[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

SI3184523T1 - N-((4,6 dimetil-2-okso-L,2-dihidropiridin-3-IL)metil)-5-(etil (tetrahidro-2H-piran-4-IL)amino)-4-metil-4'-(morfolinometil)-(L, 1'- bifen IL)-3-karboksamid hidrobromid za uporabo pri zdravljenju celične proliferativne motnje hematološkega sistema - Google Patents

N-((4,6 dimetil-2-okso-L,2-dihidropiridin-3-IL)metil)-5-(etil (tetrahidro-2H-piran-4-IL)amino)-4-metil-4'-(morfolinometil)-(L, 1'- bifen IL)-3-karboksamid hidrobromid za uporabo pri zdravljenju celične proliferativne motnje hematološkega sistema

Info

Publication number
SI3184523T1
SI3184523T1 SI201331566T SI201331566T SI3184523T1 SI 3184523 T1 SI3184523 T1 SI 3184523T1 SI 201331566 T SI201331566 T SI 201331566T SI 201331566 T SI201331566 T SI 201331566T SI 3184523 T1 SI3184523 T1 SI 3184523T1
Authority
SI
Slovenia
Prior art keywords
methyl
dihydropyridin
morpholinomethyl
pyran
tetrahydro
Prior art date
Application number
SI201331566T
Other languages
English (en)
Inventor
Kevin Wayne Kuntz
Kuan-Chun Huang
Hyeong Wook Choi
Kristen Sanders
Steven Mathieu
Arani Chanda
Frank Fang
Original Assignee
Epizyme Inc
Eisai R&D Management Co., 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 Epizyme Inc, Eisai R&D Management Co., Ltd. filed Critical Epizyme Inc
Publication of SI3184523T1 publication Critical patent/SI3184523T1/sl

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • C07D405/02Heterocyclic 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 two hetero rings
    • C07D405/12Heterocyclic 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 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
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen 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
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyridine Compounds (AREA)
SI201331566T 2012-04-13 2013-04-11 N-((4,6 dimetil-2-okso-L,2-dihidropiridin-3-IL)metil)-5-(etil (tetrahidro-2H-piran-4-IL)amino)-4-metil-4'-(morfolinometil)-(L, 1'- bifen IL)-3-karboksamid hidrobromid za uporabo pri zdravljenju celične proliferativne motnje hematološkega sistema SI3184523T1 (sl)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201261624215P 2012-04-13 2012-04-13
EP16191716.6A EP3184523B1 (en) 2012-04-13 2013-04-11 N-((4,6-dimethyl-2-oxo-l,2-dihydropyridin-3-yl)methyl)-5-(ethyl (tetrahydro-2h-pyran-4-yl)amino)-4-methyl-4'-(morpholinomethyl)-[l,1'-biphenyl]-3-carboxamide hydrobromide for use in the treatment of a cell proliferative disorder of the hematologic system

Publications (1)

Publication Number Publication Date
SI3184523T1 true SI3184523T1 (sl) 2020-04-30

Family

ID=49328166

Family Applications (2)

Application Number Title Priority Date Filing Date
SI201330551A SI2836491T1 (sl) 2012-04-13 2013-04-11 Oblike soli inhibitorja humane histon metiltransferaze EZH2
SI201331566T SI3184523T1 (sl) 2012-04-13 2013-04-11 N-((4,6 dimetil-2-okso-L,2-dihidropiridin-3-IL)metil)-5-(etil (tetrahidro-2H-piran-4-IL)amino)-4-metil-4'-(morfolinometil)-(L, 1'- bifen IL)-3-karboksamid hidrobromid za uporabo pri zdravljenju celične proliferativne motnje hematološkega sistema

Family Applications Before (1)

Application Number Title Priority Date Filing Date
SI201330551A SI2836491T1 (sl) 2012-04-13 2013-04-11 Oblike soli inhibitorja humane histon metiltransferaze EZH2

Country Status (26)

Country Link
US (6) US9394283B2 (sl)
EP (4) EP2836491B1 (sl)
JP (3) JP6255382B2 (sl)
KR (4) KR102438340B1 (sl)
CN (2) CN104603130B (sl)
AU (2) AU2013245878B2 (sl)
BR (1) BR112014025508B1 (sl)
CA (1) CA2870005C (sl)
CY (2) CY1119383T1 (sl)
DK (3) DK3184523T3 (sl)
ES (3) ES2931316T3 (sl)
HR (2) HRP20170295T1 (sl)
HU (3) HUE045353T2 (sl)
IL (4) IL296199B2 (sl)
IN (1) IN2014DN09068A (sl)
LT (2) LT2836491T (sl)
MX (1) MX362339B (sl)
NZ (1) NZ700761A (sl)
PL (3) PL2836491T3 (sl)
PT (3) PT2836491T (sl)
RS (2) RS59392B1 (sl)
RU (1) RU2658911C2 (sl)
SG (3) SG10201608577RA (sl)
SI (2) SI2836491T1 (sl)
SM (2) SMT201900501T1 (sl)
WO (1) WO2013155317A1 (sl)

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO3438B1 (ar) 2011-04-13 2019-10-20 Epizyme Inc مركبات بنزين مستبدلة بأريل أو أريل غير متجانس
WO2013075084A1 (en) 2011-11-18 2013-05-23 Constellation Pharmaceuticals Modulators of methyl modifying enzymes, compositions and uses thereof
EP2812001B1 (en) 2012-02-10 2017-06-14 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
SG10201912111TA (en) 2012-04-13 2020-02-27 Epizyme Inc Combination therapy for treating cancer
US9394283B2 (en) * 2012-04-13 2016-07-19 Epizyme, Inc. Salt form of a human histone methyltransferase EZH2 inhibitor
US9562041B2 (en) 2012-05-16 2017-02-07 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
KR102057365B1 (ko) * 2012-10-15 2019-12-18 에피자임, 인코포레이티드 치환된 벤젠 화합물
KR20190105669A (ko) 2012-10-15 2019-09-17 에피자임, 인코포레이티드 암을 치료하는 방법
EP2970305B1 (en) 2013-03-15 2017-02-22 Constellation Pharmaceuticals, Inc. Modulators of methyl modifying enzymes, compositions and uses thereof
CA2910873A1 (en) 2013-04-30 2014-11-06 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
US9556157B2 (en) 2013-07-10 2017-01-31 Glaxosmithkline Intellectual Property (No.2) Limited Enhancer of zeste homolog 2 inhibitors
EP3033334A1 (en) 2013-08-15 2016-06-22 Constellation Pharmaceuticals, Inc. Indole derivatives as modulators of methyl modifying enzymes, compositions and uses thereof
WO2015057859A1 (en) 2013-10-16 2015-04-23 Epizyme, Inc. Hydrochloride salt form for ezh2 inhibition
JP2016533364A (ja) * 2013-10-18 2016-10-27 エピザイム,インコーポレイティド 癌を処置する方法
US9738630B2 (en) 2013-11-19 2017-08-22 Bristol-Myers Squibb Company Inhibitors of lysine methyl transferase
ES2863996T3 (es) 2013-12-06 2021-10-13 Epizyme Inc Terapia de combinación para el tratamiento del cáncer
KR20230031963A (ko) 2014-06-17 2023-03-07 에피자임, 인코포레이티드 림프종 치료를 위한 ezh2 억제제
DK3157928T3 (da) 2014-06-20 2019-05-20 Constellation Pharmaceuticals Inc Krystallinske former af 2-((4s)-6-(4-chlorphenyl)-1-methyl-4h-benzo[c]isoxazolo[4,5-e]azepin-4-yl)acetamid
AU2015331729A1 (en) 2014-10-16 2017-04-13 Epizyme, Inc. Method for treating cancer
ES2947819T3 (es) * 2014-11-17 2023-08-21 Epizyme Inc Método para el tratamiento del cáncer con N-((4,6-dimetil-2-oxo-1,2-dihidropiridin-3-il)metil)-5-(etil(tetrahidro-2H-piran-4-il)amino)-4-metil-4'-(morfolinometil)-[1,1'-bifenil]-3-carboxamida
AR102767A1 (es) 2014-12-05 2017-03-22 Lilly Co Eli Inhibidores de ezh2
SG10201902664RA (en) 2015-04-20 2019-04-29 Epizyme Inc Combination therapy for treating cancer
AU2016275051A1 (en) 2015-06-10 2017-12-07 Epizyme, Inc. EZH2 inhibitors for treating lymphoma
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
US10577350B2 (en) 2015-08-28 2020-03-03 Constellation Pharmaceuticals, Inc. Crystalline forms of (R)-N-((4-methoxy-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-2-methyl-1-(1-(1-(2,2,2-trifluoroethyl)piperidin-4-yl)ethyl)-1H-indole-3-carboxamide
CA3011186A1 (en) 2016-01-29 2017-08-03 Epizyme, Inc. Combination therapy for treating cancer
AU2017273726B2 (en) 2016-06-01 2023-10-19 Epizyme, Inc. Use of EZH2 inhibitors for treating cancer
MA45406A (fr) 2016-06-17 2019-04-24 Epizyme Inc Inhibiteurs d'ezh2 pour traiter le cancer
EP3529242A1 (en) 2016-10-19 2019-08-28 Constellation Pharmaceuticals, Inc. Synthesis of inhibitors of ezh2
WO2018137639A1 (zh) * 2017-01-25 2018-08-02 恩瑞生物医药科技(上海)有限公司 一种组蛋白甲基转移酶ezh2抑制剂、其制备方法及其医药用途
US11642346B2 (en) 2017-03-31 2023-05-09 Epizyme, Inc. Combination therapy for treating cancer
US11602529B2 (en) 2017-06-02 2023-03-14 Epizyme, Inc. Use of EZH2 inhibitors for treating cancer
JP7399079B2 (ja) 2017-09-05 2023-12-15 エピザイム,インコーポレイティド 癌を処置するための併用療法
CN112399857A (zh) 2018-07-09 2021-02-23 盲人庇护基金会 Prc2亚单位的抑制治疗眼失调
JP2022545467A (ja) 2019-08-22 2022-10-27 ジュノー セラピューティクス インコーポレイテッド T細胞療法とzesteホモログ2エンハンサー(EZH2)阻害剤との併用療法および関連方法
IL294108A (en) * 2019-12-20 2022-08-01 Epizyme Inc Crystalline hydrobromide salt of a ezh2 inhibitor, its preparation and pharmaceutical composition useful for the treatment of cancer
WO2022208552A1 (en) * 2021-03-31 2022-10-06 Msn Laboratories Private Limited, R&D Center Crystalline forms of [1,1'-Biphenyl]-3-carboxamide, N-[(1,2-dihydro-4,6-dimethyl-2-oxo-3-pyridinyl)methyl]-5-[ethyl(tetrahydro-2H-pyran-4-yl)amino]-4-methyl-4'-(4-morpholinylmethyl)-, hydrobromide (1:1) and process for its preparation thereof
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder

Family Cites Families (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0733729A (ja) 1993-07-26 1995-02-03 Kirin Brewery Co Ltd N−シアノ−n′−置換−アリールカルボキシイミダミド化合物の製造法
HUT74450A (en) 1993-12-27 1996-12-30 Eisai Co Ltd Anthranilic acid derivative and pharmaceutical compns. contg. such compds.
DE19516776A1 (de) 1995-05-10 1996-11-14 Boehringer Ingelheim Int Chromatin-Regulatorgene
US5741819A (en) 1995-06-07 1998-04-21 3-Dimensional Pharmaceuticals, Inc. Arylsulfonylaminobenzene derivatives and the use thereof as factor Xa inhibitors
JP3906935B2 (ja) 1995-12-18 2007-04-18 杏林製薬株式会社 N−置換ジオキソチアゾリジルベンズアミド誘導体及びその製造法
BR9914207A (pt) 1998-09-30 2001-07-03 Procter & Gamble Ceto-amidas 2-substituìdas
UA71587C2 (uk) 1998-11-10 2004-12-15 Шерінг Акцієнгезелльшафт Аміди антранілової кислоти та їхнє застосування як лікарських засобів
US6710058B2 (en) 2000-11-06 2004-03-23 Bristol-Myers Squibb Pharma Company Monocyclic or bicyclic carbocycles and heterocycles as factor Xa inhibitors
KR20030070082A (ko) 2000-12-28 2003-08-27 시오노기세이야쿠가부시키가이샤 칸나비노이드 2형 수용체 친화 작용을 갖는 피리돈 유도체
US7700293B2 (en) 2001-08-02 2010-04-20 The Regents Of The University Of Michigan Expression profile of prostate cancer
TW200303304A (en) * 2002-02-18 2003-09-01 Astrazeneca Ab Chemical compounds
JPWO2003070277A1 (ja) 2002-02-19 2005-06-09 塩野義製薬株式会社 抗掻痒剤
TW200306155A (en) 2002-03-19 2003-11-16 Du Pont Benzamides and advantageous compositions thereof for use as fungicides
US7442685B2 (en) 2003-06-13 2008-10-28 The University Of North Carolina At Chapel Hill DOT1 histone methyltransferases as a target for identifying therapeutic agents for leukemia
CN1989131A (zh) * 2004-03-30 2007-06-27 希龙公司 取代的噻吩衍生物用作抗癌药
WO2005118796A2 (en) 2004-06-01 2005-12-15 The University Of North Carolina At Chapel Hill Reconstituted histone methyltransferase complex and methods of identifying modulators thereof
JO2787B1 (en) 2005-04-27 2014-03-15 امجين إنك, Alternative amide derivatives and methods of use
WO2006130720A2 (en) 2005-06-02 2006-12-07 University Of North Carolina At Chapel Hill Purification, characterization and reconstitution of a ubiquitin e3 ligase
FR2889526B1 (fr) 2005-08-04 2012-02-17 Aventis Pharma Sa 7-aza-indazoles substitues, compositions les contenant, procede de fabrication et utilisation
PT1940821E (pt) 2005-10-19 2013-05-29 Gruenenthal Gmbh Novos ligandos do receptor de vanilóide e seu uso para a produção de medicamentos
ATE510822T1 (de) 2005-10-21 2011-06-15 Merck Sharp & Dohme Kaliumkanalinhibitoren
CA2622615A1 (en) 2005-10-28 2007-05-10 The University Of North Carolina At Chapel Hill Protein demethylases comprising a jmjc domain
EP1966141A1 (en) 2005-12-14 2008-09-10 Brystol-Myers Squibb Company Six-membered heterocycles useful as serine protease inhibitors
EP1974055A4 (en) 2006-01-20 2010-01-27 Univ North Carolina DIAGNOSTIC AND THERAPEUTIC OBJECTIVES AGAINST LEUKEMIA
MX2008014616A (es) 2006-05-15 2008-11-28 Irm Llc Compuestos y composiciones de tereftalamato, y su uso como inhibidores de integrasa de vih.
US20070287706A1 (en) 2006-05-18 2007-12-13 Dickson John K Jr Certain substituted quinolones, compositions, and uses thereof
JP2010505958A (ja) 2006-10-10 2010-02-25 バーンハム インスティトゥート フォー メディカル リサーチ 神経防護作用組成物および方法
JP2010519204A (ja) 2007-02-16 2010-06-03 アムジエン・インコーポレーテツド 窒素含有複素環ケトン類およびそれらのc−Met阻害薬としての使用
WO2008104077A1 (en) 2007-02-28 2008-09-04 Methylgene Inc. Small molecule inhibitors of protein arginine methyltransferases (prmts)
WO2008113006A1 (en) 2007-03-14 2008-09-18 Xenon Pharmaceuticals Inc. Methods of using quinolinone compounds in treating sodium channel-mediated diseases or conditions
DE102007017884A1 (de) 2007-04-13 2008-10-16 Grünethal GmbH Neue Vanilloid-Rezeptor Liganden und ihre Verwendung zur Herstellung von Arzneimitteln
WO2009006577A2 (en) 2007-07-03 2009-01-08 The Regents Of The University Of Michigan Compositions and methods for inhibiting ezh2
DE102007047737A1 (de) * 2007-10-05 2009-04-30 Merck Patent Gmbh Piperidin- und Piperazinderivate
WO2009058298A1 (en) 2007-10-31 2009-05-07 Merck & Co., Inc. P2x3, receptor antagonists for treatment of pain
PL2229391T3 (pl) 2007-12-19 2015-02-27 Cancer Research Tech Ltd Pirydo[2,3-b]pirazyno-8-podstawione związki i ich zastosowanie
WO2009124137A2 (en) 2008-04-01 2009-10-08 Mount Sinai School Of Medicine Of New York University Method of suppressing gene transcription through histone lysine methylation
US20100113415A1 (en) 2008-05-29 2010-05-06 Rajapakse Hemaka A Epha4 rtk inhibitors for treatment of neurological and neurodegenerative disorders and cancer
EP2323660A2 (en) 2008-08-08 2011-05-25 New York Blood Center Small molecule inhibitors of retroviral assembly and maturation
FR2934995B1 (fr) 2008-08-14 2010-08-27 Sanofi Aventis Composes d'azetidines polysubstitues, leur preparation et leur application en therapeutique
US20120065247A1 (en) 2009-03-27 2012-03-15 Discoverybiomed, Inc. Modulating ires-mediated translation
US20110021362A1 (en) 2009-07-20 2011-01-27 Constellation Pharmaceuticals Agents for stimulating activity of methyl modifying enzymes and methods of use thereof
CA2784899A1 (en) 2009-12-30 2011-07-07 Avon Products, Inc. Topical lightening composition and uses thereof
US8846935B2 (en) * 2010-05-07 2014-09-30 Glaxosmithkline Llc Indazoles
WO2012005805A1 (en) * 2010-05-07 2012-01-12 Glaxosmithkline Llc Azaindazoles
LT2566327T (lt) * 2010-05-07 2017-05-25 Glaxosmithkline Llc Indolai
US9175331B2 (en) 2010-09-10 2015-11-03 Epizyme, Inc. Inhibitors of human EZH2, and methods of use thereof
BR112013005806B1 (pt) 2010-09-10 2022-05-10 Epizyme, Inc Métodos para detectar se um indivíduo é um candidato para o tratamento com ou responsivo a um inibidor de ezh2 e usos terapêuticos do dito inibidor de ezh2
US20130310379A1 (en) 2010-11-19 2013-11-21 Constellation Pharmaceuticals Modulators of methyl modifying enzymes, compositions and uses thereof
WO2012075080A1 (en) 2010-12-01 2012-06-07 Glaxosmithkline Llc Indoles
RU2013130253A (ru) 2010-12-03 2015-01-10 Эпизайм, Инк. 7-деазапуриновые регуляторы метилтрансферазы гистонов и способы их применения
EP2681216B1 (en) 2011-02-28 2017-09-27 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
EP2825161B1 (en) 2012-03-12 2019-01-02 Epizyme, Inc. Inhibitors of human ezh2, and methods of use thereof
SG10201912111TA (en) 2012-04-13 2020-02-27 Epizyme Inc Combination therapy for treating cancer
US9394283B2 (en) * 2012-04-13 2016-07-19 Epizyme, Inc. Salt form of a human histone methyltransferase EZH2 inhibitor
US9562041B2 (en) 2012-05-16 2017-02-07 Glaxosmithkline Llc Enhancer of zeste homolog 2 inhibitors
KR20190105669A (ko) 2012-10-15 2019-09-17 에피자임, 인코포레이티드 암을 치료하는 방법
WO2015057859A1 (en) 2013-10-16 2015-04-23 Epizyme, Inc. Hydrochloride salt form for ezh2 inhibition

Also Published As

Publication number Publication date
AU2018200168A1 (en) 2018-02-01
CN104603130B (zh) 2018-04-27
US20180243316A1 (en) 2018-08-30
HUE045353T2 (hu) 2019-12-30
KR20150002730A (ko) 2015-01-07
ES2617379T3 (es) 2017-06-16
PL3628670T3 (pl) 2023-02-20
KR20200066380A (ko) 2020-06-09
KR20250005505A (ko) 2025-01-09
IL296199B1 (en) 2024-08-01
KR102438340B1 (ko) 2022-08-30
MX2014012380A (es) 2015-07-23
CN108358899A (zh) 2018-08-03
CA2870005C (en) 2021-06-22
IL282732B (en) 2022-12-01
RS59392B1 (sr) 2019-11-29
US9394283B2 (en) 2016-07-19
JP2018199740A (ja) 2018-12-20
US11491163B2 (en) 2022-11-08
US10245269B2 (en) 2019-04-02
IN2014DN09068A (sl) 2015-05-22
IL235045A0 (en) 2014-12-31
DK2836491T3 (en) 2017-03-06
PL2836491T3 (pl) 2017-08-31
EP4190777A1 (en) 2023-06-07
PT3628670T (pt) 2022-12-02
JP2018002742A (ja) 2018-01-11
EP3184523B1 (en) 2019-06-19
RS55690B1 (sr) 2017-07-31
SMT201700132T1 (it) 2017-05-08
IL282732B2 (en) 2023-04-01
AU2018200168B2 (en) 2019-08-29
SMT201900501T1 (it) 2019-11-13
WO2013155317A1 (en) 2013-10-17
US20150065503A1 (en) 2015-03-05
EP3184523A1 (en) 2017-06-28
SI2836491T1 (sl) 2017-06-30
CN108358899B (zh) 2021-07-27
ES2745016T3 (es) 2020-02-27
IL282732A (en) 2021-06-30
IL266165A (en) 2019-06-30
HUE060881T2 (hu) 2023-04-28
KR102120883B1 (ko) 2020-06-09
EP3628670B1 (en) 2022-10-12
SG10201608577RA (en) 2016-12-29
US20170143729A1 (en) 2017-05-25
EP2836491A1 (en) 2015-02-18
HUE031976T2 (en) 2017-08-28
ES2931316T3 (es) 2022-12-28
CY1122883T1 (el) 2022-03-24
LT3184523T (lt) 2020-02-10
IL296199A (en) 2022-11-01
LT2836491T (lt) 2017-03-27
BR112014025508B1 (pt) 2020-11-17
CA2870005A1 (en) 2013-10-17
SG11201406468YA (en) 2015-01-29
AU2013245878B2 (en) 2017-10-12
JP2015512942A (ja) 2015-04-30
KR102744039B1 (ko) 2024-12-17
EP3628670A1 (en) 2020-04-01
EP2836491A4 (en) 2015-09-16
KR20220123339A (ko) 2022-09-06
DK3184523T3 (da) 2019-08-19
PL3184523T3 (pl) 2019-12-31
US20190269692A1 (en) 2019-09-05
IL235045B (en) 2019-05-30
DK3628670T3 (da) 2022-12-05
PT3184523T (pt) 2019-09-26
HRP20191653T1 (hr) 2020-02-21
JP6634058B2 (ja) 2020-01-22
RU2658911C2 (ru) 2018-06-26
EP2836491B1 (en) 2016-12-07
US20230140327A1 (en) 2023-05-04
CY1119383T1 (el) 2018-02-14
AU2013245878A1 (en) 2014-10-30
IL266165B (en) 2021-06-30
PT2836491T (pt) 2017-02-08
US20210137936A1 (en) 2021-05-13
NZ700761A (en) 2016-09-30
MX362339B (es) 2019-01-11
SG10201912109QA (en) 2020-02-27
US9872862B2 (en) 2018-01-23
US10821113B2 (en) 2020-11-03
RU2014145544A (ru) 2016-06-10
HRP20170295T1 (hr) 2017-04-21
IL296199B2 (en) 2024-12-01
JP6255382B2 (ja) 2017-12-27
CN104603130A (zh) 2015-05-06

Similar Documents

Publication Publication Date Title
SI3184523T1 (sl) N-((4,6 dimetil-2-okso-L,2-dihidropiridin-3-IL)metil)-5-(etil (tetrahidro-2H-piran-4-IL)amino)-4-metil-4'-(morfolinometil)-(L, 1'- bifen IL)-3-karboksamid hidrobromid za uporabo pri zdravljenju celične proliferativne motnje hematološkega sistema
SI3220916T1 (sl) Postopek zdravljenja raka z n-((4,6-dimetil-2-okso-1,2-dihidropiridin-3 -il)metil)-5-(etil(tetrahidro-2h-piran-4-il) amino)-4-metil-4'- (morfolinometil)-(1,1'-bifenil)-3-karboksamidom
BR112015003332A2 (pt) composto, composição farmacêutica, uso do composto e método para tratar uma doença ou condição mediada por rorgammat em um paciente
BR112015003398A2 (pt) composto, composição farmacêutica, uso do composto e método para tratar uma doença ou condição mediada por rorgammat em um paciente
HK1246159A1 (zh) 用於治療中樞系統疾病的包含依匹哌唑或其鹽和第二種藥物的組合
BR112013025386A2 (pt) combinação de um composto, composto de fórmula ia ou um sal farmaceuticamente aceitável do mesmo, método para tratamento de uma doença ou afecção modulada por mutação braf v600e e altos níveis de pakt em um mamífero e uso
BR112015003376A2 (pt) composto ou sal farmaceuticamente aceitável do mesmo , composição farmacêutica e usos de quantidade eficiente
BR112015003397A2 (pt) composto, composição farmacêutica, uso do composto e método para tratar uma doença ou condição mediada por rorgammat em um paciente.
IL237369B (en) N-]2-(6-fluoro-h1-indol-3-yl)ethyl]-3-(2, 2, 3, 3- tetrafluoropropoxy) benzylamine in combination with an acetylcholinesterase inhibitor for the treatment of Alzheimer's disease
EP2739337A4 (en) ARRANGEMENTS, SYSTEMS AND METHOD FOR INFUSING THERAPEUTICS IN THE BODY
BR112015002541A2 (pt) composto, composição farmacêutica, uso de um composto, e, método para tratamento de hcv em um paciente.
EP2726141A4 (en) DEVICE, SYSTEM AND METHODS FOR ORAL DELIVERY OF THERAPEUTIC COMPOUNDS
HK1199712A1 (en) 18-methyl-6,7-methylene-3-oxo-17-pregn-4-ene-21,17-carbolactones, pharmaceutical preparations comprising said compounds and use thereof in the treatment of endometriosis 18--67--3--17--4--2117-
HK1245833B (zh) 用於治療、預防或緩解疼痛的融合蛋白和方法
IL228600B (en) (Aralkylamino and heteroarylalkylamino alpha-converted) pyrimidinyl and 1,3,5-triazinyl benzaimidazoles, pharmaceutical preparations containing them and use of these compounds in the treatment of proliferative diseases
BR112014029705A2 (pt) composto ou sal, medicamento, métodos para inibir quinase de janus em um mamífero, e para a profilaxia ou tratamento de doenças autoimunes, e, uso de um composto ou sal
ZA201408836B (en) N-(tetrazol-5-yl)-and n-(triazol-5-yl)arylcarboxamide salts and use thereof as herbicides
HK1196819A1 (zh) 雜環化合物、含有所述化合物的藥物及其用途和其製備方法
IL232333A0 (en) N-(pyrid-4-yl)amides and n-(pyrimidin-4-yl)amides and their pharmaceutical and cosmetic use
PL2905268T3 (pl) Kompozycja do traktowania stref zaszpachlowanych gipsem, wykańczanych gipsem albo tynkowanych gipsem i jej zastosowanie do traktowania stref zaszpachlowanych gipsem, wykańczanych gipsem albo tynkowanych gipsem
EA201491609A1 (ru) Модуляторы x рецепторов печени
BR112013025397A2 (pt) combinação de um composto, composto de fórmula i ou um sal farmaceuticamente aceitável do mesmo, uso, kit, produto, método para tratamento de um distúrbio hiperproliferativo e método para tratamento de uma doença ou afecção modulada por quinase akt em um mamífero
BRPI0806529A2 (pt) Composto ou um sal farmaceuticamente aceitável do mesmo, composição farmacêutica, uso de um composto, e, método de tratamento de um distúrbio de agregação de plaqueta
NZ630033A (en) Crystalline forms of 1-(3-tert-butyl-1-p-tolyl-1h-pyrazol-5-yl)-3-(5-fluoro-2-(1-(2-hydroxyethyl)-indazol-5-yloxy)benzyl)urea hydrochloride
PL396023A1 (pl) Nowy 2"-(2"'-hydroksyizopropylo) -dihydrofurano[2", 3";3',4']-2',4-dihydroksy-6'-metoksydihydrochalkon i sposób jego wytwarzania