IS4121A - Hliðstæð aðferð til framleiðslu á 2,6-Díamínópúrín afleiðum - Google Patents
Hliðstæð aðferð til framleiðslu á 2,6-Díamínópúrín afleiðumInfo
- Publication number
- IS4121A IS4121A IS4121A IS4121A IS4121A IS 4121 A IS4121 A IS 4121A IS 4121 A IS4121 A IS 4121A IS 4121 A IS4121 A IS 4121A IS 4121 A IS4121 A IS 4121A
- Authority
- IS
- Iceland
- Prior art keywords
- preparation
- analogous method
- diaminopurine derivatives
- diaminopurine
- derivatives
- Prior art date
Links
Classifications
-
- 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
- C07H19/16—Purine radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- 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
- C07H19/16—Purine radicals
- C07H19/167—Purine radicals with ribosyl as the saccharide radical
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Pulmonology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Oncology (AREA)
- Cardiology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Saccharide Compounds (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Hydrogenated Pyridines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB939301000A GB9301000D0 (en) | 1993-01-20 | 1993-01-20 | Chemical compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IS4121A true IS4121A (is) | 1994-07-21 |
Family
ID=10728948
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IS4121A IS4121A (is) | 1993-01-20 | 1994-01-14 | Hliðstæð aðferð til framleiðslu á 2,6-Díamínópúrín afleiðum |
Country Status (29)
| Country | Link |
|---|---|
| US (2) | US5925624A (OSRAM) |
| EP (1) | EP0680488B1 (OSRAM) |
| JP (1) | JP3768232B2 (OSRAM) |
| KR (1) | KR960700261A (OSRAM) |
| CN (1) | CN1043997C (OSRAM) |
| AP (1) | AP457A (OSRAM) |
| AT (1) | ATE164849T1 (OSRAM) |
| AU (1) | AU679714B2 (OSRAM) |
| CA (1) | CA2153688A1 (OSRAM) |
| CZ (1) | CZ187995A3 (OSRAM) |
| DE (1) | DE69409503T2 (OSRAM) |
| DK (1) | DK0680488T3 (OSRAM) |
| EC (1) | ECSP941104A (OSRAM) |
| ES (1) | ES2117249T3 (OSRAM) |
| FI (1) | FI953489L (OSRAM) |
| GB (1) | GB9301000D0 (OSRAM) |
| HU (1) | HU211914A9 (OSRAM) |
| IL (1) | IL108372A (OSRAM) |
| IS (1) | IS4121A (OSRAM) |
| NO (1) | NO305603B1 (OSRAM) |
| NZ (1) | NZ259880A (OSRAM) |
| PE (1) | PE54194A1 (OSRAM) |
| PL (1) | PL309975A1 (OSRAM) |
| RU (1) | RU2129561C1 (OSRAM) |
| SI (1) | SI9400021A (OSRAM) |
| SK (1) | SK281229B6 (OSRAM) |
| TW (1) | TW267168B (OSRAM) |
| WO (1) | WO1994017090A1 (OSRAM) |
| ZA (1) | ZA94335B (OSRAM) |
Families Citing this family (101)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI0828740T1 (en) * | 1995-05-30 | 2001-12-31 | Aventis Pharma Sa | 2-azabicyclo(2.2.1)heptane derivatives, preparation and application thereof |
| TW528755B (en) | 1996-12-24 | 2003-04-21 | Glaxo Group Ltd | 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives |
| JP3861413B2 (ja) * | 1997-11-05 | 2006-12-20 | ソニー株式会社 | 情報配信システム、情報処理端末装置、携帯端末装置 |
| YU44900A (sh) | 1998-01-31 | 2003-01-31 | Glaxo Group Limited | Derivati 2-(purin-9-il)tetrahidrofuran-3,4-diola |
| US6413974B1 (en) | 1998-02-26 | 2002-07-02 | Aventis Pharmaceuticals Inc. | 6,9,-disubstituted 2-[trans-(4-aminocyclohexyl) amino] purines |
| WO1999043676A2 (en) * | 1998-02-26 | 1999-09-02 | Aventis Pharmaceuticals Inc. | 6,9-disubstituted 2-[trans-(4- aminocyclohexyl) amino]purines |
| US6479487B1 (en) | 1998-02-26 | 2002-11-12 | Aventis Pharmaceuticals Inc. | 6, 9-disubstituted 2-[trans-(4-aminocyclohexyl)amino] purines |
| US6878716B1 (en) | 1998-06-02 | 2005-04-12 | Osi Pharmaceuticals, Inc. | Compounds specific to adenosine A1 receptor and uses thereof |
| PL204628B1 (pl) | 1998-06-02 | 2010-01-29 | Osi Pharmaceuticals | Pochodna pirolo[2,3d]pirymidyny, jej zastosowanie i sposoby wytwarzania tej pochodnej i preparaty farmaceutyczne |
| US6686366B1 (en) | 1998-06-02 | 2004-02-03 | Osi Pharmaceuticals, Inc. | Compounds specific to adenosine A3 receptor and uses thereof |
| GB9813540D0 (en) * | 1998-06-23 | 1998-08-19 | Glaxo Group Ltd | Chemical compounds |
| GB9813554D0 (en) * | 1998-06-23 | 1998-08-19 | Glaxo Group Ltd | Chemical compounds |
| GB9813535D0 (en) * | 1998-06-23 | 1998-08-19 | Glaxo Group Ltd | Chemical compounds |
| HRP20000894A2 (en) | 1998-06-23 | 2001-12-31 | Glaxo Group Ltd | 2-(purin-9-yl)-tetrahydrofuran-3,4-diol derivatives |
| GB9813565D0 (en) * | 1998-06-23 | 1998-08-19 | Glaxo Group Ltd | Chemical compounds |
| RU2258071C2 (ru) * | 1999-05-24 | 2005-08-10 | Юниверсити Оф Вирджиния Пэйтент Фаундейшн | Производные 2-алкиниладенозина для борьбы с воспалительной реакцией |
| US6664252B2 (en) | 1999-12-02 | 2003-12-16 | Osi Pharmaceuticals, Inc. | 4-aminopyrrolo[2,3-d]pyrimidine compounds specific to adenosine A2a receptor and uses thereof |
| US7160890B2 (en) | 1999-12-02 | 2007-01-09 | Osi Pharmaceuticals, Inc. | Compounds specific to adenosine A3 receptor and uses thereof |
| US6680322B2 (en) | 1999-12-02 | 2004-01-20 | Osi Pharmaceuticals, Inc. | Compounds specific to adenosine A1 receptors and uses thereof |
| CA2394654A1 (en) | 1999-12-17 | 2001-06-21 | Manfred Weigele | Proton pump inhibitors |
| CN1440408B (zh) * | 2000-04-25 | 2012-07-18 | 艾科斯有限公司 | 人磷脂酰肌醇3-激酶δ的抑制剂 |
| US6667300B2 (en) | 2000-04-25 | 2003-12-23 | Icos Corporation | Inhibitors of human phosphatidylinositol 3-kinase delta |
| EP1939203B1 (en) * | 2000-04-25 | 2014-11-19 | ICOS Corporation | Inhibitors of human phosphatidyl-inositol 3-kinase delta isoform |
| US6861524B2 (en) | 2000-10-31 | 2005-03-01 | Aventis Pharmaceuticals Inc. | Acyl and sulfonyl derivatives of 6,9-disubstituted 2-(trans-1,4-diaminocyclohexyl)-purines and their use as antiproliferative agents |
| US6673802B2 (en) | 2000-12-01 | 2004-01-06 | Osi Pharmaceuticals, Inc. | Compounds specific to adenosine A3 receptor and uses thereof |
| US6680324B2 (en) | 2000-12-01 | 2004-01-20 | Osi Pharmaceuticals, Inc. | Compounds specific to adenosine A1 receptors and uses thereof |
| WO2002088079A2 (en) * | 2001-05-01 | 2002-11-07 | Bristol-Myers Squibb Company | Dual inhibitors of pde 7 and pde 4 |
| PE20030008A1 (es) * | 2001-06-19 | 2003-01-22 | Bristol Myers Squibb Co | Inhibidores duales de pde 7 y pde 4 |
| ES2301659T3 (es) * | 2001-07-06 | 2008-07-01 | Topigen Pharmaceuticals Inc. | Metodos para aumentar la eficacia in vivo de oligonucleotidos e inhibir la inflamacion en mamiferos. |
| US6825349B2 (en) * | 2001-11-09 | 2004-11-30 | Cv Therapeutics Inc. | A2B adenosine receptor antagonists |
| US7321033B2 (en) | 2001-11-27 | 2008-01-22 | Anadys Pharmaceuticals, Inc. | 3-B-D-ribofuranosylthiazolo [4,5-d] pyrimidine nucleosides and uses thereof |
| US6924271B2 (en) | 2001-11-27 | 2005-08-02 | Anadys Pharmaceuticals, Inc. | 3-β-D-ribofuranosylthiazolo[4-5-d]pyridimine nucleosides and uses thereof |
| ATE446298T1 (de) | 2001-11-30 | 2009-11-15 | Osi Pharm Inc | Verbindungen, die für adenosin a1 und a3 rezeptoren spezifisch sind, und deren anwendungen |
| US20030229067A1 (en) | 2001-12-20 | 2003-12-11 | Arlindo Castelhano | Pyrrolopyrimidine A2b selective antagonist compounds, their synthesis and use |
| US6916804B2 (en) | 2001-12-20 | 2005-07-12 | Osi Pharmaceuticals, Inc. | Pyrimidine A2b selective antagonist compounds, their synthesis and use |
| ES2237234B1 (es) * | 2002-08-02 | 2006-11-01 | Universidad De Oviedo | Preparacion de (+) y (-)-trans-ciclopentano-1,2-diamina. |
| AU2003263846B2 (en) * | 2002-08-15 | 2009-12-17 | Gilead Palo Alto, Inc. | Partial and full agonists of A1 adenosine receptors |
| TW200519106A (en) | 2003-05-02 | 2005-06-16 | Novartis Ag | Organic compounds |
| GB0328319D0 (en) * | 2003-12-05 | 2004-01-07 | Cambridge Biotechnology Ltd | Improved synthesis of 2-substituted adenosines |
| GB0401334D0 (en) | 2004-01-21 | 2004-02-25 | Novartis Ag | Organic compounds |
| DK2612862T3 (en) | 2004-05-13 | 2016-12-05 | Icos Corp | Quinazolinones as inhibitors of human phosphatidylinositol 3-kinase delta |
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| PE20060272A1 (es) | 2004-05-24 | 2006-05-22 | Glaxo Group Ltd | (2r,3r,4s,5r,2'r,3'r,4's,5's)-2,2'-{trans-1,4-ciclohexanodiilbis-[imino(2-{[2-(1-metil-1h-imidazol-4-il)etil]amino}-9h-purin-6,9-diil)]}bis[5-(2-etil-2h-tetrazol-5-il)tetrahidro-3,4-furanodiol] como agonista a2a |
| DK1758596T3 (da) * | 2004-05-26 | 2010-07-26 | Inotek Pharmaceuticals Corp | Purinderivater som adenosin-A1-receptoragonister og fremgangsmåder til anvendelse deraf |
| FR2874014B1 (fr) * | 2004-08-03 | 2010-05-14 | Univ Paris Descartes | Analogues d'aminoglycosides, leur utilisation et leur synthese |
| ES2450929T3 (es) | 2004-10-29 | 2014-03-25 | Topigen Pharmaceuticals Inc. | Oligonucleótidos antisentido para tratar la alergia y la proliferación de las células neoplásicas |
| GB0424284D0 (en) | 2004-11-02 | 2004-12-01 | Novartis Ag | Organic compounds |
| GB0426164D0 (en) | 2004-11-29 | 2004-12-29 | Novartis Ag | Organic compounds |
| DK2561872T3 (en) | 2004-12-17 | 2014-12-08 | Anadys Pharmaceuticals Inc | 3,5-DISUBSTITUTED AND 3,5,7-TRISUBSTITUTED 3H-OXAZOLO- [4,5-d] PYRIMIDIN-2-ON COMPOUNDS AND PRODRUGS THEREOF |
| GB0500785D0 (en) * | 2005-01-14 | 2005-02-23 | Novartis Ag | Organic compounds |
| GB0510390D0 (en) | 2005-05-20 | 2005-06-29 | Novartis Ag | Organic compounds |
| GB0514809D0 (en) | 2005-07-19 | 2005-08-24 | Glaxo Group Ltd | Compounds |
| AR058104A1 (es) | 2005-10-21 | 2008-01-23 | Novartis Ag | Compuestos organicos |
| DE602006015700D1 (de) | 2005-11-21 | 2010-09-02 | Anadys Pharmaceuticals Inc | Neues verfahren zur herstellung von 5-amino-3h-thiazoloä4,5-düpyrimidin-2-on |
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| KR101461604B1 (ko) | 2006-06-22 | 2014-11-18 | 애나디스 파마슈티칼스, 인코포레이티드 | 5-아미노-3-(3''-데옥시-β-D-리보퓨라노실)-티아졸로[4,5-d]파이리미딘-2,7-다이온의 프로드럭 |
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| EP2081933B1 (en) | 2006-09-29 | 2011-03-23 | Novartis AG | Pyrazolopyrimidines as pi3k lipid kinase inhibitors |
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| US8796241B2 (en) | 2007-08-29 | 2014-08-05 | Adam Lubin | Therapy of tumors and infectious agents deficient in methylthioadenosine phosphorylase |
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| AU2010283806A1 (en) | 2009-08-12 | 2012-03-01 | Novartis Ag | Heterocyclic hydrazone compounds and their uses to treat cancer and inflammation |
| BR112012003709B1 (pt) | 2009-08-17 | 2021-05-18 | Intellikine Llc | compostos heterocíclicos e usos dos mesmos |
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| WO2012116237A2 (en) | 2011-02-23 | 2012-08-30 | Intellikine, Llc | Heterocyclic compounds and uses thereof |
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| WO2013007768A1 (en) | 2011-07-13 | 2013-01-17 | F. Hoffmann-La Roche Ag | Tricyclic heterocyclic compounds, compositions and methods of use thereof as jak inhibitors |
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| JP6130391B2 (ja) | 2011-11-23 | 2017-05-17 | インテリカイン, エルエルシー | Mtor阻害剤を使用する強化された治療レジメン |
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| CN106632339B (zh) * | 2016-12-16 | 2018-11-27 | 温州医科大学 | 一种6-取代-9h-嘌呤类衍生物及其制备方法和应用 |
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| CN119798352B (zh) * | 2024-01-15 | 2025-11-11 | 中国医学科学院药物研究所 | 化合物yzg-331的晶型及其制备方法 |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE789773A (fr) * | 1971-10-08 | 1973-04-06 | Schering Ag | Adenosines n6 -substituees et leur procede de |
| CA1239397A (en) * | 1983-08-01 | 1988-07-19 | James A. Bristol | N.sup.6-substituted adenosines |
| DE3406533A1 (de) * | 1984-02-23 | 1985-08-29 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verwendung von adenosin-derivaten als antiallergica und arzneimittel, die diese enthalten |
| WO1985004882A1 (en) * | 1984-04-18 | 1985-11-07 | Nelson Research And Development Company | N-6 substituted adenosine derivatives as cardiac vasodilators |
| US4663313A (en) * | 1984-10-26 | 1987-05-05 | Warner-Lambert Company | N6 -tricyclic adenosines for treating hypertension |
| US4738954A (en) | 1985-11-06 | 1988-04-19 | Warner-Lambert Company | Novel N6 -substituted-5'-oxidized adenosine analogs |
| US5106837A (en) * | 1988-03-16 | 1992-04-21 | The Scripps Research Institute | Adenosine derivatives with therapeutic activity |
| US4757747A (en) * | 1986-04-08 | 1988-07-19 | Vickers, Incorporated | Power transmission |
| AU8274187A (en) * | 1986-10-31 | 1988-05-25 | Warner-Lambert Company | Heteroaromatic derivatives of adenosine |
| PT86660B (pt) * | 1987-02-04 | 1992-02-28 | Ciba Geigy Ag | Processo para a preparacao de derivados de adenosina-5'-carboxamida |
| US4968697A (en) * | 1987-02-04 | 1990-11-06 | Ciba-Geigy Corporation | 2-substituted adenosine 5'-carboxamides as antihypertensive agents |
| LU87181A1 (fr) * | 1987-04-06 | 1988-11-17 | Sandoz Sa | Nouveaux derives de l'acide furannuronique,leur preparation et leur utilisation comme medicaments |
| DE3810551A1 (de) * | 1987-04-06 | 1988-11-03 | Sandoz Ag | Neue ribofuranuronsaeure-derivate |
| US5219840A (en) * | 1987-04-06 | 1993-06-15 | Sandoz Ltd. | Antihypertensive 9-(2,N6 -disubstituted adenyl) ribofuranuronic acid derivatives |
| ATE128141T1 (de) * | 1988-03-16 | 1995-10-15 | Scripps Research Inst | Als therapeutische mittel verwendbare substituierte adeninderivate. |
| JPH0725785B2 (ja) * | 1989-01-11 | 1995-03-22 | 日本臓器製薬株式会社 | アデノシン誘導体及び該化合物を有効成分として含有する医薬組成物 |
| DE3924424A1 (de) * | 1989-07-24 | 1991-01-31 | Boehringer Mannheim Gmbh | Nucleosid-derivate, verfahren zu deren herstellung, deren verwendung als arzneimittel sowie deren verwendung bei der nucleinsaeure-sequenzierung |
| CA2028002A1 (en) * | 1989-10-19 | 1991-04-20 | Daniel P. Becker | Method of treating gastrointestinal motility disorders |
| US5459255A (en) * | 1990-01-11 | 1995-10-17 | Isis Pharmaceuticals, Inc. | N-2 substituted purines |
| DE4025879A1 (de) * | 1990-08-16 | 1992-02-20 | Sandoz Ag | Neue adenosin derivate, deren herstellung und verwendung |
| FR2687678B1 (fr) * | 1992-01-31 | 1995-03-31 | Union Pharma Scient Appl | Nouveaux derives de l'adenosine, leurs procedes de preparation, compositions pharmaceutiques les contenant. |
| EP0708781B1 (en) * | 1993-07-13 | 2001-10-04 | THE UNITED STATES OF AMERICA, as represented by THE SECRETARY, Department of Health and Human Services | A 3 adenosine receptor agonists |
-
1993
- 1993-01-20 GB GB939301000A patent/GB9301000D0/en active Pending
-
1994
- 1994-01-14 IS IS4121A patent/IS4121A/is unknown
- 1994-01-18 AT AT94905100T patent/ATE164849T1/de not_active IP Right Cessation
- 1994-01-18 AP APAP/P/1994/000613A patent/AP457A/en active
- 1994-01-18 RU RU95122754A patent/RU2129561C1/ru active
- 1994-01-18 US US08/446,727 patent/US5925624A/en not_active Expired - Fee Related
- 1994-01-18 PL PL94309975A patent/PL309975A1/xx unknown
- 1994-01-18 CA CA002153688A patent/CA2153688A1/en not_active Abandoned
- 1994-01-18 KR KR1019950702963A patent/KR960700261A/ko not_active Abandoned
- 1994-01-18 CZ CZ951879A patent/CZ187995A3/cs unknown
- 1994-01-18 AU AU58851/94A patent/AU679714B2/en not_active Ceased
- 1994-01-18 FI FI953489A patent/FI953489L/fi unknown
- 1994-01-18 DE DE69409503T patent/DE69409503T2/de not_active Expired - Lifetime
- 1994-01-18 NZ NZ259880A patent/NZ259880A/en unknown
- 1994-01-18 WO PCT/EP1994/000145 patent/WO1994017090A1/en not_active Ceased
- 1994-01-18 EP EP94905100A patent/EP0680488B1/en not_active Expired - Lifetime
- 1994-01-18 SK SK918-95A patent/SK281229B6/sk unknown
- 1994-01-18 ES ES94905100T patent/ES2117249T3/es not_active Expired - Lifetime
- 1994-01-18 ZA ZA94335A patent/ZA94335B/xx unknown
- 1994-01-18 DK DK94905100T patent/DK0680488T3/da active
- 1994-01-18 CN CN94191527A patent/CN1043997C/zh not_active Expired - Fee Related
- 1994-01-18 JP JP51665294A patent/JP3768232B2/ja not_active Expired - Fee Related
- 1994-01-19 IL IL108372A patent/IL108372A/en not_active IP Right Cessation
- 1994-01-19 SI SI9400021A patent/SI9400021A/sl unknown
- 1994-05-30 TW TW083104895A patent/TW267168B/zh active
- 1994-06-14 EC EC1994001104A patent/ECSP941104A/es unknown
- 1994-06-15 PE PE1994244634A patent/PE54194A1/es not_active Application Discontinuation
-
1995
- 1995-06-28 HU HU95P/P00514P patent/HU211914A9/hu unknown
- 1995-07-19 NO NO952872A patent/NO305603B1/no not_active IP Right Cessation
-
1997
- 1997-09-22 US US08/934,540 patent/US5889178A/en not_active Expired - Lifetime
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