JP2004523561A5 - - Google Patents
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- Publication number
- 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.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims 43
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 33
- 150000003839 salts Chemical class 0.000 claims 33
- 125000000217 alkyl group Chemical group 0.000 claims 22
- 229910052739 hydrogen Inorganic materials 0.000 claims 20
- 239000001257 hydrogen Substances 0.000 claims 20
- 229910052736 halogen Inorganic materials 0.000 claims 17
- 150000002367 halogens Chemical class 0.000 claims 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 16
- 150000002431 hydrogen Chemical group 0.000 claims 16
- 239000000203 mixture Substances 0.000 claims 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 12
- 239000002253 acid Substances 0.000 claims 10
- 150000001413 amino acids Chemical class 0.000 claims 10
- 125000003884 phenylalkyl group Chemical group 0.000 claims 10
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 10
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 8
- 125000005233 alkylalcohol group Chemical group 0.000 claims 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 8
- 229910052757 nitrogen Inorganic materials 0.000 claims 8
- 229910052760 oxygen Inorganic materials 0.000 claims 8
- 239000001301 oxygen Substances 0.000 claims 8
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims 8
- 229910052717 sulfur Inorganic materials 0.000 claims 8
- 239000011593 sulfur Substances 0.000 claims 8
- 125000003282 alkyl amino group Chemical group 0.000 claims 7
- 239000003937 drug carrier Substances 0.000 claims 7
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims 7
- 239000008194 pharmaceutical composition Substances 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical group O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 125000004367 cycloalkylaryl group Chemical group 0.000 claims 4
- 150000004673 fluoride salts Chemical class 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 229960002317 succinimide Drugs 0.000 claims 4
- 150000003973 alkyl amines Chemical class 0.000 claims 3
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 3
- 230000033115 angiogenesis Effects 0.000 claims 3
- 125000000524 functional group Chemical group 0.000 claims 3
- 230000002401 inhibitory effect Effects 0.000 claims 2
- 125000001041 indolyl group Chemical group 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
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 (enExample) | 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 (enExample) |
| EP (1) | EP1389203B8 (enExample) |
| JP (2) | JP4361273B2 (enExample) |
| AT (1) | ATE450529T1 (enExample) |
| AU (1) | AU2002306596B2 (enExample) |
| CA (1) | CA2439410C (enExample) |
| DE (1) | DE60234585D1 (enExample) |
| ES (1) | ES2338534T3 (enExample) |
| WO (1) | WO2002068414A2 (enExample) |
Families Citing this family (83)
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| AU2002253795B2 (en) * | 2000-11-30 | 2007-02-01 | The Children's Medical Center Corporation | Synthesis of 4-Amino-Thalidomide enantiomers |
| JP4361273B2 (ja) | 2001-02-27 | 2009-11-11 | アメリカ合衆国 | 潜在的な血管形成阻害剤としてのサリドマイド類似体 |
| US20100129363A1 (en) * | 2002-05-17 | 2010-05-27 | Zeldis Jerome B | Methods and compositions using pde4 inhibitors for the treatment and management of cancers |
| 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 |
| 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 |
| 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 |
| CN1668296A (zh) * | 2002-05-17 | 2005-09-14 | 细胞基因公司 | 使用选择性细胞因子抑制性药物用于治疗和控制癌症和其它疾病的方法及组合物 |
| 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 |
| US8404717B2 (en) * | 2002-10-15 | 2013-03-26 | Celgene Corporation | Methods of treating myelodysplastic syndromes using lenalidomide |
| CN1713905A (zh) * | 2002-10-15 | 2005-12-28 | 细胞基因公司 | 用于治疗骨髓增生异常综合征的选择性细胞因子抑制药 |
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| US11116782B2 (en) | 2002-10-15 | 2021-09-14 | Celgene Corporation | Methods of treating myelodysplastic syndromes with a combination therapy using lenalidomide and azacitidine |
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| US20070208057A1 (en) * | 2003-11-06 | 2007-09-06 | Zeldis Jerome B | Methods And Compositions Using Thalidomide For The Treatment And Management Of Cancers And Other Diseases |
| 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 |
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-
2002
- 2002-02-26 JP JP2002567927A patent/JP4361273B2/ja not_active Expired - Fee Related
- 2002-02-26 CA CA2439410A patent/CA2439410C/en not_active Expired - Fee Related
- 2002-02-26 ES ES02780964T patent/ES2338534T3/es not_active Expired - Lifetime
- 2002-02-26 EP EP02780964A patent/EP1389203B8/en not_active Expired - Lifetime
- 2002-02-26 AU AU2002306596A patent/AU2002306596B2/en not_active Ceased
- 2002-02-26 US US10/469,359 patent/US7320991B2/en not_active Expired - Fee Related
- 2002-02-26 AT AT02780964T patent/ATE450529T1/de not_active IP Right Cessation
- 2002-02-26 WO PCT/US2002/005868 patent/WO2002068414A2/en not_active Ceased
- 2002-02-26 DE DE60234585T patent/DE60234585D1/de not_active Expired - Lifetime
-
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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