EP0804192A1 - Pharmazeutische präparate zur tnf-inhibition - Google Patents
Pharmazeutische präparate zur tnf-inhibitionInfo
- Publication number
- EP0804192A1 EP0804192A1 EP96902870A EP96902870A EP0804192A1 EP 0804192 A1 EP0804192 A1 EP 0804192A1 EP 96902870 A EP96902870 A EP 96902870A EP 96902870 A EP96902870 A EP 96902870A EP 0804192 A1 EP0804192 A1 EP 0804192A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- compounds
- formula
- alkyl
- treatment
- diseases
- 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.)
- Withdrawn
Links
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- 108050007852 Tumour necrosis factor Proteins 0.000 title abstract 3
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- -1 Hydroxy, carboxy Chemical group 0.000 claims description 12
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Classifications
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/42—Oxazoles
- A61K31/421—1,3-Oxazoles, e.g. pemoline, trimethadione
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/12—Antidiuretics, e.g. drugs for diabetes insipidus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Definitions
- the invention relates to the use of the compounds of the formula I for the production of medicaments for the treatment of diseases which are mediated by activation of the tumor necrosis factor (TNF).
- TNF tumor necrosis factor
- the compounds of formula I are described, for example, in USP-4,186,129 and WO 8602268. From these patents it is known that the compounds of the formula I have phosphodiesterase inhibitory activity and have central depressive, antidopaminergic, antinociceptive and anticonvulsive activity and are suitable for the local treatment of inflammation. It is also known from USP -4,824,838 that compounds of the formula I can be used as antidepressants.
- R ⁇ is hydrogen or C ⁇ .g-alkyl.
- the compounds of formula I can contain one or more chiral centers and also include the racemic diastereomeric mixtures and the individual optical isomers.
- Alkyl means in each case straight-chain or branched alkyl groups, such as, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, pentyl, 2-methyl-butyl, 2,2-dimethylpropyl and hexyl .
- Alkyl residues with 1 to 4 carbon atoms are to be regarded as preferred.
- Alkenyl means for example 1-propenyl, 2-propenyl or 3-methyl-2-propenyl and alkynyl means for example propargyl.
- Cycloalkyl is understood to mean, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or cycloheptyl, in particular C3_5-cycloalkyls.
- Aryl or aralkyl each mean an aromatic ring or an aromatic ring system having 6 to 10 carbon atoms, such as, for example, phenyl, benzyl, phenethyl or naphthyl.
- a monocycle is to be regarded as preferred.
- Acyl is to be understood as meaning aliphatic and aromatic carboxylic acids, for example C 1-6 -alkanoyl, benzoyl.
- heterocycle encompasses a 5- or 6-membered saturated heterocycle having an oxygen, sulfur or nitrogen atom, for example 2- or 3-tetrahydropyranyl, 2- or 3-tetrahydrofuranyl, 2- or 3-tetrahydrothienyl, dihydropyranyl , Pyrrolidinyl, pvrrolinyl, piperidinyl and N-alkyl-pyrrolidinyl and N-alkyl-piperidinyl in which the alkyl radical contains 1-4 carbon atoms, preferably tetrahydrofuranyl.
- Halogen means chlorine, fluorine, bromine and iodine.
- Rl is methyl and R3 is hydrogen.
- R ⁇ is hydrogen
- R 2 is alkyl or cycloalkyl
- R 3 in the meaning CH 3 being preferred in particular.
- TNF Diseases that are mediated by TNF are understood to mean both diseases that are triggered by the production of TNF and diseases in which other cytokines such as 11-1 or 11-6 are influenced by TNF.
- TNF means both TNF- ⁇ and TNF- ⁇ , both of which are antagonized by the compounds of the formula I. TNF- ⁇ is preferably inhibited.
- the compounds of the formula I are therefore suitable for producing a pharmaceutical preparation which is used for the treatment and prophylaxis of diseases in living things which are triggered by stimulation of TNF.
- Diseases which are influenced by excessive or unregulated TNF stimulation are, for example, allergic and inflammatory diseases, autoimmune diseases, pulmonary diseases, infectious diseases and bone resorption diseases such as rheumatoid arthritis, rheumatoid spondylitis, osteoarthritis, gout, sepsis, septic shock, endotoxin shock, Gram-negative sepsis, toxic shock syndrome, ARDS (acute respiratory distress syndrome), pulmonary sarcoidosis, asthma, silicosis, cachexia, ulcerative colitis, Crohn's disease, osteoporosis, organ damage after reperfusion, inflammatory diseases of the CNS such as cerebral infectious diseases, panalitis, multiple sclerosis, such as multiple sclerosis Mad cow disease, inflammatory skin diseases such as urticaria, psoriasis,
- the agents are produced by customary processes by bringing the active ingredient into the form of a pharmaceutical preparation with suitable carriers, auxiliaries and / or additives which is suitable for enteral or parenteral administration.
- the preparations thus obtained can be used as pharmaceuticals in human or veterinary medicine be used.
- the application can be administered orally or sublingually as a solid in the form of capsules or tablets or as a liquid in the form of solutions, suspensions, elixirs, aerosols or emulsions or rectally in the form of suppositories or in the form of injection solutions which can also be used subcutaneously, intramuscularly or intravenously, or topically or intrathecally.
- auxiliary organic and inorganic carrier materials are suitable as auxiliaries for the desired pharmaceutical formulation, such as, for. As water, gelatin, gum arabic, milk sugar, starch, magnesium stearate, talc, vegetable oils, polyalkylene glycols, etc. If necessary, preservatives, stabilizers, wetting agents, emulsifiers or salts for changing the osmotic pressure or buffer may also be included.
- the pharmaceutical preparations can be in solid form, for example as tablets, dragees, suppositories, capsules or in liquid form, for. B. present as solutions, suspensions or emulsions.
- Auxiliary materials such as salts, bile acids or animal or vegetable phospholipids and their mixtures as well as liposomes or their components can also be used as carrier systems.
- tablets, coated tablets or capsules with talc and / or hydrocarbon carrier or binder such as. B. lactose, corn or potato starch, suitable.
- the application can also be in liquid form, such as. B. as juice to which sweetener may be added.
- the compounds of formula I are used in doses sufficient to reduce TNF production to normal or lower levels.
- the dosage of the active ingredients can vary depending on the route of administration, age and weight of the patient, type and severity of the disease to be treated and similar factors.
- the daily dose is 0.5-50 mg, preferably 0J- 5 mg, whereby the dose can be given as a single dose to be administered once or divided into 2 or more daily doses.
- the activity of the compounds according to the invention can be demonstrated, for example, in animals suffering from experimental allergic encephalomyelitis (EAE), a CNS disease which is caused by T lymphocytes.
- EAE allergic encephalomyelitis
- the illness can be triggered on rodents and primates by immunization and histopathologically and symptomatically resembles the disease states in humans.
- the course of the disease can be followed using magnetic resonance imaging.
- Macrophages and microglial cells which have macrophage functions in the brain, mediate the release of TNF- ⁇ during experimental allergic encephalomyelitis (EAE). If macrophages are stimulated, for example by lipopolysaccharide (LPS), TNF- ⁇ is secreted in vitro and in vivo within hours.
- LPS lipopolysaccharide
- a urine macrophage Zeil line (RAW 264) was preincubated for 30 minutes in the presence and in the absence of various concentrations of PDE-IV inhibitors and then stimulated with LPS (10 ng / ml). The culture medium was removed 18 hours after stimulation and the TNF- ⁇ release was measured using a specific Elisa test.
- the test is available from various companies, including British Biotechnology, Genzyme, and is performed as described by the manufacturer.
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Physical Education & Sports Medicine (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Diabetes (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Virology (AREA)
- Pain & Pain Management (AREA)
- AIDS & HIV (AREA)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Cardiology (AREA)
- Vascular Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Dermatology (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19505516 | 1995-02-10 | ||
| DE19505516 | 1995-02-10 | ||
| PCT/DE1996/000257 WO1996024350A1 (de) | 1995-02-10 | 1996-02-09 | Pharmazeutische präparate zur tnf-inhibition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0804192A1 true EP0804192A1 (de) | 1997-11-05 |
Family
ID=7754327
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP96902870A Withdrawn EP0804192A1 (de) | 1995-02-10 | 1996-02-09 | Pharmazeutische präparate zur tnf-inhibition |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6117895A (fi) |
| EP (1) | EP0804192A1 (fi) |
| JP (1) | JPH11500110A (fi) |
| KR (1) | KR19980702116A (fi) |
| CN (1) | CN1173818A (fi) |
| AU (1) | AU706159B2 (fi) |
| CZ (1) | CZ290671B6 (fi) |
| FI (1) | FI973277A0 (fi) |
| HU (1) | HUP9702408A3 (fi) |
| IL (1) | IL117090A (fi) |
| MX (1) | MX9706086A (fi) |
| SK (1) | SK283821B6 (fi) |
| WO (1) | WO1996024350A1 (fi) |
| ZA (1) | ZA961081B (fi) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2300813A1 (en) * | 1997-08-21 | 1999-03-04 | Hiroyuki Odaka | Anti-inflammatory agent |
| US20040220103A1 (en) * | 1999-04-19 | 2004-11-04 | Immunex Corporation | Soluble tumor necrosis factor receptor treatment of medical disorders |
| DOP2005000123A (es) * | 2004-07-02 | 2011-07-15 | Merck Sharp & Dohme | Inhibidores de cetp |
| TW200732313A (en) * | 2005-12-15 | 2007-09-01 | Astrazeneca Ab | Oxazolidinone compounds and their use as metabotropic glutamate receptor potentiators |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2413935A1 (de) * | 1974-03-20 | 1975-10-16 | Schering Ag | 4-(polyalkoxy-phenyl)-2-pyrrolidone |
| DE2541855A1 (de) * | 1975-09-18 | 1977-03-31 | Schering Ag | 4-(polyalkoxy-phenyl)-2-pyrrolidone ii |
| FR2358155A1 (fr) * | 1976-07-15 | 1978-02-10 | Lapinet Eugene | Composition pour le traitement et la prevention de l'irritation et de l'inflammation de la peau, de l'oeil et des muqueuses |
| DE2655369A1 (de) * | 1976-12-03 | 1978-06-08 | Schering Ag | 5-(subst. phenyl)-oxazolidinone und deren schwefelanaloga sowie verfahren zu deren herstellung |
| DE3438839A1 (de) * | 1984-10-19 | 1986-04-24 | Schering AG, 1000 Berlin und 4709 Bergkamen | Pharmazeutische praeparate |
| US5783591A (en) * | 1984-10-19 | 1998-07-21 | Schering Aktiengesellschaft | Administration of oxazolidinone and pyrolidinone compounds for the treatment of inflammation |
| US5310732A (en) * | 1986-02-03 | 1994-05-10 | The Scripps Research Institute | 2-halo-2'-deoxyadenosines in the treatment of rheumatoid arthritis |
| DE3639225A1 (de) * | 1986-11-14 | 1988-05-19 | Schering Ag | Verwendung von 5-(subst. phenyl)-oxazolidinonderiaten als psychopharmaka |
| WO1991000092A1 (en) * | 1989-06-13 | 1991-01-10 | Smithkline Beecham Corporation | Inhibition of interleukin-1 and tumor necrosis factor production by monocytes and/or macrophages |
| US5420154A (en) * | 1990-08-03 | 1995-05-30 | Smithkline Beecham Corp. | TNF inhibitors |
| PT100441A (pt) * | 1991-05-02 | 1993-09-30 | Smithkline Beecham Corp | Pirrolidinonas, seu processo de preparacao, composicoes farmaceuticas que as contem e uso |
| US5227369A (en) * | 1991-07-11 | 1993-07-13 | The Regents Of The University Of California | Compositions and methods for inhibiting leukocyte adhesion to cns myelin |
| GB9204808D0 (en) * | 1992-03-04 | 1992-04-15 | Rhone Poulenc Rorer Ltd | Novel compositions of matter |
| US5264437A (en) * | 1992-03-20 | 1993-11-23 | Syntex (U.S.A.) Inc. | Optionally substituted pyrido[2,3-d]pyridine-2,4(1H,3H)-diones and pyrido[2,]pyrimidine-2(1H,3H)-ones |
| US5672622A (en) * | 1994-04-21 | 1997-09-30 | Berlex Laboratories, Inc. | Treatment of multiple sclerosis |
-
1996
- 1996-02-09 HU HU9702408A patent/HUP9702408A3/hu unknown
- 1996-02-09 WO PCT/DE1996/000257 patent/WO1996024350A1/de not_active Application Discontinuation
- 1996-02-09 MX MX9706086A patent/MX9706086A/es not_active IP Right Cessation
- 1996-02-09 IL IL11709096A patent/IL117090A/xx not_active IP Right Cessation
- 1996-02-09 CN CN96191868A patent/CN1173818A/zh active Pending
- 1996-02-09 EP EP96902870A patent/EP0804192A1/de not_active Withdrawn
- 1996-02-09 JP JP8523903A patent/JPH11500110A/ja not_active Ceased
- 1996-02-09 SK SK1073-97A patent/SK283821B6/sk unknown
- 1996-02-09 ZA ZA961081A patent/ZA961081B/xx unknown
- 1996-02-09 CZ CZ19972513A patent/CZ290671B6/cs not_active IP Right Cessation
- 1996-02-09 AU AU47122/96A patent/AU706159B2/en not_active Ceased
- 1996-02-10 KR KR1019970705511A patent/KR19980702116A/ko not_active Application Discontinuation
- 1996-07-18 US US08/683,467 patent/US6117895A/en not_active Expired - Fee Related
-
1997
- 1997-08-08 FI FI973277A patent/FI973277A0/fi not_active IP Right Cessation
Non-Patent Citations (5)
| Title |
|---|
| BEERS: "The Merck Manual of Diagnosis and Therapy, Fourteenth Edition", 1982, MERCK & CO., RAHWAY, N.J. * |
| BRUUNSGAARD H. ET AL.: "A high plasma concentration of TNFalpha is associated with dementia in centenarians", JOURNAL OF GERONTOLOGY: MEDICAL SCIENCES, vol. 54A, no. 7, 1999, pages M357 - M364 * |
| CACABELOS R. ET AL.: "Serum tumor necrosis factor (TNF) in Alzheimer's disease and multi-infarct dementia", METH. FIND. EXP. CLIN. PHARMACOL., vol. 16, no. 1, 1994, pages 29 - 35, XP000569366 * |
| KORDEK R. ET AL.: "Heightened expression of tumor necrosis factor alpha, interleukin 1alpha, and glial fibrillary acidic protein in experimental Creutzfeldt-Jacob disease in mice", PROC. NATL. ACAD. SCI. USA, vol. 93, 1996, pages 9754 - 9758 * |
| See also references of WO9624350A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| MX9706086A (es) | 1997-10-31 |
| IL117090A0 (en) | 1996-06-18 |
| AU4712296A (en) | 1996-08-27 |
| FI973277A (fi) | 1997-08-08 |
| KR19980702116A (ko) | 1998-07-15 |
| HUP9702408A3 (en) | 2000-08-28 |
| JPH11500110A (ja) | 1999-01-06 |
| SK107397A3 (en) | 1997-12-10 |
| AU706159B2 (en) | 1999-06-10 |
| ZA961081B (en) | 1996-10-15 |
| WO1996024350A1 (de) | 1996-08-15 |
| CZ290671B6 (cs) | 2002-09-11 |
| US6117895A (en) | 2000-09-12 |
| SK283821B6 (sk) | 2004-02-03 |
| CZ251397A3 (en) | 1997-12-17 |
| IL117090A (en) | 2000-07-26 |
| CN1173818A (zh) | 1998-02-18 |
| HUP9702408A2 (hu) | 1998-05-28 |
| FI973277A0 (fi) | 1997-08-08 |
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