MX9704059A - Derivado de amidinonaftilo novedoso o sal del mismo. - Google Patents
Derivado de amidinonaftilo novedoso o sal del mismo.Info
- Publication number
- MX9704059A MX9704059A MX9704059A MX9704059A MX9704059A MX 9704059 A MX9704059 A MX 9704059A MX 9704059 A MX9704059 A MX 9704059A MX 9704059 A MX9704059 A MX 9704059A MX 9704059 A MX9704059 A MX 9704059A
- Authority
- MX
- Mexico
- Prior art keywords
- group
- formula
- represented
- hydrogen atom
- group represented
- Prior art date
Links
- 150000003839 salts Chemical class 0.000 title abstract 3
- -1 amidinonaphthyl Chemical class 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 108010074860 Factor Xa Proteins 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 230000009805 platelet accumulation Effects 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004434 sulfur atom 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)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un derivado de amidinonaftilo representado por la siguiente formula general (I), que tiene una accion inhibidora de la acumulacion de plaquetas basada en la accion inhibidora del factor X de coagulacion sanguínea activado, y es util como un agente contra trombos y similares, una sal del mismo, un intermediario del mismo, y una composicion farmacéutica que comprende al derivado de amidinonaftilo. Un derivado de amidinonaftilo representado por la siguiente formula general (I), o una sal farmacéuticamente aceptable del mismo: (Ver Formula) (los símbolos en la formula tienen los siguientes significados: R1; un átomo de hidrogeno o un grupo representado por la formula -A-W-R4, A: un grupo representado por la formula (Ver Formula) un grupo representado por la formula, o un grupo representado por la formula -SO2-, X: un átomo de oxígeno o un átomo de azufre, W: un enlace sencillo o un grupo representado por la formula -NR5-; R4: un grupo hidroxilo, un grupo alcoxi inferior, etcétera; R5: un átomo de hidrogeno, un grupo carbamoilo, un grupo alcoxi inferior-carbonilo, etcétera; R2: un grupo alquilo inferior, R3: un átomo de hidrogeno, un átomo de halogeno, un grupo carboxilo; B: un grupo alquileno inferior o un grupo carbonilo; y n: 0 o 1.
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP29996394 | 1994-12-02 | ||
| JP10520595 | 1995-04-28 | ||
| JP19881695 | 1995-08-03 | ||
| PCT/JP1995/002458 WO1996016940A1 (en) | 1994-12-02 | 1995-12-01 | Novel amidinonaphthyl derivative or salt thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX9704059A true MX9704059A (es) | 1997-08-30 |
Family
ID=27310425
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX9704059A MX9704059A (es) | 1994-12-02 | 1995-12-01 | Derivado de amidinonaftilo novedoso o sal del mismo. |
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 |
|---|---|---|---|---|
| DK0813525T3 (da) | 1995-03-10 | 2004-02-16 | Berlex Lab | Benzamidinderivater, deres fremstilling og anvendelse som antikoagulanter |
| SE9602646D0 (sv) * | 1996-07-04 | 1996-07-04 | Astra Ab | Pharmaceutically-useful compounds |
| IL128524A0 (en) | 1996-08-15 | 2000-01-31 | Schering Corp | Ether muscarinic antagonists |
| 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 |
| WO1999011617A1 (en) * | 1997-09-01 | 1999-03-11 | 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 |
| EP1048652A4 (en) * | 1997-12-26 | 2001-05-09 | Mochida Pharm Co Ltd | AROMATIC COMPOUNDS WITH A CYCLIC AMINO GROUP OR THEIR SALTS |
| AU2074699A (en) * | 1998-01-26 | 1999-08-09 | 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 |
| ATE272630T1 (de) | 1998-04-10 | 2004-08-15 | Japan Tobacco Inc | Amidin-verbindungen |
| 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 |
| WO2000038683A1 (en) | 1998-12-23 | 2000-07-06 | Du Pont Pharmaceuticals Company | THROMBIN OR FACTOR Xa INHIBITORS |
| US6472393B1 (en) | 1999-01-13 | 2002-10-29 | Genentech, Inc. | Serine protease inhibitors |
| JP4599714B2 (ja) * | 1999-01-22 | 2010-12-15 | アステラス製薬株式会社 | 経口吸収改善医薬用組成物 |
| JP2002538151A (ja) | 1999-03-02 | 2002-11-12 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | カテプシンの可逆的インヒビターとして有用な化合物 |
| 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 |
| CN1572882A (zh) | 1999-10-28 | 2005-02-02 | 三共株式会社 | 苯甲脒衍生物 |
| 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 |
| WO2001064643A2 (en) | 2000-02-29 | 2001-09-07 | Cor Therapeutics, Inc. | BENZAMIDES AND RELATED INHIBITORS OF FACTOR Xa |
| US6548517B2 (en) * | 2000-03-24 | 2003-04-15 | Millennium Pharmaceuticals, 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 |
| AU2001288819A1 (en) | 2000-09-11 | 2002-03-26 | Genentech, Inc. | Amidine inhibitors of serine proteases |
| DE60118774T2 (de) * | 2000-11-22 | 2007-03-15 | Astellas Pharma Inc. | Substituierte phenolderivate und deren salze als hemmstoffe von koagulations faktor x |
| US6710061B2 (en) | 2001-03-09 | 2004-03-23 | Ortho-Mcneil Pharamceutical, Inc. | Aminopyrrolidine sulfonamides as serine protease inhibitors |
| WO2002076945A1 (en) | 2001-03-09 | 2002-10-03 | Ortho-Mcneil Pharmaceutical, 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 |
| KR100922041B1 (ko) * | 2002-01-29 | 2009-10-19 | 라보라토리스 세로노 에스.에이. | 단백질 티로신 포스파타제의 모듈레이터로서의 치환된메틸렌 아미드 유도체 |
| RU2226392C1 (ru) * | 2002-10-23 | 2004-04-10 | Биологический факультет Московского государственного университета им. М.В. Ломоносова | Способ ингибирования агрегации тромбоцитов |
| AU2003284596A1 (en) | 2002-11-22 | 2004-06-18 | Takeda Pharmaceutical Company Limited | Imidazole derivative, process for producing the same, and use |
| AU2003302238A1 (en) | 2002-12-03 | 2004-06-23 | Axys Pharmaceuticals, Inc. | 2-(2-hydroxybiphenyl-3-yl)-1h-benzoimidazole-5-carboxamidine derivatives as factor viia inhibitors |
| JP4601053B2 (ja) * | 2002-12-24 | 2010-12-22 | 第一三共株式会社 | 新規なエチレンジアミン誘導体 |
| WO2004113316A1 (en) | 2003-05-20 | 2004-12-29 | Genentech, Inc. | Benzofuran inhibitors of factor viia |
| JP2007505160A (ja) | 2003-05-20 | 2007-03-08 | ジェネンテック・インコーポレーテッド | 第VIIa因子のアシルスルファミド阻害剤 |
| ATE453626T1 (de) | 2003-10-09 | 2010-01-15 | Millennium Pharm Inc | Thioethersubstituierte benzamide als inhibitoren von faktor xa |
| 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 |
| EP1893572B1 (en) | 2004-06-18 | 2016-12-14 | Millennium Pharmaceuticals, Inc. | Factor xa inhibitors |
| WO2006055951A2 (en) | 2004-11-19 | 2006-05-26 | Portola Pharmaceuticals, Inc. | Tetrahydroisoquinolines as factor xa inhibitors |
| US20060160790A1 (en) * | 2004-12-07 | 2006-07-20 | Portola Pharmaceuticals, Inc. | Thioureas as factor Xa inhibitors |
| WO2006063113A2 (en) | 2004-12-07 | 2006-06-15 | Portola Pharmaceuticals, Inc. | Ureas 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 |
| NZ592533A (en) | 2005-11-08 | 2012-08-31 | Millennium Pharm Inc | METHOD FOR THE PREPARATION OF N-(5-CHLORO-2-PYRIDINYL)-2-[[4-[(DIMETHYLAMINO) IMINOMETHYL] BENZOYL] AMINO]-5-METHOXY-BENZAMIDE, A FACTOR Xa INHIBITOR |
| JP2009531364A (ja) * | 2006-03-28 | 2009-09-03 | ノバルティス アクチエンゲゼルシャフト | アミド誘導体およびgタンパク質関連疾患の処置のためのそれらの使用 |
| EP2072498A4 (en) * | 2006-10-12 | 2012-07-18 | Inst Med Molecular Design Inc | N-PHENYLOXAMIDINSÄUREDERIVAT |
| ES2382055T3 (es) | 2006-11-02 | 2012-06-04 | Millennium Pharmaceuticals, Inc. | Métodos para sintetizar sales farmacéuticas de un inhibidor del factor 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 |
| EP2311810A4 (en) * | 2008-07-11 | 2012-04-04 | Ajinomoto Kk | AMIDINE DERIVATIVE |
| EA015918B1 (ru) | 2010-03-03 | 2011-12-30 | Дмитрий Геннадьевич ТОВБИН | УРЕТАНЫ, МОЧЕВИНЫ, АМИДЫ И РОДСТВЕННЫЕ ИНГИБИТОРЫ ФАКТОРА Xa |
| US11679093B2 (en) | 2018-06-11 | 2023-06-20 | 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 HU HU9702028A patent/HUT77313A/hu unknown
- 1995-12-01 PT PT95938625T patent/PT798295E/pt unknown
- 1995-12-01 TW TW084112820A patent/TW300888B/zh active
- 1995-12-01 AT AT95938625T patent/ATE233240T1/de not_active IP Right Cessation
- 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 CN CN95196546A patent/CN1087736C/zh not_active Expired - Fee Related
- 1995-12-01 AU AU39942/95A patent/AU688628B2/en not_active Ceased
- 1995-12-01 ES ES95938625T patent/ES2193202T3/es not_active Expired - Lifetime
- 1995-12-01 PL PL95320486A patent/PL184824B1/pl not_active IP Right Cessation
- 1995-12-01 NZ NZ296210A patent/NZ296210A/en unknown
- 1995-12-01 RU RU97108576/04A patent/RU2154633C2/ru not_active IP Right Cessation
- 1995-12-01 WO PCT/JP1995/002458 patent/WO1996016940A1/ja not_active Ceased
- 1995-12-01 EP EP95938625A patent/EP0798295B1/en not_active Expired - Lifetime
- 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 DE DE69529770T patent/DE69529770T2/de not_active Expired - Fee Related
- 1995-12-01 CA CA002206532A patent/CA2206532C/en not_active Expired - Fee Related
-
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 |
|---|---|
| FI972326A7 (fi) | 1997-06-02 |
| PL184824B1 (pl) | 2002-12-31 |
| CA2206532A1 (en) | 1996-06-06 |
| CA2206532C (en) | 2006-07-11 |
| ATE233240T1 (de) | 2003-03-15 |
| FI115051B (fi) | 2005-02-28 |
| US5869501A (en) | 1999-02-09 |
| PL320486A1 (en) | 1997-09-29 |
| PT798295E (pt) | 2003-07-31 |
| NZ296210A (en) | 1998-05-27 |
| AU688628B2 (en) | 1998-03-12 |
| EP0798295A1 (en) | 1997-10-01 |
| DE69529770T2 (de) | 2003-12-24 |
| TW300888B (es) | 1997-03-21 |
| RU2154633C2 (ru) | 2000-08-20 |
| FI972326A0 (fi) | 1997-06-02 |
| JP3004362B2 (ja) | 2000-01-31 |
| HUT77313A (hu) | 1998-03-30 |
| EP0798295B1 (en) | 2003-02-26 |
| WO1996016940A1 (en) | 1996-06-06 |
| NO972482L (no) | 1997-08-01 |
| EP0798295A4 (en) | 1998-03-04 |
| NO309566B1 (no) | 2001-02-19 |
| NO972482D0 (no) | 1997-05-30 |
| CN1167484A (zh) | 1997-12-10 |
| KR100383161B1 (ko) | 2003-12-24 |
| AU3994295A (en) | 1996-06-19 |
| CN1087736C (zh) | 2002-07-17 |
| DE69529770D1 (de) | 2003-04-03 |
| ES2193202T3 (es) | 2003-11-01 |
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