NO905300D0 - Pyrimidin-nukleosider og mellomprodukter. - Google Patents
Pyrimidin-nukleosider og mellomprodukter.Info
- Publication number
- NO905300D0 NO905300D0 NO1990905300A NO905300A NO905300D0 NO 905300 D0 NO905300 D0 NO 905300D0 NO 1990905300 A NO1990905300 A NO 1990905300A NO 905300 A NO905300 A NO 905300A NO 905300 D0 NO905300 D0 NO 905300D0
- Authority
- NO
- Norway
- Prior art keywords
- compounds
- chem
- och3
- ether
- intermediates
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/34—One oxygen atom
- C07D239/36—One oxygen atom as doubly bound oxygen atom or as unsubstituted hydroxy radical
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- 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
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
- C07H19/10—Pyrimidine radicals with the saccharide radical esterified by phosphoric or polyphosphoric acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Pharmacology & Pharmacy (AREA)
- Virology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Communicable Diseases (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8802173A SE8802173D0 (sv) | 1988-06-10 | 1988-06-10 | Pyrimidine derivatives |
| PCT/SE1989/000322 WO1989012061A1 (en) | 1988-06-10 | 1989-06-07 | Pyrimidine nucleosides and intermediates |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| NO905300D0 true NO905300D0 (no) | 1990-12-07 |
| NO905300L NO905300L (no) | 1991-02-06 |
| NO175981B NO175981B (no) | 1994-10-03 |
| NO175981C NO175981C (no) | 1995-01-11 |
Family
ID=20372582
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO905300A NO175981C (no) | 1988-06-10 | 1990-12-07 | Analogifremgangsmåte ved fremstilling av pyrimidin-nukleosider og mellomprodukter som anvendes deri |
Country Status (20)
| Country | Link |
|---|---|
| US (2) | US5440040A (no) |
| EP (2) | EP0691333A2 (no) |
| JP (1) | JP2851094B2 (no) |
| KR (1) | KR900701815A (no) |
| AT (1) | ATE136308T1 (no) |
| AU (1) | AU637574B2 (no) |
| CA (1) | CA1339313C (no) |
| DE (1) | DE68926137T2 (no) |
| DK (1) | DK291890A (no) |
| ES (1) | ES2087090T3 (no) |
| FI (1) | FI94643C (no) |
| GR (1) | GR3020212T3 (no) |
| HU (1) | HU211736B (no) |
| IE (1) | IE62914B1 (no) |
| MY (1) | MY109743A (no) |
| NO (1) | NO175981C (no) |
| PH (1) | PH27219A (no) |
| PT (1) | PT90803B (no) |
| SE (1) | SE8802173D0 (no) |
| WO (1) | WO1989012061A1 (no) |
Families Citing this family (58)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5159067A (en) * | 1987-01-28 | 1992-10-27 | University Of Georgia Research Foundation Inc. | 5'-Diphosphohexose nucleoside pharmaceutical compositions |
| SE8802173D0 (sv) * | 1988-06-10 | 1988-06-10 | Astra Ab | Pyrimidine derivatives |
| US5688778A (en) * | 1989-05-15 | 1997-11-18 | Institute Of Organic Chemistry And Biochemistry Of The Academy Of Sciences Of The Czech Republic | Nucleoside analogs |
| CA2479846C (en) * | 1989-05-15 | 2007-07-24 | Institute Of Organic Chemistry And Biochemistry Of The Academy Of Scienc Es Of The Czech Republic | Phosphonomethoxymethylpurine/pyrimidine derivatives |
| US5118672A (en) * | 1989-07-10 | 1992-06-02 | University Of Georgia Research Foundation | 5'-diphosphohexose nucleoside pharmaceutical compositions |
| FR2656867A1 (fr) * | 1990-01-09 | 1991-07-12 | Centre Nat Rech Scient | Nouveau derives de la thymidine, leur preparation et les compositions qui les contiennent. |
| CA2039403A1 (en) * | 1990-04-04 | 1991-10-05 | Gerald Saischek | Process for the manufacture of 2-deoxy-d-threo-pentofuranosides, intermediates for their manufacture and their use |
| US5128458A (en) * | 1990-04-20 | 1992-07-07 | Southern Research Institute | 2',3'-dideoxy-4'-thioribonucleosides as antiviral agents |
| ZA914894B (en) * | 1990-07-02 | 1992-04-29 | Squibb & Sons Inc | Purinyl and pyrimidinyl tetrahydrofurans |
| EP0477454A1 (en) * | 1990-09-28 | 1992-04-01 | Merrell Dow Pharmaceuticals Inc. | Novel phosphonate derivatives of certain nucleosides |
| SE9003151D0 (sv) * | 1990-10-02 | 1990-10-02 | Medivir Ab | Nucleoside derivatives |
| US5672697A (en) * | 1991-02-08 | 1997-09-30 | Gilead Sciences, Inc. | Nucleoside 5'-methylene phosphonates |
| DE4110977A1 (de) * | 1991-04-05 | 1992-10-08 | Bayer Ag | Substituierte 2',3'-didesoxy-5-trifluormethyluridine, verfahren zu ihrer herstellung und ihre verwendung in arzneimitteln |
| EP0637965B1 (en) * | 1991-11-26 | 2002-10-16 | Isis Pharmaceuticals, Inc. | Enhanced triple-helix and double-helix formation with oligomers containing modified pyrimidines |
| US6235887B1 (en) | 1991-11-26 | 2001-05-22 | Isis Pharmaceuticals, Inc. | Enhanced triple-helix and double-helix formation directed by oligonucleotides containing modified pyrimidines |
| TW393513B (en) * | 1991-11-26 | 2000-06-11 | Isis Pharmaceuticals Inc | Enhanced triple-helix and double-helix formation with oligomers containing modified pyrimidines |
| AU4671193A (en) * | 1992-07-13 | 1994-01-31 | Kenneth E. Sherman | Composition and method of treating hepatitis b |
| US6200952B1 (en) * | 1993-06-02 | 2001-03-13 | Sciclone Pharmaceuticals, Inc. | Combination therapy method for treating chronic hepatitis B |
| US5502177A (en) * | 1993-09-17 | 1996-03-26 | Gilead Sciences, Inc. | Pyrimidine derivatives for labeled binding partners |
| US6432924B1 (en) | 1993-12-26 | 2002-08-13 | East Carolina University | Method of treating disorders characterized by overexpression of cytidine deaminase or deoxycytidine deaminase |
| JPH10501809A (ja) * | 1994-06-22 | 1998-02-17 | ネクスター ファーマスーティカルズ，インコーポレイテッド | 分子内求核置換による公知および新規２′−ヌクレオシドの新規製造方法 |
| DE4430401A1 (de) * | 1994-08-26 | 1996-02-29 | Chemprosa Holding Ag | D-Xylofuranose-Derivate, Verfahren zu deren Herstellung, deren Verwendung und neue Zwischenverbindungen für das Verfahren |
| EP0876149A4 (en) * | 1995-12-22 | 2001-09-26 | Univ East Carolina | PROCESS FOR THE TREATMENT OF CHARACTERIZED DISORDERS BY OVEREXPRESSION OF CYTIDINE-DESAMINASE OR DESOXYCYTIDINE-DESAMINASE |
| US5747526A (en) * | 1996-01-25 | 1998-05-05 | Hollinshead; Ariel C. | Anti-HIV /Aids Chemo(C)-, immuno(I)-, or ci-therapy using tur (or related compounds) and/or NVA (or EPV) |
| US5869493A (en) | 1996-02-16 | 1999-02-09 | Medivir Ab | Acyclic nucleoside derivatives |
| JP3613424B2 (ja) * | 1996-09-27 | 2005-01-26 | 財団法人国際超電導産業技術研究センター | 酸化物超電導体の製造方法 |
| US6737236B1 (en) | 1997-01-08 | 2004-05-18 | Proligo, Llc | Bioconjugation of macromolecules |
| US7427678B2 (en) * | 1998-01-08 | 2008-09-23 | Sigma-Aldrich Co. | Method for immobilizing oligonucleotides employing the cycloaddition bioconjugation method |
| US6090602A (en) * | 1998-02-18 | 2000-07-18 | Promelas Research Corporation | Levo-monosaccharide in a nucleoside analog for use as an anti-retroviral agent |
| EA008609B1 (ru) | 1998-02-25 | 2007-06-29 | Эмори Юниверсити | 2'-фторнуклеозиды |
| EP1057831B1 (en) | 1999-05-26 | 2004-09-22 | F. Hoffmann-La Roche Ag | Process for the preparation of vinyl pyrimidine derivatives |
| PT1411954E (pt) | 2000-10-18 | 2011-03-16 | Pharmasset Inc | Nucleosídeos modificados para o tratamento de infecções virais e proliferação celular anormal |
| WO2003000200A2 (en) | 2001-06-22 | 2003-01-03 | Pharmasset Ltd. | β-2'-OR 3'-HALONUCLEOSIDES |
| WO2003062452A2 (en) * | 2002-01-23 | 2003-07-31 | Proligo, Llc | Methods for the integrated synthesis and purification of oligonucleotides |
| WO2003072757A2 (en) | 2002-02-28 | 2003-09-04 | Biota, Inc. | Nucleotide mimics and their prodrugs |
| WO2004058794A1 (en) * | 2002-12-31 | 2004-07-15 | Proligo Llc | Methods and compositions for the tandem synthesis of two or more oligonuleotides on the same solid support |
| US7262214B2 (en) | 2003-02-26 | 2007-08-28 | Merial Limited | 1-N-arylpyrazole derivatives in prevention of arthropod-borne and mosquito-borne diseases |
| US7531186B2 (en) * | 2003-12-17 | 2009-05-12 | Merial Limited | Topical formulations comprising 1-N-arylpyrazole derivatives and amitraz |
| DE602005015466D1 (de) | 2004-08-23 | 2009-08-27 | Hoffmann La Roche | Antivirale 4'-azidonucleoside |
| US20080261823A1 (en) * | 2004-12-10 | 2008-10-23 | Yitzhak Tor | Fluorescent Nucleoside Analogs That Mimic Naturally Occurring Nucleosides |
| US8895531B2 (en) | 2006-03-23 | 2014-11-25 | Rfs Pharma Llc | 2′-fluoronucleoside phosphonates as antiviral agents |
| WO2007122634A2 (en) * | 2006-04-24 | 2007-11-01 | Jubilant Biosys Limited | Pyrimidinediones as tyrosine kinase inhibitors |
| DK2035390T3 (en) | 2006-07-05 | 2016-01-04 | Merial Inc | 1-aryl-5-alkylpyrazolderivatforbindelser, methods of making and methods of use thereof |
| EP2361922B1 (en) | 2006-10-10 | 2012-08-22 | Janssen Products, L.P. | Intermediate to HCV-Nucleoside Inhibitors |
| US7947447B2 (en) | 2007-01-16 | 2011-05-24 | Somalogic, Inc. | Method for generating aptamers with improved off-rates |
| US8404830B2 (en) * | 2007-07-17 | 2013-03-26 | Somalogic, Inc. | Method for generating aptamers with improved off-rates |
| GB0815968D0 (en) * | 2008-09-03 | 2008-10-08 | Angeletti P Ist Richerche Bio | Antiviral agents |
| MY155497A (en) | 2008-11-19 | 2015-10-30 | Merial Inc | Compositions comprising an aryl pyrazole and/or a formamidine, methods and use thereof |
| KR101246911B1 (ko) * | 2009-11-02 | 2013-03-25 | 한국화학연구원 | 신규한 2,4-피리미딘 유도체 및 이의 용도 |
| CA2784141C (en) | 2009-12-17 | 2017-10-24 | Merial Limited | Compositions comprising macrocyclic lactone compounds and spirodioxepinoindoles |
| UA108641C2 (uk) | 2010-04-02 | 2015-05-25 | Паразитицидна композиція, яка містить чотири активних агенти, та спосіб її застосування | |
| NO2558478T3 (no) | 2010-04-12 | 2018-08-04 | ||
| CA2855954C (en) | 2011-11-17 | 2020-09-01 | Merial Limited | Compositions comprising an aryl pyrazole and a substituted imidazole, methods and uses thereof. |
| JO3626B1 (ar) | 2012-02-23 | 2020-08-27 | Merial Inc | تركيبات موضعية تحتوي على فيبرونيل و بيرميثرين و طرق استخدامها |
| TWI579274B (zh) | 2012-04-20 | 2017-04-21 | 龍馬躍公司 | 製備１－芳基－５－烷基吡唑化合物的改良方法 |
| KR102290214B1 (ko) | 2013-11-21 | 2021-08-18 | 소마로직, 인크. | 시티딘-5-카르복스아미드 변형된 뉴클레오티드 조성물 및 그와 관련된 방법들 |
| AU2015339096B2 (en) | 2014-10-31 | 2018-08-02 | Boehringer Ingelheim Animal Health USA Inc. | Parasiticidal composition comprising fipronil |
| CN104892706A (zh) * | 2015-04-27 | 2015-09-09 | 河南师范大学 | 具有抗寄生虫活性的异噁唑-核苷杂化体及其制备方法和应用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2721466A1 (de) * | 1977-05-12 | 1978-11-16 | Robugen Gmbh | Verfahren zur herstellung von 2'-desoxyribofuranosylnucleosiden |
| JPS54112880A (en) * | 1978-02-21 | 1979-09-04 | Matsura Teruo | Novel uracil derivative and its manufacture |
| US4211773A (en) * | 1978-10-02 | 1980-07-08 | Sloan Kettering Institute For Cancer Research | 5-Substituted 1-(2'-Deoxy-2'-substituted-β-D-arabinofuranosyl)pyrimidine nucleosides |
| HU198393B (en) * | 1984-03-06 | 1989-10-30 | Sloan Kettering Inst Cancer | Process for production of medical composition suitable for treatment of hepatitis containing as active substance derivatives of piramidin-nucleoside |
| US4666892A (en) * | 1984-03-06 | 1987-05-19 | Sloan-Kettering Memorial Cancer Center | Method and composition for hepatitis treatment with pyrimidine nucleoside compounds |
| SE8605503D0 (sv) * | 1986-12-19 | 1986-12-19 | Astra Laekemedel Ab | Novel medicinal use |
| SE8802173D0 (sv) * | 1988-06-10 | 1988-06-10 | Astra Ab | Pyrimidine derivatives |
-
1988
- 1988-06-10 SE SE8802173A patent/SE8802173D0/xx unknown
-
1989
- 1989-06-06 CA CA000601897A patent/CA1339313C/en not_active Expired - Fee Related
- 1989-06-07 HU HU894340A patent/HU211736B/hu not_active IP Right Cessation
- 1989-06-07 AU AU37504/89A patent/AU637574B2/en not_active Ceased
- 1989-06-07 KR KR1019900700287A patent/KR900701815A/ko not_active Application Discontinuation
- 1989-06-07 WO PCT/SE1989/000322 patent/WO1989012061A1/en active IP Right Grant
- 1989-06-07 JP JP1506227A patent/JP2851094B2/ja not_active Expired - Lifetime
- 1989-06-07 EP EP95113626A patent/EP0691333A2/en not_active Withdrawn
- 1989-06-07 AT AT89850184T patent/ATE136308T1/de not_active IP Right Cessation
- 1989-06-07 EP EP89850184A patent/EP0357571B1/en not_active Expired - Lifetime
- 1989-06-07 US US07/613,900 patent/US5440040A/en not_active Expired - Fee Related
- 1989-06-07 DE DE68926137T patent/DE68926137T2/de not_active Expired - Fee Related
- 1989-06-07 ES ES89850184T patent/ES2087090T3/es not_active Expired - Lifetime
- 1989-06-09 MY MYPI89000776A patent/MY109743A/en unknown
- 1989-06-09 PH PH38770A patent/PH27219A/en unknown
- 1989-06-09 PT PT90803A patent/PT90803B/pt not_active IP Right Cessation
- 1989-06-12 IE IE181689A patent/IE62914B1/en not_active IP Right Cessation
-
1990
- 1990-12-07 DK DK291890A patent/DK291890A/da not_active Application Discontinuation
- 1990-12-07 NO NO905300A patent/NO175981C/no not_active IP Right Cessation
- 1990-12-07 FI FI906053A patent/FI94643C/fi not_active IP Right Cessation
-
1995
- 1995-02-28 US US08/395,877 patent/US5576429A/en not_active Expired - Lifetime
-
1996
- 1996-06-12 GR GR960401591T patent/GR3020212T3/el unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |
Free format text: LAPSED IN DECEMBER 2000 |