NO971423L - Bestemte aminometyl-fenylimidazol-derivater; en ny klasse spesifikke dopaminreseptor-undertype-ligander - Google Patents
Bestemte aminometyl-fenylimidazol-derivater; en ny klasse spesifikke dopaminreseptor-undertype-liganderInfo
- Publication number
- NO971423L NO971423L NO971423A NO971423A NO971423L NO 971423 L NO971423 L NO 971423L NO 971423 A NO971423 A NO 971423A NO 971423 A NO971423 A NO 971423A NO 971423 L NO971423 L NO 971423L
- Authority
- NO
- Norway
- Prior art keywords
- straight
- chain
- carbon atoms
- branched lower
- lower alkyl
- Prior art date
Links
- 108050004812 Dopamine receptor Proteins 0.000 title description 18
- 102000015554 Dopamine receptor Human genes 0.000 title description 18
- CNIIMCXFZSUBJC-UHFFFAOYSA-N (2-phenyl-1h-imidazol-5-yl)methanamine Chemical class NCC1=CNC(C=2C=CC=CC=2)=N1 CNIIMCXFZSUBJC-UHFFFAOYSA-N 0.000 title description 5
- 239000003446 ligand Substances 0.000 title description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 182
- 125000000217 alkyl group Chemical group 0.000 claims description 162
- 239000001257 hydrogen Substances 0.000 claims description 134
- 229910052739 hydrogen Inorganic materials 0.000 claims description 134
- 150000001875 compounds Chemical class 0.000 claims description 126
- IAOGWYABFHUNKI-UHFFFAOYSA-N 1h-imidazole;dihydrochloride Chemical compound Cl.[Cl-].C1=C[NH+]=CN1 IAOGWYABFHUNKI-UHFFFAOYSA-N 0.000 claims description 121
- 150000002431 hydrogen Chemical class 0.000 claims description 94
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 claims description 84
- 229910052736 halogen Inorganic materials 0.000 claims description 81
- 150000002367 halogens Chemical class 0.000 claims description 80
- 125000003545 alkoxy group Chemical group 0.000 claims description 76
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 66
- -1 4-(2methoxyphenyl)piperazin-1-yl Chemical group 0.000 claims description 57
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 39
- ZXTHWIZHGLNEPG-UHFFFAOYSA-N 2-phenyl-4,5-dihydro-1,3-oxazole Chemical compound O1CCN=C1C1=CC=CC=C1 ZXTHWIZHGLNEPG-UHFFFAOYSA-N 0.000 claims description 37
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 34
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 30
- 125000004076 pyridyl group Chemical group 0.000 claims description 30
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- 230000015654 memory Effects 0.000 claims description 22
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 20
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- 239000001301 oxygen Substances 0.000 claims description 14
- 229910052760 oxygen Inorganic materials 0.000 claims description 14
- 238000002360 preparation method Methods 0.000 claims description 12
- 229910052717 sulfur Chemical group 0.000 claims description 12
- 239000011593 sulfur Chemical group 0.000 claims description 12
- 231100000252 nontoxic Toxicity 0.000 claims description 11
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- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- 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
-
- 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
- C07D401/06—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 linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- Chemical & Material Sciences (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Neurosurgery (AREA)
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- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Biomedical Technology (AREA)
- Public Health (AREA)
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- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/313,435 US5633376A (en) | 1990-12-28 | 1994-09-27 | Certain aminomethyl phenylimidazole derivatives; and 4-aryl substituted piperazinyl and piperidinylmethyl phenylimidazole derivatives; a new class of dopamine receptor subtype ligands |
| US08/401,201 US5681956A (en) | 1990-12-28 | 1995-03-09 | 4-aryl substituted piperazinylmethyl phenylimidazole derivatives; a new class of dopamine receptor subtype specific ligands |
| PCT/US1995/012272 WO1996010018A1 (fr) | 1994-09-27 | 1995-09-26 | Derives de l'aminomethylphenylimidazole et nouvelle categorie de ligands specifiques du sous-type du recepteur de la dopamine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO971423D0 NO971423D0 (no) | 1997-03-25 |
| NO971423L true NO971423L (no) | 1997-05-23 |
Family
ID=26978872
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO971423A NO971423L (no) | 1994-09-27 | 1997-03-25 | Bestemte aminometyl-fenylimidazol-derivater; en ny klasse spesifikke dopaminreseptor-undertype-ligander |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US5681956A (fr) |
| EP (1) | EP0783494A1 (fr) |
| JP (1) | JP2927967B2 (fr) |
| KR (1) | KR970706259A (fr) |
| CN (1) | CN1092643C (fr) |
| AU (1) | AU705585B2 (fr) |
| BR (1) | BR9509101A (fr) |
| CA (1) | CA2201140A1 (fr) |
| CZ (1) | CZ87397A3 (fr) |
| HU (1) | HUT76928A (fr) |
| MX (1) | MX9702234A (fr) |
| NO (1) | NO971423L (fr) |
| NZ (1) | NZ294447A (fr) |
| PL (1) | PL319637A1 (fr) |
| SK (1) | SK40797A3 (fr) |
| WO (1) | WO1996010018A1 (fr) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5646281A (en) * | 1990-12-28 | 1997-07-08 | Neurogen Corporation | Certain 4-piperidino- and piperazinomethyl-2-phenyl imidazole derivatives; dopamine receptor subtype specific ligands |
| TW504510B (en) * | 1996-05-10 | 2002-10-01 | Janssen Pharmaceutica Nv | 2,4-diaminopyrimidine derivatives |
| US5905152A (en) * | 1996-08-08 | 1999-05-18 | Schering Corporation | Preparation of aminomethyl-phenylimidazoles |
| DE19637237A1 (de) | 1996-09-13 | 1998-03-19 | Merck Patent Gmbh | Piperazin-Derivate |
| US6313141B1 (en) | 1997-06-13 | 2001-11-06 | Neurogen Corporation | 2-aminoalkylaminoquinolines as dopamine D4 ligands |
| JP2002504125A (ja) * | 1997-06-13 | 2002-02-05 | ニューロゲン コーポレイション | ドーパミンｄ▲下４▼リガンドとしての２−アミノアルキルアミノキノリン |
| US5972945A (en) * | 1997-06-13 | 1999-10-26 | Neurogen Corporation | 2-aminoalkylaminoquinolines; dopamine receptor subtype specific ligands |
| AU6242999A (en) * | 1998-09-02 | 2000-03-21 | Neurogen Corporation | 2-aryl-4-(1-(4-heteroaryl)piperazin-1-yl) methylimidazoles: dopamine d4 receptor subtype ligands |
| WO2000018763A2 (fr) * | 1998-09-29 | 2000-04-06 | Neurogen Corporation | 2-(2,3-dihydrobenzofuran-5-yl)-4-aminomethylimidazoles; ligands specifiques du sous-type du recepteur de dopamine |
| US6288230B1 (en) | 1998-09-29 | 2001-09-11 | Neurogen Corporation | 2-(2, 3-dihydrobenzofuran-5-yl)-4-aminomethylimidazoles: dopamine receptor subtype specific ligands |
| US6284759B1 (en) | 1998-09-30 | 2001-09-04 | Neurogen Corporation | 2-piperazinoalkylaminobenzo-azole derivatives: dopamine receptor subtype specific ligands |
| JP2002527433A (ja) | 1998-10-08 | 2002-08-27 | スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー | ドーパミンｄ３受容体のモジュレーター（抗精神病薬）として有用なテトラヒドロベンズアゼピン誘導体 |
| WO2002049993A2 (fr) * | 2000-09-29 | 2002-06-27 | Neurogen Corporation | Petites molecules modulatrices des recepteurs c5a a haute affinite |
| US6723743B1 (en) | 1999-09-28 | 2004-04-20 | Neurogen Corporation | High affinity small molecule C5a receptor modulators |
| US6884815B1 (en) * | 1999-09-28 | 2005-04-26 | Neurogen Corporation | High affinity small molecule C5a receptor modulators |
| US6613901B2 (en) | 2000-03-08 | 2003-09-02 | Neurogen Corporation | 2-aminoalkylaminoquinolines as dopamine D4 ligands |
| DE10041479A1 (de) * | 2000-08-24 | 2002-03-14 | Sanol Arznei Schwarz Gmbh | Neue pharmazeutische Zusammensetzung zur Verabreichung von N-0923 |
| US6861440B2 (en) | 2001-10-26 | 2005-03-01 | Hoffmann-La Roche Inc. | DPP IV inhibitors |
| IL164355A0 (en) | 2002-03-29 | 2005-12-18 | Neurogen Corp | New aryl imidazoles and related compounds as cra receptor modulators |
| CA2480082A1 (fr) * | 2002-03-29 | 2003-10-16 | Neurogen Corporation | Therapie combinatoire pour le traitement de maladies faisant intervenir des composants inflammatoires |
| US20040048779A1 (en) * | 2002-05-06 | 2004-03-11 | Erwin Schollmayer | Use of rotigotine for treating the restless leg syndrome |
| EP1613615A2 (fr) * | 2003-04-03 | 2006-01-11 | Merck & Co., Inc. | Derives d'imidazole a 4 cycles utilises en tant que modulateurs du recepteur 5 metabotropique du glutamate |
| ES2327740T3 (es) | 2003-06-20 | 2009-11-03 | F. Hoffmann-La Roche Ag | Hexahidropiridoisoquinolinas como inhibidoras de la dpp-iv. |
| AU2004251830B8 (en) | 2003-06-20 | 2009-11-26 | F. Hoffmann-La Roche Ag | Pyrido[2, 1-A]-isoquinoline derivatives as DPP-IV inhibitors |
| DE10334187A1 (de) * | 2003-07-26 | 2005-03-03 | Schwarz Pharma Ag | Substituierte 2-Aminotetraline zur Behandlung von Depressionen |
| DE10334188B4 (de) * | 2003-07-26 | 2007-07-05 | Schwarz Pharma Ag | Verwendung von Rotigotin zur Behandlung von Depressionen |
| RU2006105717A (ru) * | 2003-07-30 | 2007-09-20 | Зинон Фармасьютиклз Инк. (Ca) | Производные пиперазина и их применение в качестве терапевтических агентов |
| JP2007516290A (ja) * | 2003-12-23 | 2007-06-21 | シェーリング コーポレイション | 肥満およびｃｎｓ障害の処置のための選択的ｄ１ドーパミンレセプターアンタゴニストとしての置換ｎ−アリールアミジン |
| DE10361258A1 (de) * | 2003-12-24 | 2005-07-28 | Schwarz Pharma Ag | Verwendung von substituierten 2-Aminotetralinen zur vorbeugenden Behandlung von Morbus Parkinson |
| US20050197385A1 (en) * | 2004-02-20 | 2005-09-08 | Schwarz Pharma Ag | Use of rotigotine for treatment or prevention of dopaminergic neuron loss |
| DE102004014841B4 (de) * | 2004-03-24 | 2006-07-06 | Schwarz Pharma Ag | Verwendung von Rotigotin zur Behandlung und Prävention des Parkinson-Plus-Syndroms |
| WO2006089076A2 (fr) * | 2005-02-18 | 2006-08-24 | Neurogen Corporation | Thiazole amides, imidazole amides et analogues associes |
| TW200800946A (en) * | 2005-08-15 | 2008-01-01 | Astrazeneca Ab | Substituted piperazines as metabotropic glutamate receptor antagonists |
| EP1987815A1 (fr) * | 2007-05-04 | 2008-11-05 | Schwarz Pharma Ag | Compositions pharmaceutiques à base d'agonistes dopaminergiques administrables par voie oro-naso-pharyngale pour la prévention et/ou le traitement de membres sans repos |
| EP3083595B1 (fr) * | 2013-12-20 | 2020-05-27 | Esteve Pharmaceuticals, S.A. | Composés de pipéridine ayant une activité multimodale contre la douleur |
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| US3304306A (en) * | 1964-01-02 | 1967-02-14 | Ciba Geigy Corp | Nu (amidino-lower alkyl)-benzhydryl piperidines |
| US3491098A (en) * | 1967-05-29 | 1970-01-20 | Sterling Drug Inc | 1-((imidazolyl)-lower-alkyl)-4-substituted-piperazines |
| US4080503A (en) * | 1972-07-19 | 1978-03-21 | Boehringer Ingelheim Gmbh | 2-Amino-4-phenyl-2-imidazolines and salts thereof |
| US4404382A (en) * | 1980-09-17 | 1983-09-13 | The Upjohn Company | Piperazinyl-substituted imidazoles |
| US4605655A (en) * | 1984-03-06 | 1986-08-12 | Bristol-Myers Company | Antipsychotic 1-fluorophenylbutyl-4-(2-pyrimidinyl)piperazine derivatives |
| DE3411997A1 (de) * | 1984-03-31 | 1985-10-17 | Boehringer Mannheim Gmbh, 6800 Mannheim | Neue redox-indikatoren |
| US5206257A (en) * | 1987-03-05 | 1993-04-27 | May & Baker Limited | Pesticidal method using 2-phenylimidazole derivatives |
| US5043447A (en) * | 1987-04-24 | 1991-08-27 | Syntex Pharmaceuticals, Ltd. | Substituted imidazolyl-alkyl-piperazine and -diazepine derivatives |
| US4829065A (en) * | 1987-04-24 | 1989-05-09 | Syntex Pharmaceuticals, Ltd. | Substituted imidazolyl-alkyl-piperazine and -diazepine derivatives |
| JPS63269445A (ja) * | 1987-04-28 | 1988-11-07 | Canon Inc | 電子ビーム発生素子 |
| JP2700475B2 (ja) * | 1988-07-30 | 1998-01-21 | コニカ株式会社 | 非線形光学材料および非線形光学素子 |
| IT1230703B (it) * | 1989-01-26 | 1991-10-29 | Luso Farmaco Inst | Derivati imidazolonici ad attivita' antiipertensiva, loro metodi di preparazione e composizioni farmaceutiche che li contengono. |
| FR2642759B1 (fr) * | 1989-02-09 | 1991-05-17 | Laboratorios Esteve Sa | Derives de pyrimidyl-piperazinyl-alkyl azoles avec activite anxiolytique et/ou tranquillisante |
| FR2642758B1 (fr) * | 1989-02-09 | 1991-05-17 | Esteve Labor Dr | Derives de pyrimidine,2-(4-((alpha)-heteroaryl-(alpha) aryl-((alpha)-alkyl)-methoxy)-butyl)-1-piperazinyl), avec activite serotoninergique |
| AU621245B2 (en) * | 1989-10-17 | 1992-03-05 | Boehringer Mannheim Gmbh | Hydrolase substrates, a process for the preparation thereof and agents containing them |
| FR2654621B1 (fr) * | 1989-11-22 | 1994-09-23 | Esteve Labor Dr | Inhibition du syndrome d'abstinence. |
| FR2672052B1 (fr) * | 1991-01-28 | 1995-05-24 | Esteve Labor Dr | Derives d'aryl (ou heteroaryl)-piperazinyl-alkyl-azoles, leur preparation et leur application en tant que medicaments. |
| GB9021453D0 (en) * | 1990-10-03 | 1990-11-14 | Wyeth John & Brother Ltd | Piperazine derivatives |
| US5159083A (en) * | 1990-12-28 | 1992-10-27 | Neurogen Corporation | Certain aminomethyl phenylimidazole derivatives; a class of dopamine receptor subtype specific ligands |
| FR2671972B1 (fr) * | 1991-01-25 | 1995-03-03 | Esteve Labor Dr | Utilisation de derives 1-h-azole-(omega-(4-(2-pyrimidinyl)-1-piperazinyl)-alkyl) pour la preparation de medicaments destines au traitement des troubles des fonctions cognitives. |
| FR2673628B1 (fr) * | 1991-03-07 | 1993-07-09 | Esteve Labor Dr | Procede de preparation de derives d'aryl (ou heteroaryl)-piperazinyl-butyl-azoles. |
| US5093333A (en) * | 1991-04-29 | 1992-03-03 | American Home Products Corporation | N-substituted-2-aminoquinolines useful for treating hypofunction of the cholinergic system |
| NZ246295A (en) * | 1991-12-18 | 1996-06-25 | Schering Corp | Imidazolylalkyl derivatives and pharmaceutical compositions; histamine h3 agonists and antagonists |
| JP3393891B2 (ja) * | 1992-08-18 | 2003-04-07 | 塩野義製薬株式会社 | イミダゾール類の製造方法 |
| FR2701260B1 (fr) * | 1993-02-05 | 1995-05-05 | Esteve Labor Dr | Dérivés de 2-[4-(4-azolylbutyl)-1-pipérazinyl]-5-hydroxypyrimidine, leur préparation et leur application en tant que médicaments. |
| US5296609A (en) * | 1993-04-09 | 1994-03-22 | Syntex Pharmaceuticals, Ltd. | Process for the preparation of 1,2,4-substituted imidazoles and related aminoalkylimidazole derivatives |
| FR2705098B1 (fr) * | 1993-05-10 | 1995-08-04 | Esteve Labor Dr | Procédé de préparation de 2-{4-[4-(chloro-1-pyrazolyl)butyl]1-pipérazinyl}pyrimidine (Lesopitron) . |
| WO1994028933A1 (fr) * | 1993-06-04 | 1994-12-22 | New York University | Anticorps monoclonaux humains a double specificite, specifiques contre le virus de l'immunodeficience humaine |
| FR2712808B1 (fr) * | 1993-11-25 | 1996-02-16 | Esteve Labor Dr | Utilisation des dérivés de 1-{4-[4-aryl(ou hétéroaryl)-1-pipérazinyl]-butyl}-1-H-azole pour la préparation de médicaments destinés au traitement des troubles de la sécrétion gastrique . |
-
1995
- 1995-03-09 US US08/401,201 patent/US5681956A/en not_active Expired - Fee Related
- 1995-09-26 MX MX9702234A patent/MX9702234A/es unknown
- 1995-09-26 BR BR9509101A patent/BR9509101A/pt not_active Application Discontinuation
- 1995-09-26 PL PL95319637A patent/PL319637A1/xx unknown
- 1995-09-26 SK SK407-97A patent/SK40797A3/sk unknown
- 1995-09-26 CZ CZ97873A patent/CZ87397A3/cs unknown
- 1995-09-26 CA CA002201140A patent/CA2201140A1/fr not_active Abandoned
- 1995-09-26 HU HU9701497A patent/HUT76928A/hu unknown
- 1995-09-26 WO PCT/US1995/012272 patent/WO1996010018A1/fr not_active Application Discontinuation
- 1995-09-26 EP EP95935121A patent/EP0783494A1/fr not_active Withdrawn
- 1995-09-26 AU AU37259/95A patent/AU705585B2/en not_active Ceased
- 1995-09-26 JP JP8511959A patent/JP2927967B2/ja not_active Ceased
- 1995-09-26 CN CN95195289A patent/CN1092643C/zh not_active Expired - Fee Related
- 1995-09-26 NZ NZ294447A patent/NZ294447A/xx unknown
- 1995-09-26 KR KR1019970702005A patent/KR970706259A/ko not_active Application Discontinuation
-
1997
- 1997-03-25 NO NO971423A patent/NO971423L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| BR9509101A (pt) | 1998-07-14 |
| US5681956A (en) | 1997-10-28 |
| CZ87397A3 (en) | 1997-08-13 |
| PL319637A1 (en) | 1997-08-18 |
| MX9702234A (es) | 1997-12-31 |
| KR970706259A (ko) | 1997-11-03 |
| CN1158608A (zh) | 1997-09-03 |
| NO971423D0 (no) | 1997-03-25 |
| WO1996010018A1 (fr) | 1996-04-04 |
| JPH10501819A (ja) | 1998-02-17 |
| CA2201140A1 (fr) | 1996-04-04 |
| AU705585B2 (en) | 1999-05-27 |
| CN1092643C (zh) | 2002-10-16 |
| SK40797A3 (en) | 1997-10-08 |
| NZ294447A (en) | 1998-10-28 |
| EP0783494A1 (fr) | 1997-07-16 |
| AU3725995A (en) | 1996-04-19 |
| JP2927967B2 (ja) | 1999-07-28 |
| HUT76928A (hu) | 1998-01-28 |
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| FC2A | Withdrawal, rejection or dismissal of laid open patent application |