NO931118L - Uracil reduktase inaktivatorer - Google Patents
Uracil reduktase inaktivatorerInfo
- Publication number
- NO931118L NO931118L NO93931118A NO931118A NO931118L NO 931118 L NO931118 L NO 931118L NO 93931118 A NO93931118 A NO 93931118A NO 931118 A NO931118 A NO 931118A NO 931118 L NO931118 L NO 931118L
- Authority
- NO
- Norway
- Prior art keywords
- halo
- uracil reductase
- uracil
- inactivators
- substd
- Prior art date
Links
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 title abstract 4
- 229940035893 uracil Drugs 0.000 title abstract 2
- 125000001475 halogen functional group Chemical group 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- UJBCLAXPPIDQEE-UHFFFAOYSA-N 5-prop-1-ynyl-1h-pyrimidine-2,4-dione Chemical compound CC#CC1=CNC(=O)NC1=O UJBCLAXPPIDQEE-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000000937 inactivator Effects 0.000 abstract 1
- 238000013160 medical therapy Methods 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
Classifications
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/513—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
-
- 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
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
- A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
- A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
- A61K31/7072—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0031—Rectum, anus
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
- A61K9/1623—Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1635—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1629—Organic macromolecular compounds
- A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Molecular Biology (AREA)
- Biophysics (AREA)
- Biochemistry (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cephalosporin Compounds (AREA)
- Saccharide Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Semiconductor Lasers (AREA)
- Vibration Dampers (AREA)
- Springs (AREA)
- Compounds Of Unknown Constitution (AREA)
- Laminated Bodies (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Transformer Cooling (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB909020930A GB9020930D0 (en) | 1990-09-26 | 1990-09-26 | Pharmaceutical combinations |
PCT/GB1991/001650 WO1992004901A1 (en) | 1990-09-26 | 1991-09-25 | Uracil reductase inactivators |
Publications (3)
Publication Number | Publication Date |
---|---|
NO931118L true NO931118L (no) | 1993-03-25 |
NO931118D0 NO931118D0 (no) | 1993-03-25 |
NO313175B1 NO313175B1 (no) | 2002-08-26 |
Family
ID=10682770
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19931118A NO313175B1 (no) | 1990-09-26 | 1993-03-25 | Fremgangsmåte for fremstilling av en 5-fluoruracil farmasöytisk kombinasjon med forbedret stabilitet mot uracilreduktase |
NO980717A NO980717D0 (no) | 1990-09-26 | 1998-02-20 | Uracil reduktase inaktivatorer |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO980717A NO980717D0 (no) | 1990-09-26 | 1998-02-20 | Uracil reduktase inaktivatorer |
Country Status (30)
Country | Link |
---|---|
US (5) | US6268374B1 (no) |
EP (2) | EP0550580B1 (no) |
JP (2) | JP2682739B2 (no) |
KR (1) | KR100222329B1 (no) |
AT (1) | ATE190489T1 (no) |
BR (1) | BR1100356A (no) |
CA (2) | CA2390654A1 (no) |
CZ (4) | CZ16196A3 (no) |
DE (1) | DE69132052T2 (no) |
DK (1) | DK0550580T3 (no) |
ES (1) | ES2143465T3 (no) |
FI (1) | FI112601B (no) |
GB (1) | GB9020930D0 (no) |
GR (1) | GR3033388T3 (no) |
HK (1) | HK1004188A1 (no) |
HU (1) | HU219589B (no) |
IE (1) | IE20010101A1 (no) |
IL (2) | IL99562A (no) |
MC (1) | MC2307A1 (no) |
MY (1) | MY128980A (no) |
NO (2) | NO313175B1 (no) |
NZ (2) | NZ239927A (no) |
PT (1) | PT99041B (no) |
RU (1) | RU2194511C2 (no) |
SG (1) | SG47912A1 (no) |
SK (1) | SK281894B6 (no) |
TW (1) | TW271397B (no) |
UA (1) | UA42679C2 (no) |
WO (1) | WO1992004901A1 (no) |
ZA (1) | ZA917667B (no) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6337209B1 (en) | 1992-02-26 | 2002-01-08 | Glaxo Wellcome Inc. | Molecular constructs containing a carcinoembryonic antigen regulatory sequence |
GB9020930D0 (en) * | 1990-09-26 | 1990-11-07 | Wellcome Found | Pharmaceutical combinations |
WO1992020816A1 (en) * | 1991-05-15 | 1992-11-26 | Yale University | Determination of prodrugs metabolizable by the liver and therapeutic use thereof |
GB9322795D0 (en) * | 1993-11-05 | 1993-12-22 | Wellcome Found | Novel compounds |
US6849602B1 (en) * | 1996-03-05 | 2005-02-01 | The Regents Of The University Of California | Compositions for alleviating neuropathic pain with prosaposin receptor agonists |
NZ330360A (en) * | 1997-06-02 | 1999-03-29 | Hoffmann La Roche | 5'-deoxy-cytidine derivatives, their manufacture and use as antitumoral agents |
US6005098A (en) * | 1998-02-06 | 1999-12-21 | Hoffmann-La Roche Inc. | 5'deoxycytidine derivatives |
US7026301B2 (en) * | 2002-10-17 | 2006-04-11 | New York University | Method of orally treating inflammatory skin conditions with prodrugs of 5-fluorouracil |
US20080255168A1 (en) * | 2004-12-03 | 2008-10-16 | Adherex Technologies, Inc. | Methods for administering dpd inhibitors in combination with 5-fu and 5-fu prodrugs |
KR20070098798A (ko) * | 2004-12-03 | 2007-10-05 | 애드헤렉스 테크놀로지스 인크. | Dpd 억제제를 5-fu 및 5-fu 전구약물과 조합한투여방법 |
AU2012200856B2 (en) * | 2004-12-03 | 2013-10-10 | Adherex Technologies Inc. | Methods for administering DPD inhibitors in combination with 5-FU and 5-FU prodrugs |
US20090196833A1 (en) * | 2008-02-06 | 2009-08-06 | Adherex Technologies Inc. | Compositions comprising topical dpd inhibitors and methods of using same in the treatment of hand-foot syndrome |
US8658618B2 (en) * | 2009-10-14 | 2014-02-25 | Adherex Technologies, Inc. | Methods for preventing or reducing neurotoxicity associated with administering DPD inhibitors in combination with 5-FU and 5-FU prodrugs |
US10556872B2 (en) | 2017-03-17 | 2020-02-11 | Hampton University | Fatty acid synthase inhibitors and methods of use |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3324126A (en) * | 1963-08-07 | 1967-06-06 | Univ Kansas State | Production of 5-trifluoromethyluracil |
US4124765A (en) | 1975-05-13 | 1978-11-07 | Ono Pharmaceutical Co., Ltd. | 5-Fluorouracil derivatives |
DE2522369A1 (de) | 1975-05-21 | 1976-12-02 | Ono Pharmaceutical Co | 5-fluoruracilderivate und verfahren zu ihrer herstellung |
DD122381A1 (no) * | 1975-10-03 | 1976-10-05 | ||
JPS55111420A (en) * | 1979-02-20 | 1980-08-28 | Ono Pharmaceut Co Ltd | Antitumorigenic agent |
US4381344A (en) | 1980-04-25 | 1983-04-26 | Burroughs Wellcome Co. | Process for producing deoxyribosides using bacterial phosphorylase |
JPS6094971A (ja) * | 1983-10-31 | 1985-05-28 | Sagami Chem Res Center | 5−ペルフルオロアルキルウラシル類の製造方法 |
US4719214A (en) | 1985-07-25 | 1988-01-12 | Southern Research Institute | Carbocyclic analogues of thymine nucleosides |
GB8629892D0 (en) * | 1986-12-15 | 1987-01-28 | Wellcome Found | Antiviral compounds |
US4863927A (en) * | 1987-05-11 | 1989-09-05 | Merck & Co., Inc. | 1-(2-hydroxymethyl)cycloalkylmethyl)-5-substituted uracils |
US4874602A (en) | 1988-02-22 | 1989-10-17 | Paul Calabresi | Reduction of the severity 3'-azido-3'-deoxythymidine-induced anemia using benzylacyclouridine |
CA1334535C (en) | 1988-03-31 | 1995-02-21 | Tadashi Miyasaka | 6-substituted acyclopyrimidine nucleoside derivative and antiviral agent containing the same as active ingredient thereof |
US5077280A (en) | 1988-04-12 | 1991-12-31 | Brown University Research Foundation | Treatment of viral infections |
US5157114A (en) * | 1988-08-19 | 1992-10-20 | Burroughs Wellcome Co. | 2',3'-dideoxy-3'-fluoro-5-ethyngluridine |
US5198539A (en) * | 1988-08-19 | 1993-03-30 | Burroughs Wellcome Co. | 5'-esters of 2',3'-dideoxy-3'-fluoro-5-ethynyluridine |
EP0566162B1 (en) * | 1988-08-25 | 1997-06-11 | Yoshitomi Pharmaceutical Industries, Ltd. | 2'-Methylidenepyrimidine Nucleoside Compounds, their use and method for production thereof |
NZ234534A (en) * | 1989-07-17 | 1994-12-22 | Univ Birmingham | Pyrimidine 4'-thionucleoside derivatives and their preparation; intermediates therefor |
EP0711555A2 (en) * | 1990-07-19 | 1996-05-15 | The Wellcome Foundation Limited | Enzyme inactivators |
US5643913A (en) * | 1990-07-19 | 1997-07-01 | Glaxo Wellcome Inc. | Pharmaceutical compositions of 5-substituted uracil compounds |
GB9020930D0 (en) * | 1990-09-26 | 1990-11-07 | Wellcome Found | Pharmaceutical combinations |
-
1990
- 1990-09-26 GB GB909020930A patent/GB9020930D0/en active Pending
-
1991
- 1991-09-25 MC MC912307D patent/MC2307A1/xx unknown
- 1991-09-25 MY MYPI91001733A patent/MY128980A/en unknown
- 1991-09-25 RU RU99101342/14A patent/RU2194511C2/ru not_active IP Right Cessation
- 1991-09-25 AT AT91917260T patent/ATE190489T1/de not_active IP Right Cessation
- 1991-09-25 CZ CZ96161A patent/CZ16196A3/cs unknown
- 1991-09-25 EP EP91917260A patent/EP0550580B1/en not_active Expired - Lifetime
- 1991-09-25 PT PT99041A patent/PT99041B/pt not_active IP Right Cessation
- 1991-09-25 JP JP3515549A patent/JP2682739B2/ja not_active Expired - Fee Related
- 1991-09-25 DK DK91917260T patent/DK0550580T3/da active
- 1991-09-25 CZ CZ96162A patent/CZ16296A3/cs unknown
- 1991-09-25 TW TW080107580A patent/TW271397B/zh active
- 1991-09-25 CA CA002390654A patent/CA2390654A1/en not_active Abandoned
- 1991-09-25 EP EP99202472A patent/EP0985415A1/en not_active Withdrawn
- 1991-09-25 CA CA002092435A patent/CA2092435C/en not_active Expired - Fee Related
- 1991-09-25 ES ES91917260T patent/ES2143465T3/es not_active Expired - Lifetime
- 1991-09-25 HU HU9300863A patent/HU219589B/hu unknown
- 1991-09-25 ZA ZA917667A patent/ZA917667B/xx unknown
- 1991-09-25 SK SK233-93A patent/SK281894B6/sk unknown
- 1991-09-25 DE DE69132052T patent/DE69132052T2/de not_active Expired - Lifetime
- 1991-09-25 US US08/030,259 patent/US6268374B1/en not_active Expired - Lifetime
- 1991-09-25 UA UA93101215A patent/UA42679C2/uk unknown
- 1991-09-25 WO PCT/GB1991/001650 patent/WO1992004901A1/en active IP Right Grant
- 1991-09-25 IL IL9956291A patent/IL99562A/en not_active IP Right Cessation
- 1991-09-25 CZ CZ1993506A patent/CZ288515B6/cs not_active IP Right Cessation
- 1991-09-26 SG SG1996005207A patent/SG47912A1/en unknown
-
1993
- 1993-03-23 KR KR1019930700875A patent/KR100222329B1/ko not_active IP Right Cessation
- 1993-03-24 IE IE20010101A patent/IE20010101A1/en unknown
- 1993-03-24 NZ NZ239927A patent/NZ239927A/en not_active IP Right Cessation
- 1993-03-24 NZ NZ250799A patent/NZ250799A/en unknown
- 1993-03-25 FI FI931337A patent/FI112601B/fi not_active IP Right Cessation
- 1993-03-25 NO NO19931118A patent/NO313175B1/no not_active IP Right Cessation
-
1995
- 1995-06-06 US US08/470,317 patent/US5817664A/en not_active Expired - Lifetime
- 1995-06-29 CZ CZ19951709A patent/CZ288520B6/cs not_active IP Right Cessation
-
1997
- 1997-04-28 BR BR1100356-1A patent/BR1100356A/pt active IP Right Grant
- 1997-05-12 JP JP9120730A patent/JP3003993B2/ja not_active Expired - Fee Related
- 1997-10-10 IL IL12194797A patent/IL121947A0/xx unknown
-
1998
- 1998-02-20 NO NO980717A patent/NO980717D0/no not_active Application Discontinuation
- 1998-04-22 HK HK98103371A patent/HK1004188A1/xx not_active IP Right Cessation
-
2000
- 2000-05-09 GR GR20000401075T patent/GR3033388T3/el not_active IP Right Cessation
- 2000-06-30 US US09/608,972 patent/US6297223B1/en not_active Expired - Fee Related
-
2001
- 2001-10-01 US US09/968,472 patent/US7119096B2/en not_active Expired - Fee Related
-
2006
- 2006-09-01 US US11/469,515 patent/US7704971B2/en not_active Expired - Fee Related
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