JP2010540525A5 - - Google Patents

Download PDF

Info

Publication number
JP2010540525A5
JP2010540525A5 JP2010526944A JP2010526944A JP2010540525A5 JP 2010540525 A5 JP2010540525 A5 JP 2010540525A5 JP 2010526944 A JP2010526944 A JP 2010526944A JP 2010526944 A JP2010526944 A JP 2010526944A JP 2010540525 A5 JP2010540525 A5 JP 2010540525A5
Authority
JP
Japan
Prior art keywords
halo
optionally substituted
alkyl
hydrogen
compound according
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
JP2010526944A
Other languages
English (en)
Japanese (ja)
Other versions
JP2010540525A (ja
JP5637852B2 (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2008/011124 external-priority patent/WO2009042177A1/en
Publication of JP2010540525A publication Critical patent/JP2010540525A/ja
Publication of JP2010540525A5 publication Critical patent/JP2010540525A5/ja
Application granted granted Critical
Publication of JP5637852B2 publication Critical patent/JP5637852B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2010526944A 2007-09-26 2008-09-25 6、7又は8置換キナゾリノン誘導体並びにそれらを含有する組成物及びそれらを使用する方法 Active JP5637852B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US99567607P 2007-09-26 2007-09-26
US60/995,676 2007-09-26
PCT/US2008/011124 WO2009042177A1 (en) 2007-09-26 2008-09-25 6-, 7-, or 8-substituted quinazolinone derivatives and compositions comprising and methods of using the same

Publications (3)

Publication Number Publication Date
JP2010540525A JP2010540525A (ja) 2010-12-24
JP2010540525A5 true JP2010540525A5 (US07794700-20100914-C00152.png) 2011-11-17
JP5637852B2 JP5637852B2 (ja) 2014-12-10

Family

ID=40225265

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010526944A Active JP5637852B2 (ja) 2007-09-26 2008-09-25 6、7又は8置換キナゾリノン誘導体並びにそれらを含有する組成物及びそれらを使用する方法

Country Status (22)

Country Link
US (5) US8492395B2 (US07794700-20100914-C00152.png)
EP (1) EP2200999B1 (US07794700-20100914-C00152.png)
JP (1) JP5637852B2 (US07794700-20100914-C00152.png)
KR (1) KR101593242B1 (US07794700-20100914-C00152.png)
CN (2) CN104211684A (US07794700-20100914-C00152.png)
AU (1) AU2008305581C1 (US07794700-20100914-C00152.png)
BR (1) BRPI0817525A2 (US07794700-20100914-C00152.png)
CA (1) CA2704710C (US07794700-20100914-C00152.png)
CO (1) CO6270228A2 (US07794700-20100914-C00152.png)
CR (1) CR11355A (US07794700-20100914-C00152.png)
ES (1) ES2523925T3 (US07794700-20100914-C00152.png)
HK (1) HK1139934A1 (US07794700-20100914-C00152.png)
IL (2) IL204763A (US07794700-20100914-C00152.png)
MX (1) MX347987B (US07794700-20100914-C00152.png)
MY (1) MY157495A (US07794700-20100914-C00152.png)
NI (1) NI201000041A (US07794700-20100914-C00152.png)
NZ (1) NZ584425A (US07794700-20100914-C00152.png)
RU (1) RU2476432C2 (US07794700-20100914-C00152.png)
SG (2) SG10201503486XA (US07794700-20100914-C00152.png)
UA (1) UA102078C2 (US07794700-20100914-C00152.png)
WO (1) WO2009042177A1 (US07794700-20100914-C00152.png)
ZA (1) ZA201002303B (US07794700-20100914-C00152.png)

Families Citing this family (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5388854B2 (ja) 2006-09-26 2014-01-15 セルジーン コーポレイション 5−置換キナゾリノン誘導体、それを含む組成物、及びその使用方法
US8354417B2 (en) * 2007-09-26 2013-01-15 Celgene Corporation Solid forms comprising 3-(2,5-dimethyl-4-oxo-4H-quinazolin-3-yl)-piperidine-2,6-dione, compositions comprising the same, and methods of using the same
ME02151B (me) * 2009-08-31 2015-10-20 Merck Sharp & Dohme Piranil aril metil benzohinazolinon kao pozitivni alosterni modulatori receptora m1
WO2011049731A1 (en) 2009-10-21 2011-04-28 Merck Sharp & Dohme Corp. Quinolinone-pyrazolone m1 receptor positive allosteric modulators
DK2683708T3 (da) 2011-03-11 2018-01-29 Celgene Corp Faste former af 3-(5-amino-2-methyl-4-oxo-4h-quinazolin-3-yl)-piperidin-2,6-dion og farmaceutiske sammensætninger og anvendelser deraf
AR085651A1 (es) * 2011-03-11 2013-10-16 Celgene Corp Metodos para tratar cancer usando 3-(5-amino-2-metil-4-oxo-4h-quinazolin-3-il)-piperidin-2,6-diona
AU2012236655B2 (en) 2011-03-28 2016-09-22 Deuterx, Llc, 2',6'-dioxo-3'-deutero-piperdin-3-yl-isoindoline compounds
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
EP2968334A4 (en) * 2013-03-14 2016-08-03 Deuterx Llc 3- (SUBSTITIERTES-4-OXO-quinazolin-3 (4H) -yl) -3-deutero-PIPERIDINE-2,6-DIONE DERIVATIVES
CA2909625C (en) 2013-04-17 2021-06-01 Signal Pharmaceuticals, Llc Combination therapy comprising a tor kinase inhibitor and a 5-substituted quinazolinone compound for treating cancer
TW201534305A (zh) * 2013-05-03 2015-09-16 Celgene Corp 使用組合療法治療癌症之方法
HUE061382T2 (hu) 2014-08-22 2023-06-28 Celgene Corp Eljárás myeloma multiplex kezelésére immunomoduláló vegyületekkel, antestekkel kombinálva
KR20180023968A (ko) 2015-07-02 2018-03-07 셀진 코포레이션 혈액암 및 충실성 종양의 치료를 위한 병용 요법
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
EP3404024B1 (en) 2016-01-14 2020-11-18 Kangpu Biopharmaceuticals, Ltd. Quinazolinone derivative, preparation method therefor, pharmaceutical composition, and applications
WO2017197055A1 (en) 2016-05-10 2017-11-16 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
CN109562113A (zh) 2016-05-10 2019-04-02 C4医药公司 用于靶蛋白降解的螺环降解决定子体
WO2018208123A1 (ko) * 2017-05-12 2018-11-15 한국화학연구원 신규한 피페리딘-2,6-디온 유도체 및 이의 용도
KR102014478B1 (ko) 2017-05-12 2019-08-26 한국화학연구원 신규한 피페리딘-2,6-디온 유도체 및 이의 용도
WO2018237026A1 (en) 2017-06-20 2018-12-27 C4 Therapeutics, Inc. N / O-LINKED DEGRONS AND DEGRONIMERS FOR DEGRADATION OF PROTEINS
CN111278816B (zh) 2017-09-04 2024-03-15 C4医药公司 二氢喹啉酮
EP3679026A1 (en) 2017-09-04 2020-07-15 C4 Therapeutics, Inc. Glutarimide
CN111315735B (zh) 2017-09-04 2024-03-08 C4医药公司 二氢苯并咪唑酮
CA3079959A1 (en) * 2017-10-27 2018-10-26 Transfusion Health, Llc Compositions and methods of making expanded hematopoietic stem cells using derivatives of fluorene
WO2019099868A2 (en) 2017-11-16 2019-05-23 C4 Therapeutics, Inc. Degraders and degrons for targeted protein degradation
WO2019191112A1 (en) 2018-03-26 2019-10-03 C4 Therapeutics, Inc. Cereblon binders for the degradation of ikaros
CN112312904A (zh) 2018-04-16 2021-02-02 C4医药公司 螺环化合物
EP3578561A1 (en) 2018-06-04 2019-12-11 F. Hoffmann-La Roche AG Spiro compounds
CN113677664A (zh) 2019-04-12 2021-11-19 C4医药公司 Ikaros和aiolos的三环降解物
US11807620B2 (en) 2020-02-21 2023-11-07 Plexium, Inc. Quinazolinone compounds and related compounds
WO2022033548A1 (zh) * 2020-08-14 2022-02-17 上海科技大学 免疫调节化合物及其抗肿瘤应用

Family Cites Families (55)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3536809A (en) 1969-02-17 1970-10-27 Alza Corp Medication method
US3598123A (en) 1969-04-01 1971-08-10 Alza Corp Bandage for administering drugs
US3845770A (en) 1972-06-05 1974-11-05 Alza Corp Osmatic dispensing device for releasing beneficial agent
US3916899A (en) 1973-04-25 1975-11-04 Alza Corp Osmotic dispensing device with maximum and minimum sizes for the passageway
US4008719A (en) 1976-02-02 1977-02-22 Alza Corporation Osmotic system having laminar arrangement for programming delivery of active agent
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
IE58110B1 (en) 1984-10-30 1993-07-14 Elan Corp Plc Controlled release powder and process for its preparation
US5073543A (en) 1988-07-21 1991-12-17 G. D. Searle & Co. Controlled release formulations of trophic factors in ganglioside-lipsome vehicle
IT1229203B (it) 1989-03-22 1991-07-25 Bioresearch Spa Impiego di acido 5 metiltetraidrofolico, di acido 5 formiltetraidrofolico e dei loro sali farmaceuticamente accettabili per la preparazione di composizioni farmaceutiche in forma a rilascio controllato attive nella terapia dei disturbi mentali organici e composizioni farmaceutiche relative.
US5120548A (en) 1989-11-07 1992-06-09 Merck & Co., Inc. Swelling modulated polymeric drug delivery device
KR0166088B1 (ko) 1990-01-23 1999-01-15 . 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도
US5733566A (en) 1990-05-15 1998-03-31 Alkermes Controlled Therapeutics Inc. Ii Controlled release of antiparasitic agents in animals
US5580578A (en) 1992-01-27 1996-12-03 Euro-Celtique, S.A. Controlled release formulations coated with aqueous dispersions of acrylic polymers
US5591767A (en) 1993-01-25 1997-01-07 Pharmetrix Corporation Liquid reservoir transdermal patch for the administration of ketorolac
WO1995003009A1 (en) 1993-07-22 1995-02-02 Oculex Pharmaceuticals, Inc. Method of treatment of macular degeneration
US5770589A (en) 1993-07-27 1998-06-23 The University Of Sydney Treatment of macular degeneration
IT1270594B (it) 1994-07-07 1997-05-07 Recordati Chem Pharm Composizione farmaceutica a rilascio controllato di moguisteina in sospensione liquida
IT1274549B (it) 1995-05-23 1997-07-17 Indena Spa Uso di flavanolignani per la preparazione di medicamenti ad attivita' antiproliferativa nei tumori dell'utero,dell'ovaio e del seno
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
EA002905B1 (ru) * 1996-05-15 2002-10-31 Пфайзер Инк. 2,3-двузамещенные-4(3н)-хиназолиноны и содержащая их фармацевтическая композиция
US6281230B1 (en) 1996-07-24 2001-08-28 Celgene Corporation Isoindolines, method of use, and pharmaceutical compositions
HU228769B1 (en) 1996-07-24 2013-05-28 Celgene Corp Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1-oxoisoindolines and their use for production of pharmaceutical compositions for mammals to reduce the level of tnf-alpha
US5635517B1 (en) * 1996-07-24 1999-06-29 Celgene Corp Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines
DE69740140D1 (de) 1996-07-24 2011-04-14 Celgene Corp Substituierte 2-(2,6-Dioxopiperidin-3-yl)-phthalimide und Oxoisoindoline und Verfahren zur Verringerung der TNF-Alpha-Stufen
HUP0102113A3 (en) * 1998-03-16 2003-03-28 Celgene Corp Warren 2-(2,6-dioxopiperidin-3-yl)isoindoline derivatives, their preparation and their use as inhibitors of inflammatory cytokines
US6015803A (en) 1998-05-04 2000-01-18 Wirostko; Emil Antibiotic treatment of age-related macular degeneration
US6225348B1 (en) 1998-08-20 2001-05-01 Alfred W. Paulsen Method of treating macular degeneration with a prostaglandin derivative
US6001368A (en) 1998-09-03 1999-12-14 Protein Technologies International, Inc. Method for inhibiting or reducing the risk of macular degeneration
US7182953B2 (en) 1999-12-15 2007-02-27 Celgene Corporation Methods and compositions for the prevention and treatment of atherosclerosis restenosis and related disorders
US20030045552A1 (en) 2000-12-27 2003-03-06 Robarge Michael J. Isoindole-imide compounds, compositions, and uses thereof
CN1511420A (zh) 2001-11-09 2004-07-07 松下电器产业株式会社 运动图像编码方法和装置
US7381730B2 (en) 2002-03-15 2008-06-03 Bristol-Myers Squibb Company 3-arylquinazoline derivatives as selective estrogen receptor beta modulators
US7393862B2 (en) 2002-05-17 2008-07-01 Celgene Corporation Method using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for treatment of certain leukemias
US7968569B2 (en) 2002-05-17 2011-06-28 Celgene Corporation Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione
US7323479B2 (en) 2002-05-17 2008-01-29 Celgene Corporation Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline
US7211580B2 (en) * 2002-07-23 2007-05-01 Cytokinetics, Incorporated Compounds, compositions, and methods
US7189740B2 (en) 2002-10-15 2007-03-13 Celgene Corporation Methods of using 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myelodysplastic syndromes
US20050203142A1 (en) 2002-10-24 2005-09-15 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for treatment, modification and management of pain
US20040091455A1 (en) 2002-10-31 2004-05-13 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for treatment and management of macular degeneration
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
GB0324790D0 (en) * 2003-10-24 2003-11-26 Astrazeneca Ab Amide derivatives
US20050100529A1 (en) 2003-11-06 2005-05-12 Zeldis Jerome B. Methods of using and compositions comprising immunomodulatory compounds for the treatment and management of asbestos-related diseases and disorders
MXPA06006061A (es) 2003-12-02 2006-08-11 Celgene Corp Metodos y composiciones para el tratamiento y manejo de la hemoglinopatia y la anemia.
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
EP1737453A4 (en) 2004-03-22 2008-11-26 Celgene Corp METHOD FOR THE USE OF IMMUNOMODULATORY COMPOUNDS AND COMPOSITIONS CONTAINING THEREOF FOR THE TREATMENT AND SUPPLY OF SKIN DISEASES OR DISORDERS
CA2563038C (en) * 2004-04-02 2013-10-29 Gaik Beng Kok Neurologically-active compounds
AU2005237490A1 (en) 2004-04-23 2005-11-10 Celgene Corporation Methods of using and compositions comprising immunomodulatory compounds for the treatment and management of pulmonary hypertension
MXPA06014696A (es) * 2004-06-15 2007-02-12 Astrazeneca Ab Quinazolonas sustituidas como agentes anticancerosos.
WO2006053160A2 (en) 2004-11-12 2006-05-18 Celgene Corporation Methods and compositions using immunomodulatory compounds for treatment and management of parasitic diseases
CN101102771A (zh) 2004-11-23 2008-01-09 细胞基因公司 用免疫调节化合物治疗和控制中枢神经系统损伤的方法和组合物
JP5775245B2 (ja) 2004-12-01 2015-09-09 セルジーン コーポレイション 免疫不全障害の治療のために免疫調節化合物を用いる方法及び組成物
CA2620085C (en) 2005-08-31 2016-07-12 Celgene Corporation Isoindole-imide compounds and compositions comprising and methods of using the same
DE602006020300D1 (de) 2005-09-01 2011-04-07 Celgene Corp Immunologische verwendungen von immunmodulatorischen verbindungen für einen impfstoff und therapie gegen infektionskrankheiten
JP5388854B2 (ja) * 2006-09-26 2014-01-15 セルジーン コーポレイション 5−置換キナゾリノン誘導体、それを含む組成物、及びその使用方法

Similar Documents

Publication Publication Date Title
JP2010540525A5 (US07794700-20100914-C00152.png)
JP2014508811A5 (US07794700-20100914-C00152.png)
JP2013544860A5 (US07794700-20100914-C00152.png)
RU2012127334A (ru) Производные 5-замещенного хиназолинона, содержащие их композиции и способы их применения
JP2008546770A5 (US07794700-20100914-C00152.png)
JP2007508360A5 (US07794700-20100914-C00152.png)
JP2020502047A5 (US07794700-20100914-C00152.png)
JP2009501745A5 (US07794700-20100914-C00152.png)
JP2010503688A5 (US07794700-20100914-C00152.png)
JP2013513613A5 (US07794700-20100914-C00152.png)
JP2006524660A5 (US07794700-20100914-C00152.png)
JP2011519854A5 (US07794700-20100914-C00152.png)
JP2014530900A5 (US07794700-20100914-C00152.png)
JP2007508361A5 (US07794700-20100914-C00152.png)
JP2016506960A5 (US07794700-20100914-C00152.png)
JP2008539268A5 (US07794700-20100914-C00152.png)
JP2009514823A5 (US07794700-20100914-C00152.png)
NZ599199A (en) 4'-o-substituted isoindoline derivatives and compositions comprising and methods of using the same
RU2014121090A (ru) Модуляторы рецептора нмда и их применение
NO20076498L (no) Derivater av 4-(2-amino-1-hydroksyetyl)fenol som agonister av den betta2-adrenerge reseptoren
JP2013505969A5 (US07794700-20100914-C00152.png)
RU2010116273A (ru) 6-, 7-, или 8-замещенные производные хиназолинона и композиции, включающие их и способы их использования
JP2011509309A5 (US07794700-20100914-C00152.png)
JP2018135343A5 (US07794700-20100914-C00152.png)
JP2014516033A5 (US07794700-20100914-C00152.png)