EP0927035A4 - Thrombin inhibitors - Google Patents
Thrombin inhibitorsInfo
- Publication number
- EP0927035A4 EP0927035A4 EP97942415A EP97942415A EP0927035A4 EP 0927035 A4 EP0927035 A4 EP 0927035A4 EP 97942415 A EP97942415 A EP 97942415A EP 97942415 A EP97942415 A EP 97942415A EP 0927035 A4 EP0927035 A4 EP 0927035A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- thrombin inhibitors
- thrombin
- inhibitors
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/10—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines
- C07C257/18—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. amidines having carbon atoms of amidino groups bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/22—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
- C07D295/26—Sulfur atoms
-
- 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
- C07D405/12—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 linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US2603396P | 1996-09-13 | 1996-09-13 | |
US26033P | 1996-09-13 | ||
GBGB9624278.9A GB9624278D0 (en) | 1996-11-22 | 1996-11-22 | Thrombin inhibitors |
GB9624278 | 1996-11-22 | ||
PCT/US1997/015989 WO1998010763A1 (en) | 1996-09-13 | 1997-09-09 | Thrombin inhibitors |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0927035A1 EP0927035A1 (en) | 1999-07-07 |
EP0927035A4 true EP0927035A4 (en) | 2002-11-13 |
Family
ID=26310456
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97942415A Withdrawn EP0927035A4 (en) | 1996-09-13 | 1997-09-09 | Thrombin inhibitors |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0927035A4 (en) |
JP (1) | JP2001500864A (en) |
AU (1) | AU725403B2 (en) |
CA (1) | CA2264037A1 (en) |
WO (1) | WO1998010763A1 (en) |
Families Citing this family (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6133297A (en) * | 1997-09-30 | 2000-10-17 | Merck & Co., Inc. | Thrombin inhibitors |
US7015230B1 (en) | 1999-05-19 | 2006-03-21 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade |
US6653316B1 (en) | 1999-05-19 | 2003-11-25 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyrimidinones useful for selective inhibition of the coagulation cascade |
US6458952B1 (en) | 1999-05-19 | 2002-10-01 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl uracils useful for selective inhibition of the coagulation cascade |
US6716838B1 (en) | 1999-05-19 | 2004-04-06 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl uracils as anticoagulative agents |
US6867217B1 (en) | 1999-05-19 | 2005-03-15 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyridones useful for selective inhibition of the coagulation cascade |
US6750342B1 (en) | 1999-05-19 | 2004-06-15 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyrimidinones useful for selective inhibition of the coagulation cascade |
US6664255B1 (en) | 1999-05-19 | 2003-12-16 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl pyrazinones useful for selective inhibition of the coagulation cascade |
AU2001243598A1 (en) | 2000-03-13 | 2001-09-24 | Pharmacia Corporation | Polycyclic aryl and heteroaryl substituted benzenes useful for selective inhibition of the coagulation cascade |
EP1268428A2 (en) | 2000-04-05 | 2003-01-02 | Pharmacia Corporation | Polycyclic aryl and heteroaryl substituted 4-pyridones useful for selective inhibition of the coagulation cascade |
AU2001249870A1 (en) | 2000-04-05 | 2001-10-23 | Pharmacia Corporation | Polycyclic aryl and heteroaryl substituted 4-pyrones useful for selective inhibition of the coagulation cascade |
AU2001253363A1 (en) | 2000-04-17 | 2001-10-30 | Pharmacia Corporation | Polycyclic aryl and heteroaryl substituted 1,4-quinones useful for selective inhibition of the coagulation cascade |
MXPA03004458A (en) | 2000-11-20 | 2005-01-25 | Pharmacia Corp | Substituted polycyclic aryl and heteroaryl pyridines useful for selective inhibition of the coagulation cascade. |
US7015223B1 (en) | 2000-11-20 | 2006-03-21 | Pharmacia Corporation | Substituted polycyclic aryl and heteroaryl 1,2,4-triazinones useful for selective inhibition of the coagulation cascade |
US7119094B1 (en) | 2000-11-20 | 2006-10-10 | Warner-Lambert Company | Substituted polycyclic aryl and heteroarpyl pyrazinones useful for selective inhibition of the coagulation cascade |
US7507767B2 (en) | 2001-02-08 | 2009-03-24 | Schering Corporation | Cannabinoid receptor ligands |
US7067539B2 (en) | 2001-02-08 | 2006-06-27 | Schering Corporation | Cannabinoid receptor ligands |
WO2002100341A2 (en) * | 2001-06-12 | 2002-12-19 | Wellstat Therapeutics Corporation | Compounds for the treatment of metabolic disorders |
US6969715B2 (en) | 2001-10-03 | 2005-11-29 | Pharmacia Corporation | 6-membered heterocyclic compounds useful for selective inhibition of the coagulation cascade |
EP1432687A2 (en) | 2001-10-03 | 2004-06-30 | Pharmacia Corporation | Substituted 5-membered polycyclic compounds useful for selective inhibition of the coagulation cascade |
IL161439A0 (en) | 2001-11-14 | 2004-09-27 | Schering Corp | Cannabinoid receptor ligands |
DE60319714T2 (en) | 2002-06-19 | 2009-04-02 | Schering Corp. | AGONISTS OF CANNABINOID RECEPTOR |
US7120327B2 (en) | 2002-11-27 | 2006-10-10 | International Business Machines Corporation | Backplane assembly with board to board optical interconnections |
WO2004073611A2 (en) * | 2003-02-13 | 2004-09-02 | Wellstat Therapeutics Corporation | Compounds for the treatment of metabolic disorders |
TW200505902A (en) | 2003-03-20 | 2005-02-16 | Schering Corp | Cannabinoid receptor ligands |
AU2007210014B2 (en) * | 2006-02-01 | 2012-11-01 | Merck Sharp & Dohme Corp. | Potassium channel inhibitors |
JP5180843B2 (en) * | 2006-02-01 | 2013-04-10 | メルク・シャープ・エンド・ドーム・コーポレイション | Potassium channel inhibitor |
JP5268652B2 (en) * | 2006-02-01 | 2013-08-21 | メルク・シャープ・アンド・ドーム・コーポレーション | Potassium channel inhibitor |
RU2354647C2 (en) * | 2007-06-28 | 2009-05-10 | Общество С Ограниченной Ответственностью "Бионика" | New compounds with thrombin inhibiting function, and based pharmaceutical compositions |
RU2353619C2 (en) * | 2007-06-28 | 2009-04-27 | Общество С Ограниченной Ответственностью "Бионика" | Novel compounds possessing anticoagulant function, based on them pharmaceutical compositions for treatment of thrombotic conditions and plasma-substituting solution for correction of hypercoagulation disorders in hemodilution |
RU2469029C2 (en) * | 2010-12-30 | 2012-12-10 | Закрытое Акционерное Общество "Вертекс" | Substance showing combined antiagregant, anticoagulant and vasodilator activities, n,n'-substituted piperazines and method for preparing them (versions) |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5283532A (en) * | 1976-01-01 | 1977-07-12 | Teijin Ltd | Novel aromatic compounds |
EP0302792A2 (en) * | 1987-08-07 | 1989-02-08 | Sanofi | Alkylaminoalkoxyphenyl derivatives, process of preparation and compositions containing the same |
EP0524781A1 (en) * | 1991-07-25 | 1993-01-27 | Zeneca Limited | Therapeutic amides |
WO1994020467A1 (en) * | 1993-03-03 | 1994-09-15 | Boehringer Mannheim Gmbh | New 4-aminopyridines, process for preparing the same and medicaments containing the same |
EP0718286A1 (en) * | 1994-12-22 | 1996-06-26 | Bristol-Myers Squibb Company | 3-Alkoxybenzylpiperidine derivatives as melatonergic agents |
WO1996026196A2 (en) * | 1995-02-23 | 1996-08-29 | Schering Corporation | Benzylpiperidines and piperazines as muscarinic antagonists |
WO1998005644A1 (en) * | 1996-08-02 | 1998-02-12 | Universidad De Granada | New compounds having a selective antitumour, antiviral, antiparasite and antifungic activity, which block biosynthesis of phosphorilcholine by selective inhibition of intracellular choline kinase or its use as second messenger in cellular proliferation |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5084466A (en) * | 1989-01-31 | 1992-01-28 | Hoffmann-La Roche Inc. | Novel carboxamide pyridine compounds which have useful pharmaceutical utility |
EP0511347A1 (en) * | 1990-11-15 | 1992-11-04 | Pentapharm A.G. | Meta-substituted phenyl alanine derivatives |
US5612363A (en) * | 1995-06-02 | 1997-03-18 | Berlex Laboratories, Inc. | N,N-di(aryl) cyclic urea derivatives as anti-coagulants |
-
1997
- 1997-09-09 AU AU44117/97A patent/AU725403B2/en not_active Ceased
- 1997-09-09 JP JP10513809A patent/JP2001500864A/en active Pending
- 1997-09-09 EP EP97942415A patent/EP0927035A4/en not_active Withdrawn
- 1997-09-09 WO PCT/US1997/015989 patent/WO1998010763A1/en not_active Application Discontinuation
- 1997-09-09 CA CA002264037A patent/CA2264037A1/en not_active Abandoned
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5283532A (en) * | 1976-01-01 | 1977-07-12 | Teijin Ltd | Novel aromatic compounds |
EP0302792A2 (en) * | 1987-08-07 | 1989-02-08 | Sanofi | Alkylaminoalkoxyphenyl derivatives, process of preparation and compositions containing the same |
EP0524781A1 (en) * | 1991-07-25 | 1993-01-27 | Zeneca Limited | Therapeutic amides |
WO1994020467A1 (en) * | 1993-03-03 | 1994-09-15 | Boehringer Mannheim Gmbh | New 4-aminopyridines, process for preparing the same and medicaments containing the same |
EP0718286A1 (en) * | 1994-12-22 | 1996-06-26 | Bristol-Myers Squibb Company | 3-Alkoxybenzylpiperidine derivatives as melatonergic agents |
WO1996026196A2 (en) * | 1995-02-23 | 1996-08-29 | Schering Corporation | Benzylpiperidines and piperazines as muscarinic antagonists |
WO1998005644A1 (en) * | 1996-08-02 | 1998-02-12 | Universidad De Granada | New compounds having a selective antitumour, antiviral, antiparasite and antifungic activity, which block biosynthesis of phosphorilcholine by selective inhibition of intracellular choline kinase or its use as second messenger in cellular proliferation |
Non-Patent Citations (9)
Title |
---|
DATABASE CROSSFIRE BEILSTEIN Beilstein Institut zur Förderung der Chemischen Wissenschaften, Frankfurt am Main, DE; 27 June 1988 (1988-06-27), XP002213631 * |
DATABASE WPI Section Ch Week 197734, Derwent World Patents Index; Class C02, AN 1977-60361Y, XP002213632 * |
EFANGE ET AL: "Flexible N-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Analogues: Synthesis Monamine Oxidase Catalyzed Bioactivation", JOURNAL OF MEDICINAL CHEMISTRY, AMERICAN CHEMICAL SOCIETY. WASHINGTON, US, vol. 33, no. 12, 1990, pages 3133 - 3142, XP002119483, ISSN: 0022-2623 * |
J. PRAKT. CHEM., vol. 325, no. 2, 1983, pages 301 - 308 * |
JAIN ET AL: "Chemical and pharmacological investigations of some.omega.-substituted alkylamino-3-aminopyridines", JOURNAL OF MEDICINAL CHEMISTRY, AMERICAN CHEMICAL SOCIETY. WASHINGTON, US, vol. 11, no. 1, 1968, pages 87 - 92, XP002093777, ISSN: 0022-2623 * |
MAO S-S: "FACTOR XA INHIBITORS", PERSPECTIVES IN DRUG DISCOVERY AND DESIGN, ESCOM SCIENCE PUBLISHERS BV, XX, vol. 1, no. 3, 1993, pages 423 - 430, XP000654087, ISSN: 0928-2866 * |
PROTIVA M ET AL: "1-ARYL- AND 1-(ARYLMETHYL)-4-GUANYLPIPERAZINES AND OTHER HETEROCYCLIC AND ALICYCLIC GUANIDINE DERIVATIVES", COLLECTION OF CZECHOSLOVAK CHEMICAL COMMUNICATIONS, ACADEMIC PRESS, LONDON, GB, vol. 40, 1975, pages 3904 - 3923, XP000574972, ISSN: 0010-0765 * |
See also references of WO9810763A1 * |
WALKER G N ET AL: "APPLICATION OF SODIUM BOROHYDRIDE, REDUCTION TO SYNTHESIS OF SUBSTITUTED AMINOPIPERIDINES, AMINOPIPERAZINES, AMINOPYRIDINES AND HYDRAZINES", JOURNAL OF ORGANIC CHEMISTRY, AMERICAN CHEMICAL SOCIETY. EASTON, US, vol. 26, no. 8, 14 August 1961 (1961-08-14), pages 2740 - 2747, XP002071843, ISSN: 0022-3263 * |
Also Published As
Publication number | Publication date |
---|---|
JP2001500864A (en) | 2001-01-23 |
CA2264037A1 (en) | 1998-03-19 |
WO1998010763A1 (en) | 1998-03-19 |
AU4411797A (en) | 1998-04-02 |
EP0927035A1 (en) | 1999-07-07 |
AU725403B2 (en) | 2000-10-12 |
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Legal Events
Date | Code | Title | Description |
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PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
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17P | Request for examination filed |
Effective date: 19990413 |
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RIC1 | Information provided on ipc code assigned before grant |
Free format text: 7A 61K 31/44 A, 7A 61K 31/155 B, 7A 61K 31/495 B, 7C 07C 257/18 B, 7C 07D 213/12 B, 7C 07D 241/04 B, 7C 07D 213/06 B, 7C 07D 213/30 B, 7C 07D 213/73 B, 7C 07D 213/74 B, 7C 07D 295/22 B, 7C 07D 405/12 B |
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A4 | Supplementary search report drawn up and despatched |
Effective date: 20021002 |
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18D | Application deemed to be withdrawn |
Effective date: 20040401 |