ATE161824T1 - Anticonvulsives aminosäurederivat - Google Patents
Anticonvulsives aminosäurederivatInfo
- Publication number
- ATE161824T1 ATE161824T1 AT92913324T AT92913324T ATE161824T1 AT E161824 T1 ATE161824 T1 AT E161824T1 AT 92913324 T AT92913324 T AT 92913324T AT 92913324 T AT92913324 T AT 92913324T AT E161824 T1 ATE161824 T1 AT E161824T1
- Authority
- AT
- Austria
- Prior art keywords
- anticonvulsive
- amino acid
- acid derivative
- compounds
- cns
- Prior art date
Links
- 150000003862 amino acid derivatives Chemical class 0.000 title 1
- 230000002082 anti-convulsion Effects 0.000 title 1
- 210000003169 central nervous system Anatomy 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 208000015114 central nervous system disease Diseases 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 206010015037 epilepsy Diseases 0.000 abstract 1
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/33—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/337—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
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- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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- C07C229/30—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and unsaturated
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- C07C233/47—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
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- C07C259/04—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids
- C07C259/06—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups without replacement of the other oxygen atom of the carboxyl group, e.g. hydroxamic acids having carbon atoms of hydroxamic groups bound to hydrogen atoms or to acyclic carbon atoms
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- C07C309/17—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing carboxyl groups bound to the carbon skeleton
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- C07C317/50—Sulfones; Sulfoxides having sulfone or sulfoxide groups and carboxyl groups bound to the same carbon skeleton the carbon skeleton being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
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- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/60—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
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- Chemical & Material Sciences (AREA)
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Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/710,610 US5378729A (en) | 1985-02-15 | 1991-06-04 | Amino acid derivative anticonvulsant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE161824T1 true ATE161824T1 (de) | 1998-01-15 |
Family
ID=24854774
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT92913324T ATE161824T1 (de) | 1991-06-04 | 1992-06-04 | Anticonvulsives aminosäurederivat |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US5378729A (de) |
| EP (1) | EP0592490B1 (de) |
| JP (2) | JP3330374B2 (de) |
| AT (1) | ATE161824T1 (de) |
| AU (1) | AU657985B2 (de) |
| CA (1) | CA2110693C (de) |
| DE (1) | DE69223965T2 (de) |
| WO (1) | WO1992021648A1 (de) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5654301A (en) * | 1985-02-15 | 1997-08-05 | Research Corporation Technologies, Inc. | Amino acid derivative anticonvulsant |
| FI94339C (fi) | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
| WO1997033861A1 (en) * | 1996-03-15 | 1997-09-18 | Research Corporation Technologies, Inc. | Anticonvulsant enantiomeric amino acid derivatives |
| US5773475A (en) | 1997-03-17 | 1998-06-30 | Research Corporation Technologies, Inc. | Anticonvulsant enantiomeric amino acid derivatives |
| WO1998013336A1 (en) * | 1996-09-27 | 1998-04-02 | Research Corporation Technologies, Inc. | Propionamide derivatives and their use as anticonvulsants |
| DE69738275T2 (de) | 1996-12-18 | 2008-08-28 | Teva Pharmaceutical Industries Ltd. | Aminoindanderivate |
| US6048899A (en) * | 1997-03-17 | 2000-04-11 | Research Corporation Tech., Inc. | Anticonvulsant enantiomeric amino acid derivatives |
| ES2184300T3 (es) * | 1997-07-15 | 2003-04-01 | Res Corp Technologies Inc | Derivados de aminoacidos utiles para tratar el accidente vascular encefalico. |
| PL343770A1 (en) * | 1998-04-16 | 2001-09-10 | Texas Biotechnology Corp | N,n-disubstituted amides that inhibit the binding of integrins to their receptors |
| US6737547B1 (en) | 1998-12-31 | 2004-05-18 | Teva Pharmaceutical Industries, Ltd. | Compositions containing and methods of using N-acyl-1H-aminoindenes |
| US6645968B2 (en) | 1999-08-03 | 2003-11-11 | Abbott Laboratories | Potassium channel openers |
| ES2190305B1 (es) * | 2000-05-24 | 2004-07-01 | Medichem S.A. | Compuestos intermedios para la preparacion de mirtazapina y sus procedimientos de obtencion. |
| AU8676301A (en) * | 2000-08-25 | 2002-03-04 | Res Corp Technologies Inc | New uses for amino acid anticonvulsants |
| DK1243262T3 (da) | 2001-03-20 | 2006-10-02 | Sanol Arznei Schwarz Gmbh | Hidtil ukendt anvendelse af en peptidklasse af forbindelser til behandling af ikke-neuropatiske, inflammatoriske smerter |
| ES2185606T3 (es) | 2001-03-21 | 2003-05-01 | Sanol Arznei Schwarz Gmbh | Nuevo uso de una clase de compuestos peptidicos para tratamiento de la alodinia u otros tipos diferentes de dolor cronico o fantasma. |
| ATE392410T1 (de) * | 2001-09-14 | 2008-05-15 | Medichem Sa | Zwischenprodukte für die herstellung von mirtazapin und verfahren zu deren herstellung |
| US20040010038A1 (en) * | 2002-02-27 | 2004-01-15 | Eran Blaugrund | Propargylamino indan derivatives and propargylamino tetralin derivatives as brain-selective MAO inhibitors |
| JP4664924B2 (ja) * | 2003-12-02 | 2011-04-06 | ウーツェーベー ファルマ ゲーエムベーハー | 中枢神経因性疼痛の治療のためのペプチド化合物の新規使用 |
| US20060009384A1 (en) * | 2003-12-05 | 2006-01-12 | David Rudd | Novel use of peptide compounds for treating status epilepticus or related conditions |
| US20100256179A1 (en) * | 2004-03-26 | 2010-10-07 | Ucb Pharma Gmbh | Combination therapy for pain in painful diabetic neuropathy |
| US20070042969A1 (en) * | 2004-03-26 | 2007-02-22 | Srz Properties, Inc. | Combination therapy for pain in painful diabetic neuropathy |
| EP1579858A1 (de) * | 2004-03-26 | 2005-09-28 | Schwarz Pharma Ag | Neue Verwendung von Peptidverbindungen zur Behandlung von diabetishen Neuropathie |
| KR20070007931A (ko) * | 2004-04-16 | 2007-01-16 | 쉬바르츠파르마에이지 | 만성 두통의 예방 및 치료를 위한 펩티드 화합물의 용도 |
| EP1604654A1 (de) | 2004-05-18 | 2005-12-14 | Schwarz Pharma Ag | Neue Verwendung von Peptidverbindungen zur Behandlung von Dyskynesien |
| EP1604655A1 (de) | 2004-06-09 | 2005-12-14 | Schwarz Pharma Ag | Neue Verwendung von Peptidverbindungen zur Behandlung von Trigeminusneuralgie |
| EP1604656A1 (de) | 2004-06-09 | 2005-12-14 | Schwarz Pharma Ag | Neue Verwendung von Peptidverbindungen zur Behandlung von amyotropher Lateralsklerose (ALS) |
| US7427601B2 (en) * | 2004-06-24 | 2008-09-23 | Schwarz Pharma Ag | Method for treating tremor |
| PL1781276T3 (pl) * | 2004-08-27 | 2010-11-30 | Ucb Pharma Gmbh | Zastosowanie związków peptydowych do leczenia bólu związanego z rakiem kości, bólu indukowanego przez chemioterapię oraz nukleozydy |
| KR20070096058A (ko) | 2005-01-28 | 2007-10-01 | 쉬바르츠파르마에이지 | 정신분열증의 부가 요법용 spm 927 |
| EP1688137A1 (de) * | 2005-01-28 | 2006-08-09 | Schwarz Pharma Ag | SPM 927 zur Co-Therapie der Schizophrenie |
| US20060252749A1 (en) * | 2005-01-28 | 2006-11-09 | Srz Properties, Inc. | Lacosamide for add-on therapy of psychosis |
| AU2006258842B2 (en) * | 2005-06-13 | 2011-09-15 | Merck Sharp & Dohme Limited | Therapeutic agents |
| EP1754476A1 (de) | 2005-08-18 | 2007-02-21 | Schwarz Pharma Ag | Lacosamid (SPM 927) zur Behandlung von Myalgien, z.B. Fibromyalgie |
| US20070048372A1 (en) * | 2005-08-18 | 2007-03-01 | Srz Properties, Inc. | Method for treating non-inflammatory osteoarthritic pain |
| US20070043120A1 (en) * | 2005-08-18 | 2007-02-22 | Bettina Beyreuther | Therapeutic combination for painful medical conditions |
| AU2006326642B2 (en) * | 2005-12-09 | 2012-05-03 | Technion Research And Development Foundation Ltd. | Use of low-dose ladostigil for neuroprotection |
| US7902401B2 (en) * | 2006-12-14 | 2011-03-08 | Nps Pharmaceuticals, Inc. | Fluorinated compounds |
| JP5307550B2 (ja) * | 2005-12-20 | 2013-10-02 | エヌピーエス ファーマシューティカルズ インコーポレイテッド | フッ素化化合物 |
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| EP1925314A1 (de) * | 2006-11-22 | 2008-05-28 | Schwarz Pharma Ag | Pharmazeutische Zusammensetzung mit synergistischer antikonvulsiver Wirkung |
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| CN101466390B (zh) * | 2006-06-15 | 2014-03-12 | 优时比制药有限公司 | 用于治疗难治性癫痫持续状态的肽类化合物 |
| WO2007144195A2 (en) | 2006-06-15 | 2007-12-21 | Schwarz Pharma Ag | Pharmaceutical composition with synergistic anticonvulsant effect |
| CA2672494A1 (en) | 2006-12-14 | 2008-06-19 | Nps Pharmaceuticals, Inc. | Use of d-serine derivatives for the treatment of anxiety disorders |
| EP2214657A1 (de) | 2007-10-23 | 2010-08-11 | UCB Pharma GmbH | Verbindungen zur behandlung von demyelisationserkrankungen |
| WO2009145816A2 (en) * | 2008-04-01 | 2009-12-03 | The University Of North Carolina At Chapel Hill | Novel n-benzylamide substituted derivatives of 2-(acylamido)acetic acid and 2-(acylamido)propionic acids: potent neurological agents |
| CA2774569A1 (en) * | 2009-09-23 | 2011-03-31 | The University Of North Carolina At Chapel Hill | Novel n-benzylamide substituted derivatives of 2-(acylamido)acetic acid and 2-(acylamido)propionic acids: potent neurological agents |
| CN103201263A (zh) * | 2010-09-08 | 2013-07-10 | 匹兹堡高等教育联邦体系大学 | p53-Mdm2拮抗剂 |
| EP2621893A1 (de) | 2010-10-01 | 2013-08-07 | UCB Pharma GmbH | Verfahren zur herstellung von aminosäurederivaten |
| GB201020026D0 (en) | 2010-11-25 | 2011-01-12 | Cambrex Karlskoga Ab | New process |
| GB201219627D0 (en) | 2012-11-01 | 2012-12-12 | Cambrex Karlskoga Ab | New process |
| CN109069480A (zh) | 2015-12-30 | 2018-12-21 | 阿达玛斯医药公司 | 用于治疗与癫痫相关的病症的方法和组合物 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2676188A (en) * | 1950-12-16 | 1954-04-20 | American Home Prod | Acylated glycinamides |
| US2721197A (en) * | 1953-01-05 | 1955-10-18 | Bristol Lab Inc | Bicyclic lactams |
| DE1185194B (de) * | 1959-06-11 | 1965-01-14 | Nippon Shinyaku Co Ltd | Verfahren zur Herstellung von Abkoemmlingen des Salicylsaeureamides |
| GB1051220A (de) * | 1963-03-21 | |||
| US3340147A (en) * | 1965-06-28 | 1967-09-05 | Mead Johnson & Co | Amides of n-acylated cysteines |
| IE33790B1 (en) * | 1968-06-04 | 1974-10-30 | Beecham Group Ltd | Derivatives of n-acylaminoacid amides |
| US3887543A (en) | 1970-12-07 | 1975-06-03 | Yoshitomi Pharmaceutical | Thieno(2,3-E)(1,4)diazepine derivatives |
| US3707559A (en) * | 1971-05-14 | 1972-12-26 | Searle & Co | N-acyl phenylalanine amides |
| US4002764A (en) | 1972-11-28 | 1977-01-11 | Ciba-Geigy Corporation | Diazepine derivatives in the treatment of tension, agitation and epilepsy |
| US4209516A (en) | 1974-01-14 | 1980-06-24 | Ciba-Geigy Corporation | Triazole derivatives |
| US4018826A (en) * | 1974-11-04 | 1977-04-19 | Dynapol Corporation | Process for preparing polyvinylamine and salts thereof |
| LU75836A1 (de) | 1976-09-20 | 1978-05-12 | ||
| DE2807286A1 (de) * | 1978-02-21 | 1979-08-23 | Bayer Ag | Stereoselektive spaltung von phenylglycinderivaten und 4-hydroxyphenylglycinderivaten mit enzymharzen |
| JPS557242A (en) * | 1978-06-30 | 1980-01-19 | Tanabe Seiyaku Co Ltd | Phenethylamine derivative |
| DE2937698A1 (de) * | 1979-09-18 | 1981-04-02 | A. Nattermann & Cie GmbH, 5000 Köln | N-propionylsarcosinanilide, deren herstellungsverfahren und arzneimittel auf deren basis |
| FR2480747A1 (fr) * | 1980-04-17 | 1981-10-23 | Roques Bernard | Derives d'acides amines et leur application therapeutique |
| US4372974A (en) | 1980-06-25 | 1983-02-08 | New York University | Anticonvulsive compositions and method of treating convulsive disorders |
| FR2489319A1 (fr) * | 1980-08-27 | 1982-03-05 | Clin Midy | Derives de l'acide amino-4 butyrique et les medicaments, actifs notamment sur le systeme nerveux central, en contenant |
| BE885303A (fr) * | 1980-09-19 | 1981-03-19 | Continental Pharma | Glycinamides |
| FR2518088B1 (fr) * | 1981-12-16 | 1987-11-27 | Roques Bernard | Nouveaux derives d'aminoacides, et leur application therapeutique |
| US4595700A (en) * | 1984-12-21 | 1986-06-17 | G. D. Searle & Co. | Thiol based collagenase inhibitors |
| EP0194464B1 (de) * | 1985-02-15 | 1991-04-03 | Research Corporation Technologies, Inc. (a Delaware corp.) | Aminosäure-Derivate und ihre Anwendung zur Herstellung eines Antikrampfmittels |
| NZ222045A (en) * | 1986-08-21 | 1989-10-27 | Res Corp Technologies Inc | From diamides up to tetrapeptides for use as anticanvulsants |
| US4873241A (en) * | 1988-10-31 | 1989-10-10 | Fisons Corporation | 2-amino-N-(2-phenylindan-2-yl)acetamides useful as anti-epileptics |
| JPH03506045A (ja) | 1989-05-19 | 1991-12-26 | リサーチ・コーポレイション・テクノロジーズ・インコーポレイテッド | アミノ酸誘導体抗けいれん薬 |
| DE3920618A1 (de) * | 1989-06-02 | 1991-02-21 | Grafenwald Kunststoff | Flaschen und umverpackung enthaltende anordnung |
-
1991
- 1991-06-04 US US07/710,610 patent/US5378729A/en not_active Expired - Lifetime
-
1992
- 1992-06-04 EP EP92913324A patent/EP0592490B1/de not_active Expired - Lifetime
- 1992-06-04 DE DE69223965T patent/DE69223965T2/de not_active Expired - Lifetime
- 1992-06-04 WO PCT/US1992/004687 patent/WO1992021648A1/en not_active Ceased
- 1992-06-04 AT AT92913324T patent/ATE161824T1/de not_active IP Right Cessation
- 1992-06-04 AU AU21621/92A patent/AU657985B2/en not_active Expired
- 1992-06-04 JP JP50065093A patent/JP3330374B2/ja not_active Expired - Lifetime
- 1992-06-04 CA CA002110693A patent/CA2110693C/en not_active Expired - Lifetime
-
2001
- 2001-12-05 JP JP2001371994A patent/JP2002241355A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002241355A (ja) | 2002-08-28 |
| EP0592490A1 (de) | 1994-04-20 |
| AU2162192A (en) | 1993-01-08 |
| JPH06510985A (ja) | 1994-12-08 |
| DE69223965T2 (de) | 1998-04-30 |
| EP0592490B1 (de) | 1998-01-07 |
| JP3330374B2 (ja) | 2002-09-30 |
| CA2110693A1 (en) | 1992-12-10 |
| CA2110693C (en) | 2003-05-20 |
| DE69223965D1 (de) | 1998-02-12 |
| AU657985B2 (en) | 1995-03-30 |
| WO1992021648A1 (en) | 1992-12-10 |
| EP0592490A4 (en) | 1994-08-17 |
| US5378729A (en) | 1995-01-03 |
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| RER | Ceased as to paragraph 5 lit. 3 law introducing patent treaties |