SK7382000A3 - Substituted 2-(2,6-dioxo-3-fluoropiperidin-3-yl)-isoindolines, pharmaceutical composition containing the same and their use - Google Patents
Substituted 2-(2,6-dioxo-3-fluoropiperidin-3-yl)-isoindolines, pharmaceutical composition containing the same and their use Download PDFInfo
- Publication number
- SK7382000A3 SK7382000A3 SK738-2000A SK7382000A SK7382000A3 SK 7382000 A3 SK7382000 A3 SK 7382000A3 SK 7382000 A SK7382000 A SK 7382000A SK 7382000 A3 SK7382000 A3 SK 7382000A3
- Authority
- SK
- Slovakia
- Prior art keywords
- dioxo
- fluoropiperidin
- isoindoline
- substituted
- oxo
- Prior art date
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- MWBYARISMFKTSP-UHFFFAOYSA-N 3-(1,3-dihydroisoindol-2-yl)-3-fluoropiperidine-2,6-dione Chemical class C1C2=CC=CC=C2CN1C1(F)CCC(=O)NC1=O MWBYARISMFKTSP-UHFFFAOYSA-N 0.000 title claims description 31
- 239000008194 pharmaceutical composition Chemical class 0.000 title claims description 5
- SCJORWDJJJWLJD-UHFFFAOYSA-N 2-(3-fluoro-2,6-dioxopiperidin-3-yl)isoindole-1,3-dione Chemical class O=C1C2=CC=CC=C2C(=O)N1C1(F)CCC(=O)NC1=O SCJORWDJJJWLJD-UHFFFAOYSA-N 0.000 claims abstract description 14
- 108090000695 Cytokines Proteins 0.000 claims abstract description 13
- 102000004127 Cytokines Human genes 0.000 claims abstract description 12
- QNHYEPANFMRYAK-UHFFFAOYSA-N 3-fluoro-3-(3-oxo-1h-isoindol-2-yl)piperidine-2,6-dione Chemical class C1C2=CC=CC=C2C(=O)N1C1(F)CCC(=O)NC1=O QNHYEPANFMRYAK-UHFFFAOYSA-N 0.000 claims abstract description 9
- 230000002757 inflammatory effect Effects 0.000 claims abstract description 8
- 241000124008 Mammalia Species 0.000 claims abstract description 6
- -1 2,6-dioxo-3-fluoropiperidin-3-yl Chemical group 0.000 claims description 34
- 239000003814 drug Substances 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- RZYZVYYEAJEWCD-UHFFFAOYSA-N 3-(6-amino-3-oxo-1h-isoindol-2-yl)-3-fluoropiperidine-2,6-dione Chemical compound C1C2=CC(N)=CC=C2C(=O)N1C1(F)CCC(=O)NC1=O RZYZVYYEAJEWCD-UHFFFAOYSA-N 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 150000003839 salts Chemical class 0.000 claims description 5
- YYSHXGPLFIHOKV-UHFFFAOYSA-N 4,5,6,7-tetrafluoro-2-(3-fluoro-2,6-dioxopiperidin-3-yl)isoindole-1,3-dione Chemical compound O=C1C2=C(F)C(F)=C(F)C(F)=C2C(=O)N1C1(F)CCC(=O)NC1=O YYSHXGPLFIHOKV-UHFFFAOYSA-N 0.000 claims description 4
- GGBRXFWJIGJFPD-UHFFFAOYSA-N 3-(7-amino-3-oxo-1h-isoindol-2-yl)-3-fluoropiperidine-2,6-dione Chemical compound C1C=2C(N)=CC=CC=2C(=O)N1C1(F)CCC(=O)NC1=O GGBRXFWJIGJFPD-UHFFFAOYSA-N 0.000 claims description 3
- PSXYVZFBPHMZMA-UHFFFAOYSA-N 3-fluoro-3-(4,5,6,7-tetrafluoro-3-oxo-1h-isoindol-2-yl)piperidine-2,6-dione Chemical compound O=C1C2=C(F)C(F)=C(F)C(F)=C2CN1C1(F)CCC(=O)NC1=O PSXYVZFBPHMZMA-UHFFFAOYSA-N 0.000 claims description 3
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- GLGOUXNCDPGRTK-UHFFFAOYSA-N 3-fluoro-3-(4,5,6,7-tetramethoxy-3-oxo-1h-isoindol-2-yl)piperidine-2,6-dione Chemical compound O=C1C2=C(OC)C(OC)=C(OC)C(OC)=C2CN1C1(F)CCC(=O)NC1=O GLGOUXNCDPGRTK-UHFFFAOYSA-N 0.000 claims description 2
- WTTDIUSTBRWKGX-UHFFFAOYSA-N 3-fluoro-3-(4,5,6,7-tetramethyl-3-oxo-1h-isoindol-2-yl)piperidine-2,6-dione Chemical compound O=C1C2=C(C)C(C)=C(C)C(C)=C2CN1C1(F)CCC(=O)NC1=O WTTDIUSTBRWKGX-UHFFFAOYSA-N 0.000 claims description 2
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- C07—ORGANIC CHEMISTRY
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
- A61P31/08—Antibacterial agents for leprosy
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/976,140 US5874448A (en) | 1997-11-18 | 1997-11-18 | Substituted 2-(2,6 dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing TNFα levels |
US09/042,274 US5955476A (en) | 1997-11-18 | 1998-03-13 | Substituted 2-(2,6-dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing inflammatory cytokine levels |
PCT/US1998/024453 WO1999046258A1 (en) | 1998-03-13 | 1998-11-17 | SUBSTITUTED 2-(2,6-DIOXO-3-FLUOROPIPERIDIN-3-YL)-ISOINDOLINES AND THEIR USE TO REDUCE TNFα LEVELS |
Publications (1)
Publication Number | Publication Date |
---|---|
SK7382000A3 true SK7382000A3 (en) | 2000-12-11 |
Family
ID=26719049
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SK738-2000A SK7382000A3 (en) | 1997-11-18 | 1998-11-17 | Substituted 2-(2,6-dioxo-3-fluoropiperidin-3-yl)-isoindolines, pharmaceutical composition containing the same and their use |
Country Status (14)
Country | Link |
---|---|
EP (3) | EP1062214B1 (no) |
AT (2) | ATE233753T1 (no) |
AU (1) | AU752958B2 (no) |
CY (1) | CY1106100T1 (no) |
CZ (1) | CZ299808B6 (no) |
DE (2) | DE69834668T2 (no) |
DK (1) | DK1308444T3 (no) |
ES (2) | ES2192342T3 (no) |
FI (1) | FI20001192A (no) |
HK (1) | HK1054381B (no) |
NO (1) | NO318737B1 (no) |
PT (1) | PT1308444E (no) |
SI (1) | SI1308444T1 (no) |
SK (1) | SK7382000A3 (no) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CZ299253B6 (cs) * | 1998-03-16 | 2008-05-28 | Celgene Corporation | Isoindolinový derivát, jeho použití pro výrobu léciva a farmaceutická kompozice tento derivát obsahující |
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 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU1531492A (en) * | 1991-02-14 | 1992-09-15 | Rockefeller University, The | Method for controlling abnormal concentration tnf alpha in human tissues |
US5629327A (en) * | 1993-03-01 | 1997-05-13 | Childrens Hospital Medical Center Corp. | Methods and compositions for inhibition of angiogenesis |
US5463063A (en) * | 1993-07-02 | 1995-10-31 | Celgene Corporation | Ring closure of N-phthaloylglutamines |
DE4422237A1 (de) * | 1994-06-24 | 1996-01-04 | Gruenenthal Gmbh | Verwendung von Lactamverbindungen als pharmazeutische Wirkstoffe |
DE19613976C1 (de) * | 1996-04-09 | 1997-11-20 | Gruenenthal Gmbh | Thalidomid-Prodrugs mit immunmodulatorischer Wirkung |
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 |
ES2339425T3 (es) * | 1996-07-24 | 2010-05-20 | Celgene Corporation | 2-(2,6-dioxopiperidin-3-il)-ftalimidas y -1-oxoisoindolinas sustituidas y procedimiento para reducir los niveles de tnf-alfa. |
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 |
-
1998
- 1998-11-17 ES ES98958016T patent/ES2192342T3/es not_active Expired - Lifetime
- 1998-11-17 DE DE69834668T patent/DE69834668T2/de not_active Expired - Lifetime
- 1998-11-17 DE DE69811962T patent/DE69811962T2/de not_active Expired - Lifetime
- 1998-11-17 CZ CZ20001822A patent/CZ299808B6/cs not_active IP Right Cessation
- 1998-11-17 SI SI9830846T patent/SI1308444T1/sl unknown
- 1998-11-17 EP EP98958016A patent/EP1062214B1/en not_active Expired - Lifetime
- 1998-11-17 EP EP02028237A patent/EP1308444B1/en not_active Expired - Lifetime
- 1998-11-17 AU AU14138/99A patent/AU752958B2/en not_active Ceased
- 1998-11-17 AT AT98958016T patent/ATE233753T1/de not_active IP Right Cessation
- 1998-11-17 SK SK738-2000A patent/SK7382000A3/sk unknown
- 1998-11-17 DK DK02028237T patent/DK1308444T3/da active
- 1998-11-17 AT AT02028237T patent/ATE327228T1/de not_active IP Right Cessation
- 1998-11-17 ES ES02028237T patent/ES2262753T3/es not_active Expired - Lifetime
- 1998-11-17 PT PT02028237T patent/PT1308444E/pt unknown
- 1998-11-17 EP EP06009666A patent/EP1710242A1/en not_active Withdrawn
-
2000
- 2000-05-16 NO NO20002529A patent/NO318737B1/no not_active IP Right Cessation
- 2000-05-18 FI FI20001192A patent/FI20001192A/fi not_active Application Discontinuation
-
2003
- 2003-09-15 HK HK03106604.2A patent/HK1054381B/zh not_active IP Right Cessation
-
2006
- 2006-06-19 CY CY20061100821T patent/CY1106100T1/el unknown
Also Published As
Publication number | Publication date |
---|---|
EP1062214A1 (en) | 2000-12-27 |
EP1308444A1 (en) | 2003-05-07 |
DE69811962T2 (de) | 2003-08-28 |
CY1106100T1 (el) | 2011-06-08 |
CZ299808B6 (cs) | 2008-12-03 |
CZ20001822A3 (cs) | 2000-11-15 |
AU1413899A (en) | 1999-09-27 |
ATE327228T1 (de) | 2006-06-15 |
PT1308444E (pt) | 2006-08-31 |
NO318737B1 (no) | 2005-05-02 |
HK1054381A1 (en) | 2003-11-28 |
AU752958B2 (en) | 2002-10-03 |
ES2262753T3 (es) | 2006-12-01 |
DK1308444T3 (da) | 2006-09-18 |
EP1710242A1 (en) | 2006-10-11 |
ES2192342T3 (es) | 2003-10-01 |
SI1308444T1 (sl) | 2007-04-30 |
FI20001192A (fi) | 2000-07-14 |
EP1308444B1 (en) | 2006-05-24 |
DE69811962D1 (de) | 2003-04-10 |
DE69834668D1 (de) | 2006-06-29 |
DE69834668T2 (de) | 2007-01-11 |
HK1054381B (zh) | 2006-10-13 |
ATE233753T1 (de) | 2003-03-15 |
NO20002529D0 (no) | 2000-05-16 |
EP1062214B1 (en) | 2003-03-05 |
NO20002529L (no) | 2000-06-30 |
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