JP2020531481A - エーテル化合物およびその使用 - Google Patents

エーテル化合物およびその使用 Download PDF

Info

Publication number
JP2020531481A
JP2020531481A JP2020509482A JP2020509482A JP2020531481A JP 2020531481 A JP2020531481 A JP 2020531481A JP 2020509482 A JP2020509482 A JP 2020509482A JP 2020509482 A JP2020509482 A JP 2020509482A JP 2020531481 A JP2020531481 A JP 2020531481A
Authority
JP
Japan
Prior art keywords
substituted
unsubstituted
compound according
mmol
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.)
Pending
Application number
JP2020509482A
Other languages
English (en)
Japanese (ja)
Other versions
JP2020531481A5 (enExample
Inventor
カイル ダブリュー.エイチ. チャン,
カイル ダブリュー.エイチ. チャン,
ポール イー. エルドマン,
ポール イー. エルドマン,
リア ファン,
リア ファン,
デイビッド アーロン ヘクト,
デイビッド アーロン ヘクト,
フランク メルキューリオ,
フランク メルキューリオ,
ロバート サリバン,
ロバート サリバン,
Original Assignee
バイオセリックス, インコーポレイテッド
バイオセリックス, インコーポレイテッド
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 バイオセリックス, インコーポレイテッド, バイオセリックス, インコーポレイテッド filed Critical バイオセリックス, インコーポレイテッド
Publication of JP2020531481A publication Critical patent/JP2020531481A/ja
Publication of JP2020531481A5 publication Critical patent/JP2020531481A5/ja
Pending legal-status Critical Current

Links

Classifications

    • 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
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • 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
    • 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
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/12Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D495/14Ortho-condensed systems

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
JP2020509482A 2017-08-25 2018-08-07 エーテル化合物およびその使用 Pending JP2020531481A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201762550489P 2017-08-25 2017-08-25
US62/550,489 2017-08-25
PCT/US2018/045626 WO2019040274A1 (en) 2017-08-25 2018-08-07 ETHER COMPOUNDS AND USES THEREOF

Publications (2)

Publication Number Publication Date
JP2020531481A true JP2020531481A (ja) 2020-11-05
JP2020531481A5 JP2020531481A5 (enExample) 2021-09-16

Family

ID=63350615

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2020509482A Pending JP2020531481A (ja) 2017-08-25 2018-08-07 エーテル化合物およびその使用

Country Status (8)

Country Link
US (2) US10513515B2 (enExample)
EP (1) EP3672955A1 (enExample)
JP (1) JP2020531481A (enExample)
CN (1) CN111247138A (enExample)
AU (1) AU2018321567A1 (enExample)
CA (1) CA3072543A1 (enExample)
TW (2) TWI742303B (enExample)
WO (1) WO2019040274A1 (enExample)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4467143B1 (en) 2017-07-10 2026-03-11 Celgene Corporation Method for preparing 4-(4-(4-(((2-(2,6-dioxopiperidin-3-yl)-l-oxoisoindolin-4-yl)oxy)methyl)benzyl)piperazin-l-yl)-3-fluorobenzonitrile
CA3106239A1 (en) 2018-07-27 2020-01-30 Biotheryx, Inc. Bifunctional compounds as cdk modulators
US20230093099A1 (en) * 2019-04-02 2023-03-23 Cullgen (Shanghai), Inc. Compounds and methods of treating cancers
WO2021222150A2 (en) 2020-04-28 2021-11-04 Anwita Biosciences, Inc. Interleukin-2 polypeptides and fusion proteins thereof, and their pharmaceutical compositions and therapeutic applications
CN113896711A (zh) * 2020-07-06 2022-01-07 北京诺诚健华医药科技有限公司 杂环类免疫调节剂
WO2022012622A1 (en) * 2020-07-16 2022-01-20 Beigene, Ltd. Degradation of (egfr) by conjugation of egfr inhibitors with e3 ligase ligand and methods of use
BR112023000817A2 (pt) 2020-07-20 2023-02-07 Jiangsu Hengrui Pharmaceuticals Co Ltd Derivado de isoindolina contendo enxofre, e método de preparação do mesmo e uso médico do mesmo
US20240025863A1 (en) 2020-09-16 2024-01-25 Biotheryx, Inc. Sos1 protein degraders, pharmaceutical compositions thereof, and their therapeutic applications
WO2022087335A1 (en) 2020-10-23 2022-04-28 Biotheryx, Inc. Kras protein degraders, pharmaceutical compositions thereof, and their therapeutic applications
CN117203196A (zh) 2020-12-14 2023-12-08 拜欧斯瑞克斯公司 Pde4降解剂、药物组合物和治疗应用
KR20240020735A (ko) 2021-05-07 2024-02-15 카이메라 쎄라퓨틱스 인코포레이티드 Cdk2 분해제 및 그 용도
WO2022251588A1 (en) * 2021-05-27 2022-12-01 Halda Therapeutics Opco, Inc. Heterobifunctional compounds and methods of treating disease
KR20240053589A (ko) * 2021-07-30 2024-04-24 하이노바 파마슈티컬스 인코포레이티드 이중 기능성 키메라 헤테로 고리 화합물 및 이의 안드로겐 수용체 분해제로서의 용도
WO2023025136A1 (zh) * 2021-08-27 2023-03-02 杭州格博生物医药有限公司 异吲哚啉酮化合物及其用途
US12419962B2 (en) 2022-03-16 2025-09-23 Biotheryx, Inc. Quinazolines, pharmaceutical compositions, and therapeutic applications
CN118019736A (zh) * 2022-09-08 2024-05-10 标新生物医药科技(上海)有限公司 基于cereblon蛋白设计的分子胶化合物及其应用
WO2024064358A1 (en) 2022-09-23 2024-03-28 Ifm Due, Inc. Compounds and compositions for treating conditions associated with sting activity
CN119684303A (zh) * 2023-12-28 2025-03-25 上海超阳药业有限公司 一种双功能可降解雄激素受体的杂环化合物及其应用
TW202543650A (zh) 2024-03-08 2025-11-16 美商海爾達醫療運營公司 異雙官能化合物及其在治療疾病中之用途
DE102024129145A1 (de) 2024-10-09 2026-04-09 Balluff Gmbh Sensorelement

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013519675A (ja) * 2010-02-11 2013-05-30 セルジーン コーポレイション アリールメトキシイソインドリン誘導体、それを含む組成物、及びその使用方法
WO2014116573A1 (en) * 2013-01-22 2014-07-31 Celgene Corporation Processes for the preparation of isotopologues of 3-(4-((4-(morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione and pharmaceutically acceptable salts thereof
WO2016065980A1 (zh) * 2014-10-30 2016-05-06 康朴生物医药技术(上海)有限公司 异吲哚啉衍生物、其中间体、制备方法、药物组合物及应用
WO2016191178A1 (en) * 2015-05-22 2016-12-01 Biotheryx, Inc. Compounds targeting proteins, compositions, methods, and uses thereof
WO2017024318A1 (en) * 2015-08-06 2017-02-09 Dana-Farber Cancer Institute, Inc. Targeted protein degradation to attenuate adoptive t-cell therapy associated adverse inflammatory responses

Family Cites Families (106)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE292451C (enExample)
CA793864A (en) 1968-09-03 G. Bassiri Taghi Epsilon-caprolactams
US3331835A (en) 1965-01-07 1967-07-18 Allied Chem Novel epsilon-caprolactams
BE793517A (fr) 1972-01-03 1973-06-29 Bayer Ag Colorants anthraquinoniques
US4339600A (en) 1976-05-10 1982-07-13 E. R. Squibb & Sons, Inc. Compounds for alleviating angiotensin related hypertension
US4415496A (en) 1981-03-23 1983-11-15 Merck & Co., Inc. Bicyclic lactams
US4644069A (en) 1984-08-15 1987-02-17 Ciba-Geigy Corporation Process for the preparation of dimethylmaleic anhydride
DE3833892A1 (de) 1988-10-05 1990-04-12 Bayer Ag Basische 4-aryl-dhp-amide, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln
SU1708812A1 (ru) 1989-10-03 1992-01-30 Отдел Тонкого Органического Синтеза Института Химии Башкирского Научного Центра Уральского Отделения Ан Ссср @ , @ -Фталимидо- @ -капролактамы как промежуточные продукты дл синтеза N @ -метил- @ -лизина гидрохлорида
EP0446899A1 (en) 1990-03-16 1991-09-18 Konica Corporation Silver halide photographic material
DE4125292A1 (de) 1991-07-31 1993-02-04 Kali Chemie Pharma Gmbh 6-oxo-azepinoindol-verbindungen sowie verfahren und zwischenprodukte zu ihrer herstellung und diese verbindungen enthaltende arzneimittel
US5272158A (en) 1991-10-29 1993-12-21 Merck & Co., Inc. Fibrinogen receptor antagonists
US5504080A (en) 1992-10-28 1996-04-02 Bristol-Myers Squibb Co. Benzo-fused lactams
DE69329701T2 (de) 1992-10-30 2001-05-10 Merrell Pharmaceuticals Inc., Cincinnati Mercaptoacetylamid substituiertes bizyclisches laktam zur verwendung als enkephalinase und ace-hemmer
EP0678106A4 (en) 1993-01-11 1995-12-27 Univ Pennsylvania POLYCYCLIC AROMATIC COMPOUNDS WITH NON-LINEAR OPTICAL PROPERTIES.
US5629327A (en) 1993-03-01 1997-05-13 Childrens Hospital Medical Center Corp. Methods and compositions for inhibition of angiogenesis
US5463063A (en) 1993-07-02 1995-10-31 Celgene Corporation Ring closure of N-phthaloylglutamines
US5631280A (en) 1995-03-29 1997-05-20 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
US5932582A (en) 1996-06-28 1999-08-03 Merck & Co., Inc. Fibrinogen receptor antagonist prodrugs
US6281230B1 (en) 1996-07-24 2001-08-28 Celgene Corporation Isoindolines, method of use, and pharmaceutical compositions
US6429212B1 (en) 1996-08-16 2002-08-06 Ishihara Sangyo Kaisha Ltd. Medicinal composition
ATE493983T1 (de) 1996-11-05 2011-01-15 Childrens Medical Center Thalidomide und dexamethason für die behandlung von tumors
US5977134A (en) 1996-12-05 1999-11-02 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
CA2285264A1 (en) 1997-04-25 1998-11-05 Michiyo Gyoten Condensed pyridazine derivatives, their production and use
EP0927992A4 (en) 1997-07-17 1999-09-15 Sony Corp MAGNETIC RECORDING MEDIUM AND MAGNETIC RECORDING / REPRODUCING DEVICE COMPRISING SAME
AU9309898A (en) 1997-09-09 1999-03-29 Du Pont Pharmaceuticals Company Benzimidazolinones, benzoxazolinones, benzopiperazinones, indanones, and derivatives thereof as inhibitors of factor xa
JP2000159761A (ja) 1998-11-30 2000-06-13 Yoshio Takeuchi フルオロサリドマイド
WO2000034437A2 (en) 1998-12-08 2000-06-15 Merck & Co., Inc. Inhibitors of prenyl-protein transferase
AU4485400A (en) 1999-04-26 2000-11-10 Advanced Life Sciences Inc. Synthetic indolocarbazole regioisomers and uses thereof
US6492380B1 (en) 1999-05-17 2002-12-10 Queen's University At Kingston Method of inhibiting neurotrophin-receptor binding
ATE277048T1 (de) 1999-06-15 2004-10-15 Bristol Myers Squibb Pharma Co Substituierte hetercyclisch kondensierte gamma carboline
FR2800739B1 (fr) 1999-11-04 2002-10-11 Corning Sa Naphtopyranes avec un heterocycle en position 5,6, preparation et compositions et matrices (co) polymeres les renfermant
FR2801054B1 (fr) 1999-11-17 2003-06-13 Adir Nouveaux derives de 12,13-(pyranosyl)-indolo[2,3-a]pyrrolo [3,4-c]carbazole et 12,13-(pyranosyl)-furo[3,4-c]indolo [2,3-a]carbazole, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
US6388090B2 (en) 2000-01-14 2002-05-14 Orion Corporation Imidazole derivatives
US6686477B2 (en) 2000-09-29 2004-02-03 Eastman Chemical Company Highly enantiomerically pure lactam-substituted propanoic acid derivatives and methods of making and using same
US7071181B2 (en) 2001-01-26 2006-07-04 Schering Corporation Methods and therapeutic combinations for the treatment of diabetes using sterol absorption inhibitors
AU2002254375A1 (en) 2001-03-30 2002-10-15 Merck And Co., Inc. Inhibitors of prenyl-protein transferase
US20030114448A1 (en) 2001-05-31 2003-06-19 Millennium Pharmaceuticals, Inc. Inhibitors of factor Xa
DE10137163A1 (de) 2001-07-30 2003-02-13 Bayer Ag Substituierte Isoindole und ihre Verwendung
WO2003027314A2 (en) 2001-09-27 2003-04-03 Linden Technologies, Inc. Protected linker compounds
US20040110757A1 (en) 2002-03-21 2004-06-10 Thomas Arrhenius Flt-1 ligands and their uses in the treatment of diseases regulatable by angiogenesis
WO2004080983A1 (en) 2003-03-14 2004-09-23 Astrazeneca Ab Novel lactams and uses thereof
WO2004087153A2 (en) 2003-03-28 2004-10-14 Chiron Corporation Use of organic compounds for immunopotentiation
DE10317817A1 (de) 2003-04-16 2004-11-04 Chromeon Gmbh Pyrrolopyrrole als fluoreszente Marker für Biomoleküle und sphärische Partikel
AU2004234087A1 (en) 2003-04-28 2004-11-11 Tibotec Pharmaceuticals Ltd. HIV integrase inhibitors
WO2005016326A2 (en) 2003-07-11 2005-02-24 The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Analogs of thalidomide as potential angiogenesis inhibitors
US7320992B2 (en) 2003-08-25 2008-01-22 Amgen Inc. Substituted 2,3-dihydro-1h-isoindol-1-one derivatives and methods of use
WO2005121138A2 (en) 2004-06-03 2005-12-22 Rigel Pharmaceuticals, Inc. Heterotricyclic compounds for use as hcv inhibitors
WO2006034419A2 (en) 2004-09-21 2006-03-30 Athersys, Inc. Indole acetic acids exhibiting crth2 receptor antagonism and uses thereof
AU2006212765B2 (en) 2005-02-09 2012-02-02 3M Innovative Properties Company Alkyloxy substituted thiazoloquinolines and thiazolonaphthyridines
AR056968A1 (es) 2005-04-11 2007-11-07 Xenon Pharmaceuticals Inc Compuestos espiro-oxindol y composiciones farmacéuticas
US7592467B2 (en) 2005-04-11 2009-09-22 Probiodrug Ag Inhibitors of prolyl endopeptidase
TW200728277A (en) 2005-06-29 2007-08-01 Palau Pharma Sa Bicyclic derivatives as P38 inhibitors
WO2007000337A1 (en) 2005-06-29 2007-01-04 Palau Pharma, S.A. Bicyclic derivatives as p38 kinase inhibitors
BRPI0613958A2 (pt) 2005-06-29 2011-02-22 Palau Pharma Sa composto bicìclico, seu uso como inibidor p38 e composição farmacêutica contendo o mesmo
WO2007028789A1 (en) 2005-09-07 2007-03-15 Istituto Di Ricerche Di Biologia Molecolare P. Angeletti Spa Quinazoline derivatives as antiviral agents
WO2007126941A2 (en) 2006-03-24 2007-11-08 Archemix Corp. Solid support reagents for synthesis
US20100297046A1 (en) 2006-03-31 2010-11-25 Dynamis Therapeutics, Inc. Compositions and Methods Related to Fructosamine-3-Kinase Inhibitors
US8063225B2 (en) 2006-08-14 2011-11-22 Chembridge Corporation Tricyclic compound derivatives useful in the treatment of neoplastic diseases, inflammatory disorders and immunomodulatory disorders
WO2008037266A1 (en) 2006-09-25 2008-04-03 Universite Libre De Bruxelles Inhibitors of conventional protein kinase c isozymes and use thereof for treating inflammatory diseases
US8143284B2 (en) 2006-10-05 2012-03-27 Abbott Laboratories Poly(ADP-ribose)polymerase inhibitors
AR063311A1 (es) 2006-10-18 2009-01-21 Novartis Ag Compuestos organicos
JP2009023986A (ja) 2006-11-08 2009-02-05 Pharma Ip 抗癌剤としてのビアリール誘導体
CN101186611B (zh) 2006-11-15 2011-05-18 天津和美生物技术有限公司 可抑制细胞释放肿瘤坏死因子的吡咯啉-2-酮衍生物及其制备和应用
WO2008073865A2 (en) 2006-12-11 2008-06-19 Novartis Ag Method of preventing or treating myocardial ischemia
KR20090117730A (ko) 2007-01-08 2009-11-12 폴리에라 코퍼레이션 아렌-비스(디카르복스이미드)-기재 반도체 물질, 및 이를 제조하기 위한 관련된 중간체의 제조 방법
GB0707051D0 (en) 2007-04-12 2007-05-30 Istituto Di Ricerche D Biolog Antiviral agents
WO2009039635A1 (en) 2007-09-24 2009-04-02 Painceptor Pharma Corporation Methods of modulating neurotrophin-mediated activity
KR101124350B1 (ko) 2007-10-17 2012-03-15 한국화학연구원 항암 활성을 갖는 페난트렌 락탐 유도체, 이의 제조방법 및이를 포함하는 약학 조성물
WO2009070533A1 (en) 2007-11-29 2009-06-04 Complegen, Inc. Methods of inhibiting steroyl coa desaturase
JP5632612B2 (ja) 2007-12-05 2014-11-26 あすか製薬株式会社 ラクタム化合物又はその塩及びppar活性化剤
EP2072506A1 (de) 2007-12-21 2009-06-24 Bayer CropScience AG Thiazolyloxyphenylamidine oder Thiadiazolyloxyphenylamidine und deren Verwendung als Fungizide
RU2544856C2 (ru) 2008-01-25 2015-03-20 Сергей Олегович Бачурин НОВЫЕ ПРОИЗВОДНЫЕ 2,3,4,5-ТЕТРАГИДРО-1-ПИРИДО[4,3-b]ИНДОЛА И СПОСОБЫ ИХ ПРИМЕНЕНИЯ
US9446995B2 (en) 2012-05-21 2016-09-20 Illinois Institute Of Technology Synthesis of therapeutic and diagnostic drugs centered on regioselective and stereoselective ring opening of aziridinium ions
WO2009112445A1 (en) 2008-03-10 2009-09-17 Novartis Ag Method of increasing cellular phosphatidyl choline by dgat1 inhibition
MX2010010272A (es) 2008-03-19 2011-05-25 Chembridge Corp Nuevos inhibidores de tirosina quinasa.
WO2009156098A2 (de) 2008-06-27 2009-12-30 Bayer Cropscience Ag Thiadiazolyloxyphenylamidine und deren verwendung als fungizide
WO2010011924A2 (en) 2008-07-24 2010-01-28 Draths Corporation Monomers derived from alpha-or beta-amino-e-caprolactam and polymers made therefrom
EP2373645A4 (en) 2008-12-08 2012-05-02 Sirtris Pharmaceuticals Inc ISOINDOLINONE AND RELATED ANALOGUES AS SIRTUIN MODULATORS
CA2774871C (en) 2009-10-20 2018-05-29 Tokyo Institute Of Technology Screening method utilizing thalidomide-targeting factor
JP5734570B2 (ja) 2010-01-28 2015-06-17 富士フイルム株式会社 顔料微粒子の製造方法
KR20110119282A (ko) 2010-04-27 2011-11-02 다우어드밴스드디스플레이머티리얼 유한회사 신규한 유기 전자재료용 화합물 및 이를 채용하고 있는 유기 전계 발광 소자
US8697690B2 (en) 2010-07-01 2014-04-15 Merck Sharp & Dohme Corp. Isoindolone M1 receptor positive allosteric modulators
WO2012037155A2 (en) 2010-09-13 2012-03-22 Gtx, Inc. Tyrosine kinase inhibitors
US8742097B2 (en) 2010-11-09 2014-06-03 Hoffmann-La Roche Inc. Triazole compounds I
TWI445696B (zh) 2010-11-29 2014-07-21 Univ Nat Yang Ming 標靶人類胸線核苷酸激酶誘導惡性腫瘤中的dna修復毒性
JP5728921B2 (ja) 2010-12-10 2015-06-03 コニカミノルタ株式会社 光学フィルム、及びそれを用いた偏光板、液晶表示装置
US9464065B2 (en) 2011-03-24 2016-10-11 The Scripps Research Institute Compounds and methods for inducing chondrogenesis
WO2012158475A1 (en) 2011-05-17 2012-11-22 Merck Sharp & Dohme Corp. N-linked lactam m1 receptor positive allosteric modulators
SG194770A1 (en) 2011-05-27 2013-12-30 Probiodrug Ag Radiolabelled glutaminyl cyclase inhibitors
WO2013010218A1 (en) 2011-07-15 2013-01-24 Freie Universität Berlin Inhibition of clathrin
WO2013106409A1 (en) 2012-01-10 2013-07-18 Merck Patent Gmbh Benzamide derivatives as modulators of the follicle stimulating hormone
KR20130131663A (ko) 2012-05-24 2013-12-04 코오롱생명과학 주식회사 벤질리딘 프탈이미드 단량체, 이의 제조 방법, 이를 포함하는 중합체, 이를 포함하는 광배향막 및 이를 포함하는 위상차 필름
KR101592628B1 (ko) 2012-09-20 2016-02-11 주식회사 엘지화학 이미다졸 유도체 및 이를 이용한 유기 전자 소자
AR092742A1 (es) 2012-10-02 2015-04-29 Intermune Inc Piridinonas antifibroticas
US20150272939A1 (en) 2012-10-02 2015-10-01 Yale University Identification of Small Molecule Inhibitors of Jumonji AT-Rich Interactive Domain 1A (JARID1A) and 1B (JARID1B) Histone Demethylase
BR112015015584A2 (pt) 2012-12-27 2017-12-12 Baruch S Blumberg Inst novos agentes antivirais contra infecção por hbv
US20140213538A1 (en) 2013-01-15 2014-07-31 Intermune, Inc. Lysophosphatidic acid receptor antagonists
KR20140103447A (ko) 2013-02-18 2014-08-27 코오롱생명과학 주식회사 벤질리딘 프탈이미드 단량체, 이의 제조 방법, 이를 포함하는 중합체, 이를 포함하는 광배향막 및 이를 포함하는 위상차 필름
CN104004122B (zh) 2014-05-08 2016-05-11 中国科学院长春应用化学研究所 新型温敏性聚合物及用可再生资源l-赖氨酸制备新型温敏性聚合物的方法
CA3018429A1 (en) 2016-04-22 2017-10-26 Dana-Farber Cancer Institute, Inc. Degradation of cyclin-dependent kinase 9 (cdk9) by conjugation of cdk9 inhibitors with e3 ligase ligand and methods of use
WO2017201069A1 (en) * 2016-05-18 2017-11-23 Biotheryx, Inc. Oxoindoline derivatives as protein function modulators
US10406165B2 (en) * 2017-03-14 2019-09-10 Biotheryx, Inc. Compounds targeting proteins, compositions, methods, and uses thereof
US11584734B2 (en) * 2017-08-15 2023-02-21 Global Blood Therapeutics, Inc. Tricyclic compounds as histone methyltransferase inhibitors
WO2019241271A1 (en) * 2018-06-13 2019-12-19 Biotheryx, Inc. Fused thiophene compounds
JP2022533260A (ja) * 2019-05-24 2022-07-21 バイオセリックス, インコーポレイテッド タンパク質を標的とする化合物及びその医薬組成物並びにそれらの治療的応用

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2013519675A (ja) * 2010-02-11 2013-05-30 セルジーン コーポレイション アリールメトキシイソインドリン誘導体、それを含む組成物、及びその使用方法
WO2014116573A1 (en) * 2013-01-22 2014-07-31 Celgene Corporation Processes for the preparation of isotopologues of 3-(4-((4-(morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione and pharmaceutically acceptable salts thereof
WO2016065980A1 (zh) * 2014-10-30 2016-05-06 康朴生物医药技术(上海)有限公司 异吲哚啉衍生物、其中间体、制备方法、药物组合物及应用
WO2016191178A1 (en) * 2015-05-22 2016-12-01 Biotheryx, Inc. Compounds targeting proteins, compositions, methods, and uses thereof
WO2017024318A1 (en) * 2015-08-06 2017-02-09 Dana-Farber Cancer Institute, Inc. Targeted protein degradation to attenuate adoptive t-cell therapy associated adverse inflammatory responses

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
GUTSCHOW,M. ET AL.: "Aza analogues of thalidomide: synthesis and evaluation as inhibitors of tumor necrosis factor-α pro", BIOORGANIC & MEDICINAL CHEMISTRY, vol. 9, no. 4, JPN6022016275, 2001, pages 1059 - 1065, ISSN: 0004760643 *

Also Published As

Publication number Publication date
US20190062320A1 (en) 2019-02-28
CA3072543A1 (en) 2019-02-28
EP3672955A1 (en) 2020-07-01
TWI742303B (zh) 2021-10-11
US10513515B2 (en) 2019-12-24
TW201919639A (zh) 2019-06-01
TW202222794A (zh) 2022-06-16
WO2019040274A1 (en) 2019-02-28
US10927104B2 (en) 2021-02-23
CN111247138A (zh) 2020-06-05
US20200231582A1 (en) 2020-07-23
AU2018321567A1 (en) 2020-03-19

Similar Documents

Publication Publication Date Title
JP2020531481A (ja) エーテル化合物およびその使用
US11345714B2 (en) Compounds targeting proteins, compositions, methods, and uses thereof
JP7365059B2 (ja) 縮合チオフェン化合物
CN108290893B (zh) 二氢蝶啶酮类衍生物、其制备方法及其用途
EP2029145B1 (en) Pyrrolopyrimidine compounds and their uses
AU2014318178B2 (en) Substituted 2, 3-dihydro-1H-inden-1-one retinoic acid-related orphan nuclear receptor antagonists for treating multiple sclerosis
JP2016504282A (ja) ジヒドロピラゾールgpr40モジュレーター
EP3353170A1 (en) New benzimidazoles derivatives as tec kinases family inhibitors
JP2022522890A (ja) 芳香族誘導体、その調製方法および医薬用途
KR102490140B1 (ko) 레티노이드-관련 희귀 수용체 감마의 신규한 헤테로방향족 조절제
JP2023551313A (ja) アミド化合物、医薬組成物およびその使用
TWI681960B (zh) 苯并咪唑類衍生物及其製備方法及其在醫藥上的用途
WO2024256569A1 (en) Novel cdk degraders
WO2023139164A1 (en) Cdk9 inhibitors
WO2019040512A1 (en) BENZIMIDAZOLE COMPOUNDS AS INHIBITORS OF KINASES
MXPA06008934A (en) Piperidinylcarbonyl-pyrrolidines and their use as melanocortin agonists

Legal Events

Date Code Title Description
A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20210806

A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20210806

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20220426

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20221115