JP2010540525A5 - - Google Patents
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- 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
Links
- 125000001475 halogen functional group Chemical group 0.000 claims 76
- 229910052739 hydrogen Inorganic materials 0.000 claims 39
- 239000001257 hydrogen Substances 0.000 claims 39
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 36
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 34
- 125000000217 alkyl group Chemical group 0.000 claims 25
- 150000001875 compounds Chemical class 0.000 claims 25
- 125000003118 aryl group Chemical group 0.000 claims 20
- 150000003839 salts Chemical class 0.000 claims 14
- 239000012453 solvate Substances 0.000 claims 14
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 12
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 11
- 125000001072 heteroaryl group Chemical group 0.000 claims 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 9
- 208000035475 disorder Diseases 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- 125000003545 alkoxy group Chemical group 0.000 claims 6
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 5
- 201000010099 disease Diseases 0.000 claims 4
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 201000001320 Atherosclerosis Diseases 0.000 claims 1
- 208000029462 Immunodeficiency disease Diseases 0.000 claims 1
- 208000019693 Lung disease Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 208000002193 Pain Diseases 0.000 claims 1
- 208000034189 Sclerosis Diseases 0.000 claims 1
- 108060008682 Tumor Necrosis Factor Proteins 0.000 claims 1
- 102000000852 Tumor Necrosis Factor-alpha Human genes 0.000 claims 1
- 208000027418 Wounds and injury Diseases 0.000 claims 1
- 230000002159 abnormal effect Effects 0.000 claims 1
- 230000033115 angiogenesis Effects 0.000 claims 1
- 239000010425 asbestos Substances 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 208000015114 central nervous system disease Diseases 0.000 claims 1
- 230000006378 damage Effects 0.000 claims 1
- 230000004064 dysfunction Effects 0.000 claims 1
- 208000014674 injury Diseases 0.000 claims 1
- 208000002780 macular degeneration Diseases 0.000 claims 1
- 244000045947 parasite Species 0.000 claims 1
- 229910052895 riebeckite Inorganic materials 0.000 claims 1
- 208000017520 skin disease Diseases 0.000 claims 1
- 208000011580 syndromic disease Diseases 0.000 claims 1
- 0 *C(CCC(N1)O)(C1O)N(C(*)=NC1=C2CCC=C1*)C2=O Chemical compound *C(CCC(N1)O)(C1O)N(C(*)=NC1=C2CCC=C1*)C2=O 0.000 description 1
- FZYDOMZNKUYWTR-UHFFFAOYSA-N CC(N1C(CCC(N2)=O)C2=O)=NC(C(CC(Cl)=C2)Cl)=C2C1=O Chemical compound CC(N1C(CCC(N2)=O)C2=O)=NC(C(CC(Cl)=C2)Cl)=C2C1=O FZYDOMZNKUYWTR-UHFFFAOYSA-N 0.000 description 1
- BJJPMDJZCMOFPZ-UHFFFAOYSA-N CC(N1C(CCC(N2)=O)C2=O)=Nc(cc(c(OC)c2)OC)c2C1=O Chemical compound CC(N1C(CCC(N2)=O)C2=O)=Nc(cc(c(OC)c2)OC)c2C1=O BJJPMDJZCMOFPZ-UHFFFAOYSA-N 0.000 description 1
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 (show.php) | 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 (21)
| Country | Link |
|---|---|
| US (5) | US8492395B2 (show.php) |
| EP (1) | EP2200999B1 (show.php) |
| JP (1) | JP5637852B2 (show.php) |
| KR (1) | KR101593242B1 (show.php) |
| CN (2) | CN104211684A (show.php) |
| AU (1) | AU2008305581C1 (show.php) |
| BR (1) | BRPI0817525A2 (show.php) |
| CA (1) | CA2704710C (show.php) |
| CO (1) | CO6270228A2 (show.php) |
| CR (1) | CR11355A (show.php) |
| ES (1) | ES2523925T3 (show.php) |
| IL (2) | IL204763A (show.php) |
| MX (1) | MX347987B (show.php) |
| MY (1) | MY157495A (show.php) |
| NI (1) | NI201000041A (show.php) |
| NZ (1) | NZ584425A (show.php) |
| RU (1) | RU2476432C2 (show.php) |
| SG (2) | SG176442A1 (show.php) |
| UA (1) | UA102078C2 (show.php) |
| WO (1) | WO2009042177A1 (show.php) |
| ZA (1) | ZA201002303B (show.php) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107445940A (zh) | 2006-09-26 | 2017-12-08 | 细胞基因公司 | 作为抗肿瘤剂的5‑取代的喹唑酮衍生物 |
| 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 |
| CA2770480C (en) | 2009-08-31 | 2014-11-18 | Merck Sharp & Dohme Corp. | Pyranyl aryl methyl benzoquinazolinone m1 receptor positive allosteric modulators |
| EP2490692B1 (en) | 2009-10-21 | 2016-11-16 | Merck Sharp & Dohme Corp. | Quinolinone-pyrazolone m1 receptor positive allosteric modulators |
| UA113512C2 (xx) | 2011-03-11 | 2017-02-10 | Тверда форма 3-(5-аміно-2-метил-4-оксо-4h-хіназолін-3-іл)піперидин-2,6-діону і її фармацевтична композиція та застосування | |
| EP3025715A1 (en) * | 2011-03-11 | 2016-06-01 | Celgene Corporation | Methods of treating cancer using 3-(5-amino-2-methyl-4-oxo-4h-quinazolin-3-yl)-piperidine-2,6-dione |
| EP2699091B1 (en) | 2011-03-28 | 2017-06-21 | DeuteRx, LLC | 2',6'-dioxo-3'-deutero-piperdin-3-yl-isoindoline compounds |
| US9540340B2 (en) | 2013-01-14 | 2017-01-10 | Deuterx, Llc | 3-(5-substituted-4-oxoquinazolin-3(4H)-yl)-3-deutero-piperidine-2,6-dione derivatives and compositions comprising and methods of using the same |
| WO2014152833A1 (en) | 2013-03-14 | 2014-09-25 | Deuterx, Llc | 3-(substituted-4-oxo-quinazolin-3(4h)-yl)-3-deutero-piperidine-2,6-dione derivatives |
| WO2014172436A1 (en) | 2013-04-17 | 2014-10-23 | Signal Pharmaceuticals, Llc | Combination therapy comprising a tor kinase inhibitor and a 5-substituted quinazolinone compound for treating cancer |
| EP2991651A1 (en) | 2013-05-03 | 2016-03-09 | Celgene Corporation | Methods for treating cancer using combination therapy |
| JP7120763B2 (ja) | 2014-08-22 | 2022-08-17 | セルジーン コーポレイション | 免疫調節化合物を抗体と併用する多発性骨髄腫の治療方法 |
| WO2017004532A1 (en) | 2015-07-02 | 2017-01-05 | Celgene Corporation | Combination therapy for treatment of hematological cancers and solid tumors |
| 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 |
| JP6930748B2 (ja) | 2016-01-14 | 2021-09-01 | カンプ・バイオファーマスーティカルズ、リミテッドＫａｎｇｐｕ Ｂｉｏｐｈａｒｍａｃｅｕｔｉｃａｌｓ，Ｌｔｄ | キナゾリン誘導体、そのための調製方法、医薬組成物、および適用 |
| EP3454856B1 (en) | 2016-05-10 | 2024-09-11 | C4 Therapeutics, Inc. | Heterocyclic degronimers for target protein degradation |
| WO2017197036A1 (en) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Spirocyclic degronimers for target protein degradation |
| EP3455218A4 (en) | 2016-05-10 | 2019-12-18 | C4 Therapeutics, Inc. | C3 CARBON-BASED GLUTARIMIDE DEGRONIMERS FOR TARGET PROTEIN REDUCTION |
| WO2017197051A1 (en) | 2016-05-10 | 2017-11-16 | C4 Therapeutics, Inc. | Amine-linked c3-glutarimide degronimers for target protein degradation |
| 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 |
| CN110769822A (zh) | 2017-06-20 | 2020-02-07 | C4医药公司 | 用于蛋白降解的n/o-连接的降解决定子和降解决定子体 |
| WO2019043208A1 (en) | 2017-09-04 | 2019-03-07 | F. Hoffmann-La Roche Ag | DIHYDROQUINOLINONES |
| WO2019043214A1 (en) | 2017-09-04 | 2019-03-07 | F. Hoffmann-La Roche Ag | glutarimide |
| EP3679027A1 (en) | 2017-09-04 | 2020-07-15 | C4 Therapeutics, Inc. | Dihydrobenzimidazolones |
| JP2021501198A (ja) * | 2017-10-27 | 2021-01-14 | トランスフュージョン ヘルス，リミティド ライアビリティ カンパニー | フルオレンの誘導体を用いて造血幹細胞を増殖する組成物および方法 |
| 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 |
| EP3781156A4 (en) | 2018-04-16 | 2022-05-18 | C4 Therapeutics, Inc. | SPIROCYCLIC COMPOUNDS |
| EP3578561A1 (en) | 2018-06-04 | 2019-12-11 | F. Hoffmann-La Roche AG | Spiro compounds |
| WO2020132561A1 (en) | 2018-12-20 | 2020-06-25 | C4 Therapeutics, Inc. | Targeted protein degradation |
| EA202192738A1 (ru) | 2019-04-12 | 2022-03-17 | С4 Терапьютикс, Инк. | Трициклические соединения, обеспечивающие разрушение белка ikaros и белка aiolos |
| US12280096B2 (en) | 2021-07-12 | 2025-04-22 | Penland Foundation | Treatments of cancer using nitrous oxide and botulinum toxin |
| WO2021168314A1 (en) | 2020-02-21 | 2021-08-26 | Plexium, Inc. | Quinazolinone compounds and related compounds |
| EP4198030A4 (en) * | 2020-08-14 | 2024-01-10 | Shanghaitech University | Immunoregulatory compound and antitumor application thereof |
| KR20250021314A (ko) | 2022-06-06 | 2025-02-12 | 씨4 테라퓨틱스, 인코포레이티드 | 비시클릭-치환된 글루타르이미드 세레블론 결합제 |
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| CN107445940A (zh) * | 2006-09-26 | 2017-12-08 | 细胞基因公司 | 作为抗肿瘤剂的5‑取代的喹唑酮衍生物 |
-
2008
- 2008-09-25 BR BRPI0817525-0A2A patent/BRPI0817525A2/pt not_active Application Discontinuation
- 2008-09-25 CA CA2704710A patent/CA2704710C/en not_active Expired - Fee Related
- 2008-09-25 WO PCT/US2008/011124 patent/WO2009042177A1/en not_active Ceased
- 2008-09-25 UA UAA201004853A patent/UA102078C2/ru unknown
- 2008-09-25 JP JP2010526944A patent/JP5637852B2/ja active Active
- 2008-09-25 KR KR1020107008968A patent/KR101593242B1/ko not_active Expired - Fee Related
- 2008-09-25 ES ES08834539.2T patent/ES2523925T3/es active Active
- 2008-09-25 US US12/238,354 patent/US8492395B2/en active Active
- 2008-09-25 CN CN201410362879.4A patent/CN104211684A/zh active Pending
- 2008-09-25 NZ NZ584425A patent/NZ584425A/en not_active IP Right Cessation
- 2008-09-25 SG SG2011080553A patent/SG176442A1/en unknown
- 2008-09-25 MY MYPI2010001343A patent/MY157495A/en unknown
- 2008-09-25 AU AU2008305581A patent/AU2008305581C1/en not_active Ceased
- 2008-09-25 CN CN200880117819.9A patent/CN101952272B/zh not_active Expired - Fee Related
- 2008-09-25 MX MX2010003355A patent/MX347987B/es active IP Right Grant
- 2008-09-25 RU RU2010116273/04A patent/RU2476432C2/ru not_active IP Right Cessation
- 2008-09-25 EP EP08834539.2A patent/EP2200999B1/en active Active
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2010
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- 2010-04-20 CO CO10046034A patent/CO6270228A2/es not_active Application Discontinuation
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2013
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2015
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2017
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