NO301227B1 - Arylsubstituerte, heterosykliske forbindelser, anvendelser derav og farmasöytisk preparat som omfatter en slik forbindelse - Google Patents
Arylsubstituerte, heterosykliske forbindelser, anvendelser derav og farmasöytisk preparat som omfatter en slik forbindelse Download PDFInfo
- Publication number
- NO301227B1 NO301227B1 NO934760A NO934760A NO301227B1 NO 301227 B1 NO301227 B1 NO 301227B1 NO 934760 A NO934760 A NO 934760A NO 934760 A NO934760 A NO 934760A NO 301227 B1 NO301227 B1 NO 301227B1
- Authority
- NO
- Norway
- Prior art keywords
- tropane
- oxadiazol
- pyridyl
- dichlorophenyl
- normethyl
- Prior art date
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- 229940047551 haloperidol injection Drugs 0.000 description 1
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- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- WTDHULULXKLSOZ-UHFFFAOYSA-N hydroxylamine hydrochloride Substances Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 1
- WCYJQVALWQMJGE-UHFFFAOYSA-M hydroxylammonium chloride Chemical compound [Cl-].O[NH3+] WCYJQVALWQMJGE-UHFFFAOYSA-M 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
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- 238000007918 intramuscular administration Methods 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 230000002197 limbic effect Effects 0.000 description 1
- 238000005567 liquid scintillation counting Methods 0.000 description 1
- 239000003589 local anesthetic agent Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-M mandelate Chemical compound [O-]C(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-M 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000010907 mechanical stirring Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 230000003340 mental effect Effects 0.000 description 1
- AMIHUYQKNJHXPT-RBDSIQFVSA-N methyl (1s,3s,4r,5r)-3-(3,4-dichlorophenyl)-8-methyl-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1([C@@H]2[C@H]([C@]3(CC[C@@](C2)(N3C)[H])[H])C(=O)OC)=CC=C(Cl)C(Cl)=C1 AMIHUYQKNJHXPT-RBDSIQFVSA-N 0.000 description 1
- QUSLQENMLDRCTO-GBJTYRQASA-N methyl (1s,3s,4r,5r)-3-(4-fluorophenyl)-8-methyl-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1([C@@H]2[C@H]([C@]3(CC[C@@](C2)(N3C)[H])[H])C(=O)OC)=CC=C(F)C=C1 QUSLQENMLDRCTO-GBJTYRQASA-N 0.000 description 1
- LCHVZQDOKNCPDQ-BSDSXHPESA-N methyl (1s,3s,4r,5r)-3-(4-tert-butylphenyl)-8-methyl-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1([C@@H]2[C@H]([C@]3(CC[C@@](C2)(N3C)[H])[H])C(=O)OC)=CC=C(C(C)(C)C)C=C1 LCHVZQDOKNCPDQ-BSDSXHPESA-N 0.000 description 1
- MMKZDDDDODERSJ-ZJIFWQFVSA-N methyl (1s,3s,4r,5r)-8-methyl-3-(4-methylphenyl)-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1([C@@H]2[C@H]([C@]3(CC[C@@](C2)(N3C)[H])[H])C(=O)OC)=CC=C(C)C=C1 MMKZDDDDODERSJ-ZJIFWQFVSA-N 0.000 description 1
- HGNMYGRBKGXPFK-DOIPELPJSA-N methyl (1s,3s,4r,5r)-8-methyl-3-(4-phenylphenyl)-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1=CC([C@@H]2[C@H]([C@]3(CC[C@@](C2)(N3C)[H])[H])C(=O)OC)=CC=C1C1=CC=CC=C1 HGNMYGRBKGXPFK-DOIPELPJSA-N 0.000 description 1
- RVCJYYIKKXDKHI-JEDBISTDSA-N methyl (1s,3s,4r,5r)-8-methyl-3-naphthalen-1-yl-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1=CC=C2C([C@@H]3[C@H]([C@]4(CC[C@@](C3)(N4C)[H])[H])C(=O)OC)=CC=CC2=C1 RVCJYYIKKXDKHI-JEDBISTDSA-N 0.000 description 1
- ITFWLAOOLMWNLG-WJFTUGDTSA-N methyl (1s,3s,4r,5r)-8-methyl-3-naphthalen-2-yl-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1=CC=CC2=CC([C@@H]3[C@H]([C@]4(CC[C@@](C3)(N4C)[H])[H])C(=O)OC)=CC=C21 ITFWLAOOLMWNLG-WJFTUGDTSA-N 0.000 description 1
- AMIHUYQKNJHXPT-DRABBMOASA-N methyl (1s,3s,4s,5r)-3-(3,4-dichlorophenyl)-8-methyl-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1([C@@H]2[C@@H]([C@]3(CC[C@@](C2)(N3C)[H])[H])C(=O)OC)=CC=C(Cl)C(Cl)=C1 AMIHUYQKNJHXPT-DRABBMOASA-N 0.000 description 1
- LCHVZQDOKNCPDQ-MLHJIOFPSA-N methyl (1s,3s,4s,5r)-3-(4-tert-butylphenyl)-8-methyl-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1([C@@H]2[C@@H]([C@]3(CC[C@@](C2)(N3C)[H])[H])C(=O)OC)=CC=C(C(C)(C)C)C=C1 LCHVZQDOKNCPDQ-MLHJIOFPSA-N 0.000 description 1
- HGNMYGRBKGXPFK-BQJUDKOJSA-N methyl (1s,3s,4s,5r)-8-methyl-3-(4-phenylphenyl)-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1=CC([C@@H]2[C@@H]([C@]3(CC[C@@](C2)(N3C)[H])[H])C(=O)OC)=CC=C1C1=CC=CC=C1 HGNMYGRBKGXPFK-BQJUDKOJSA-N 0.000 description 1
- ITFWLAOOLMWNLG-MANSERQUSA-N methyl (1s,3s,4s,5r)-8-methyl-3-naphthalen-2-yl-8-azabicyclo[3.2.1]octane-4-carboxylate Chemical compound C1=CC=CC2=CC([C@@H]3[C@@H]([C@]4(CC[C@@](C3)(N4C)[H])[H])C(=O)OC)=CC=C21 ITFWLAOOLMWNLG-MANSERQUSA-N 0.000 description 1
- RLLMNWXOZDXKCQ-AKMJYWSESA-N methyl (5S)-3-hydroxy-8-methyl-8-azabicyclo[3.2.1]octane-2-carboxylate hydrochloride Chemical compound Cl.COC(=O)C1C2CC[C@@H](CC1O)N2C RLLMNWXOZDXKCQ-AKMJYWSESA-N 0.000 description 1
- WXEMSGQRTGSYOG-PTNSZRNDSA-N methyl (5S)-8-methyl-3-oxo-8-azabicyclo[3.2.1]octane-2-carboxylate Chemical compound C(=O)(OC)C1C2CC[C@@H](CC1=O)N2C WXEMSGQRTGSYOG-PTNSZRNDSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 230000037023 motor activity Effects 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- 229940051866 mouthwash Drugs 0.000 description 1
- FVYBAJYRRIYNBN-UHFFFAOYSA-N n'-hydroxy-2-phenylethanimidamide Chemical compound ON=C(N)CC1=CC=CC=C1 FVYBAJYRRIYNBN-UHFFFAOYSA-N 0.000 description 1
- AEXITZJSLGALNH-UHFFFAOYSA-N n'-hydroxyethanimidamide Chemical compound CC(N)=NO AEXITZJSLGALNH-UHFFFAOYSA-N 0.000 description 1
- BYRPNZFONPLHNA-UHFFFAOYSA-N n'-hydroxyfuran-2-carboximidamide Chemical compound ON=C(N)C1=CC=CO1 BYRPNZFONPLHNA-UHFFFAOYSA-N 0.000 description 1
- AQBMQGDKWIPBRF-UHFFFAOYSA-N n'-hydroxypyridine-3-carboximidamide Chemical compound ON=C(N)C1=CC=CN=C1 AQBMQGDKWIPBRF-UHFFFAOYSA-N 0.000 description 1
- NKMNPRXPUZINOM-UHFFFAOYSA-N n'-hydroxythiophene-2-carboximidamide Chemical compound ON=C(N)C1=CC=CS1 NKMNPRXPUZINOM-UHFFFAOYSA-N 0.000 description 1
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 description 1
- 235000021096 natural sweeteners Nutrition 0.000 description 1
- 239000003176 neuroleptic agent Substances 0.000 description 1
- 210000001009 nucleus accumben Anatomy 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 239000006186 oral dosage form Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
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- 239000006072 paste Substances 0.000 description 1
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- 235000010987 pectin Nutrition 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- SUSQOBVLVYHIEX-UHFFFAOYSA-N phenylacetonitrile Chemical compound N#CCC1=CC=CC=C1 SUSQOBVLVYHIEX-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 230000001242 postsynaptic effect Effects 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 230000000069 prophylactic effect Effects 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Substances CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 229960004063 propylene glycol Drugs 0.000 description 1
- 208000020016 psychiatric disease Diseases 0.000 description 1
- 210000002637 putamen Anatomy 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- MMKZDDDDODERSJ-JJXSEGSLSA-N rti-32 Chemical compound C1([C@H]2C[C@@H]3CC[C@@H](N3C)[C@H]2C(=O)OC)=CC=C(C)C=C1 MMKZDDDDODERSJ-JJXSEGSLSA-N 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000005062 synaptic transmission Effects 0.000 description 1
- 210000003568 synaptosome Anatomy 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000007885 tablet disintegrant Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003899 tartaric acid esters Chemical class 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 210000001519 tissue Anatomy 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
- 238000011200 topical administration Methods 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 238000001665 trituration Methods 0.000 description 1
- QQXLDOJGLXJCSE-KNVOCYPGSA-N tropinone Chemical compound C1C(=O)C[C@H]2CC[C@@H]1N2C QQXLDOJGLXJCSE-KNVOCYPGSA-N 0.000 description 1
- 239000011345 viscous material Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
-
- 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
- A61K31/46—8-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, cocaine
-
- 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
- A61P25/24—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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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)
- Neurosurgery (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Psychiatry (AREA)
- Addiction (AREA)
- Emergency Medicine (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK921541A DK154192D0 (da) | 1992-12-23 | 1992-12-23 | Heterocycliske forbindelser |
DK71893A DK71893D0 (da) | 1993-06-18 | 1993-06-18 | Heterocykliske forbindelser |
US08/093,184 US5554626A (en) | 1992-12-23 | 1993-07-16 | Substituted heterocyclic compounds as dopamine-reuptake inhibitors |
Publications (3)
Publication Number | Publication Date |
---|---|
NO934760D0 NO934760D0 (no) | 1993-12-22 |
NO934760L NO934760L (no) | 1994-06-24 |
NO301227B1 true NO301227B1 (no) | 1997-09-29 |
Family
ID=27220884
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO934760A NO301227B1 (no) | 1992-12-23 | 1993-12-22 | Arylsubstituerte, heterosykliske forbindelser, anvendelser derav og farmasöytisk preparat som omfatter en slik forbindelse |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0604352B1 (fi) |
JP (1) | JPH06293760A (fi) |
AT (1) | ATE225787T1 (fi) |
AU (1) | AU672644B2 (fi) |
CA (1) | CA2112083C (fi) |
DE (1) | DE69332366T2 (fi) |
FI (1) | FI935799A (fi) |
NO (1) | NO301227B1 (fi) |
NZ (1) | NZ250514A (fi) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6329520B1 (en) * | 1990-08-09 | 2001-12-11 | Research Triangle Institute | Cocaine receptor binding ligands |
ATE224392T1 (de) * | 1995-11-02 | 2002-10-15 | Neurosearch As | Kondensierte tropanderivate als neurotransmitter- reuptake-inhibitoren |
CA2244773C (en) | 1996-02-22 | 2006-01-03 | Neurosearch A/S | Tropane-derivatives, their preparation and use |
AU5790598A (en) * | 1996-12-02 | 1998-06-29 | Georgetown University | Tropane derivatives and method for their synthesis |
GB9915617D0 (en) * | 1999-07-05 | 1999-09-01 | Knoll Ag | Therapeutic agents |
WO2003045388A1 (en) | 2001-11-30 | 2003-06-05 | Neurosearch A/S | Tropane derivatives having dopamine reuptake inhibitor activity for the treatment of ischemic diseases |
EP2269608A3 (en) | 2003-10-16 | 2011-02-16 | NeuroSearch AS | Pharmaceutical composition comprising a monoamine neurotransmitter re-uptake inhibitor and an acetylcholinesterase inhibitor |
EP1779851A1 (en) | 2005-10-31 | 2007-05-02 | Boehringer Ingelheim Pharma GmbH & Co.KG | Treatment of diabetes |
US20100035914A1 (en) * | 2006-09-11 | 2010-02-11 | Barbara Bertani | Azabicyclic compounds as inhibitors of monoamines reuptake |
WO2010125033A1 (en) * | 2009-04-29 | 2010-11-04 | Glaxo Group Limited | Azabicyclo[4.1.0]heptane derivatives |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3813404A (en) * | 1972-11-15 | 1974-05-28 | Sterling Drug Inc | Tropane-2-carboxylates and derivatives |
FR2276823A1 (fr) * | 1974-07-04 | 1976-01-30 | Roussel Uclaf | Nouveaux derives de la dibenzo(b.e)thiepine et leurs sels, procede de preparation et application a titre de medicaments desdits produits |
NZ219646A (en) * | 1986-03-27 | 1990-10-26 | Merck Sharp & Dohme | Oxadiazole derivatives of azacyclics for treating cns disorders |
IL88156A (en) * | 1987-11-13 | 1997-02-18 | Novo Nordisk As | Azacyclic compounds their preparation and pharmaceutical compositions containing them |
NZ227684A (en) * | 1988-01-30 | 1991-07-26 | Merck Sharp & Dohme | Pyrazine, pyridazine, and pyrimidine derivatives and pharmaceutical compositions |
EP0398578B1 (en) * | 1989-05-17 | 1997-03-12 | Pfizer Inc. | 2-piperidino-1-alkanol derivatives as antiischemic agents |
DK198590D0 (da) * | 1990-08-21 | 1990-08-21 | Novo Nordisk As | Heterocykliske forbindelser, deres fremstilling og anvendelse |
ATE182794T1 (de) * | 1991-11-15 | 1999-08-15 | Res Triangle Inst | Kokainrezeptor bindende liganden |
US5262428A (en) * | 1992-03-13 | 1993-11-16 | Wake Forest University | Biologically active tropane derivatives |
US5268480A (en) * | 1992-09-22 | 1993-12-07 | Mayo Foundation For Medical Education And Research | Cocaine analogs |
AU671163B2 (en) * | 1992-12-23 | 1996-08-15 | Neurosearch A/S | Alkyl substituted heterocyclic compounds |
-
1993
- 1993-12-13 AU AU52363/93A patent/AU672644B2/en not_active Ceased
- 1993-12-20 NZ NZ250514A patent/NZ250514A/en unknown
- 1993-12-20 DE DE69332366T patent/DE69332366T2/de not_active Expired - Lifetime
- 1993-12-20 AT AT93610063T patent/ATE225787T1/de not_active IP Right Cessation
- 1993-12-20 EP EP93610063A patent/EP0604352B1/en not_active Expired - Lifetime
- 1993-12-21 CA CA002112083A patent/CA2112083C/en not_active Expired - Fee Related
- 1993-12-22 JP JP5324475A patent/JPH06293760A/ja not_active Ceased
- 1993-12-22 FI FI935799A patent/FI935799A/fi unknown
- 1993-12-22 NO NO934760A patent/NO301227B1/no not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
FI935799A (fi) | 1994-06-24 |
CA2112083A1 (en) | 1994-06-24 |
JPH06293760A (ja) | 1994-10-21 |
DE69332366T2 (de) | 2003-06-18 |
NO934760L (no) | 1994-06-24 |
EP0604352A2 (en) | 1994-06-29 |
CA2112083C (en) | 2002-02-19 |
EP0604352A3 (en) | 1995-02-08 |
NZ250514A (en) | 1996-03-26 |
FI935799A0 (fi) | 1993-12-22 |
AU5236393A (en) | 1994-07-07 |
NO934760D0 (no) | 1993-12-22 |
DE69332366D1 (de) | 2002-11-14 |
ATE225787T1 (de) | 2002-10-15 |
EP0604352B1 (en) | 2002-10-09 |
AU672644B2 (en) | 1996-10-10 |
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MM1K | Lapsed by not paying the annual fees |
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