NO323304B1 - Anvendelse av bioaktive metabolitter av gepiron for fremstilling av et medikament for behandling av psykologiske forstyrrelser og farmasoytisk sammensetning omfattende samme - Google Patents
Anvendelse av bioaktive metabolitter av gepiron for fremstilling av et medikament for behandling av psykologiske forstyrrelser og farmasoytisk sammensetning omfattende samme Download PDFInfo
- Publication number
- NO323304B1 NO323304B1 NO20022954A NO20022954A NO323304B1 NO 323304 B1 NO323304 B1 NO 323304B1 NO 20022954 A NO20022954 A NO 20022954A NO 20022954 A NO20022954 A NO 20022954A NO 323304 B1 NO323304 B1 NO 323304B1
- Authority
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- Prior art keywords
- gepirone
- pharmaceutical composition
- bioactive
- depression
- disorder
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- 239000008273 gelatin Substances 0.000 description 1
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- 150000004820 halides Chemical class 0.000 description 1
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 1
- KDCIHNCMPUBDKT-UHFFFAOYSA-N hexane;propan-2-one Chemical compound CC(C)=O.CCCCCC KDCIHNCMPUBDKT-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
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- 238000010253 intravenous injection Methods 0.000 description 1
- 229950003599 ipsapirone Drugs 0.000 description 1
- 229940045996 isethionic acid Drugs 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 210000001853 liver microsome Anatomy 0.000 description 1
- 238000011866 long-term treatment Methods 0.000 description 1
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- 239000000314 lubricant Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000013081 microcrystal Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- KVBGVZZKJNLNJU-UHFFFAOYSA-M naphthalene-2-sulfonate Chemical compound C1=CC=CC2=CC(S(=O)(=O)[O-])=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-M 0.000 description 1
- 230000000701 neuroleptic effect Effects 0.000 description 1
- 235000001968 nicotinic acid Nutrition 0.000 description 1
- 239000011664 nicotinic acid Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- HGASFNYMVGEKTF-UHFFFAOYSA-N octan-1-ol;hydrate Chemical compound O.CCCCCCCCO HGASFNYMVGEKTF-UHFFFAOYSA-N 0.000 description 1
- 239000012053 oil suspension Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- WLJNZVDCPSBLRP-UHFFFAOYSA-N pamoic acid Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=C(C=3O)C(=O)O)=C(O)C(C(O)=O)=CC2=C1 WLJNZVDCPSBLRP-UHFFFAOYSA-N 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229940075930 picrate Drugs 0.000 description 1
- OXNIZHLAWKMVMX-UHFFFAOYSA-M picrate anion Chemical compound [O-]C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O OXNIZHLAWKMVMX-UHFFFAOYSA-M 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- CNMOHEDUVVUVPP-UHFFFAOYSA-N piperidine-2,3-dione Chemical compound O=C1CCCNC1=O CNMOHEDUVVUVPP-UHFFFAOYSA-N 0.000 description 1
- 229950010765 pivalate Drugs 0.000 description 1
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 229940124606 potential therapeutic agent Drugs 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004089 psychotropic agent Substances 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- AWUCVROLDVIAJX-GSVOUGTGSA-N sn-glycerol 3-phosphate Chemical compound OC[C@@H](O)COP(O)(O)=O AWUCVROLDVIAJX-GSVOUGTGSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000007920 subcutaneous administration Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
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- 229940116362 tragacanth Drugs 0.000 description 1
- 230000037317 transdermal delivery Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- ZDPHROOEEOARMN-UHFFFAOYSA-N undecanoic acid Chemical compound CCCCCCCCCCC(O)=O ZDPHROOEEOARMN-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
Landscapes
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Neurosurgery (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Neurology (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Epidemiology (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17268499P | 1999-12-20 | 1999-12-20 | |
| US09/709,741 US6534507B1 (en) | 1999-12-20 | 2000-11-13 | Methods for treating psychological disorders using bioactive metabolites of gepirone |
| PCT/US2000/034131 WO2001045687A2 (en) | 1999-12-20 | 2000-12-18 | Use of bioactive metabolites of gepirone for the treatment of psychological disorders |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20022954D0 NO20022954D0 (no) | 2002-06-19 |
| NO20022954L NO20022954L (no) | 2002-06-19 |
| NO323304B1 true NO323304B1 (no) | 2007-03-05 |
Family
ID=26868346
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20022954A NO323304B1 (no) | 1999-12-20 | 2002-06-19 | Anvendelse av bioaktive metabolitter av gepiron for fremstilling av et medikament for behandling av psykologiske forstyrrelser og farmasoytisk sammensetning omfattende samme |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6534507B1 (cs) |
| EP (1) | EP1242061B1 (cs) |
| JP (1) | JP4236407B2 (cs) |
| KR (1) | KR100602976B1 (cs) |
| CN (1) | CN1411375A (cs) |
| AT (1) | ATE294572T1 (cs) |
| AU (1) | AU776409B2 (cs) |
| CA (1) | CA2395458C (cs) |
| CZ (1) | CZ300429B6 (cs) |
| DE (1) | DE60019968T2 (cs) |
| ES (1) | ES2241683T3 (cs) |
| HU (1) | HU228963B1 (cs) |
| IL (2) | IL150222A0 (cs) |
| MX (1) | MXPA02006146A (cs) |
| NO (1) | NO323304B1 (cs) |
| NZ (1) | NZ519554A (cs) |
| PL (1) | PL200378B1 (cs) |
| PT (1) | PT1242061E (cs) |
| RU (1) | RU2282448C2 (cs) |
| WO (1) | WO2001045687A2 (cs) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002016347A1 (en) * | 2000-08-22 | 2002-02-28 | Akzo Nobel N.V. | Active metabolite of gepirone |
| US20040002500A1 (en) * | 2002-06-28 | 2004-01-01 | Fabre Kramer Pharmaceutical, Inc. | Methods for treating attention deficit disorder |
| US20040000689A1 (en) * | 2002-06-28 | 2004-01-01 | Erh-Kun Lai | Dual-bit MONOS/SONOS memory structure with non-continuous floating gate |
| WO2004014309A2 (en) * | 2002-08-12 | 2004-02-19 | Bristol-Myers Squibb Company | Improved process for hydroxyazapirones |
| WO2004069339A1 (en) * | 2003-01-29 | 2004-08-19 | Psychogenics Inc. | Treatment for attention-deficit hyperactivity disorder |
| TW200521125A (en) * | 2003-11-18 | 2005-07-01 | Bristol Myers Squibb Co | Continuous process for producing hydroxyazapirones by oxidation |
| BRPI0419179A (pt) * | 2004-11-05 | 2007-12-18 | Fabre Kramer Pharmaceuticals I | formulação de alta dosagem de liberação prolongada de gepirona |
| BRPI0912516A2 (pt) * | 2008-05-08 | 2015-10-13 | Fabre Kramer Pharmaceuticals Inc | 3-hidróxi gepirona para o tratamento de distúrbio de défict de atenção e disfunção sexual |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4423049A (en) | 1981-12-28 | 1983-12-27 | Mead Johnson & Company | 2-[4-[(4,4-Dialkyl-2,6-piperidinedion-1-yl)butyl]-1-piperazinyl]pyrimidines |
| US5185329A (en) * | 1988-08-30 | 1993-02-09 | Bristol-Myers Squibb Company | Method for treatment of substance addiction |
| HUT61719A (en) * | 1989-05-31 | 1993-03-01 | Upjohn Co | Process for producing 2-aminotetraline derivatives and pharmaceutical compositions comprising such compounds |
| US4956368A (en) | 1989-07-24 | 1990-09-11 | Bristol-Myers Company | Metabolites and prodrug formulations of 8-[4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]butyl]-8-azaspiro[4.5]decane-7,9-dione |
| US5478572A (en) | 1994-09-06 | 1995-12-26 | Bristol-Myers Squibb Co. | Gepirone dosage form |
-
2000
- 2000-11-13 US US09/709,741 patent/US6534507B1/en not_active Expired - Lifetime
- 2000-12-18 AU AU22687/01A patent/AU776409B2/en not_active Expired
- 2000-12-18 PT PT00986449T patent/PT1242061E/pt unknown
- 2000-12-18 PL PL364936A patent/PL200378B1/pl unknown
- 2000-12-18 MX MXPA02006146A patent/MXPA02006146A/es active IP Right Grant
- 2000-12-18 DE DE60019968T patent/DE60019968T2/de not_active Expired - Lifetime
- 2000-12-18 CA CA002395458A patent/CA2395458C/en not_active Expired - Lifetime
- 2000-12-18 EP EP00986449A patent/EP1242061B1/en not_active Expired - Lifetime
- 2000-12-18 IL IL15022200A patent/IL150222A0/xx unknown
- 2000-12-18 HU HU0301831A patent/HU228963B1/hu unknown
- 2000-12-18 KR KR1020027007927A patent/KR100602976B1/ko not_active Expired - Lifetime
- 2000-12-18 AT AT00986449T patent/ATE294572T1/de active
- 2000-12-18 ES ES00986449T patent/ES2241683T3/es not_active Expired - Lifetime
- 2000-12-18 RU RU2002119400/14A patent/RU2282448C2/ru active
- 2000-12-18 CZ CZ20022137A patent/CZ300429B6/cs not_active IP Right Cessation
- 2000-12-18 CN CN00817455A patent/CN1411375A/zh active Pending
- 2000-12-18 NZ NZ519554A patent/NZ519554A/en not_active IP Right Cessation
- 2000-12-18 JP JP2001546426A patent/JP4236407B2/ja not_active Expired - Lifetime
- 2000-12-18 WO PCT/US2000/034131 patent/WO2001045687A2/en not_active Ceased
-
2002
- 2002-06-13 IL IL150222A patent/IL150222A/en active IP Right Grant
- 2002-06-19 NO NO20022954A patent/NO323304B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| PL200378B1 (pl) | 2008-12-31 |
| PT1242061E (pt) | 2005-09-30 |
| ES2241683T3 (es) | 2005-11-01 |
| JP2004500362A (ja) | 2004-01-08 |
| KR100602976B1 (ko) | 2006-07-20 |
| JP4236407B2 (ja) | 2009-03-11 |
| RU2002119400A (ru) | 2004-01-27 |
| DE60019968D1 (de) | 2005-06-09 |
| EP1242061B1 (en) | 2005-05-04 |
| CZ20022137A3 (cs) | 2003-03-12 |
| PL364936A1 (en) | 2004-12-27 |
| CN1411375A (zh) | 2003-04-16 |
| CA2395458A1 (en) | 2001-06-28 |
| WO2001045687A2 (en) | 2001-06-28 |
| EP1242061A2 (en) | 2002-09-25 |
| AU2268701A (en) | 2001-07-03 |
| DE60019968T2 (de) | 2006-02-02 |
| WO2001045687A3 (en) | 2002-04-25 |
| MXPA02006146A (es) | 2004-08-23 |
| NZ519554A (en) | 2005-01-28 |
| CZ300429B6 (cs) | 2009-05-20 |
| US6534507B1 (en) | 2003-03-18 |
| AU776409B2 (en) | 2004-09-09 |
| IL150222A (en) | 2009-09-22 |
| HUP0301831A2 (hu) | 2003-09-29 |
| NO20022954D0 (no) | 2002-06-19 |
| IL150222A0 (en) | 2002-12-01 |
| CA2395458C (en) | 2009-05-12 |
| RU2282448C2 (ru) | 2006-08-27 |
| ATE294572T1 (de) | 2005-05-15 |
| KR20020082470A (ko) | 2002-10-31 |
| HU228963B1 (en) | 2013-07-29 |
| NO20022954L (no) | 2002-06-19 |
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