BRPI0607239A2 - usos de uma quantidade terapeuticamente ou profilaticamente eficaz de 4-amino-2-(3-metil-2,6-dioxopiperidin-3-il)-isoindol-1,3-d iona, de (3r)-4-amino-2-(3-metil-2,6-dioxopiperidin-3-il)-isoindol- 1,3-diona, e de (3s)-4-amino-2-(3-metil-2,6-dioxopiperidin-3-il)-isoindol- 1,3-diona, ou um sal ou solvato farmaceuticamente aceitável das mesmas, composição farmacêutica, e, forma de dosagem unitária simples - Google Patents
usos de uma quantidade terapeuticamente ou profilaticamente eficaz de 4-amino-2-(3-metil-2,6-dioxopiperidin-3-il)-isoindol-1,3-d iona, de (3r)-4-amino-2-(3-metil-2,6-dioxopiperidin-3-il)-isoindol- 1,3-diona, e de (3s)-4-amino-2-(3-metil-2,6-dioxopiperidin-3-il)-isoindol- 1,3-diona, ou um sal ou solvato farmaceuticamente aceitável das mesmas, composição farmacêutica, e, forma de dosagem unitária simplesInfo
- Publication number
- BRPI0607239A2 BRPI0607239A2 BRPI0607239-9A BRPI0607239A BRPI0607239A2 BR PI0607239 A2 BRPI0607239 A2 BR PI0607239A2 BR PI0607239 A BRPI0607239 A BR PI0607239A BR PI0607239 A2 BRPI0607239 A2 BR PI0607239A2
- Authority
- BR
- Brazil
- Prior art keywords
- isoindol
- amino
- methyl
- dioxopiperidin
- dione
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title abstract 4
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 3
- 239000012453 solvate Substances 0.000 title abstract 3
- 239000002552 dosage form Substances 0.000 title abstract 2
- VZTDWPXKIYLLAT-UHFFFAOYSA-N 4-amino-2-(3-methyl-2,6-dioxopiperidin-3-yl)isoindole-1,3-dione Chemical compound O=C1C2=CC=CC(N)=C2C(=O)N1C1(C)CCC(=O)NC1=O VZTDWPXKIYLLAT-UHFFFAOYSA-N 0.000 abstract 2
- 239000000651 prodrug Substances 0.000 abstract 2
- 229940002612 prodrug Drugs 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
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- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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Abstract
USOS DE UMA QUANTIDADE TERAPEUTICAMENTE OU PROFILATICAMENTE EFICAZ DE 4-AMINO-2-(3-MIETIL-2,6- DIOXOPIPERIDIN-3-IL)-ISOINDOL- 1 ,3-DIONA, DE (3R)-4-AMINO-2- (3-METIL-2,6-DIOXOPIPERIDIIN-3-IL)-ISOINDOL- 1 ,3-DIONA, E DE (3 S)-4-AMINO-2-(3 -METIL-2,6-DIOXOPIPERIDIN-3 -IL)-ISOINDOL- 1,3- DIONA, OU UM SAL OU SOL VATO FARMACEUTICAMENTE ACEITáVEL DAS MESMAS, COMPOSIçãO FARMACêUTICA, E, FORMA DE DOSAGEM UNITáRIA SIMPLES. Esta invenção refere-se a 4-amino-2-(3-metil-2,6- dioxopiperidin-3 -il)-i soindol- 1,3 -diona racêmica e estereomericamente pura, e pró-drogas, sais e solvatos da mesma. Revela-se a síntese, métodos de uso, e composições farmacêuticas de 4-amino-2-(3 -metil-2 ,6-dioxo-piperidin-3 -il)-isoindol- 1 ,3-diona racêmica e estereomericamente pura, e pró-drogas, sais e solvatos da mesma.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US64650505P | 2005-01-25 | 2005-01-25 | |
| PCT/US2006/002503 WO2006081251A2 (en) | 2005-01-25 | 2006-01-24 | Methods and compositions using 4-amino-2-(3-methyl-2,6-dioxopiperidin-3-yl)-isoindole-1-3-dione |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0607239A2 true BRPI0607239A2 (pt) | 2009-08-25 |
Family
ID=36609267
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0607239-9A BRPI0607239A2 (pt) | 2005-01-25 | 2006-01-24 | usos de uma quantidade terapeuticamente ou profilaticamente eficaz de 4-amino-2-(3-metil-2,6-dioxopiperidin-3-il)-isoindol-1,3-d iona, de (3r)-4-amino-2-(3-metil-2,6-dioxopiperidin-3-il)-isoindol- 1,3-diona, e de (3s)-4-amino-2-(3-metil-2,6-dioxopiperidin-3-il)-isoindol- 1,3-diona, ou um sal ou solvato farmaceuticamente aceitável das mesmas, composição farmacêutica, e, forma de dosagem unitária simples |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US20060205787A1 (pt) |
| EP (1) | EP1848433A2 (pt) |
| JP (1) | JP2008528514A (pt) |
| KR (1) | KR20070099031A (pt) |
| CN (1) | CN101141960A (pt) |
| AR (1) | AR052196A1 (pt) |
| AU (1) | AU2006208201A1 (pt) |
| BR (1) | BRPI0607239A2 (pt) |
| CA (1) | CA2595711A1 (pt) |
| IL (1) | IL184821A0 (pt) |
| MX (1) | MX2007008903A (pt) |
| WO (1) | WO2006081251A2 (pt) |
| ZA (1) | ZA200707010B (pt) |
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| WO2007059111A2 (en) * | 2005-11-14 | 2007-05-24 | Entremed, Inc. | Anti-angiogenic activity of 2-methoxyestradiol in combination with anti-cancer agents |
| US20070253960A1 (en) * | 2006-04-28 | 2007-11-01 | Josee Roy | Pharmaceutical removal of vascular extensions from a degenerating disc |
| WO2008094665A1 (en) * | 2007-01-31 | 2008-08-07 | Entremed, Inc. | Method of treating amyloidosis mediated diseases |
| US7579464B2 (en) * | 2007-05-25 | 2009-08-25 | Hoffmann-La Roche Inc. | Process for preparation of enantiomerically pure compounds |
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| US20120134969A1 (en) | 2009-05-25 | 2012-05-31 | Hiroshi Handa | Pharmaceutical composition containing nuclear factor involved in proliferation and differentiation of central neuronal cells |
| WO2011069608A1 (en) * | 2009-12-09 | 2011-06-16 | Ratiopharm Gmbh | S-lenalidomide, polymorphic forms thereof and blend comprising s- und r-lenalidomide |
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| WO2012149299A2 (en) | 2011-04-29 | 2012-11-01 | Celgene Corporaiton | Methods for the treatment of cancer and inflammatory diseases using cereblon as a predictor |
| ES2872967T3 (es) | 2012-06-29 | 2021-11-03 | Celgene Corp | Métodos para determinar la eficacia de fármacos usando IKZF3 (AIOLOS) |
| US9587281B2 (en) | 2012-08-14 | 2017-03-07 | Celgene Corporation | Cereblon isoforms and their use as biomarkers for therapeutic treatment |
| WO2014107622A1 (en) | 2013-01-07 | 2014-07-10 | University Of Southern California | Deoxyuridine triphosphatase inhibitors |
| WO2014145192A1 (en) | 2013-03-15 | 2014-09-18 | Intra-Cellular Therapies, Inc. | Organic compounds |
| US20150031697A1 (en) * | 2013-07-26 | 2015-01-29 | Wisconsin Alumni Research Foundation | Method for preventing ultraviolet radiation-induced cutaneous damage and development of squamous cell carcinomas |
| CN104557858B (zh) * | 2013-10-29 | 2018-06-01 | 上海医药工业研究院 | 一种泊利度胺的制备方法 |
| KR102967223B1 (ko) | 2013-12-03 | 2026-05-19 | 인트라-셀룰라 써래피스, 인코퍼레이티드. | 신규한 방법 |
| WO2015103489A1 (en) | 2014-01-03 | 2015-07-09 | University Of Southern California | Heteroatom containing deoxyuridine triphosphatase inhibitors |
| KR20220054908A (ko) | 2014-04-04 | 2022-05-03 | 인트라-셀룰라 써래피스, 인코퍼레이티드. | 유기 화합물 |
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| WO2016073184A1 (en) | 2014-11-04 | 2016-05-12 | Dana Farber Cancer Institute, Inc. | Compositions and methods for treating multiple myeloma |
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| WO2019023062A1 (en) | 2017-07-26 | 2019-01-31 | Intra-Cellular Therapies, Inc. | ORGANIC COMPOUNDS |
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| SMT202600133T1 (it) | 2018-03-23 | 2026-05-12 | Intra Cellular Therapies Inc | Composti organici |
| AU2019240226B2 (en) | 2018-03-23 | 2024-11-28 | Intra-Cellular Therapies, Inc. | Organic compounds |
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Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| US6281230B1 (en) * | 1996-07-24 | 2001-08-28 | Celgene Corporation | Isoindolines, method of use, and pharmaceutical compositions |
| 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 |
| US7091353B2 (en) * | 2000-12-27 | 2006-08-15 | Celgene Corporation | Isoindole-imide compounds, compositions, and uses thereof |
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2006
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- 2006-01-24 JP JP2007552380A patent/JP2008528514A/ja not_active Abandoned
- 2006-01-24 ZA ZA200707010A patent/ZA200707010B/xx unknown
- 2006-01-24 WO PCT/US2006/002503 patent/WO2006081251A2/en not_active Ceased
- 2006-01-24 EP EP06719389A patent/EP1848433A2/en not_active Withdrawn
- 2006-01-24 CN CNA2006800081712A patent/CN101141960A/zh active Pending
- 2006-01-24 AR ARP060100261A patent/AR052196A1/es not_active Application Discontinuation
- 2006-01-24 KR KR1020077019386A patent/KR20070099031A/ko not_active Withdrawn
- 2006-01-24 AU AU2006208201A patent/AU2006208201A1/en not_active Abandoned
- 2006-01-24 CA CA002595711A patent/CA2595711A1/en not_active Abandoned
- 2006-01-24 MX MX2007008903A patent/MX2007008903A/es not_active Application Discontinuation
- 2006-01-25 US US11/338,688 patent/US20060205787A1/en not_active Abandoned
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2007
- 2007-07-24 IL IL184821A patent/IL184821A0/en unknown
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| JP2008528514A (ja) | 2008-07-31 |
| ZA200707010B (en) | 2009-01-28 |
| MX2007008903A (es) | 2007-09-07 |
| IL184821A0 (en) | 2007-12-03 |
| CN101141960A (zh) | 2008-03-12 |
| EP1848433A2 (en) | 2007-10-31 |
| AR052196A1 (es) | 2007-03-07 |
| KR20070099031A (ko) | 2007-10-08 |
| WO2006081251A3 (en) | 2006-12-28 |
| CA2595711A1 (en) | 2006-08-03 |
| WO2006081251A2 (en) | 2006-08-03 |
| AU2006208201A1 (en) | 2006-08-03 |
| US20060205787A1 (en) | 2006-09-14 |
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