MA52288A - Modulateurs d'enzymes de modification de méthyle, compositions et utilisations de ceux-ci - Google Patents

Modulateurs d'enzymes de modification de méthyle, compositions et utilisations de ceux-ci

Info

Publication number
MA52288A
MA52288A MA052288A MA52288A MA52288A MA 52288 A MA52288 A MA 52288A MA 052288 A MA052288 A MA 052288A MA 52288 A MA52288 A MA 52288A MA 52288 A MA52288 A MA 52288A
Authority
MA
Morocco
Prior art keywords
compositions
methyl modification
modification enzyme
enzyme modulators
modulators
Prior art date
Application number
MA052288A
Other languages
English (en)
Inventor
Alexandre Côté
Victor S Gehling
Avinash Khanna
Ludivine Moine
Jacob I Stuckey
Original Assignee
Constellation Pharmaceuticals Inc
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 Constellation Pharmaceuticals Inc filed Critical Constellation Pharmaceuticals Inc
Publication of MA52288A publication Critical patent/MA52288A/fr

Links

Classifications

    • 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
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/443Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with oxygen as a ring hetero atom
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • 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
    • 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
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
MA052288A 2018-04-18 2019-04-17 Modulateurs d'enzymes de modification de méthyle, compositions et utilisations de ceux-ci MA52288A (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201862659408P 2018-04-18 2018-04-18

Publications (1)

Publication Number Publication Date
MA52288A true MA52288A (fr) 2021-04-07

Family

ID=66429588

Family Applications (1)

Application Number Title Priority Date Filing Date
MA052288A MA52288A (fr) 2018-04-18 2019-04-17 Modulateurs d'enzymes de modification de méthyle, compositions et utilisations de ceux-ci

Country Status (22)

Country Link
US (3) US10689371B2 (fr)
EP (1) EP3781561B1 (fr)
JP (2) JP7256823B2 (fr)
KR (1) KR20210003160A (fr)
CN (1) CN111989325A (fr)
AR (1) AR114793A1 (fr)
AU (1) AU2019255310B2 (fr)
BR (1) BR112020021194A2 (fr)
CA (1) CA3098428A1 (fr)
CL (1) CL2020002698A1 (fr)
CO (1) CO2020014217A2 (fr)
CR (1) CR20200553A (fr)
EA (1) EA202092490A1 (fr)
IL (1) IL278013B2 (fr)
MA (1) MA52288A (fr)
MX (1) MX2020010999A (fr)
PE (1) PE20201448A1 (fr)
PH (1) PH12020551578A1 (fr)
SG (1) SG11202009438UA (fr)
TW (1) TWI828677B (fr)
UA (1) UA127357C2 (fr)
WO (1) WO2019204490A1 (fr)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20210003160A (ko) 2018-04-18 2021-01-11 콘스텔레이션 파마슈티칼스, 인크. 메틸 변형 효소 조절제, 이의 조성물 및 용도
CN112262143A (zh) 2018-05-21 2021-01-22 星座制药公司 甲基修饰酶的调节剂、其组合物和用途
BR112022001154A2 (pt) * 2019-07-24 2022-06-07 Constellation Pharmaceuticals Inc Terapias de inibição de ezh2 para o tratamento de cânceres
CA3148447A1 (fr) * 2019-07-24 2021-01-28 Constellation Pharmaceuticals, Inc. Formes cristallines de 7-chloro-2-(4-(3-methoxyazetidine-1-yl))cyclohexyl) 2,4-dimethyl-n-((6-methyl-4-(methylthio)-2-oxo-1,2-dihydropyridine-3-yl) methyl)benzo[d][1,3]dioxole-5-c arboxamide
CN115175905A (zh) * 2020-03-13 2022-10-11 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
CN116018335A (zh) * 2020-07-08 2023-04-25 第一三共株式会社 用于制备1,3-苯并二氧杂环戊烯衍生物的方法
WO2022109106A1 (fr) * 2020-11-18 2022-05-27 Constellation Pharmaceuticals, Inc Thérapies d'inhibition de l'ezh2 pour le traitement de cancers de la prostate ayant subi une mutation du récepteur des androgènes
KR20220101295A (ko) 2021-01-11 2022-07-19 주식회사 엘지에너지솔루션 전극 슬러리의 유량 제어가 가능한 전극 슬러리 코팅 시스템 및 이를 이용한 전극 슬러리 코팅 방법
KR20230110210A (ko) * 2022-01-14 2023-07-21 동화약품주식회사 1,3-벤조다이옥솔 유도체 화합물 및 이를 포함하는 약학적 조성물
CN116496263A (zh) * 2022-01-27 2023-07-28 江苏天士力帝益药业有限公司 Ezh1/2抑制剂及其制备和抗肿瘤治疗中的应用
WO2023217018A1 (fr) * 2022-05-07 2023-11-16 贝达药业股份有限公司 Inhibiteur d'ezh2 et son utilisation en médecine
WO2023244917A1 (fr) 2022-06-13 2023-12-21 Treeline Biosciences, Inc. Agents dégradant bcl6 hétérobifonctionnels 1,8-naphthyridin-2-one
WO2023244918A1 (fr) 2022-06-13 2023-12-21 Treeline Biosciences, Inc. Agents de dégradation bifonctionnels de quinolone bcl6
WO2024038115A1 (fr) 2022-08-17 2024-02-22 Morphosys Ag Thérapie comprenant un anticorps anti-cd19 et des modulateurs d'ezh2

Family Cites Families (131)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6317850A (ja) 1986-07-11 1988-01-25 Fuji Photo Film Co Ltd 3−フエノキシカテコ−ル類の製造方法
DK611489A (da) 1988-12-08 1990-06-09 Duphar Int Res Anxiolytisk aktive piperazinderivater og farmaceutiske praeparater med indhold af saadanne forbindelser
JPH02255674A (ja) 1989-03-27 1990-10-16 Fuji Photo Film Co Ltd 4―アリールオキシ―1,3―ベンゾジオキソール類およびその製造方法
JPH02255673A (ja) 1989-03-27 1990-10-16 Fuji Photo Film Co Ltd 4―アリールオキシー1,3―ベンゾジオキソール類およびその製造方法
JPH02269352A (ja) 1989-04-10 1990-11-02 Fuji Photo Film Co Ltd 感光材料
JP2537682B2 (ja) 1989-04-21 1996-09-25 富士写真フイルム株式会社 3―アリ―ルオキシカテコ―ル類の製造方法
US5296497A (en) 1989-05-16 1994-03-22 Duphar International Research B.V. 3,4-dehydropiperidine derivatives having psychotropic activity
JPH03130280A (ja) 1989-10-17 1991-06-04 Fuji Photo Film Co Ltd 4―アリールオキシ―1,3―ベンゾジオキソール類の製造方法
JP2816492B2 (ja) 1990-05-23 1998-10-27 コニカ株式会社 ハロゲン化銀写真感光材料
JPH0446175A (ja) 1990-06-14 1992-02-17 Fuji Photo Film Co Ltd 5―ヒドロキシ―3,4―メチレンジオキシ安息香酸誘導体の製造法
JPH0641038A (ja) 1992-07-17 1994-02-15 Mitsubishi Kasei Corp カルボン酸誘導体
DE4326151A1 (de) 1993-08-04 1995-02-09 Hoechst Ag Aromatische Verbindungen und ihre Verwendung in flüssigkristallinen Mischungen
US5629200A (en) 1993-11-18 1997-05-13 Daicel Chemical Industries, Ltd. Production of optically active 2-amino-1-phenylethanol derivatives by asymetrical assimilation
US5514505A (en) 1995-05-15 1996-05-07 Xerox Corporation Method for obtaining improved image contrast in migration imaging members
NZ331549A (en) 1996-01-29 2000-09-29 Univ California Compounds useful in treating sexual dysfunction
US5968929A (en) 1996-10-30 1999-10-19 Schering Corporation Piperazino derivatives as neurokinin antagonists
JPH10287654A (ja) 1997-04-11 1998-10-27 Nissan Chem Ind Ltd ピラゾロン誘導体及び除草剤
BR9814106A (pt) 1997-10-27 2000-10-03 Cortex Pharma Inc Processo para tratar da esquizofrenia em um indivìduo, e, conjunto
KR100705142B1 (ko) 1998-09-29 2007-04-06 와이어쓰 홀딩스 코포레이션 단백질 티로신 키나제 억제제로서 치환 3-시아노퀴놀린
EP1384713B1 (fr) * 1998-12-23 2008-10-15 SmithKline Beecham Corporation Derives de 4-amino-azepan-3-one comme inhibiteurs de protease
US7977333B2 (en) 2000-04-20 2011-07-12 Bayer Healthcare Llc Substituted pyridines and pyridazines with angiogenesis inhibiting activity
US6451814B1 (en) 2000-07-17 2002-09-17 Wyeth Heterocyclic β-3 adrenergic receptor agonists
EE05387B1 (et) 2000-08-21 2011-02-15 Astrazenecaab KinasoliiniÁderivaadid,ÁnendeÁvalmistamismeetodÁjaÁkasutamine
AU2001281246A1 (en) 2000-08-23 2002-03-04 The Procter And Gamble Company Benzimidazoles and analogues and their use as neutrophil inhibitors
AU2001286702B2 (en) 2000-08-24 2008-03-13 University Of Pittsburgh Thioflavin derivatives and their use in diagnosis and theraphy of alzheimer's disease
AUPR255401A0 (en) 2001-01-16 2001-02-08 Novogen Research Pty Ltd Regulation of lipids and/or bone density and compositions therefor
EP1368024A4 (fr) 2001-03-16 2009-03-18 Novogen Res Pty Ltd Traitement de la restenose
JP4172541B2 (ja) 2001-04-09 2008-10-29 ノバルティス バクシンズ アンド ダイアグノスティックス, インコーポレーテッド グアニジノ化合物
EP1381599B1 (fr) 2001-04-19 2008-09-24 Astrazeneca AB Derives quinazoline
DE10148618B4 (de) 2001-09-25 2007-05-03 Schering Ag Substituierte N-(1,4,5,6-Tetrahydro-cyclopentapyrazol-3-yl)-Derivate, deren Herstellung und Verwendung als Arzneimittel
DE10148617A1 (de) 2001-09-25 2003-04-24 Schering Ag Substituierte N-(1,4,5,6-Tetrahydro-cyclopentapyrazol-3-yl)-Derivate, deren Herstellung und Verwendung als Arzneimittel
AUPR846401A0 (en) 2001-10-25 2001-11-15 Novogen Research Pty Ltd 6-Hydroxy isoflavones, derivatives and medicaments involving same
EP1503986B1 (fr) 2001-12-21 2015-09-30 Cytokinetics, Inc. Compositions et methodes permettant de traiter l'insuffisance cardiaque
AU2003219652A1 (en) 2002-01-08 2003-07-30 Eisai Co. Ltd. Eponemycin and epoxomicin analogs and uses thereof
WO2003062392A2 (fr) 2002-01-18 2003-07-31 Ceretek Llc Procedes pour traiter des pathologies associees a un recepteur d'edg
US7196108B2 (en) 2002-03-08 2007-03-27 Incyte San Diego Inc. Bicyclic heterocycles for the treatment of diabetes and other diseases
WO2003086386A1 (fr) 2002-04-09 2003-10-23 Novogen Research Pty Ltd Procedes therapeutiques et compositions associees contenant des structures isoflav-3-ene et isoflavan
DE10219294A1 (de) 2002-04-25 2003-11-13 Schering Ag Substituierte N-(1,4,5,6-Tetrahydro-cyclopentapyrazol-3-yl)-Derivate, deren Herstellung und Verwendung als Arzneimittel
CN100486973C (zh) 2002-07-29 2009-05-13 霍夫曼-拉罗奇有限公司 新苯并间二氧杂环戊烯类
AU2002951271A0 (en) 2002-09-06 2002-09-19 Novogen Research Pty Ltd Repair of dna mutagenic damage
JP2006508058A (ja) 2002-09-23 2006-03-09 ノボジェン・リサーチ・プロプライエタリー・リミテッド 皮膚光老化および光線性損傷の治療
JP4908210B2 (ja) 2003-07-28 2012-04-04 メルク セローノ ソシエテ アノニム Pi3キナーゼ阻害剤として使用するための2−イミノ−4−(チオ)オキソ−5−ポリシクロビニルアゾリン類
CA2539117A1 (fr) 2003-09-24 2005-04-07 Methylgene Inc. Inhibiteurs d'histone deacetylase
CA2546643A1 (fr) 2003-11-18 2005-06-02 Novogen Research Pty Ltd Promedicaments a base d'isoflavonoides, compositions de ces promedicaments et procedes therapeutiques les impliquant
EP1686981A4 (fr) 2003-11-19 2011-02-23 Novogen Res Pty Ltd Compositions et procedes de radiotherapie et de chimiotherapie combinatoires
GT200500008A (es) 2004-01-16 2005-08-16 Intermediarios de quinolina como inhibidores de receptores de tirosina quinasas y la sintesis de los mismos
AR048528A1 (es) 2004-04-07 2006-05-03 Millennium Pharm Inc Compuestos derivados de quinolina como antagonistas del receptor de pgd2 para el tratamiento de enfermedades inflamatorias y composiciones farmacéuticas que los contienen.
US20050245529A1 (en) 2004-04-14 2005-11-03 Boehringer Ingelheim International Gmbh Alkyne compounds with MCH antagonistic activity and medicaments comprising these compounds
US7846959B2 (en) 2004-05-07 2010-12-07 Exelixis, Inc. Raf modulators and methods of use
MXPA06013250A (es) 2004-05-14 2007-02-28 Abbott Lab Inhibidores de quinasa como agentes terapeuticos.
ITMI20041347A1 (it) 2004-07-05 2004-10-05 Italfarmaco Spa Derivati di alfa-amminoacidi ad attivita'antiinfiammatoria
SE0401971D0 (sv) 2004-08-02 2004-08-02 Astrazeneca Ab Piperidne derivatives
MX2007004302A (es) 2004-10-12 2007-06-07 Applied Research Systems Inhibidores de pi3 cinasa gamma para el tratamiento de anemia.
SE0402635D0 (sv) 2004-10-29 2004-10-29 Astrazeneca Ab Chemical compounds
JP2006145294A (ja) 2004-11-17 2006-06-08 Univ Nagoya 蛍光標識を行うラベル化試薬、リガンドを表面にもつ基材の製造方法及びラベル化試薬を用いた測定方法
US7524870B2 (en) 2004-12-03 2009-04-28 Hoffmann-La Roche Inc. Biaryloxymethylarenecarboxylic acids as glycogen synthase activators
SI1859793T1 (sl) 2005-02-28 2011-08-31 Eisai R&D Man Co Ltd Nova kombinirana uporaba sulfonamidne spojine za zdravljenje raka
US20060223846A1 (en) 2005-03-08 2006-10-05 Dyatkin Alexey B Aza-bridged-bicyclic amino acid derivatives as alpha4 integrin antagonists
EP1893605A2 (fr) 2005-03-31 2008-03-05 AstraZeneca AB Derives de s-aminopyrimidine inhibiteurs de tie2
KR20070120182A (ko) 2005-04-08 2007-12-21 바이엘 파마슈티칼스 코포레이션 피리미딘 유도체 및 암의 치료에서의 이의 용도
ES2614080T3 (es) 2005-05-17 2017-05-29 Sarcode Bioscience Inc. Composiciones y métodos para el tratamiento de trastornos oculares
RU2007139544A (ru) 2005-05-25 2009-06-27 Вайет (Us) Способ получения 3-цианохинолинов и промежуточные соединения, полученные согласно данному способу
WO2006129609A1 (fr) 2005-05-30 2006-12-07 Shionogi & Co., Ltd. Derive 2-naphtylimino-5,5-disubstitue-1,3-thiazine
AU2006252768A1 (en) 2005-06-02 2006-12-07 Bayer Cropscience Ag Phenylalkyl substituted heteroaryl devivatives
WO2006138418A2 (fr) 2005-06-14 2006-12-28 President And Fellows Of Harvard College Amelioration de la performance cognitive avec des activateurs de sirtuine
EP1904069B1 (fr) 2005-07-15 2018-06-13 Albany Molecular Research, Inc. Tetrahydrobenzazepines substituees par aryle et heteroaryle, et leur utilisation pour bloquer la reabsorption de la noradrenaline, de la dopamine, et de la serotonine
CA2616224A1 (fr) 2005-07-21 2007-02-01 Paratek Pharmaceuticals, Inc. Tetracyclines 10-substituees et leurs procedes d'utilisation
WO2007019083A1 (fr) 2005-08-04 2007-02-15 Janssen Pharmaceutica N.V. Composes de pyrimidine utiles comme modulateurs des recepteurs de la serotonine
US7737166B2 (en) 2005-08-17 2010-06-15 Daiichi Sankyo Company, Limited Antifungal bicyclic hetero ring compounds
WO2007081630A2 (fr) 2005-12-21 2007-07-19 Janssen Pharmaceutica, N.V. Inhibiteurs substitues de la pyrimidinyl kinase
CN101007798B (zh) 2006-01-24 2011-01-26 中国人民解放军军事医学科学院毒物药物研究所 苯并间二氧杂环戊烯衍生物及其制备方法和医药用途
EA015198B1 (ru) 2006-03-23 2011-06-30 Биота Юроп Лимитед Антибактериальные агенты
KR101458194B1 (ko) 2006-05-30 2014-11-03 뉴로서치 에이/에스 신규한 1,4―디아자―비사이클로[3.2.2]노닐 옥사디아졸릴 유도체 및 이의 의학적 용도
US20100035877A1 (en) 2006-06-26 2010-02-11 Katz David M Methods and compositions for treating pathologies associated with bdnf signaling
WO2008029168A2 (fr) 2006-09-08 2008-03-13 Summit Corporation Plc Traitement de la dystrophie musculaire de duchenne
CA2668008A1 (fr) 2006-10-30 2008-05-08 Novogen Research Pty Ltd Prevention et inversion de la neuropathie peripherique induite par une chimiotherapie
RU2333211C1 (ru) 2006-11-01 2008-09-10 Институт физиологически активных веществ Российской Академии наук N,n`-замещенные 3, 7-диазабицикло[3.3.1]нонаны, обладающие фармакологической активностью, фармацевтические композиции на их основе и способ их применения
MX2009011923A (es) 2007-05-10 2009-11-18 Amr Technology Inc Tetrahidrobenzo-1,4-diazepinas aril- y heteroaril-sustituidas y uso de las mismas para bloquear reabsorcion de norepinefrina, dopamina y serotonina.
BRPI0704074B8 (pt) 2007-08-29 2021-05-25 Univ Estadual Paulista Julio De Mesquita Filho Unesp derivados piperidínicos da (-)-cassina e (-)-spectalina, composições farmacêuticas contendo os mesmos e processos para sua preparação
ES2830024T3 (es) 2007-10-19 2021-06-02 Novartis Ag Composiciones y métodos para el tratamiento del edema macular
KR20100132550A (ko) 2008-04-16 2010-12-17 포톨라 파마슈티컬스, 인코포레이티드 syk 또는 JAK 키나제 억제제로서의 2,6-디아미노-피리미딘-5-일-카르복스아미드
WO2010008761A1 (fr) 2008-06-23 2010-01-21 Janssen Pharmaceutica Nv Antagonistes pipéridyl-acrylamide de ccr2
WO2010019772A2 (fr) 2008-08-14 2010-02-18 The United States Of America, As Represented By The Secretary, Department Of Health And Human Services Oxadiazole-2-oxydes en tant qu'agents antischistosomiaux
JP2010254629A (ja) 2009-04-27 2010-11-11 Bayer Cropscience Ag 光学活性アゾリン誘導体
US9206173B2 (en) 2009-05-28 2015-12-08 Otsuka Pharmaceutical Co., Ltd. Heterocyclic compounds for the treatment of stress-related conditions
AU2010270153A1 (en) 2009-07-10 2012-02-02 Vivalis Substituted pyrrolidinone as inhibitors of hepatitis C NS5B polymerase, the pharmaceutical composition thereof and their therapeutic use
RU2417082C2 (ru) 2009-07-14 2011-04-27 Учреждение Российской Академии Наук Институт Физиологически Активных Веществ Ран (Ифав Ран) Средство для восстановления утраченной памяти в норме и патологии у пациентов всех возрастных групп на основе n, n'-замещенных 3, 7-диазабицикло[3.3.1]нонанов, фармацевтическая композиция на его основе и способ ее применения
US9150813B2 (en) 2009-12-17 2015-10-06 The Lubrizol Corporation Lubricating composition containing an aromatic compound
RU2535664C2 (ru) 2010-01-27 2014-12-20 Аб Фарма Лтд Полигетероциклические соединения, используемые в качестве высокоэффективных ингибиторов вируса гепатита с
CN101851218B (zh) 2010-04-27 2014-10-15 沈阳药科大学 4,5-二取代芳基异硒唑类衍生物及其用途
US20130338153A1 (en) 2010-06-10 2013-12-19 Afraxis, Inc. 8-(2'-heterocycyl)pyrido[2.3-d]pyrimidin-7(8h)-ones for the treatment of cns disorders
DK2582674T3 (en) 2010-06-16 2014-12-15 Cymabay Therapeutics Inc GPR120 receptor agonists and uses thereof.
CA2806006A1 (fr) 2010-07-28 2012-02-02 Medizinische Universitaet Wien Derives de chalcone vinylogue et leur utilisation medicale
US9132136B2 (en) 2010-08-02 2015-09-15 Hoffmann-La Roche Inc. Pharmaceutical combination
JPWO2012036278A1 (ja) 2010-09-17 2014-02-03 大正製薬株式会社 グリシントランスポーター阻害物質
WO2012045196A1 (fr) 2010-10-09 2012-04-12 Abbott Laboratories Inhibiteurs de la phosphoglycérate kinase
US8802673B2 (en) 2011-03-24 2014-08-12 Hoffmann-La Roche Inc Heterocyclic amine derivatives
WO2013025484A1 (fr) 2011-08-12 2013-02-21 Lapchak Paul A Analogues de polyphénol pour traiter une ischémie
US8791108B2 (en) 2011-08-18 2014-07-29 Bristol-Myers Squibb Company Inhibitors of human immunodeficiency virus replication
EP2774917A4 (fr) 2011-11-04 2015-05-06 Ajinomoto Kk Composition pharmaceutique destinée au traitement du diabète
CA2862289C (fr) 2012-02-10 2019-11-26 Constellation Pharmaceuticals, Inc. Modulateurs d'enzymes de modification par methylation, leurs compositions et utilisations
AU2013235038A1 (en) 2012-03-21 2014-10-09 Malvika Kaul Antimicrobial agents
RU2509770C2 (ru) 2012-06-22 2014-03-20 Общество с ограниченной ответственностью "Молекулярные Технологии" Новые химические соединения производные 2,4-диамино-1,3,5-триазина для профилактики и лечения заболеваний человека и животных
WO2014034898A1 (fr) 2012-08-30 2014-03-06 日本新薬株式会社 Dérivé de pyridine et médicament
EP2909214B1 (fr) 2012-10-22 2020-07-22 City of Hope Dérivés d'étoposide
AU2014243869A1 (en) 2013-03-13 2015-09-24 Boston Biomedical, Inc. 3-(aryl or heteroaryl) methyleneindolin-2-one derivatives as inhibitors of cancer stem cell pathway kinases for the treatment of cancer
US20160108031A1 (en) 2013-04-30 2016-04-21 Heinrich-Heine-Universitat Dusseldorf Inhibitors of nhr2 and/or runx1/eto-tetramerization
KR20150027922A (ko) 2013-09-04 2015-03-13 주식회사 대웅제약 신규한 항진균성 피리디닐하이드라자이드 유도체
US10011627B2 (en) 2013-09-09 2018-07-03 Youngene Therapeutics Co., Ltd C-aryl glucoside derivative, preparation methods thereof, and medical applications thereof
WO2015069110A1 (fr) 2013-11-07 2015-05-14 Aapa B.V. Multiples a(nta)gonistes de d2/antagonistes de h3 pour le traitement de troubles associés au snc
DK3121175T3 (da) * 2014-03-17 2020-03-09 Daiichi Sankyo Co Ltd 1,3-benzodioxolderivater som ezh1- og/eller ezh2-hæmmere
AU2015275826B2 (en) 2014-06-17 2019-05-16 Pfizer Inc. Substituted dihydroisoquinolinone compounds
CA2960757C (fr) 2014-09-11 2022-09-06 Piramal Enterprises Limited Composes heterocycliques condenses a titre d'agonistes du gpr120
WO2016130396A1 (fr) * 2015-02-13 2016-08-18 Constellation Pharmaceuticals, Inc. Modulateurs d'enzymes de modification méthylique, compositions et utilisations associées
BR112018001688B1 (pt) 2015-07-30 2023-05-02 Daiichi Sankyo Company, Limited Uso de um composto
US10759787B2 (en) 2015-11-19 2020-09-01 Jiangsu Hengrui Medicine Co., Ltd. Benzofuran derivative, preparation method thereof and use thereof in medicine
RS60315B1 (sr) 2016-01-13 2020-07-31 Gruenenthal Gmbh Derivati 3-((hetero-)aril)-alkil-8-amino-2-okso-1,3-diaza-spiro-[4.5]-dekana
MX2018009633A (es) 2016-02-09 2018-12-17 Inventisbio Inc Inhibidor de indoleamina-2,3-dioxigenasa (ido).
US20170355708A1 (en) * 2016-06-09 2017-12-14 Cadent Therapeutics, Inc. Potassium channel modulators
US20180016260A1 (en) 2016-07-14 2018-01-18 Incyte Corporation Heterocyclic compounds as immunomodulators
CN106727549A (zh) 2016-11-26 2017-05-31 李�荣 一种治疗抑郁症的药物
KR20190105602A (ko) 2017-01-19 2019-09-17 다이이찌 산쿄 가부시키가이샤 Htlv-1 관련 척수증을 치료하는 것에 사용하기 위한 의약 조성물
US11466020B2 (en) 2017-03-17 2022-10-11 Cornell University Compounds and compositions for inhibition and elimination of Zika infection and uses for same
BR112019024674A2 (pt) 2017-05-25 2020-06-16 Araxes Pharma Llc Inibidores covalentes da kras
EP3700527A4 (fr) 2017-10-25 2021-03-10 Children's Medical Center Corporation Inhibiteurs de papd5 et leurs méthodes d'utilisation
GB201718285D0 (en) 2017-11-03 2017-12-20 Discuva Ltd Antibacterial Compounds
JP2021035913A (ja) 2017-12-21 2021-03-04 石原産業株式会社 N−メトキシアミド化合物又はその塩、及びそれらを含有する農園芸用殺菌剤
WO2019140322A1 (fr) 2018-01-12 2019-07-18 KDAc Therapeutics, Inc. Combinaison d'un inhibiteur sélectif de désacétylase d'histone 3 (hdac3) et d'un agent d'immunothérapie pour le traitement du cancer
JP2019168611A (ja) 2018-03-23 2019-10-03 株式会社Adeka 光学フィルタ
US20210093591A1 (en) 2018-03-30 2021-04-01 San Diego State University (SDSU) Foundation, dba San Diego State University Research Foundation Methods for mitigating and preventing proteostasis-based injuries
KR20210003160A (ko) 2018-04-18 2021-01-11 콘스텔레이션 파마슈티칼스, 인크. 메틸 변형 효소 조절제, 이의 조성물 및 용도

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