JP2018021046A5 - - Google Patents

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JP2018021046A5
JP2018021046A5 JP2017155657A JP2017155657A JP2018021046A5 JP 2018021046 A5 JP2018021046 A5 JP 2018021046A5 JP 2017155657 A JP2017155657 A JP 2017155657A JP 2017155657 A JP2017155657 A JP 2017155657A JP 2018021046 A5 JP2018021046 A5 JP 2018021046A5
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pharmaceutical composition
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compound
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JP2017155657A
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JP2018021046A (ja
JP6448726B2 (ja
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JP2017155657A 2007-03-20 2017-08-10 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法 Active JP6448726B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US91932307P 2007-03-20 2007-03-20
US60/919,323 2007-03-20

Related Parent Applications (1)

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JP2015211991A Division JP6373818B2 (ja) 2007-03-20 2015-10-28 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法

Publications (3)

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JP2018021046A JP2018021046A (ja) 2018-02-08
JP2018021046A5 true JP2018021046A5 (enExample) 2018-06-14
JP6448726B2 JP6448726B2 (ja) 2019-01-09

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Family Applications (4)

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JP2009554563A Withdrawn JP2010522170A (ja) 2007-03-20 2008-03-19 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法
JP2014129790A Active JP5927241B2 (ja) 2007-03-20 2014-06-25 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法
JP2015211991A Active JP6373818B2 (ja) 2007-03-20 2015-10-28 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法
JP2017155657A Active JP6448726B2 (ja) 2007-03-20 2017-08-10 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法

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Application Number Title Priority Date Filing Date
JP2009554563A Withdrawn JP2010522170A (ja) 2007-03-20 2008-03-19 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法
JP2014129790A Active JP5927241B2 (ja) 2007-03-20 2014-06-25 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法
JP2015211991A Active JP6373818B2 (ja) 2007-03-20 2015-10-28 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法

Country Status (25)

Country Link
US (6) US8153659B2 (enExample)
EP (2) EP3101017B1 (enExample)
JP (4) JP2010522170A (enExample)
KR (3) KR101791757B1 (enExample)
CN (2) CN103641814A (enExample)
AR (1) AR065810A1 (enExample)
AU (1) AU2008229383B2 (enExample)
BR (1) BRPI0809011A8 (enExample)
CA (1) CA2681633C (enExample)
CL (1) CL2008000805A1 (enExample)
CO (1) CO6231033A2 (enExample)
CR (2) CR11036A (enExample)
EC (1) ECSP099663A (enExample)
ES (2) ES2734253T3 (enExample)
IL (1) IL200990A (enExample)
MX (1) MX2009010082A (enExample)
MY (1) MY180812A (enExample)
NI (1) NI200900170A (enExample)
NZ (2) NZ599199A (enExample)
PE (1) PE20081894A1 (enExample)
RU (1) RU2471794C2 (enExample)
UA (1) UA97976C2 (enExample)
UY (1) UY30977A1 (enExample)
WO (1) WO2008115516A2 (enExample)
ZA (1) ZA200906497B (enExample)

Families Citing this family (69)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2929331B2 (ja) * 1990-07-18 1999-08-03 丸善石油化学株式会社 トラクションドライブ用流体
NZ555886A (en) * 2004-12-01 2009-12-24 Celgene Corp Methods and compositions using immunomodulatory compounds for the treatment of immunodeficiency disorders
BRPI0809011A8 (pt) 2007-03-20 2019-01-15 Celgene Corp composto, composição farmacêutica, método de tratamento, controle ou prevenção de uma doença ou distúrbio, e, forma de dosagem unitária única
CA2710196A1 (en) * 2007-12-20 2009-07-09 Celgene Corporation Use of micro-rna as a biomarker of immunomodulatory drug activity
CA2781888C (en) * 2009-12-11 2019-06-18 Nono Inc. Agents and methods for treating ischemic and other diseases
AU2016203826B2 (en) * 2010-02-11 2018-05-17 Celgene Corporation Arylmethoxy isoindoline derivatives and compositions comprising and methods of using the same
AU2013245487B2 (en) * 2010-02-11 2016-03-10 Celgene Corporation Arylmethoxy isoindoline derivatives and compositions comprising and methods of using the same
ES2730763T3 (es) * 2010-02-11 2019-11-12 Celgene Corp Derivados de arilmetoxi isoindolina y composiciones que los comprenden y métodos de uso de los mismos
AU2012236655B2 (en) 2011-03-28 2016-09-22 Deuterx, Llc, 2',6'-dioxo-3'-deutero-piperdin-3-yl-isoindoline compounds
CA2839438C (en) * 2011-06-15 2020-08-04 Nono Inc. Agents and methods for treating ischemic and other diseases
CN102731851B (zh) * 2012-06-28 2013-11-27 芜湖宏达橡塑阀门制造有限公司 一种耐油橡胶
CN102731853B (zh) * 2012-06-28 2013-11-27 芜湖宏达橡塑阀门制造有限公司 耐油橡胶
CN102731850B (zh) * 2012-06-28 2013-11-27 芜湖宏达橡塑阀门制造有限公司 耐油耐磨橡胶
WO2014018866A1 (en) * 2012-07-27 2014-01-30 Celgene Corporation Processes for preparing isoindoline-1,3-dione compounds
AU2013299625B2 (en) 2012-08-09 2018-02-01 Celgene Corporation Treatment of immune-related and inflammatory diseases
EP2882442B1 (en) * 2012-08-09 2021-06-09 Celgene Corporation Methods of treating cancer using 3-(4-((4-(morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione
US20150038511A1 (en) 2012-08-09 2015-02-05 Celgene Corporation Treatment of immune-related and inflammatory diseases
KR20150041650A (ko) 2012-08-09 2015-04-16 셀진 코포레이션 (s)-3-(4-((4-(모르폴리노메틸)벤질)옥시)-1-옥소이소인돌린-2-일)피페리딘-2,6-디온 및 이의 약학적으로 허용가능한 형태의 제조를 위한 공정
EP2943201B2 (en) 2013-01-14 2020-07-29 Deuterx, LLC 3-(5-substituted-4-oxoquinazolin-3(4h)-yl)-3-deutero-piperidine-2,6-dione derivatives
US9695145B2 (en) 2013-01-22 2017-07-04 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
US9242966B2 (en) 2013-03-11 2016-01-26 Bristol-Myers Squibb Company Phthalazines as potassium ion channel inhibitors
CA2941560A1 (en) 2013-03-14 2014-09-25 Deuterx, Llc 3-(substituted-4-oxo-quinazolin-3(4h)-yl)-3-deutero-piperidine-2,6-dione derivatives
KR102223060B1 (ko) 2013-04-17 2021-03-05 시그날 파마소티칼 엘엘씨 암 치료를 위한 TOR 키나제 억제제 및 IMiD 화합물을 포함하는 조합요법
UA117141C2 (uk) 2013-10-08 2018-06-25 Селджин Корпорейшн Склади (s)-3-(4-((4-(морфолінометил)бензил)оксі)-1-оксоізоіндолін-2-іл)піперидин-2,6-діону
EP3145513B1 (en) 2014-05-19 2023-11-15 Celgene Corporation 3-(4-((4-(morpholinomethyl-benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione for the treatment of systemic lupus erythematosus
AU2015341301B2 (en) * 2014-10-30 2019-05-16 Kangpu Biopharmaceuticals, Ltd. Isoindoline derivative, intermediate, preparation method, pharmaceutical composition and use thereof
US9809603B1 (en) 2015-08-18 2017-11-07 Deuterx, Llc Deuterium-enriched isoindolinonyl-piperidinonyl conjugates and oxoquinazolin-3(4H)-yl-piperidinonyl conjugates and methods of treating medical disorders using same
WO2017165572A1 (en) * 2016-03-23 2017-09-28 Louis Habash Increasing expression level of apoptosis-related genes by treating a human subject with a nitroxide
US20180078539A1 (en) 2016-03-23 2018-03-22 Louis Habash T-cell regulation in t-cell mediated diseases by reducing pathogenic function of th17 in a human subject through treatment with a nitroxide
US10159665B2 (en) 2016-03-23 2018-12-25 Louis Habash Preventing amyloid plaque formation by treating a human subject with a nitroxide
US10231959B2 (en) 2016-03-23 2019-03-19 Louis Habash Increasing expression level of apoptosis-related genes by treating a human subject with a nitroxide
CN109790143A (zh) 2016-05-10 2019-05-21 C4医药公司 用于靶蛋白降解的胺连接的c3-戊二酰亚胺降解决定子体
EP3454856B1 (en) 2016-05-10 2024-09-11 C4 Therapeutics, Inc. Heterocyclic degronimers for target protein degradation
WO2017197046A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. C3-carbon linked glutarimide degronimers for target protein degradation
WO2017197036A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Spirocyclic degronimers for target protein degradation
CN110049765B (zh) * 2016-12-16 2022-02-01 康朴生物医药技术(上海)有限公司 一种组合、其应用及治疗方法
EP3641762A4 (en) 2017-06-20 2021-03-10 C4 Therapeutics, Inc. N / O-LINKED DEGRONES AND DEGRONIMERS FOR PROTEIN DEGRADATION
RS66162B1 (sr) 2017-07-10 2024-12-31 Celgene Corp 4-(4-(4-(((2-(2,6-dioksopiperidin-3-il)-l-oksoizoindolin-4-il)oksi)metil)benzil)piperazin-l-il)-3-fluorobenzonitril kao antiproliferativno jedinjenje
CN111315735B (zh) 2017-09-04 2024-03-08 C4医药公司 二氢苯并咪唑酮
WO2019043214A1 (en) 2017-09-04 2019-03-07 F. Hoffmann-La Roche Ag glutarimide
EP3679028A1 (en) 2017-09-04 2020-07-15 C4 Therapeutics, Inc. Dihydroquinolinones
CN111372585A (zh) 2017-11-16 2020-07-03 C4医药公司 用于靶蛋白降解的降解剂和降解决定子
KR20210018199A (ko) 2018-03-26 2021-02-17 씨4 테라퓨틱스, 인코포레이티드 이카로스의 분해를 위한 세레블론 결합제
US12226424B2 (en) * 2018-04-09 2025-02-18 Shanghaitech University Target protein degradation compounds, their anti-tumor use, their intermediates and use of intermediates
CN119751456A (zh) 2018-04-16 2025-04-04 C4医药公司 螺环化合物
MX2020011183A (es) 2018-04-23 2020-11-12 Celgene Corp Compuestos de 4-aminoisoindolina-1,3-diona sustituidos y su uso para el tratamiento de linfoma.
EP3578561A1 (en) 2018-06-04 2019-12-11 F. Hoffmann-La Roche AG Spiro compounds
KR102873348B1 (ko) * 2018-07-10 2025-10-20 노파르티스 아게 3-(5-하이드록시-1-옥소이소인돌린-2-일)피페리딘-2,6-디온 유도체 및 ikaros 패밀리 아연 핑거 2(ikzf2)-의존성 질환의 치료에 있어서의 이의 용도
EP3862348A4 (en) * 2018-09-30 2022-06-22 Shanghai Institute of Materia Medica, Chinese Academy of Sciences ISOINDOLINE COMPOUND, PROCESS OF MANUFACTURE, PHARMACEUTICAL COMPOSITION AND USE THEREOF
WO2020072334A1 (en) 2018-10-01 2020-04-09 Celgene Corporation Combination therapy for the treatment of cancer
WO2020092950A1 (en) * 2018-11-01 2020-05-07 Northwestern University Targeting pleckstrin-2 for treating cancer
WO2020118098A1 (en) * 2018-12-05 2020-06-11 Vividion Therapeutics, Inc. Substituted isoindolinones as modulators of cereblon-mediated neo-substrate recruitment
AU2019392231B2 (en) 2018-12-06 2022-10-20 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Isoindoline compound, and preparation method, pharmaceutical composition, and application of isoindoline compound
EP3897631A4 (en) 2018-12-20 2022-11-23 C4 Therapeutics, Inc. TARGETED PROTEIN BREAKDOWN
JP7524203B2 (ja) * 2019-02-22 2024-07-29 エルケム・シリコーンズ・ユーエスエイ・コーポレーション 有効成分の溶出を改善するための薬デリバリーシリコーン組成物
EP4470618A3 (en) 2019-03-06 2025-03-05 C4 Therapeutics, Inc. Heterocyclic compounds for medical treatment
CN111747924B (zh) * 2019-03-29 2023-11-10 华东师范大学 一类来那度胺/泊马度胺类似物及其应用
CN113677664B (zh) 2019-04-12 2025-04-04 C4医药公司 Ikaros和aiolos的三环降解物
CN113544130B (zh) * 2019-05-31 2024-01-09 西藏海思科制药有限公司 一种btk抑制剂环衍生物及其制备方法和药学上的应用
CN113372327B (zh) * 2020-02-25 2023-07-18 上海科技大学 基于戊二酰亚胺骨架的化合物及其应用
CN115397412B (zh) * 2020-04-17 2025-03-25 伊赛恩特制药公司 Mas相关g蛋白受体x4的调节剂及相关产物和方法
WO2022017365A1 (zh) 2020-07-20 2022-01-27 江苏恒瑞医药股份有限公司 含硫异吲哚啉类衍生物、其制备方法及其在医药上的应用
CN116669736B (zh) * 2021-01-05 2025-11-11 江苏恒瑞医药股份有限公司 稠杂环基取代的环己二酰亚胺衍生物、其制备方法及其在医药上的应用
JP2024504932A (ja) 2021-01-13 2024-02-02 モンテ ローザ セラピューティクス, インコーポレイテッド イソインドリノン化合物
CN115504963A (zh) * 2021-06-22 2022-12-23 苏州开拓药业股份有限公司 一种c-Myc蛋白降解剂
CA3248757A1 (en) 2022-01-19 2025-07-09 Jiangsu Hengrui Pharmaceuticals Co., Ltd. CRYSTALLINE FORM OF A SULFUR-CONTAINING ISOINDOLINE DERIVATIVE
EP4536656A1 (en) 2022-06-06 2025-04-16 C4 Therapeutics, Inc. Bicyclic-substituted glutarimide cereblon binders
AR130961A1 (es) * 2022-11-04 2025-02-05 Bristol Myers Squibb Co Compuestos y su uso para el tratamiento de hemoglobinopatías
CN116675786A (zh) * 2023-07-10 2023-09-01 盐城师范学院 一种靶向传递喜树碱的环糊精超分子药物及其制备方法和应用

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5001116A (en) 1982-12-20 1991-03-19 The Children's Medical Center Corporation Inhibition of angiogenesis
US4994443A (en) 1982-12-20 1991-02-19 The Children's Medical Center Corporation Inhibition of angiogenesis
US5800819A (en) 1996-01-25 1998-09-01 National Institute For Pharmaceutical Research And Development Federal Ministry Of Science And Technology Piper guineense, pterocarpus osun, eugenia caryophyllata, and sorghum bicolor extracts for treating sickle cell disease
KR19980074060A (ko) * 1997-03-21 1998-11-05 김윤배 신규한 치환된 3,4-디알콕시페닐 유도체
TR200101505T2 (tr) * 1998-03-16 2002-06-21 Celgene Corporation 2-(2,6-dioksopiperidin-3-il) izoindolin türevleri, bunların hazırlanması ve enflamatuar sitokinlerin inhibitörleri olarak kullanımı
US6458810B1 (en) * 2000-11-14 2002-10-01 George Muller Pharmaceutically active isoindoline derivatives
US20030045552A1 (en) * 2000-12-27 2003-03-06 Robarge Michael J. Isoindole-imide compounds, compositions, and uses thereof
US7320992B2 (en) 2003-08-25 2008-01-22 Amgen Inc. Substituted 2,3-dihydro-1h-isoindol-1-one derivatives and methods of use
EP1663223B1 (en) * 2003-09-17 2014-01-01 The Government of the United States of America, as represented by the Secretary of the Department of Health and Human Services Thalidomide analogs as tnf-alpha modulators
GB0324790D0 (en) * 2003-10-24 2003-11-26 Astrazeneca Ab Amide derivatives
NZ555886A (en) 2004-12-01 2009-12-24 Celgene Corp Methods and compositions using immunomodulatory compounds for the treatment of immunodeficiency disorders
RU2396259C2 (ru) * 2004-12-24 2010-08-10 Астразенека Аб Амидные производные
BRPI0809011A8 (pt) 2007-03-20 2019-01-15 Celgene Corp composto, composição farmacêutica, método de tratamento, controle ou prevenção de uma doença ou distúrbio, e, forma de dosagem unitária única

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