) * 2020-03-18 2021-08-03 徐州圣元化工有限公司 一种3-(二氟甲基)-1-甲基-1h-吡唑-4-羧酸乙酯的制备方法
WO2023230205A1 (en) 2022-05-25 2023-11-30 Ikena Oncology, Inc. Mek inhibitors and uses thereof

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005074642A2 (en) * 2004-01-30 2005-08-18 Smithkline Beecham Corporation Chemical compounds
MXPA06010520A (es) * 2004-03-30 2007-03-26 Chiron Corp Derivados de tiofeno sustituidos como agentes anticancerosos.
US7696352B2 (en) * 2004-06-18 2010-04-13 Millennium Pharmaceuticals, Inc. Factor Xa inhibitors
AU2006325746A1 (en) 2005-12-14 2007-06-21 Bristol-Myers Squibb Company Six-membered heterocycles useful as serine protease inhibitors
AU2010281503B2 (en) * 2009-08-07 2016-01-28 Merck Patent Gmbh Novel azaheterocyclic compounds
WO2012005805A1 (en) * 2010-05-07 2012-01-12 Glaxosmithkline Llc Azaindazoles
PH12012502194A1 (en) 2010-05-07 2014-09-05 Glaxosmithkline Llc Indoles
WO2011140325A1 (en) * 2010-05-07 2011-11-10 Glaxosmithkline Llc Indazoles
WO2012075080A1 (en) 2010-12-01 2012-06-07 Glaxosmithkline Llc Indoles
AU2012223448B2 (en) * 2011-02-28 2017-03-16 Epizyme, Inc. Substituted 6,5-fused bicyclic heteroaryl compounds
JO3438B1 (ar) 2011-04-13 2019-10-20 Epizyme Inc مركبات بنزين مستبدلة بأريل أو أريل غير متجانس
TWI598336B (zh) * 2011-04-13 2017-09-11 雅酶股份有限公司 經取代之苯化合物
KR20140082742A (ko) * 2011-09-30 2014-07-02 글락소스미스클라인 엘엘씨 암을 치료하는 방법
CA2862289C (en) 2012-02-10 2019-11-26 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
DK3628670T3 (da) 2012-04-13 2022-12-05 Epizyme Inc Saltform til ezh2-hæmning
US9562041B2 (en) 2012-05-16 2017-02-07 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
CA2910873A1 (en) * 2013-04-30 2014-11-06 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors

Also Published As

Publication number Publication date
CN105308038B (zh) 2018-05-29
PE20151981A1 (es) 2016-01-14
US9505745B2 (en) 2016-11-29
EP2991980A1 (en) 2016-03-09
EA030196B1 (ru) 2018-07-31
JP2016517878A (ja) 2016-06-20
EP2991980B1 (en) 2019-01-02
CL2015003200A1 (es) 2016-04-22
AU2014261075A1 (en) 2015-11-05
US20170029412A1 (en) 2017-02-02
CA2910873A1 (en) 2014-11-06
BR112015027527A2 (pt) 2017-07-25
PH12015502414A1 (en) 2016-02-22
ZA201507398B (en) 2017-01-25
WO2014177982A1 (en) 2014-11-06
KR20160003115A (ko) 2016-01-08
JP6373973B2 (ja) 2018-08-15
ES2717680T3 (es) 2019-06-24
EA201592068A1 (ru) 2016-05-31
SG11201508203TA (en) 2015-11-27
HK1214815A1 (zh) 2016-08-05
DOP2015000270A (es) 2016-02-15
US20160102083A1 (en) 2016-04-14
AU2014261075B2 (en) 2017-01-19
US9790212B2 (en) 2017-10-17
CN105308038A (zh) 2016-02-03
MX2015015144A (es) 2016-02-18

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PSEA Patent sealed
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Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 25 APR 2019 BY THOMSON REUTERS

Effective date: 20180321

LAPS Patent lapsed