JP2004523561A5 - - Google Patents
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- JP2004523561A5 JP2004523561A5 JP2002567927A JP2002567927A JP2004523561A5 JP 2004523561 A5 JP2004523561 A5 JP 2004523561A5 JP 2002567927 A JP2002567927 A JP 2002567927A JP 2002567927 A JP2002567927 A JP 2002567927A JP 2004523561 A5 JP2004523561 A5 JP 2004523561A5
- Authority
- JP
- Japan
- Prior art keywords
- pharmaceutically acceptable
- substituted
- compound
- acceptable salt
- alkyl
- 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.)
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US27194101P | 2001-02-27 | 2001-02-27 | |
| PCT/US2002/005868 WO2002068414A2 (en) | 2001-02-27 | 2002-02-26 | Analogs of thalidomide as potential angiogenesis inhibitors |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009143087A Division JP2009263376A (ja) | 2001-02-27 | 2009-06-16 | 潜在的な血管形成阻害剤としてのサリドマイド類似体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004523561A JP2004523561A (ja) | 2004-08-05 |
| JP2004523561A5 true JP2004523561A5 (https=) | 2005-12-22 |
| JP4361273B2 JP4361273B2 (ja) | 2009-11-11 |
Family
ID=23037728
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002567927A Expired - Fee Related JP4361273B2 (ja) | 2001-02-27 | 2002-02-26 | 潜在的な血管形成阻害剤としてのサリドマイド類似体 |
| JP2009143087A Pending JP2009263376A (ja) | 2001-02-27 | 2009-06-16 | 潜在的な血管形成阻害剤としてのサリドマイド類似体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009143087A Pending JP2009263376A (ja) | 2001-02-27 | 2009-06-16 | 潜在的な血管形成阻害剤としてのサリドマイド類似体 |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US7320991B2 (https=) |
| EP (1) | EP1389203B8 (https=) |
| JP (2) | JP4361273B2 (https=) |
| AT (1) | ATE450529T1 (https=) |
| AU (1) | AU2002306596B2 (https=) |
| CA (1) | CA2439410C (https=) |
| DE (1) | DE60234585D1 (https=) |
| ES (1) | ES2338534T3 (https=) |
| WO (1) | WO2002068414A2 (https=) |
Families Citing this family (83)
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| ATE374609T1 (de) * | 2000-11-30 | 2007-10-15 | Childrens Medical Center | Synthese von 4-aminothalidomid enantiomeren |
| US7320991B2 (en) | 2001-02-27 | 2008-01-22 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services, National Institutes Of Health | Analogs of thalidomide as potential angiogenesis inhibitors |
| USRE48890E1 (en) | 2002-05-17 | 2022-01-11 | Celgene Corporation | Methods for treating multiple myeloma with 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione after stem cell transplantation |
| EP2258363A1 (en) * | 2002-05-17 | 2010-12-08 | Celgene Corporation | Compositions for treatment of cancers |
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| TW200501945A (en) | 2002-11-06 | 2005-01-16 | Celgene Corp | Methods and compositions using selective cytokine inhibitory drugs for treatment and management of cancers and other diseases |
| US8034831B2 (en) * | 2002-11-06 | 2011-10-11 | Celgene Corporation | Methods for the treatment and management of myeloproliferative diseases using 4-(amino)-2-(2,6-Dioxo(3-piperidyl)-isoindoline-1,3-dione in combination with other therapies |
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| US8952895B2 (en) | 2011-06-03 | 2015-02-10 | Apple Inc. | Motion-based device operations |
| US7973057B2 (en) | 2003-09-17 | 2011-07-05 | The United States Of America As Represented By The Department Of Health And Human Services | Thalidomide analogs |
| US20080027113A1 (en) * | 2003-09-23 | 2008-01-31 | Zeldis Jerome B | Methods of Using and Compositions Comprising Immunomodulatory Compounds for Treatment and Management of Macular Degeneration |
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| 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 |
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| US20080213213A1 (en) * | 2004-04-14 | 2008-09-04 | Zeldis Jerome B | Method For the Treatment of Myelodysplastic Syndromes Using (+)-2-[1-(3-Ethoxy-4-Methoxyphenyl)-2-Methylsulfonylethyl]-4-Acetylaminoisoindoline-1,3-Dione |
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| ES2194640T3 (es) | 1999-03-31 | 2003-12-01 | Gruenenthal Chemie | Solucion acuosa estable del derivado de la talidomida (em 12), para su administracion parenteral, y su procedimiento de preparacion. |
| US6310360B1 (en) * | 1999-07-21 | 2001-10-30 | The Trustees Of Princeton University | Intersystem crossing agents for efficient utilization of excitons in organic light emitting devices |
| WO2001041755A2 (en) | 1999-12-02 | 2001-06-14 | The Regents Of The University Of Michigan | Topical compositions comprising thalidomide for the treatment of inflammatory diseases |
| KR20030003708A (ko) | 2000-03-31 | 2003-01-10 | 셀진 코포레이션 | 시클로옥시게나제-2 활성의 저해 |
| US6458810B1 (en) | 2000-11-14 | 2002-10-01 | George Muller | Pharmaceutically active isoindoline derivatives |
| ATE374609T1 (de) | 2000-11-30 | 2007-10-15 | Childrens Medical Center | Synthese von 4-aminothalidomid enantiomeren |
| US7320991B2 (en) | 2001-02-27 | 2008-01-22 | The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services, National Institutes Of Health | Analogs of thalidomide as potential angiogenesis inhibitors |
| NZ531294A (en) | 2001-08-06 | 2005-11-25 | Childrens Medical Center | Synthesis and anti-tumor activity of nitrogen substituted thalidomide analogs |
| EP1336602A1 (en) | 2002-02-13 | 2003-08-20 | Giovanni Scaramuzzino | Nitrate prodrugs able to release nitric oxide in a controlled and selective way and their use for prevention and treatment of inflammatory, ischemic and proliferative diseases |
| CA2752124A1 (en) | 2002-05-17 | 2003-11-27 | Celgene Corporation | Methods and compositions using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for treatment and management of head and neck cancer |
| CN100488959C (zh) | 2003-03-27 | 2009-05-20 | 天津和美生物技术有限公司 | 水溶性的酞胺哌啶酮衍生物 |
| WO2005016325A2 (en) | 2003-06-03 | 2005-02-24 | Teva Pharmaceutical Industries Ltd. | CRISTALLINE ZIPRASIDONE HCl AND PROCESSES FOR PREPARATION THEREOF |
| WO2005016326A2 (en) | 2003-07-11 | 2005-02-24 | The Government Of The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services | Analogs of thalidomide as potential angiogenesis inhibitors |
-
2002
- 2002-02-26 US US10/469,359 patent/US7320991B2/en not_active Expired - Fee Related
- 2002-02-26 CA CA2439410A patent/CA2439410C/en not_active Expired - Fee Related
- 2002-02-26 EP EP02780964A patent/EP1389203B8/en not_active Expired - Lifetime
- 2002-02-26 ES ES02780964T patent/ES2338534T3/es not_active Expired - Lifetime
- 2002-02-26 AU AU2002306596A patent/AU2002306596B2/en not_active Ceased
- 2002-02-26 DE DE60234585T patent/DE60234585D1/de not_active Expired - Lifetime
- 2002-02-26 AT AT02780964T patent/ATE450529T1/de not_active IP Right Cessation
- 2002-02-26 JP JP2002567927A patent/JP4361273B2/ja not_active Expired - Fee Related
- 2002-02-26 WO PCT/US2002/005868 patent/WO2002068414A2/en not_active Ceased
-
2007
- 2007-07-19 US US11/880,404 patent/US8716315B2/en not_active Expired - Fee Related
-
2009
- 2009-06-16 JP JP2009143087A patent/JP2009263376A/ja active Pending
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