JP2018021046A5 - - Google Patents

Download PDF

Info

Publication number
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
Authority
JP
Japan
Prior art keywords
disorder
pharmaceutical composition
dosage form
unit dosage
compound
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.)
Granted
Application number
JP2017155657A
Other languages
English (en)
Japanese (ja)
Other versions
JP2018021046A (ja
JP6448726B2 (ja
Filing date
Publication date
Application filed filed Critical
Publication of JP2018021046A publication Critical patent/JP2018021046A/ja
Publication of JP2018021046A5 publication Critical patent/JP2018021046A5/ja
Application granted granted Critical
Publication of JP6448726B2 publication Critical patent/JP6448726B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

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)

Application Number Title Priority Date Filing Date
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)

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

Family

ID=39719168

Family Applications (4)

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JP2009554563A Withdrawn JP2010522170A (ja) 2007-03-20 2008-03-19 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法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
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

Family Applications Before (3)

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JP2009554563A Withdrawn JP2010522170A (ja) 2007-03-20 2008-03-19 4’−o−置換イソインドリン誘導体および該誘導体を含有する組成物およびその使用方法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) CN101679380A (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) NZ579890A (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 (71)

* 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
CN101111234A (zh) * 2004-12-01 2008-01-23 细胞基因公司 包含免疫调节化合物的组合物及其治疗免疫缺陷疾病的用途
AU2008229383B2 (en) 2007-03-20 2013-09-05 Celgene Corporation 4'-O-substituted isoindoline derivatives and compositions comprising and methods of using the same
US7964354B2 (en) * 2007-12-20 2011-06-21 Celgene Corporation Use of micro-RNA as a biomarker of immunomodulatory drug activity
AU2010327936B2 (en) 2009-12-11 2015-08-20 Nono Inc. Agents and methods for treating ischemic and other diseases
SG10201501062SA (en) 2010-02-11 2015-04-29 Celgene Corp 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
AU2016203826B2 (en) * 2010-02-11 2018-05-17 Celgene Corporation Arylmethoxy isoindoline derivatives and compositions comprising and methods of using the same
AU2012236655B2 (en) * 2011-03-28 2016-09-22 Deuterx, Llc, 2',6'-dioxo-3'-deutero-piperdin-3-yl-isoindoline compounds
US9334256B2 (en) 2011-06-15 2016-05-10 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
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
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
ES2755748T3 (es) * 2012-07-27 2020-04-23 Celgene Corp Procedimientos para preparar compuestos de isoindolin-1,3-diona
CN114366746A (zh) * 2012-08-09 2022-04-19 细胞基因公司 使用氧代异吲哚化合物治疗癌症
US20150038511A1 (en) 2012-08-09 2015-02-05 Celgene Corporation Treatment of immune-related and inflammatory diseases
CN114939119A (zh) 2012-08-09 2022-08-26 细胞基因公司 免疫相关和炎性疾病的治疗
CA3108974C (en) 2012-08-09 2023-04-04 Celgene Corporation Processes for the preparation of (s)-3-(4-((4-(morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione and pharmaceutically acceptable forms thereof
CA2935495C (en) 2013-01-14 2021-04-20 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
US9290475B2 (en) 2013-03-14 2016-03-22 Deuterx, Llc 3-(substituted-4-oxoquinazolin-3(4H)-yl)-3-deutero-piperidine-2,6-dione derivatives and compositions comprising and methods of using the same
EP2986318A1 (en) 2013-04-17 2016-02-24 Signal Pharmaceuticals, LLC Combination therapy comprising a tor kinase inhibitor and an imid compound for treating cancer
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
TWI745271B (zh) 2014-05-19 2021-11-11 美商西建公司 全身紅斑性狼瘡之治療
ES2901509T3 (es) * 2014-10-30 2022-03-22 Kangpu Biopharmaceuticals Ltd Derivado de isoindolina, compuesto intermedio, métodos de preparación, composición farmacéutica y uso del mismo
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
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
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
EP3455219A4 (en) 2016-05-10 2019-12-18 C4 Therapeutics, Inc. AMINE-RELATED C3-GLUTARIMIDE DEGRONIMERS FOR TARGET PROTEIN REDUCTION
EP4483875A3 (en) 2016-05-10 2025-04-02 C4 Therapeutics, Inc. Spirocyclic degronimers for target protein degradation
CN109562107A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的杂环降解决定子体
CN109641874A (zh) 2016-05-10 2019-04-16 C4医药公司 用于靶蛋白降解的c3-碳连接的戊二酰亚胺降解决定子体
US10933059B2 (en) * 2016-12-16 2021-03-02 Kangpu Biopharmaceuticals. Ltd. Combination, application thereof and treatment method
EP3641762B1 (en) 2017-06-20 2026-02-18 C4 Therapeutics, Inc. N/o-linked degrons and degronimers for protein degradation
JP7258009B2 (ja) 2017-07-10 2023-04-14 セルジーン コーポレイション 抗増殖化合物及びその使用方法
EP3679028A1 (en) 2017-09-04 2020-07-15 C4 Therapeutics, Inc. Dihydroquinolinones
CN111315735B (zh) 2017-09-04 2024-03-08 C4医药公司 二氢苯并咪唑酮
EP3679026A1 (en) 2017-09-04 2020-07-15 C4 Therapeutics, Inc. Glutarimide
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
WO2019204354A1 (en) 2018-04-16 2019-10-24 C4 Therapeutics, Inc. Spirocyclic compounds
FI3784663T3 (fi) 2018-04-23 2023-10-06 Celgene Corp Substituoituja 4-aminoisoindoliini-1,3-dioniyhdisteitä ja niiden käyttö lymfooman hoitamiseksi
EP3578561A1 (en) 2018-06-04 2019-12-11 F. Hoffmann-La Roche AG Spiro compounds
CU20210002A7 (es) * 2018-07-10 2021-08-06 Novartis Ag Derivados de 3-(5-hidroxi-1-oxoisoindolin-2-il)piperidina-2,6-diona y su uso en el tratamiento de trastornos dependientes de la proteína con dedos de zinc 2 de la familia ikaros (ikzf2)
US12459921B2 (en) * 2018-09-30 2025-11-04 Shanghai Institute Of Materia Medica, Chinese Academy Of Sciences Isoindoline compound, preparation method, pharmaceutical composition and use thereof
AU2019351811B2 (en) 2018-10-01 2025-01-02 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
US20230045737A1 (en) * 2018-12-05 2023-02-09 Vividion Therapeutics, Inc. Substituted isoindolinones as modulators of cereblon-mediated neo-substrate recruitment
EP3896062A4 (en) 2018-12-06 2022-06-15 Shanghai Institute of Materia Medica, Chinese Academy of Sciences ISOINDOLINE COMPOUND, METHOD FOR PREPARATION, PHARMACEUTICAL COMPOSITION AND USE OF ISOINDOLINE COMPOUND
CN120698983A (zh) 2018-12-20 2025-09-26 C4医药公司 靶向蛋白降解
FI3962489T3 (fi) * 2019-02-22 2023-06-09 Elkem Silicones Usa Corp Lääkeaineen antamiseen tarkoitettu silikonikoostumus vaikuttavan aineen eluution parantamiseksi
US12582641B2 (en) 2019-02-25 2026-03-24 Shanghaitech University Sulfur-containing compound based on glutarimide skeleton and application thereof
ES2995214T3 (en) 2019-03-06 2025-02-07 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
MA55628A (fr) 2019-04-12 2022-02-16 C4 Therapeutics Inc Agents de dégradation tricycliques d'ikaros et d'aiolos
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
CN112321566B (zh) 2019-08-05 2022-06-10 上海科技大学 Egfr蛋白降解剂及其抗肿瘤应用
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
KR20230042057A (ko) * 2020-07-20 2023-03-27 지앙수 헨그루이 파마슈티컬스 컴퍼니 리미티드 황-함유 이소인돌린 유도체, 및 이의 제조 방법 및 이의 의학적 용도
WO2022148358A1 (zh) * 2021-01-05 2022-07-14 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
WO2023138647A1 (zh) 2022-01-19 2023-07-27 江苏恒瑞医药股份有限公司 一种含硫异吲哚啉类衍生物的晶型
CA3249074A1 (en) 2022-06-06 2023-12-14 C4 Therapeutics, Inc. BICYCLIC SUBSTITUTION GLUTARIMIDE CEREBLON BINDERS
PE20251697A1 (es) 2022-11-04 2025-07-02 Bristol Myers Squibb Co Compuestos y su uso para el tratamiento de hemoglobinopatias
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
US20010006973A1 (en) * 1998-03-16 2001-07-05 Hon-Wah Man 1-oxo- and 1,3-dioxoisoindolines and method of reducing inflammatory cytokine levels
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
WO2005028436A2 (en) * 2003-09-17 2005-03-31 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
CN101111234A (zh) 2004-12-01 2008-01-23 细胞基因公司 包含免疫调节化合物的组合物及其治疗免疫缺陷疾病的用途
NZ555768A (en) * 2004-12-24 2009-12-24 Astrazeneca Ab Benzamide derivatives as inhibitors of cytokine mediated disease
AU2008229383B2 (en) * 2007-03-20 2013-09-05 Celgene Corporation 4'-O-substituted isoindoline derivatives and compositions comprising and methods of using the same

Similar Documents

Publication Publication Date Title
JP2018048154A5 (enExample)
RU2018133298A (ru) Способы применения агонистов fxr
CN113767106A (zh) 氧杂氮杂喹唑啉-7(8h)-酮类化合物,其制法与医药上的用途
JP2013519675A5 (enExample)
ES2656696T3 (es) Compuestos heterocíclicos tricíclicos condensados como inhibidores de la integrasa del VIH
JP2010504973A5 (enExample)
JP2016528301A5 (enExample)
JP2017528503A5 (enExample)
JP2017528507A5 (enExample)
WO2014205229A8 (en) Use of high dose pridopidine for treating huntington's disease
RU2017114346A (ru) АНТАГОНИСТЫ ИНТЕГРИНА ανβ6
CN110036005A (zh) 酰胺衍生物及其在药物中的应用
JP2017504611A5 (enExample)
MX2018008021A (es) Metodos y composiciones para el tratamiento de trastornos relacionados con convulsiones.
JP2018537507A5 (enExample)
JP2016515628A5 (enExample)
JP2017522300A5 (enExample)
JP2015510916A5 (enExample)
JP2016510326A5 (enExample)
RU2019100037A (ru) Способ лечения рассеянного склероза с использованием ингибитора lsd1
JP2020529995A5 (enExample)
HRP20241716T1 (hr) Postupci liječenja promjena u ponašanju
PH12017501829A1 (en) Pharmaceutical formulations
BR112022008551A2 (pt) Forma de dosagem farmacêutica de desintegração oral, e, processo para a preparação de uma forma de dosagem de desintegração oral
JP2019085364A5 (enExample)