ES2193202T3 - Nuevo derivado de amidinonaftilo o sal de este. - Google Patents
Nuevo derivado de amidinonaftilo o sal de este.Info
- Publication number
- ES2193202T3 ES2193202T3 ES95938625T ES95938625T ES2193202T3 ES 2193202 T3 ES2193202 T3 ES 2193202T3 ES 95938625 T ES95938625 T ES 95938625T ES 95938625 T ES95938625 T ES 95938625T ES 2193202 T3 ES2193202 T3 ES 2193202T3
- Authority
- ES
- Spain
- Prior art keywords
- group
- sup
- formula
- represented
- derivative
- 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.)
- Expired - Lifetime
Links
- -1 HYDROXYL GROUP Chemical group 0.000 abstract 4
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 abstract 2
- 102000015081 Blood Coagulation Factors Human genes 0.000 abstract 1
- 108010039209 Blood Coagulation Factors Proteins 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 230000002776 aggregation Effects 0.000 abstract 1
- 238000004220 aggregation Methods 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 239000003114 blood coagulation factor Substances 0.000 abstract 1
- 229940019700 blood coagulation factors Drugs 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 239000013067 intermediate product Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Chemical group 0.000 abstract 1
Classifications
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
-
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
-
- 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
- C07D409/12—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 linked by a chain containing hetero atoms as chain links
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
UN DERIVADO DE AMIDINONAFTILO REPRESENTADO POR LA SIGUIENTE FORMULA GENERAL (I) QUE TIENE UNA ACCION INHIBIDORA DE LA AGREGACION PLAQUETARIA BASADA EN LA ACCION INHIBIDORA ACTIVADA DEL FACTOR X DE COAGULACION DE LA SANGRE Y UTIL COMO AGENTE ANTITROMBOTICO Y SIMILAR, UNA SAL DE ESTE, UN PRODUCTO INTERMEDIO DE ESTE Y UNA COMPOSICION FARMACEUTICA QUE CONTIENE EL DERIVADO DE AMIDINONAFTILO. LA INVENCION SE REFIERE ASIMISMO A UN DERIVADO DE AMIDINONAFTILO REPRESENTADO POR LA SIGUIENTE FORMULA GENERAL (I) O UNA SAL ACEPTABLE FARMACEUTICAMENTE DE ESTE. (LOS SIMBOLOS DE LA FORMULA TIENEN LOS SIGUIENTES SIGNIFICADOS: R{SUP,1}): ATOMO DE HIDROGENO O UN GRUPO REPRESENTADO POR LA FORMULA - A - W - R {SUP,4}, A: UN GRUPO REPRESENTADO POR LA FORMULA: UN GRUPO REPRESENTADO POR LA FORMULA: O UN GRUPO REPRESENTADO POR LA FORMULA - SO {SUB,2}-, X ES UN ATOMO DE OXIGENO O UN ATOMO DE AZUFRE, W ES UN ENLACE SENCILLO O UN GRUPO REPRESENTADO POR LA FORMULA - NR{SUP,5} -, R{SUP,4} ES UN GRUPO HIDROXILO, UN GRUPOALCOXI INFERIOR, ETC., NO UN GRUPO HIDROXILO O UN GRUPO ALCOXI INFERIOR, R{SUP,5} ES UN ATOMO DE HIDROGENO, UN GRUPO CARBAMOILO, UN GRUPO ALCOXICARBONILO INFERIOR, ETC.; R{SUP,2} ES UN GRUPO ALQUILO INFERIOR, R{SUP,3} ES UN ATOMO DE HIDROGENO, UN ATOMO DE HALOGENO, UN GRUPO CARBOXILO, B ES UN GRUPO ALQUILENO INFERIOR O UN GRUPO CARBONILO, Y N ES 0 O 1).
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29996394 | 1994-12-02 | ||
| JP10520595 | 1995-04-28 | ||
| JP19881695 | 1995-08-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2193202T3 true ES2193202T3 (es) | 2003-11-01 |
Family
ID=27310425
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES95938625T Expired - Lifetime ES2193202T3 (es) | 1994-12-02 | 1995-12-01 | Nuevo derivado de amidinonaftilo o sal de este. |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US5869501A (es) |
| EP (1) | EP0798295B1 (es) |
| JP (1) | JP3004362B2 (es) |
| KR (1) | KR100383161B1 (es) |
| CN (1) | CN1087736C (es) |
| AT (1) | ATE233240T1 (es) |
| AU (1) | AU688628B2 (es) |
| CA (1) | CA2206532C (es) |
| DE (1) | DE69529770T2 (es) |
| ES (1) | ES2193202T3 (es) |
| FI (1) | FI115051B (es) |
| HU (1) | HUT77313A (es) |
| MX (1) | MX9704059A (es) |
| NO (1) | NO309566B1 (es) |
| NZ (1) | NZ296210A (es) |
| PL (1) | PL184824B1 (es) |
| PT (1) | PT798295E (es) |
| RU (1) | RU2154633C2 (es) |
| TW (1) | TW300888B (es) |
| WO (1) | WO1996016940A1 (es) |
Families Citing this family (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69630214T2 (de) | 1995-03-10 | 2004-07-15 | Berlex Laboratories, Inc., Richmond | Benzamidin-derivate, deren herstellung und deren verwendung als anti-koagulantien |
| SE9602646D0 (sv) | 1996-07-04 | 1996-07-04 | Astra Ab | Pharmaceutically-useful compounds |
| CZ43399A3 (cs) | 1996-08-15 | 1999-07-14 | Schering Corporation | Etheroví muskarinní antagonisté |
| EP0842941A1 (de) | 1996-11-16 | 1998-05-20 | Roche Diagnostics GmbH | Neue Phosphonate, Verfahren zu ihrer Herstellung und Arzneimittel |
| US6653340B1 (en) | 1997-06-03 | 2003-11-25 | Biocryst Pharmaceuticals, Inc. | Compounds useful in the complement, coagulat and kallikrein pathways and method for their preparation |
| EP0993448A1 (en) * | 1997-06-19 | 2000-04-19 | The Du Pont Merck Pharmaceutical Company | (AMIDINO)6-MEMBERED AROMATICS AS FACTOR Xa INHIBITORS |
| US6060491A (en) * | 1997-06-19 | 2000-05-09 | Dupont Pharmaceuticals | 6-membered aromatics as factor Xa inhibitors |
| ZA986594B (en) * | 1997-07-25 | 1999-01-27 | Abbott Lab | Urokinase inhibitors |
| US6258822B1 (en) | 1997-08-06 | 2001-07-10 | Abbott Laboratories | Urokinase inhibitors |
| AU8886698A (en) * | 1997-09-01 | 1999-03-22 | Yamanouchi Pharmaceutical Co., Ltd. | Novel naphthamide derivatives or salts thereof |
| US6686364B2 (en) | 1997-12-08 | 2004-02-03 | Berlex Laboratories, Inc. | Benzamidine derivatives and their use as anti-coagulants |
| DE19754490A1 (de) * | 1997-12-09 | 1999-06-10 | Boehringer Ingelheim Pharma | Durch einen Aminocarbonylrest substituierte Bicyclen, ihre Herstellung und ihre Verwendung als Arzneimittel |
| CA2318351A1 (en) * | 1997-12-26 | 1999-07-08 | Hidemitsu Nishida | Aromatic compounds having cyclic amino or salts thereof |
| WO1999037643A1 (en) * | 1998-01-26 | 1999-07-29 | Yamanouchi Pharmaceutical Co., Ltd. | Novel benzene-fused heterocyclic derivatives or salts thereof |
| EP0937723A1 (de) * | 1998-02-18 | 1999-08-25 | Roche Diagnostics GmbH | Neue Sulfonamide, Verfahren zu ihrer Herstellung sowie diese enthaltende Arzneimittel |
| EP1066272A4 (en) * | 1998-03-27 | 2002-03-13 | Biocryst Pharm Inc | NEW CONNECTIONS USEFUL IN THE COMPLEMENT, COAGULATE AND KALLIKREIN REACTION WAY AND METHOD FOR THEIR PRODUCTION |
| TR200002904T2 (tr) * | 1998-04-10 | 2001-02-21 | Japan Tobacco Inc. | Amidin bileşikleri |
| US6284796B1 (en) | 1998-08-06 | 2001-09-04 | Abbott Laboratories | Ukokinase inhibitors |
| US6504031B1 (en) | 1998-08-06 | 2003-01-07 | Milan Bruncko | Naphthamidine urokinase inhibitors |
| US6262088B1 (en) | 1998-11-19 | 2001-07-17 | Berlex Laboratories, Inc. | Polyhydroxylated monocyclic N-heterocyclic derivatives as anti-coagulants |
| CA2348740A1 (en) | 1998-12-23 | 2000-07-06 | Ruth R. Wexler | Thrombin or factor xa inhibitors |
| CN100488947C (zh) | 1999-01-13 | 2009-05-20 | 杰南技术公司 | 丝氨酸蛋白酶抑制剂 |
| WO2000043041A1 (fr) * | 1999-01-22 | 2000-07-27 | Yamanouchi Pharmaceutical Co., Ltd. | Compositions medicamenteuses presentant une meilleure absorption orale |
| WO2000051998A1 (en) | 1999-03-02 | 2000-09-08 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compounds useful as reversible inhibitors of cathepsin s |
| FR2793247B1 (fr) * | 1999-05-04 | 2001-06-22 | Synthelabo | Derives de 6-[[(aryl et heteroaryl)oxy]methyl]naphtalene-2- carboximidamide, leur preparation et leur application en therapeutique |
| US6858599B2 (en) * | 1999-06-30 | 2005-02-22 | Mochida Pharmaceutical Co., Ltd. | Tricyclic compound having spiro union |
| AU5570900A (en) * | 1999-07-01 | 2001-01-22 | Sankyo Company Limited | Indoline or tetrahydroquinoline derivatives |
| US6350761B1 (en) | 1999-07-30 | 2002-02-26 | Berlex Laboratories, Inc. | Benzenamine derivatives as anti-coagulants |
| US6420364B1 (en) | 1999-09-13 | 2002-07-16 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compound useful as reversible inhibitors of cysteine proteases |
| DE60027204T2 (de) | 1999-10-28 | 2006-11-23 | Sankyo Co., Ltd. | Benzamidinderivate |
| EP1095933A1 (en) * | 1999-10-30 | 2001-05-02 | Aventis Pharma Deutschland GmbH | Novel N-guanidinoalkylamides, their preparation, their use, and pharmaceutical preparations comprising them |
| AU2001234689A1 (en) * | 2000-02-01 | 2001-08-14 | Cor Therapeutics, Inc. | Bivalent phenylene inhibitors of factor xa |
| ES2254385T3 (es) | 2000-02-29 | 2006-06-16 | Millennium Pharmaceuticals, Inc. | Benzamidas e inhibidores relacionados del factor xa. |
| AU2001249397A1 (en) * | 2000-03-24 | 2001-10-08 | Cor Therapeutics, Inc. | Oxindole inhibitors of factor xa |
| AU776053B2 (en) * | 2000-03-31 | 2004-08-26 | Astellas Pharma Inc. | Diazepan derivatives or salts thereof |
| US6495562B1 (en) | 2000-04-25 | 2002-12-17 | Abbott Laboratories | Naphthamidine urokinase inhibitors |
| US6410733B1 (en) | 2000-09-11 | 2002-06-25 | Genentech, Inc. | Amidine inhibitors of serine proteases |
| RU2276137C2 (ru) * | 2000-11-22 | 2006-05-10 | Астеллас Фарма Инк. | Замещенные производные бензола или их соли, фармацевтическая композиция на их основе |
| CA2440389A1 (en) | 2001-03-09 | 2002-10-03 | Ortho-Mcneil Pharmaceutical, Inc. | Aminopyrrolidine sulfonamides as serine protease inhibitors |
| US6710061B2 (en) | 2001-03-09 | 2004-03-23 | Ortho-Mcneil Pharamceutical, Inc. | Aminopyrrolidine sulfonamides as serine protease inhibitors |
| US7312235B2 (en) | 2001-03-30 | 2007-12-25 | Millennium Pharmaceuticals, Inc. | Benzamide inhibitors of factor Xa |
| RU2256652C1 (ru) | 2001-04-05 | 2005-07-20 | Санкио Компани, Лимитед | Соединение, фармацевтическая композиция, применение, способ предупреждения или лечения заболеваний |
| EP1569912B1 (en) | 2002-12-03 | 2015-04-29 | Pharmacyclics, Inc. | 2-(2-hydroxybiphenyl-3-yl)-1h-benzoimidazole-5-carboxamidine derivatives as factor viia inhibitors |
| ATE510817T1 (de) | 2002-01-29 | 2011-06-15 | Merck Serono Sa | Substituierte methylenamidderivate als modulatoren von proteintyrosinphosphatasen (ptps) |
| RU2226392C1 (ru) * | 2002-10-23 | 2004-04-10 | Биологический факультет Московского государственного университета им. М.В. Ломоносова | Способ ингибирования агрегации тромбоцитов |
| WO2004048363A1 (ja) | 2002-11-22 | 2004-06-10 | Takeda Pharmaceutical Company Limited | イミダゾール誘導体、その製造法および用途 |
| KR20050092373A (ko) * | 2002-12-24 | 2005-09-21 | 다이이찌 세이야꾸 가부시기가이샤 | 신규한 에틸렌디아민 유도체 |
| WO2004113316A1 (en) | 2003-05-20 | 2004-12-29 | Genentech, Inc. | Benzofuran inhibitors of factor viia |
| US7250447B2 (en) | 2003-05-20 | 2007-07-31 | Genentech, Inc. | Acylsulfamide inhibitors of factor VIIa |
| CN1886398A (zh) | 2003-10-09 | 2006-12-27 | 米伦纽姆医药公司 | 作为Xa因子抑制剂的经硫醚取代的苯甲酰胺 |
| TWI396686B (zh) | 2004-05-21 | 2013-05-21 | Takeda Pharmaceutical | 環狀醯胺衍生物、以及其製品和用法 |
| JP5020073B2 (ja) | 2004-06-18 | 2012-09-05 | ミレニアム ファーマシューティカルズ インク. | 第Xa因子阻害剤 |
| US7612089B2 (en) | 2004-11-19 | 2009-11-03 | Portola Pharmaceuticals, Inc. | Tetrahydroisoquinolines as factor Xa inhibitors |
| US7678913B2 (en) | 2004-12-07 | 2010-03-16 | Portola Pharmaceuticals, Inc. | Ureas as factor Xa inhibitors |
| WO2006063293A2 (en) * | 2004-12-07 | 2006-06-15 | Portola Pharmaceuticals, Inc. | THIOUREAS AS FACTOR Xa INHIBITORS |
| JP4900238B2 (ja) | 2005-02-02 | 2012-03-21 | 味の素株式会社 | 新規ベンズアミジン化合物 |
| RU2440986C2 (ru) | 2005-11-08 | 2012-01-27 | Милленниум Фамэсьютикэлс, Инк. | СОЛЬ ИНГИБИТОРА ФАКТОРА Ха, СПОСОБ ЕЕ ПОЛУЧЕНИЯ, ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ НА ЕЕ ОСНОВЕ, СОСТОЯЩИЕ ИЗ НАЗВАННОЙ КОМПОЗИЦИИ ТАБЛЕТКА, КАПСУЛА И ЛЕПЕШКА, СПОСОБ ЛЕЧЕНИЯ ТРОМБОЗА И СПОСОБ ИНГИБИРОВАНИЯ КОАГУЛЯЦИИ ОБРАЗЦОВ КРОВИ |
| US20100261758A1 (en) * | 2006-03-28 | 2010-10-14 | Novartis Ag | Heterocyclic amides for use as pharmaceuticals |
| AU2007307599A1 (en) * | 2006-10-12 | 2008-04-17 | Institute Of Medicinal Molecular Design. Inc. | N-phenyloxamic acid derivatives |
| PT2077995E (pt) | 2006-11-02 | 2012-05-10 | Millennium Pharm Inc | Métodos de sintetizar sais farmacêuticos de um inibidor de fator xa |
| US20110045028A1 (en) | 2006-11-30 | 2011-02-24 | Takeda Pharmaceutical Company Limited | Sustained release preparation |
| US8633245B2 (en) * | 2008-04-11 | 2014-01-21 | Institute Of Medicinal Molecular Design, Inc. | PAI-1 inhibitor |
| KR20110036833A (ko) | 2008-07-11 | 2011-04-11 | 아지노모토 가부시키가이샤 | 아미딘 유도체 |
| EA015918B1 (ru) | 2010-03-03 | 2011-12-30 | Дмитрий Геннадьевич ТОВБИН | УРЕТАНЫ, МОЧЕВИНЫ, АМИДЫ И РОДСТВЕННЫЕ ИНГИБИТОРЫ ФАКТОРА Xa |
| WO2019241213A1 (en) * | 2018-06-11 | 2019-12-19 | The Regents Of The University Of Colorado, A Body Corporate | 2-naphthimidamides, analogues thereof, and methods of treatment using same |
| CN117304076B (zh) * | 2023-11-28 | 2024-02-20 | 苏州大学 | 一种n-磺酰基脒化合物的制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4443462A (en) * | 1979-08-06 | 1984-04-17 | Merrell Dow Pharmaceuticals Inc. | Antipsychotic 4-(naphthalenyloxy)piperidine derivatives |
| AU527371B2 (en) * | 1980-09-16 | 1983-03-03 | Torii & Co., Ltd. | Amidine |
| JPS59139357A (ja) * | 1983-01-28 | 1984-08-10 | Torii Yakuhin Kk | アミジン誘導体 |
| US4563527A (en) * | 1984-07-19 | 1986-01-07 | Torii & Co., Ltd. | Amidine compounds |
| ZA928276B (en) * | 1991-10-31 | 1993-05-06 | Daiichi Seiyaku Co | Aromatic amidine derivates and salts thereof. |
-
1995
- 1995-12-01 NZ NZ296210A patent/NZ296210A/en unknown
- 1995-12-01 CN CN95196546A patent/CN1087736C/zh not_active Expired - Fee Related
- 1995-12-01 EP EP95938625A patent/EP0798295B1/en not_active Expired - Lifetime
- 1995-12-01 US US08/849,391 patent/US5869501A/en not_active Expired - Fee Related
- 1995-12-01 MX MX9704059A patent/MX9704059A/es not_active IP Right Cessation
- 1995-12-01 DE DE69529770T patent/DE69529770T2/de not_active Expired - Fee Related
- 1995-12-01 JP JP8518590A patent/JP3004362B2/ja not_active Expired - Fee Related
- 1995-12-01 KR KR1019970703620A patent/KR100383161B1/ko not_active Expired - Fee Related
- 1995-12-01 AU AU39942/95A patent/AU688628B2/en not_active Ceased
- 1995-12-01 RU RU97108576/04A patent/RU2154633C2/ru not_active IP Right Cessation
- 1995-12-01 ES ES95938625T patent/ES2193202T3/es not_active Expired - Lifetime
- 1995-12-01 TW TW084112820A patent/TW300888B/zh active
- 1995-12-01 PL PL95320486A patent/PL184824B1/pl not_active IP Right Cessation
- 1995-12-01 HU HU9702028A patent/HUT77313A/hu unknown
- 1995-12-01 PT PT95938625T patent/PT798295E/pt unknown
- 1995-12-01 WO PCT/JP1995/002458 patent/WO1996016940A1/ja not_active Ceased
- 1995-12-01 CA CA002206532A patent/CA2206532C/en not_active Expired - Fee Related
- 1995-12-01 AT AT95938625T patent/ATE233240T1/de not_active IP Right Cessation
-
1997
- 1997-05-30 NO NO972482A patent/NO309566B1/no not_active IP Right Cessation
- 1997-06-02 FI FI972326A patent/FI115051B/fi not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CA2206532C (en) | 2006-07-11 |
| MX9704059A (es) | 1997-08-30 |
| FI972326A0 (fi) | 1997-06-02 |
| ATE233240T1 (de) | 2003-03-15 |
| DE69529770D1 (de) | 2003-04-03 |
| US5869501A (en) | 1999-02-09 |
| EP0798295A4 (en) | 1998-03-04 |
| CA2206532A1 (en) | 1996-06-06 |
| PL184824B1 (pl) | 2002-12-31 |
| FI115051B (fi) | 2005-02-28 |
| JP3004362B2 (ja) | 2000-01-31 |
| RU2154633C2 (ru) | 2000-08-20 |
| AU688628B2 (en) | 1998-03-12 |
| NZ296210A (en) | 1998-05-27 |
| KR100383161B1 (ko) | 2003-12-24 |
| TW300888B (es) | 1997-03-21 |
| PT798295E (pt) | 2003-07-31 |
| AU3994295A (en) | 1996-06-19 |
| HUT77313A (hu) | 1998-03-30 |
| NO972482D0 (no) | 1997-05-30 |
| EP0798295B1 (en) | 2003-02-26 |
| WO1996016940A1 (en) | 1996-06-06 |
| FI972326A7 (fi) | 1997-06-02 |
| CN1087736C (zh) | 2002-07-17 |
| CN1167484A (zh) | 1997-12-10 |
| PL320486A1 (en) | 1997-09-29 |
| EP0798295A1 (en) | 1997-10-01 |
| DE69529770T2 (de) | 2003-12-24 |
| NO972482L (no) | 1997-08-01 |
| NO309566B1 (no) | 2001-02-19 |
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