WO2000051684A2 - Regulateurs de transacylase independante de la coenzyme a comme medicaments psychotropes - Google Patents
Regulateurs de transacylase independante de la coenzyme a comme medicaments psychotropes Download PDFInfo
- Publication number
- WO2000051684A2 WO2000051684A2 PCT/GB2000/000779 GB0000779W WO0051684A2 WO 2000051684 A2 WO2000051684 A2 WO 2000051684A2 GB 0000779 W GB0000779 W GB 0000779W WO 0051684 A2 WO0051684 A2 WO 0051684A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- depression
- coait
- drugs
- disease
- inhibit
- 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.)
- Ceased
Links
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
Definitions
- Schizophrenia depression and bipolar disorder (manic-depression) are the major common psychiatric disorders. Schizophrenia is usually treated by drugs which block dopamine and serotonin receptors. Bipolar disorder is usually treated by lithium or by one of a range of drugs which also have anti-epileptic actions. Depression is usually treated by drugs which in some way modify catecholamine or serotonin function or metabolism.
- Arachidonic acid is generally recognised as playing a major role in immune and inflammatory reactions. In the process of many such reactions AA is released from a phospholipid compartment. The released AA may act by itself or may be converted to a range of prostaglandin, leukotriene, or other oxygenated metabolites. This range of substances is fundamental to a normal immune response and to the stimulation of secretion of interleukins, interferons and other cytokines.
- CoAIT transfers AA from other phospholipids to particular phospholipids, usually ones with an ether linkage at the Snl position, which are the sources of the AA released during activation of macrophages, lymphocytes, polymorphonuclear leucocytes and other cells of the inflammation and immune systems.
- the donor phospholipids are often but not always phosphatidylcholines with an AA group at the Sn2 position and an acyl-link to another fatty acid at the Snl position.
- the recipient phospholipids are usually lysophospholipids from which the fatty acid at the Sn2 position has been removed.
- lysphospholipids often have an alkyl or an alkenyl group at the Snl position, and are also often of the phosphatidyl ethanolamine class.
- the recipient phospholipids become enriched in AA which is then released during immune and inflammatory reactions.
- CoAIT inhibitors have recently been developed as anti-inflammatory agents but have not been proposed to have anti-depressant actions.
- Several different classes of compound have been reported to inhibit CoAIT. They include agents which interact with cysteine, serine esterase inhibitors such as phenyl-methyl- sulfonyl fluoride and N-tosyl-L-phenylalanine chloromethyl ketone, p- nitrophenyl phosphate and M-aminophenyl boronic acid, and agents which can inhibit the enzyme lecithin choline acyltransferase which has a similar mode of action to CoAIT (Winkler & Chilton, 1995).
- SK ⁇ F98625 diethyl 7-(3,4,5-triphenyl- 2-oxo-2,3-dihydro-imidazol-l-yl)heptane-phosphate
- SK ⁇ F 45905 2-[2-[3- (4-c--doro-3-trifluoro-methylphenyl)ureido]-4,5-dichlorobenzenesulfonic acid inhibitors
- inhibitors which have been described include SK ⁇ F 105809 (2-(4-methylsulf ⁇ nylphenyl)-3-(4-pyridyl)-6,7- dihydro-[5H]-pyrrolol[l,2-a]imidazole), SK ⁇ F 105561 (2-(4-methylthiophenyl)- 3-(4-pyridyl)-6,7-dihydro-[5H]-pyrrolol[l,2-a]imidazole and other pyrroloimidazoles (PJ Marshall et al, Biochemical Pharmacology 1991 ; 42: 813-824) and a range of beta-lactam derivatives, including SB 212047 (4- methoxbenzyl(3S,4R)-6-bromo-6-[(l-methyl-l,2,3-triazol-4-yl)- hydroxymethyljpenicillanate) and SB216754 ((3S, 4R)-4-[(isobuteny
- CoAIT is overactive, in schizophrenia it is underactive.
- immune and inflammatory reactions are impaired (DF Horrobin et al, Schizophrenia Research 1994; 13:195-207), and the response to niacin, which activates arachidonic acid release, is seriously defective (P Ward et al, Schizophrenia Research 1998; 29:269-274).
- Drugs which activate CoAIT will therefore be important and effective in schizophrenia.
- CoAIT inhibitors or activators which can penetrate the brain.
- One way of dong this is to make them more lipophilic. This can be done by attaching to them fatty acids with 12-30 carbon atoms and 0-6 double bonds. It can also be done by incorporating them into compounds such as these described in international patent applications WO 96/34846 and WO 96/34855.
Landscapes
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
L'invention concerne l'utilisation de médicaments capables d'inhiber une transacylase indépendante de la coenzyme A dans le traitement ou la production d'un médicament destiné au traitement de troubles psychiatriques.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB9904895.1A GB9904895D0 (en) | 1999-03-03 | 1999-03-03 | Regulators of coenzyme-A-independent transacylase as psychotropic drugs |
| GB9904895.1 | 1999-03-03 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| WO2000051684A2 true WO2000051684A2 (fr) | 2000-09-08 |
| WO2000051684A3 WO2000051684A3 (fr) | 2001-01-04 |
Family
ID=10848886
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/GB2000/000779 Ceased WO2000051684A2 (fr) | 1999-03-03 | 2000-03-03 | Regulateurs de transacylase independante de la coenzyme a comme medicaments psychotropes |
Country Status (2)
| Country | Link |
|---|---|
| GB (1) | GB9904895D0 (fr) |
| WO (1) | WO2000051684A2 (fr) |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0289204B1 (fr) * | 1987-04-27 | 1991-07-17 | Efamol Holdings Plc | Compositions pharmaceutiques contenant des sels de lithium |
| DK0626969T3 (da) * | 1992-02-11 | 2000-10-30 | Smithkline Beecham Corp | CoA-IT- og PAF-inhibitorer |
| JPH11511130A (ja) * | 1995-07-25 | 1999-09-28 | スミスクライン・ビーチャム・コーポレイション | CoA−非依存性トランスアシラーゼの阻害およびアポトーシス |
| DK0956013T3 (da) * | 1996-10-11 | 2003-08-04 | Scarista Ltd | Farmaceutisk præparat indeholdende eicosapentaensyre og/eller stearidonsyre |
| AU7222598A (en) * | 1997-04-29 | 1998-11-24 | Scotia Holdings Plc | Treatment of depression and anxiety using docosahexaenoic acid or natural antioxidants |
-
1999
- 1999-03-03 GB GBGB9904895.1A patent/GB9904895D0/en not_active Ceased
-
2000
- 2000-03-03 WO PCT/GB2000/000779 patent/WO2000051684A2/fr not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| GB9904895D0 (en) | 1999-04-28 |
| WO2000051684A3 (fr) | 2001-01-04 |
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