ATE121730T1 - N-aryl und n-heteroarylamide und harnstoffderivate als inhibitoren von acyl- coenzym a: cholesterol-acyl-transferase. - Google Patents
N-aryl und n-heteroarylamide und harnstoffderivate als inhibitoren von acyl- coenzym a: cholesterol-acyl-transferase.Info
- Publication number
- ATE121730T1 ATE121730T1 AT90310009T AT90310009T ATE121730T1 AT E121730 T1 ATE121730 T1 AT E121730T1 AT 90310009 T AT90310009 T AT 90310009T AT 90310009 T AT90310009 T AT 90310009T AT E121730 T1 ATE121730 T1 AT E121730T1
- Authority
- AT
- Austria
- Prior art keywords
- acyl
- inhibitors
- coenzyme
- cholesterol
- heteroarylamide
- Prior art date
Links
- 102100030817 Liver carboxylesterase 1 Human genes 0.000 title abstract 2
- 101710181187 Liver carboxylesterase 1 Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical class NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 1
- 230000000879 anti-atherosclerotic effect Effects 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 230000000055 hyoplipidemic effect Effects 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
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- 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
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- C07D213/62—Oxygen or sulfur atoms
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
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- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (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)
- Urology & Nephrology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Furan Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Quinoline Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US1989/004033 WO1991004027A1 (en) | 1989-09-15 | 1989-09-15 | New n-aryl and n-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme a: cholesterol acyl transferase (acat) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE121730T1 true ATE121730T1 (de) | 1995-05-15 |
Family
ID=22215232
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT94200437T ATE177082T1 (de) | 1989-09-15 | 1990-09-13 | N-heteroarylamidederivate als inhibitoren von acyl-coenzym a: cholesterol-acyl-transferase |
| AT90310009T ATE121730T1 (de) | 1989-09-15 | 1990-09-13 | N-aryl und n-heteroarylamide und harnstoffderivate als inhibitoren von acyl- coenzym a: cholesterol-acyl-transferase. |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT94200437T ATE177082T1 (de) | 1989-09-15 | 1990-09-13 | N-heteroarylamidederivate als inhibitoren von acyl-coenzym a: cholesterol-acyl-transferase |
Country Status (24)
| Country | Link |
|---|---|
| EP (2) | EP0418071B1 (de) |
| JP (1) | JPH0825974B2 (de) |
| KR (1) | KR930011303B1 (de) |
| CN (1) | CN1050183A (de) |
| AT (2) | ATE177082T1 (de) |
| AU (1) | AU652345B2 (de) |
| CA (1) | CA2025301C (de) |
| DD (1) | DD298092A5 (de) |
| DE (2) | DE69032981T2 (de) |
| DK (2) | DK0609960T3 (de) |
| EG (1) | EG19358A (de) |
| ES (2) | ES2127878T3 (de) |
| FI (1) | FI111362B (de) |
| GR (1) | GR3029826T3 (de) |
| HU (1) | HUT70027A (de) |
| IE (1) | IE66324B1 (de) |
| IL (3) | IL95610A (de) |
| MX (1) | MX22406A (de) |
| NO (1) | NO904022L (de) |
| NZ (1) | NZ235323A (de) |
| PL (4) | PL165357B1 (de) |
| PT (1) | PT95310B (de) |
| WO (1) | WO1991004027A1 (de) |
| ZA (1) | ZA907346B (de) |
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| US5668136A (en) * | 1990-09-25 | 1997-09-16 | Eisai Co., Ltd. | Trisubstituted benzene derivatives, composition and methods of treatment |
| WO1992009572A1 (en) * | 1990-11-26 | 1992-06-11 | Taisho Pharmaceutical Co., Ltd. | Anilide derivative |
| ES2075685T3 (es) * | 1991-01-31 | 1995-10-01 | Pfizer | Sintesis de intermediarios en la preparacion de inhibidores de acat. |
| FR2674522B1 (fr) * | 1991-03-26 | 1993-07-16 | Lipha | Nouveaux derives de l'indole, procedes de preparation et medicaments les contenant. |
| AU1879792A (en) * | 1991-04-26 | 1992-12-21 | Pfizer Inc. | 4-aryl-3-(heteroarylureido)quinoline derivatives |
| US5124337A (en) * | 1991-05-20 | 1992-06-23 | Schering Corporation | N-acyl-tetrahydroisoquinolines as inhibitors of acyl-coenzyme a:cholesterol acyl transferase |
| US5238935A (en) * | 1991-05-20 | 1993-08-24 | Schering Corporation | N-acyl-tetrahydroisoquinolines as inhibitors of acyl-coenzyme A: cholesterol acyl transferase |
| ES2125325T3 (es) * | 1992-01-23 | 1999-03-01 | Pfizer | Derivados de 4-fenil-3-(heteroarilureido)-1,2-dihidro-2-oxoquinolina como agentes antihipercolesterolemicos y antiateroscleroticos. |
| FR2687402B1 (fr) * | 1992-02-14 | 1995-06-30 | Lipha | Nouveaux azaindoles, procedes de preparation et medicaments les contenant. |
| JPH05320143A (ja) * | 1992-03-18 | 1993-12-03 | Mochida Pharmaceut Co Ltd | 新規ピリミジン誘導体 |
| AU4028393A (en) * | 1992-05-28 | 1993-12-30 | Pfizer Inc. | New (N)-aryl and (N)-heteroarylurea derivatives as inhibitors of acyl coenzyme a:cholesterol acyl transferase (ACAT) |
| ATE159715T1 (de) * | 1992-07-20 | 1997-11-15 | Eisai Co Ltd | Benzolderivate |
| US5239082A (en) * | 1992-08-03 | 1993-08-24 | Warner-Lambert Company | Sulfonamide tetrazole ACAT inhibitors |
| US5565472A (en) * | 1992-12-21 | 1996-10-15 | Pfizer Inc. | 4-aryl-3-(heteroarylureido)-1,2-dihydro-2-oxo-quinoline derivatives as antihypercholesterolemic and antiatherosclerotic agents |
| DE4401893A1 (de) * | 1994-01-24 | 1995-07-27 | Bayer Ag | Substituierte Arylharnstoffe |
| US5491152A (en) * | 1994-03-23 | 1996-02-13 | The Du Pont Merck Pharmaceutical Company | Derivatives of cyclic ethers and sulfides for the treatment of atherosclerosis |
| WO1996002542A1 (en) * | 1994-07-15 | 1996-02-01 | Takeda Chemical Industries, Ltd. | Tricyclic compounds, their production and use |
| US6133326A (en) | 1994-08-31 | 2000-10-17 | Pfizer Inc | Compositions and methods for decreasing sebum production |
| WO1996026925A1 (en) * | 1995-03-01 | 1996-09-06 | Banyu Pharmaceutical Co., Ltd. | Arylthioacetamide derivatives |
| JP4191269B2 (ja) * | 1996-05-17 | 2008-12-03 | 興和株式会社 | 新規なアニリド化合物及びこれを含有する医薬 |
| EP1473292A1 (de) * | 1997-11-03 | 2004-11-03 | Boehringer Ingelheim Pharmaceuticals, Inc. | Aromatische heterocyclische Verbindungen als antiinflammatorische Mittel |
| EP1028953A1 (de) * | 1997-11-03 | 2000-08-23 | Boehringer Ingelheim Pharmaceuticals Inc. | Aromatische heterocyclische verbindungen als antiinflammatorische mittel |
| US6022884A (en) | 1997-11-07 | 2000-02-08 | Amgen Inc. | Substituted pyridine compounds and methods of use |
| WO1999043659A1 (en) * | 1998-02-25 | 1999-09-02 | Sumitomo Pharmaceuticals Co., Ltd. | Pyridone derivatives and process for producing the same |
| US6452008B2 (en) | 1998-02-25 | 2002-09-17 | Sumitomo Pharmaceuticals Company, Limited | Pyridone derivatives and process for preparing the same |
| US6184226B1 (en) | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
| UA73492C2 (en) | 1999-01-19 | 2005-08-15 | Aromatic heterocyclic compounds as antiinflammatory agents | |
| CA2360934A1 (en) | 1999-02-22 | 2000-08-31 | Lin-Hua Zhang | Polycyclo heterocyclic derivatives as antiinflammatory agents |
| ATE278674T1 (de) | 1999-03-12 | 2004-10-15 | Boehringer Ingelheim Pharma | Heterocyklischer harnstoff und verwandte verbindungen als entzündungshemmende mittel |
| JP2002539206A (ja) | 1999-03-12 | 2002-11-19 | 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 | 抗炎症剤としての芳香族複素環化合物 |
| CA2374737C (en) | 1999-07-09 | 2008-02-12 | Boehringer Ingelheim Pharmaceuticals, Inc. | Novel process for synthesis of heteroaryl-substituted urea compounds |
| EP1232150B1 (de) | 1999-11-16 | 2007-10-10 | Boehringer Ingelheim Pharmaceuticals Inc. | Harnstoff derivate als entzündungshemmende mittel |
| US6525046B1 (en) | 2000-01-18 | 2003-02-25 | Boehringer Ingelheim Pharmaceuticals, Inc. | Aromatic heterocyclic compounds as antiinflammatory agents |
| EP1263421B1 (de) | 2000-02-02 | 2005-05-18 | Warner-Lambert Company LLC | Der duale inhibitor der cholesterylester und wachsester synthese avasimibe zur behandlung von erkrankungen des talgdrüse |
| US6608052B2 (en) | 2000-02-16 | 2003-08-19 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compounds useful as anti-inflammatory agents |
| DE10050663A1 (de) † | 2000-10-13 | 2002-04-18 | Gruenenthal Gmbh | Verwendung von substituierten Imidazo[1,2-a]pyridin-, -pyrimidin- und pyrazin-3-yl-amin-Derivaten zur Herstellung von Medikamenten zur NOS-Inhibierung |
| JP2004530690A (ja) | 2001-05-16 | 2004-10-07 | 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 | 抗炎症性薬剤として有用なジアリールウレア誘導体 |
| EP1395561A1 (de) | 2001-05-25 | 2004-03-10 | Boehringer Ingelheim Pharmaceuticals Inc. | Carbamat und oxamid verbindungen als inhibitoren der cytokinproduktion |
| CA2476936A1 (en) * | 2002-02-20 | 2003-08-28 | Chih-Hung Lee | Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (vr1) receptor |
| US7074805B2 (en) * | 2002-02-20 | 2006-07-11 | Abbott Laboratories | Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor |
| EP1480973B1 (de) | 2002-02-25 | 2008-02-13 | Boehringer Ingelheim Pharmaceuticals Inc. | 1,4-disubstituierte benzokondensierte cycloalkyl-harnstoffverbindungen zur behandlung von zytokinvermittelten erkrankungen |
| AU2003243921B2 (en) | 2002-06-27 | 2009-05-07 | Novo Nordisk A/S | Aryl carbonyl derivatives as therapeutic agents |
| WO2004007459A2 (en) * | 2002-07-12 | 2004-01-22 | Janssen Pharmaceutica N.V. | Naphthol, quinoline and isoquinoline-derivatives as modulators of vanilloid vr1 receptor |
| US6933311B2 (en) | 2003-02-11 | 2005-08-23 | Abbott Laboratories | Fused azabicyclic compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor |
| AU2004298486A1 (en) | 2003-12-12 | 2005-06-30 | Wyeth | Quinolines useful in treating cardiovascular disease |
| BRPI0506662B8 (pt) | 2004-01-06 | 2021-05-25 | Novo Nordisk As | compostos ativadores de glucoquinase |
| KR20080095915A (ko) | 2004-05-06 | 2008-10-29 | 워너-램버트 캄파니 엘엘씨 | 4-페닐아미노-퀴나졸린-6-일-아미드 |
| JPWO2006003974A1 (ja) | 2004-06-30 | 2008-04-17 | 興和株式会社 | 環状ジアミン誘導体の製造法 |
| JP2009500377A (ja) | 2005-07-08 | 2009-01-08 | ノボ・ノルデイスク・エー/エス | ジシクロアルキルウレア型グルコキナーゼ活性化剤 |
| EP1904438B1 (de) | 2005-07-08 | 2012-02-29 | Novo Nordisk A/S | Dicycloalkylcarbamoyl-harnstoffe als glucokinase-aktivatoren |
| EP1904467B1 (de) | 2005-07-14 | 2013-05-01 | Novo Nordisk A/S | Harnstoff-Glucokinase-Aktivatoren |
| AU2006286654A1 (en) | 2005-07-27 | 2007-03-08 | F. Hoffmann-La Roche Ag | 4-aryloxy quinoline derivatives as 5-HT6 modulators |
| US7592461B2 (en) | 2005-12-21 | 2009-09-22 | Bristol-Myers Squibb Company | Indane modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof |
| CA2661898A1 (en) | 2006-08-25 | 2008-02-28 | Abbott Laboratories | Indazole derivatives that inhibit trpv1 and uses thereof |
| US7928123B2 (en) * | 2006-09-25 | 2011-04-19 | Boehringer Ingelheim International Gmbh | Compounds which modulate the CB2 receptor |
| CA2672196A1 (en) | 2006-12-20 | 2008-07-03 | Abbott Laboratories | Antagonists of the trpv1 receptor and uses thereof |
| EP2118083A1 (de) | 2007-01-09 | 2009-11-18 | Novo Nordisk A/S | Harnstoff-Glucokinase-Aktivatoren |
| JP5226008B2 (ja) | 2007-01-11 | 2013-07-03 | ノボ・ノルデイスク・エー/エス | ウレアグルコキナーゼアクチベーター |
| EP2489660A1 (de) | 2008-03-20 | 2012-08-22 | Abbott Laboratories | Verfahren zum Herstellen von Mitteln für das zentrale Nervensystem, die TRPV1-Antagonisten sind |
| JP5788404B2 (ja) | 2009-12-11 | 2015-09-30 | アウトイフオンイ トヘラペウトイクス リミテッド | イミダゾリジンジオン誘導体 |
| EP2649066B1 (de) | 2010-12-06 | 2015-10-21 | Autifony Therapeutics Limited | Hydantoin-derivate als kv3-inhibitoren |
| US9193704B2 (en) | 2011-06-07 | 2015-11-24 | Autifony Therapeutics Limited | Hydantoin derivatives as KV3 inhibitors |
| EP2852588B8 (de) | 2012-05-22 | 2018-01-10 | Autifony Therapeutics Limited | Hydantoinderivate als kv3-inhibitoren |
| US9422252B2 (en) | 2012-05-22 | 2016-08-23 | Autifony Therapeutics Limited | Triazoles as Kv3 inhibitors |
| CN112040945A (zh) | 2018-06-12 | 2020-12-04 | Vtv治疗有限责任公司 | 葡萄糖激酶激活剂与胰岛素或胰岛素类似物组合的治疗用途 |
| CN109553591B (zh) * | 2019-01-15 | 2020-12-15 | 山东安信制药有限公司 | 一种富马酸喹硫平中间体的制备方法 |
| GB201919213D0 (en) * | 2019-12-23 | 2020-02-05 | Ucb Biopharma Sprl | Dihydrocyclopenta-Isoquinoline-Sulfanamide derivatives compounds |
| US12391658B2 (en) | 2020-02-18 | 2025-08-19 | Vtv Therapeutics Llc | Sulfoxide and sulfone glucokinase activators and methods of use thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| NL125255C (de) * | 1964-07-31 | |||
| US3555035A (en) * | 1966-01-28 | 1971-01-12 | Geigy Chem Corp | N-(substituted pyridyl) linolamides and -linolenamides |
| CH500980A (de) * | 1966-01-28 | 1970-12-31 | Ciba Geigy Ag | Verfahren zur Herstellung von neuen Amiden aliphatischer Carbonsäuren |
| CH491112A (de) * | 1966-01-28 | 1970-05-31 | Geigy Ag J R | Verfahren zur Herstellung von neuen Amiden aliphatischer Carbonsäuren |
| US5142056A (en) * | 1989-05-23 | 1992-08-25 | Abbott Laboratories | Retroviral protease inhibiting compounds |
| US4722927A (en) * | 1986-04-28 | 1988-02-02 | Warner-Lambert Company | Pyrimidine amides of oleic or linoleic acid, composition containing them and their use as inhibitors of acyl-CoA cholesterol acyltransferase |
| US4716175A (en) * | 1987-02-24 | 1987-12-29 | Warner-Lambert Company | Saturated fatty acid amides as inhibitors of acyl-CoA:cholesterol acyltransferase |
| US5238908A (en) * | 1989-08-31 | 1993-08-24 | Rohm And Haas Company | Herbicidal glutaramic acids and derivatives |
| DE3929507A1 (de) * | 1989-09-06 | 1991-03-07 | Bayer Ag | Substituierte amino-pyridine |
| WO1991004027A1 (en) * | 1989-09-15 | 1991-04-04 | Pfizer Inc. | New n-aryl and n-heteroarylamide and urea derivatives as inhibitors of acyl coenzyme a: cholesterol acyl transferase (acat) |
-
1989
- 1989-09-15 WO PCT/US1989/004033 patent/WO1991004027A1/en not_active Ceased
- 1989-09-15 MX MX2240690A patent/MX22406A/es unknown
-
1990
- 1990-09-07 IL IL9561090A patent/IL95610A/en not_active IP Right Cessation
- 1990-09-13 DK DK94200437T patent/DK0609960T3/da active
- 1990-09-13 EP EP90310009A patent/EP0418071B1/de not_active Expired - Lifetime
- 1990-09-13 DK DK90310009.7T patent/DK0418071T3/da active
- 1990-09-13 EP EP94200437A patent/EP0609960B1/de not_active Expired - Lifetime
- 1990-09-13 AT AT94200437T patent/ATE177082T1/de not_active IP Right Cessation
- 1990-09-13 CA CA002025301A patent/CA2025301C/en not_active Expired - Fee Related
- 1990-09-13 DE DE69032981T patent/DE69032981T2/de not_active Expired - Fee Related
- 1990-09-13 EG EG54590A patent/EG19358A/xx active
- 1990-09-13 DE DE69018908T patent/DE69018908T2/de not_active Expired - Fee Related
- 1990-09-13 AT AT90310009T patent/ATE121730T1/de not_active IP Right Cessation
- 1990-09-13 ES ES94200437T patent/ES2127878T3/es not_active Expired - Lifetime
- 1990-09-13 PT PT95310A patent/PT95310B/pt not_active IP Right Cessation
- 1990-09-13 ES ES90310009T patent/ES2071033T3/es not_active Expired - Lifetime
- 1990-09-14 PL PL90291470A patent/PL165357B1/pl unknown
- 1990-09-14 CN CN90108294A patent/CN1050183A/zh active Pending
- 1990-09-14 HU HU9302945A patent/HUT70027A/hu unknown
- 1990-09-14 PL PL29147290A patent/PL291472A1/xx unknown
- 1990-09-14 FI FI904537A patent/FI111362B/fi active IP Right Grant
- 1990-09-14 IE IE333690A patent/IE66324B1/en not_active IP Right Cessation
- 1990-09-14 AU AU62553/90A patent/AU652345B2/en not_active Ceased
- 1990-09-14 JP JP2245969A patent/JPH0825974B2/ja not_active Expired - Fee Related
- 1990-09-14 ZA ZA907346A patent/ZA907346B/xx unknown
- 1990-09-14 PL PL90286899A patent/PL165370B1/pl unknown
- 1990-09-14 NZ NZ235323A patent/NZ235323A/xx unknown
- 1990-09-14 KR KR1019900014554A patent/KR930011303B1/ko not_active Expired - Fee Related
- 1990-09-14 NO NO90904022A patent/NO904022L/no unknown
- 1990-09-14 PL PL29147190A patent/PL291471A1/xx unknown
- 1990-09-27 DD DD90343971A patent/DD298092A5/de not_active IP Right Cessation
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1994
- 1994-07-14 IL IL11032194A patent/IL110321A0/xx unknown
- 1994-07-14 IL IL11032494A patent/IL110324A0/xx unknown
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1999
- 1999-03-30 GR GR990400917T patent/GR3029826T3/el unknown
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| Date | Code | Title | Description |
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| UEP | Publication of translation of european patent specification | ||
| REN | Ceased due to non-payment of the annual fee |