PE20211375A1 - Compuestos de 4-aminoisoindolina-1,3-diona sustituidos y su uso para el tratamiento de linfoma - Google Patents

Compuestos de 4-aminoisoindolina-1,3-diona sustituidos y su uso para el tratamiento de linfoma

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Publication number
PE20211375A1
PE20211375A1 PE2020001622A PE2020001622A PE20211375A1 PE 20211375 A1 PE20211375 A1 PE 20211375A1 PE 2020001622 A PE2020001622 A PE 2020001622A PE 2020001622 A PE2020001622 A PE 2020001622A PE 20211375 A1 PE20211375 A1 PE 20211375A1
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Peru
Prior art keywords
compounds
aminoisoindoline
lymphoma
diona
substituted
Prior art date
Application number
PE2020001622A
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English (en)
Inventor
Matthew D Alexander
Soraya Carrancio
Matthew D Correa
Virginia Heather Sharron Grant
Joshua Hansen
Roy L Harris
Dehua Huang
Timothy S Kercher
Antonia Lopez-Girona
Mark A Nagy
Veronique Plantevin-Krenitsky
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Celgene Corp
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Application filed by Celgene Corp filed Critical Celgene Corp
Publication of PE20211375A1 publication Critical patent/PE20211375A1/es

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    • C07D401/04Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
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    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
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Abstract

Esta referido a derivados de 4-aminoisoindolina-1,3-diona de Formula I, en donde: Anillo A es un heterociclilo no aromatico opcionalmente sustituido; R es alquilo C1-3 opcionalmente sustituido, halogeno; n es 0, 1, 2, 3, 4. Entre los compuestos preferidos tenemos los siguientes: 4-(4-((4-(2,4-difluorofenil)piperazin-1-il)metil)bencilamino)-2-(2,6-dioxopiperidin-3-il)isoindolina-1,3-diona; 2-(2,6-dioxopiperidin-3-il)-4-(4-((4-(4-fluorofenil)piperazin-1-il)metil)bencilamino)isoindolina-1,3-diona; entre otros. Estos compuestos se emplean para tratar o prevenir el linfoma difuso de celulas B grandes (DLBCL).
PE2020001622A 2018-04-23 2019-04-22 Compuestos de 4-aminoisoindolina-1,3-diona sustituidos y su uso para el tratamiento de linfoma PE20211375A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862661525P 2018-04-23 2018-04-23
PCT/US2019/028471 WO2019209692A1 (en) 2018-04-23 2019-04-22 Substituted 4-aminoisoindoline-1,3-dione compounds and their use for treating lymphoma

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PE20211375A1 true PE20211375A1 (es) 2021-07-27

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EP (2) EP4272737A3 (es)
JP (2) JP7458324B2 (es)
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Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR119715A1 (es) 2019-04-12 2022-01-05 Celgene Corp Métodos para tratar linfoma no hodgkin con el uso de 2-(2,6-dioxopiperidin-3-il)-4-((2-fluoro-4-((3-morfolinoazetidin-1-il)metil)bencil)amino)isoindolin-1,3-diona
BR112022007386A2 (pt) * 2019-10-21 2022-07-05 Celgene Corp Métodos para tratar um câncer hematológico e o uso de biomarcadores companheiros para 2-(2,6-dioxopiperidin-3-il)-4-((2-fluoro-4-((3-morfolinoazetidin-1-il)metil)benzil)amino)isoindolina-1,3-diona
BR112022007410A2 (pt) * 2019-10-21 2022-07-05 Celgene Corp Compostos de 4-aminoisoindolina-1,3-diona substituída e segundos agentes ativos para uso combinado
IL292375A (en) * 2019-10-21 2022-06-01 Celgene Corp Solid forms include (s)-2-(2,6-dioxopiperidin-3-yl)-4-((2-fluoro-4-((3-morpholinoazetidin-1-yl)metyl)benzyl)amino)isoindoline-1 3- Discussion and salts from them, and preparations that include the same and their use
CN115919871A (zh) 2019-10-21 2023-04-07 新基公司 使用化合物治疗血液恶性肿瘤的方法
WO2021080937A1 (en) 2019-10-21 2021-04-29 Celgene Corporation Pharmaceutical compositions comprising (s)-2-(2,6-dioxopiperidin-3-yl)-4-((2-fluoro-4-((3-morpholinoazetidin-1-yl)methyl)benzyl)amino)isoindoline-1,3-dione and methods of using the same
KR20220103953A (ko) * 2019-10-21 2022-07-25 셀진 코포레이션 2-(2,6-디옥소피페리딘-3-일)-4-((2-플루오로-4-((3-모르폴리노아제티딘-1-일)메틸)벤질)아미노)이소인돌린-1,3-디온을 사용하여 만성 림프구성 백혈병을 치료하는 방법
CN115038694A (zh) * 2020-01-20 2022-09-09 康朴生物医药技术(上海)有限公司 一种异吲哚啉衍生物、其药物组合物及应用
CN116669736A (zh) * 2021-01-05 2023-08-29 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
WO2022152821A1 (en) 2021-01-13 2022-07-21 Monte Rosa Therapeutics Ag Isoindolinone compounds
BR112023020012A2 (pt) 2021-03-29 2023-11-14 Juno Therapeutics Inc Combinação de uma terapia de células t que expressam car e um composto imunomodulador para o tratamento de linfoma
JP2024515108A (ja) 2021-04-21 2024-04-04 セルジーン コーポレーション 2-(2,6-ジオキソピペリジン-3-イル)-4-((2-フルオロ-4-((3-モルホリノアゼチジン-1-イル)メチル)ベンジル)アミノ)イソインドリン-1,3-ジオンを使用して非ホジキンリンパ腫を治療する方法
AU2022260522A1 (en) 2021-04-21 2023-09-21 Bristol-Myers Squibb Company Methods of treating b-cell lymphoma using combination therapy
WO2022271557A1 (en) 2021-06-21 2022-12-29 Celgene Corporation Processes for the preparation of (s)-2-(2,6-dioxopiperidin-3-yl)-4-((2-fluoro-4-((3-morpholinoazetidin-1-yl) methyl)benzyl) amino)isoindoline-1,3-dione
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
WO2023220655A1 (en) 2022-05-11 2023-11-16 Celgene Corporation Methods to overcome drug resistance by re-sensitizing cancer cells to treatment with a prior therapy via treatment with a t cell therapy
WO2023220641A2 (en) 2022-05-11 2023-11-16 Juno Therapeutics, Inc. Methods and uses related to t cell therapy and production of same
CN117088864A (zh) * 2022-05-13 2023-11-21 广州智药生物科技有限公司 一种苯并[d]异恶唑类化合物及其应用
WO2024097905A1 (en) 2022-11-02 2024-05-10 Celgene Corporation Methods of treatment with t cell therapy and immunomodulatory agent maintenance therapy

Family Cites Families (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030045552A1 (en) 2000-12-27 2003-03-06 Robarge Michael J. Isoindole-imide compounds, compositions, and uses thereof
US7091353B2 (en) 2000-12-27 2006-08-15 Celgene Corporation Isoindole-imide compounds, compositions, and uses thereof
EP1505973B1 (en) 2002-05-17 2010-03-03 Celgene Corporation Combinations for treating multiple myeloma
US7563810B2 (en) 2002-11-06 2009-07-21 Celgene Corporation Methods of using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myeloproliferative diseases
CN100398534C (zh) 2003-09-15 2008-07-02 天津和美生物技术有限公司 合成酞胺哌啶酮及其衍生物的方法
US20050143344A1 (en) 2003-12-30 2005-06-30 Zeldis Jerome B. Methods and compositions using immunomodulatory compounds for the treatment and management of central nervous system disorders or diseases
CA2579291C (en) 2004-09-03 2011-11-29 Celgene Corporation Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines
WO2006053160A2 (en) 2004-11-12 2006-05-18 Celgene Corporation Methods and compositions using immunomodulatory compounds for treatment and management of parasitic diseases
JP5366544B2 (ja) 2005-06-30 2013-12-11 セルジーン コーポレイション 4−アミノ−2−(2,6−ジオキソピペリジン−3−イル)イソインドリン−1,3−ジオン化合物を調製するための方法
ES2434946T3 (es) 2005-08-31 2013-12-18 Celgene Corporation Compuestos de isoindol imida y composiciones que los comprenden y métodos para usarlo
CA2633980A1 (en) 2005-12-29 2007-07-12 Anthrogenesis Corporation Improved composition for collecting and preserving placental stem cells and methods of using the composition
WO2007136640A2 (en) 2006-05-16 2007-11-29 Celgene Corporation Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione
US8877780B2 (en) 2006-08-30 2014-11-04 Celgene Corporation 5-substituted isoindoline compounds
ES2426350T3 (es) 2006-08-30 2013-10-22 Celgene Corporation Compuestos de isoindolina sustituidos en 5
TW200819435A (en) * 2006-09-15 2008-05-01 Celgene Corp N-methylaminomethyl isoindole compounds and compositions comprising and methods of using the same
WO2008115516A2 (en) 2007-03-20 2008-09-25 Celgene Corporation 4'-o-substituted isoindoline derivatives and compositions comprising and methods of using the same
AU2008325140A1 (en) 2007-11-08 2009-05-14 Celgene Corporation Use of immunomodulatory compounds for the treatment of disorders associated with endothelial dysfunction
NZ592425A (en) 2008-10-29 2013-04-26 Celgene Corp Isoindoline compounds for use in the treatment of cancer
RS58523B1 (sr) * 2010-02-11 2019-04-30 Celgene Corp Derivati arilmetoksi izoindolina i kombinacije koje ih obuhvataju i postupci njihove upotrebe
US20110312996A1 (en) 2010-05-17 2011-12-22 Intermune, Inc. Novel inhibitors of hepatitis c virus replication
MY162132A (en) * 2010-06-23 2017-05-31 Hanmi Science Co Ltd Novel fused pyrimidine derivatives for inhibition of tyrosine kinase activity
US20140206629A1 (en) 2011-02-17 2014-07-24 Rhode Island Hospital Stromal Derived Factor Inhibition And CXCR4 Blockade
AU2012236655B2 (en) 2011-03-28 2016-09-22 Deuterx, Llc, 2',6'-dioxo-3'-deutero-piperdin-3-yl-isoindoline compounds
WO2016040449A1 (en) 2014-09-10 2016-03-17 Raze Therapeutics, Inc. 3-phosphoglycerate dehydrogenase inhibitors and uses thereof
PL3214081T3 (pl) 2014-10-30 2021-04-06 Kangpu Biopharmaceuticals, Ltd. Pochodna izoindoliny, półprodukt, sposób wytwarzania, kompozycja farmaceutyczna i ich zastosowanie
CN107257800B (zh) 2014-12-23 2020-06-30 达纳-法伯癌症研究所股份有限公司 通过双功能分子诱导靶蛋白降解的方法
WO2017007612A1 (en) 2015-07-07 2017-01-12 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
WO2017024317A2 (en) 2015-08-06 2017-02-09 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
DK3357513T3 (da) * 2015-09-29 2023-11-27 Kangpu Biopharmaceuticals Inc Farmaceutisk sammensætning og anvendelse deraf
RU2730500C2 (ru) 2016-01-14 2020-08-24 Канпу Биофармасьютикалз, Лтд Производное хиназолинона, способ его получения, фармацевтическая композиция и применения
MX2018011105A (es) 2016-03-16 2018-11-22 Kura Oncology Inc Inhibidores sustituidos de menina-mll y metodos de uso.
US11192898B2 (en) 2016-04-06 2021-12-07 The Regents Of The University Of Michigan MDM2 protein degraders
WO2017197056A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Bromodomain targeting degronimers for target protein degradation
CA3025806C (en) 2016-06-23 2023-04-04 Dana-Farber Cancer Institute, Inc. Degradation of bromodomain-containing protein 9 (brd9) by conjugation of brd9 inhibitors with e3 ligase ligand and methods of use
US10702504B2 (en) 2016-06-23 2020-07-07 Dana-Farber Cancer Institute, Inc. Degradation of tripartite motif-containing protein 24 (TRIM24) by conjugation of TRIM24 inhibitors with E3 ligase ligand and methods of use
US10646488B2 (en) 2016-07-13 2020-05-12 Araxes Pharma Llc Conjugates of cereblon binding compounds and G12C mutant KRAS, HRAS or NRAS protein modulating compounds and methods of use thereof
WO2018071606A1 (en) 2016-10-11 2018-04-19 Arvinas, Inc. Compounds and methods for the targeted degradation of androgen receptor
SG10202104386UA (en) 2016-10-28 2021-05-28 Icahn School Med Mount Sinai Compositions and methods for treating ezh2-mediated cancer
JP7097880B2 (ja) 2016-11-01 2022-07-08 コーネル ユニバーシティー Malt1分解のための化合物
EP3544957B1 (en) 2016-11-22 2024-05-29 Dana-Farber Cancer Institute, Inc. Degradation of protein kinases by conjugation of protein kinase inhibitors with e3 ligase ligand and methods of use
EP3689868B1 (en) 2016-12-01 2023-09-27 Arvinas Operations, Inc. Tetrahydronaphthalene and tetrahydroisoquinoline derivatives as estrogen receptor degraders
CN110267659A (zh) 2016-12-08 2019-09-20 西奈山伊坎医学院 用于治疗cdk4/6介导的癌症的组合物和方法
CN107056772A (zh) 2017-01-23 2017-08-18 中国药科大学 基于cereblon配体诱导BET降解的双功能分子及其制备和应用
KR20230140606A (ko) 2017-01-26 2023-10-06 아비나스 오퍼레이션스, 인코포레이티드 에스트로겐 수용체 단백질 분해 조절제 및 관련 사용 방법
MX2019009046A (es) 2017-01-31 2019-10-30 Arvinas Operations Inc Ligandos de cereblon y compuestos bifuncionales que comprenden el mismo.
KR102125661B1 (ko) 2017-02-13 2020-06-22 강푸 바이오파마슈티칼즈 리미티드 전립선암 치료용 조합, 약학 조성물 및 치료 방법
CN108929307A (zh) * 2017-05-22 2018-12-04 苏州偶领生物医药有限公司 一类异吲哚酮-酰亚胺环-1,3-二酮-2-烯化合物、其组合物和用途
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
JP7260521B2 (ja) 2017-07-12 2023-04-18 ダナ-ファーバー キャンサー インスティテュート, インコーポレイテッド タウタンパク質分解の化合物
CN107698575A (zh) 2017-09-26 2018-02-16 中国药科大学 cereblon配体介导的新型BET蛋白降解的双功能分子及其制备和应用
US11819532B2 (en) 2018-04-23 2023-11-21 Hoffmann-La Roche Inc. Peptide macrocycles against Acinetobacter baumannii
CN108715585A (zh) 2018-04-23 2018-10-30 中国药科大学 苯基联三氮唑类mll1-wdr5蛋白-蛋白相互作用抑制剂
CN108690020A (zh) 2018-07-04 2018-10-23 清华大学 一种靶向降解bet蛋白的化合物及其应用
CN108794453A (zh) 2018-07-05 2018-11-13 清华大学 一种靶向降解fak蛋白的化合物及其应用

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