MC225A7 - 2-(2,6-Dioxopiperidine-3-yl)-phtalimides et-1-oxo-iso-indolines substitutes et methodes pour reduireles taux de tnf-alpha - Google Patents
2-(2,6-Dioxopiperidine-3-yl)-phtalimides et-1-oxo-iso-indolines substitutes et methodes pour reduireles taux de tnf-alphaInfo
- Publication number
- MC225A7 MC225A7 MC225K MC225K MC225A7 MC 225 A7 MC225 A7 MC 225A7 MC 225 K MC225 K MC 225K MC 225 K MC225 K MC 225K MC 225 A7 MC225 A7 MC 225A7
- Authority
- MC
- Monaco
- Prior art keywords
- carbon atoms
- hydrogen
- alkyl
- dioxopiperidin
- indolines
- Prior art date
Links
- FPNJYPLJTAYAMP-UHFFFAOYSA-N 7a-(2,6-dioxopiperidin-3-yl)-3ah-isoindole-1,3-dione Chemical class C1=CC=CC2C(=O)NC(=O)C21C1CCC(=O)NC1=O FPNJYPLJTAYAMP-UHFFFAOYSA-N 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 239000001257 hydrogen Substances 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 150000002431 hydrogen Chemical class 0.000 abstract 3
- -1 m -phenylene Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000005605 benzo group Chemical group 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/45—Non condensed piperidines, e.g. piperocaine having oxo groups directly attached to the heterocyclic ring, e.g. cycloheximide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
- A61K9/4841—Filling excipients; Inactive ingredients
- A61K9/4866—Organic macromolecular compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/06—Antimalarials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Engineering & Computer Science (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Biophysics (AREA)
- Molecular Biology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4827897P | 1997-05-30 | 1997-05-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
MC225A7 true MC225A7 (fr) | 2006-03-07 |
Family
ID=21953674
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MC225K MC225A7 (fr) | 1997-05-30 | 2005-08-11 | 2-(2,6-Dioxopiperidine-3-yl)-phtalimides et-1-oxo-iso-indolines substitutes et methodes pour reduireles taux de tnf-alpha |
Country Status (25)
Country | Link |
---|---|
US (3) | US6395754B1 (fr) |
EP (3) | EP1956017B1 (fr) |
JP (2) | JP4307567B2 (fr) |
KR (1) | KR100526212B1 (fr) |
CN (3) | CN1680367A (fr) |
AT (2) | ATE401319T1 (fr) |
AU (1) | AU741982B2 (fr) |
CA (2) | CA2291218C (fr) |
CY (1) | CY1108348T1 (fr) |
CZ (1) | CZ299812B6 (fr) |
DE (2) | DE69825994T2 (fr) |
DK (2) | DK1486496T3 (fr) |
ES (3) | ES2403102T3 (fr) |
FI (1) | FI19992490A (fr) |
HK (1) | HK1072248A1 (fr) |
HU (2) | HU228769B1 (fr) |
MC (1) | MC225A7 (fr) |
NO (6) | NO322080B1 (fr) |
NZ (1) | NZ501429A (fr) |
PL (1) | PL193276B1 (fr) |
PT (2) | PT1486496E (fr) |
RU (1) | RU2209207C2 (fr) |
SK (1) | SK163099A3 (fr) |
TR (4) | TR200500299T2 (fr) |
WO (1) | WO1998054170A1 (fr) |
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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 |
ATE233753T1 (de) * | 1997-11-18 | 2003-03-15 | Celgene Corp | Substituierte 2-(2,6-dioxo-3-fluoropiperidin-3- yl)-isoindoline und ihre verwendung zur verminderung des tnfa spiegels |
US5955476A (en) * | 1997-11-18 | 1999-09-21 | Celgene Corporation | Substituted 2-(2,6-dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing inflammatory cytokine levels |
EP1064277B1 (fr) * | 1998-03-16 | 2005-06-15 | Celgene Corporation | Derives de 2-(2,6-dioxopiperidin-3-yl)iso-indoline, leur preparation et leur utilisation en tant qu'inhibiteurs de cytokines inflammatoires |
RU2001121987A (ru) | 1999-03-18 | 2004-02-27 | Селджин Корпорейшн (Us) | Замещенные 1-оксо- и 1,3-диоксоизоиндолины и их применение в фармацевтических композициях для снижения уровней воспалительных цитокинов |
US7629360B2 (en) | 1999-05-07 | 2009-12-08 | Celgene Corporation | Methods for the treatment of cachexia and graft v. host disease |
US6458810B1 (en) | 2000-11-14 | 2002-10-01 | George Muller | Pharmaceutically active isoindoline derivatives |
DE60130799T2 (de) * | 2000-11-30 | 2008-07-17 | Children's Medical Center Corp., Boston | Synthese von 4-aminothalidomid enantiomeren |
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US20030045552A1 (en) * | 2000-12-27 | 2003-03-06 | Robarge Michael J. | Isoindole-imide compounds, compositions, and uses thereof |
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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 |
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 |
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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 |
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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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1997
- 1997-07-24 HU HU9903929A patent/HU228769B1/hu active Protection Beyond IP Right Term
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1998
- 1998-05-28 KR KR10-1999-7011076A patent/KR100526212B1/ko not_active IP Right Cessation
- 1998-05-28 CZ CZ0427899A patent/CZ299812B6/cs not_active IP Right Cessation
- 1998-05-28 AT AT04077432T patent/ATE401319T1/de active
- 1998-05-28 DK DK04077432T patent/DK1486496T3/da active
- 1998-05-28 PT PT04077432T patent/PT1486496E/pt unknown
- 1998-05-28 TR TR200500299T patent/TR200500299T2/xx unknown
- 1998-05-28 TR TR200801878T patent/TR200801878T2/xx unknown
- 1998-05-28 DE DE1998625994 patent/DE69825994T2/de not_active Expired - Lifetime
- 1998-05-28 ES ES08009864T patent/ES2403102T3/es not_active Expired - Lifetime
- 1998-05-28 DE DE69839739T patent/DE69839739D1/de not_active Expired - Lifetime
- 1998-05-28 CA CA 2291218 patent/CA2291218C/fr not_active Expired - Fee Related
- 1998-05-28 PL PL337124A patent/PL193276B1/pl unknown
- 1998-05-28 CN CNA2005100525903A patent/CN1680367A/zh active Pending
- 1998-05-28 AU AU77012/98A patent/AU741982B2/en not_active Ceased
- 1998-05-28 ES ES04077432T patent/ES2309443T3/es not_active Expired - Lifetime
- 1998-05-28 CA CA 2669481 patent/CA2669481C/fr not_active Expired - Fee Related
- 1998-05-28 TR TR201005282T patent/TR201005282T2/xx unknown
- 1998-05-28 US US09/445,002 patent/US6395754B1/en not_active Expired - Lifetime
- 1998-05-28 TR TR200000107T patent/TR200000107T2/xx unknown
- 1998-05-28 WO PCT/US1998/010886 patent/WO1998054170A1/fr active Application Filing
- 1998-05-28 EP EP20080009864 patent/EP1956017B1/fr not_active Expired - Lifetime
- 1998-05-28 HU HU0003217A patent/HU229578B1/hu not_active IP Right Cessation
- 1998-05-28 PT PT98924959T patent/PT984955E/pt unknown
- 1998-05-28 ES ES98924959T patent/ES2229497T3/es not_active Expired - Lifetime
- 1998-05-28 CN CNA2006101262647A patent/CN1911927A/zh active Pending
- 1998-05-28 AT AT98924959T patent/ATE275139T1/de active
- 1998-05-28 RU RU99128073A patent/RU2209207C2/ru not_active IP Right Cessation
- 1998-05-28 DK DK98924959T patent/DK0984955T3/da active
- 1998-05-28 SK SK1630-99A patent/SK163099A3/sk unknown
- 1998-05-28 JP JP50090999A patent/JP4307567B2/ja not_active Expired - Fee Related
- 1998-05-28 EP EP19980924959 patent/EP0984955B1/fr not_active Expired - Lifetime
- 1998-05-28 NZ NZ501429A patent/NZ501429A/en not_active IP Right Cessation
- 1998-05-28 CN CN98805614A patent/CN1258293A/zh active Pending
- 1998-05-28 EP EP20040077432 patent/EP1486496B1/fr not_active Expired - Lifetime
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1999
- 1999-11-23 FI FI992490A patent/FI19992490A/fi unknown
- 1999-11-23 NO NO19995751A patent/NO322080B1/no not_active IP Right Cessation
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2002
- 2002-05-10 US US10/143,416 patent/US20020173658A1/en not_active Abandoned
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2005
- 2005-01-14 US US11/035,817 patent/US7459466B2/en not_active Expired - Fee Related
- 2005-03-08 HK HK05102027A patent/HK1072248A1/xx not_active IP Right Cessation
- 2005-08-11 MC MC225K patent/MC225A7/fr unknown
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2006
- 2006-03-30 NO NO20061455A patent/NO331367B1/no not_active IP Right Cessation
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2008
- 2008-09-17 CY CY081101005T patent/CY1108348T1/el unknown
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2009
- 2009-02-06 JP JP2009025981A patent/JP2009138009A/ja active Pending
- 2009-08-18 NO NO20092860A patent/NO332270B1/no not_active IP Right Cessation
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2011
- 2011-11-08 NO NO20111536A patent/NO332271B1/no not_active IP Right Cessation
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2012
- 2012-03-06 NO NO2012004C patent/NO2012004I2/no unknown
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