IL116122A - Intermediates for the history of 0-cyclic heterocyclic amines - Google Patents

Intermediates for the history of 0-cyclic heterocyclic amines

Info

Publication number
IL116122A
IL116122A IL11612292A IL11612292A IL116122A IL 116122 A IL116122 A IL 116122A IL 11612292 A IL11612292 A IL 11612292A IL 11612292 A IL11612292 A IL 11612292A IL 116122 A IL116122 A IL 116122A
Authority
IL
Israel
Prior art keywords
mmol
formula
phenyl
alkyl
ethyl
Prior art date
Application number
IL11612292A
Other languages
English (en)
Hebrew (he)
Original Assignee
Eisai Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Eisai Co Ltd filed Critical Eisai Co Ltd
Publication of IL116122A publication Critical patent/IL116122A/en

Links

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
    • C07D401/06—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 carbon chain containing only aliphatic carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07D211/08—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/30—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
    • C07D211/32—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 hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/20—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Neurosurgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Neurology (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
IL11612292A 1991-03-28 1992-03-22 Intermediates for the history of 0-cyclic heterocyclic amines IL116122A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US67691891A 1991-03-28 1991-03-28
IL101327A IL101327A (en) 1991-03-28 1992-03-22 HISTORY OF TROCCYLIC-CYCLE AMINES AND PHARMACEUTICAL PREPARATIONS CONTAINING THEM

Publications (1)

Publication Number Publication Date
IL116122A true IL116122A (en) 1998-10-30

Family

ID=24716559

Family Applications (3)

Application Number Title Priority Date Filing Date
IL11612295A IL116122A0 (en) 1991-03-28 1992-03-22 Intermediates to heterocyclic-cyclic amine derivatives
IL11612292A IL116122A (en) 1991-03-28 1992-03-22 Intermediates for the history of 0-cyclic heterocyclic amines
IL101327A IL101327A (en) 1991-03-28 1992-03-22 HISTORY OF TROCCYLIC-CYCLE AMINES AND PHARMACEUTICAL PREPARATIONS CONTAINING THEM

Family Applications Before (1)

Application Number Title Priority Date Filing Date
IL11612295A IL116122A0 (en) 1991-03-28 1992-03-22 Intermediates to heterocyclic-cyclic amine derivatives

Family Applications After (1)

Application Number Title Priority Date Filing Date
IL101327A IL101327A (en) 1991-03-28 1992-03-22 HISTORY OF TROCCYLIC-CYCLE AMINES AND PHARMACEUTICAL PREPARATIONS CONTAINING THEM

Country Status (29)

Country Link
EP (1) EP0646115B1 (fr)
JP (3) JP2659107B2 (fr)
KR (1) KR0179054B1 (fr)
CN (1) CN1044242C (fr)
AT (1) ATE231505T1 (fr)
AU (2) AU658194B2 (fr)
BR (1) BR9205811A (fr)
CA (2) CA2107105C (fr)
CZ (1) CZ289756B6 (fr)
DE (1) DE69232907T2 (fr)
DK (1) DK0646115T3 (fr)
EG (1) EG20281A (fr)
ES (1) ES2188584T3 (fr)
FI (1) FI934223A (fr)
HU (1) HU225047B1 (fr)
IE (1) IE920980A1 (fr)
IL (3) IL116122A0 (fr)
MX (1) MX9201419A (fr)
MY (1) MY108885A (fr)
NO (1) NO304071B1 (fr)
NZ (3) NZ250987A (fr)
PL (3) PL170567B1 (fr)
PT (1) PT100300B (fr)
RU (1) RU2119920C1 (fr)
SG (1) SG49055A1 (fr)
UA (1) UA45944C2 (fr)
WO (1) WO1992017475A1 (fr)
YU (1) YU31392A (fr)
ZA (1) ZA922239B (fr)

Families Citing this family (47)

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US5750542A (en) * 1993-09-28 1998-05-12 Pfizer Benzisoxazole and benzisothizole derivatives as cholinesterase inhibitors
CA2116117A1 (fr) * 1991-08-22 1993-03-04 Hiroyuki Sueoka Compose de type benzisoxazole et son utilisation
EP0535496A1 (fr) * 1991-09-25 1993-04-07 Hoechst-Roussel Pharmaceuticals Incorporated (1-Indanon-2-yl)méthylpipéridines, produits intermédiaires et procédé pour leur préparation et leur utilisation comme médicaments
US5494908A (en) * 1992-11-23 1996-02-27 Hoechst-Roussel Pharmaceutical Incorporated Substituted 3-(aminoalkylamino)-1,2-benzisoxazoles and related compounds
JP3462501B2 (ja) * 1992-11-23 2003-11-05 アベンティス・ファーマスーティカルズ・インコーポレイテツド 置換された３−（アミノアルキルアミノ）−１，２−ベンゾイソキサゾールおよび関連化合物
GB9305623D0 (en) * 1993-03-18 1993-05-05 Merck Sharp & Dohme Therapeutic agents
ES2214506T3 (es) * 1994-10-26 2004-09-16 Pfizer Inc. Procedimientos y compuestos intermedios para la preparacion de 5,7-dihidro-3-(2-(1-bencilpiperidin-4-il)etil)-6h-pirrolo-(4,5-f)-1,2-bencisoxazol-6-ona.
EP0809642A1 (fr) * 1995-02-15 1997-12-03 PHARMACIA & UPJOHN COMPANY Imidazo 1,2-a]pyridines pour le traitement du snc et de cardiopathologies
JP3884477B2 (ja) * 1995-03-22 2007-02-21 大正製薬株式会社 チアゾール誘導体
HUP9802492A3 (en) * 1995-06-06 1999-10-28 Hoechst Marion Roussel Inc Cin Benzisoxazole and indazole derivatives as antipsychotic agents, process for their preparation and pharmaceutical compositions containing the same
JPH09124643A (ja) * 1995-08-14 1997-05-13 Bristol Myers Squibb Co 抗うつ作用を有する１−アリールアルキル−４−（アルコキシピリジニル）−又は４−（アルコキシピリミジニル）ピペラジン誘導体
US5916902A (en) * 1995-09-13 1999-06-29 Pfizer Inc. Processes and intermediates for preparing 5, 7-dihydro-3- 2-(1-benzylpiperidin-4-yl)ethyl-!6H-pyrrolo- 4, 5-F!-1, 2-benzisoxazol-6-one
US5998415A (en) * 1995-11-02 1999-12-07 Merck Sharp & Dohme Ltd. Bicyclic heteroaryl-alkylene-(homo)piperazinones and thione analogues thereof, their preparation, and their use of as selective agonists of 5-HT1 -like receptors
FR2751412B3 (fr) * 1996-07-17 1998-09-25 Valbiofrance Methodes de diagnostic in vitro de maladies neurodegeneratives et trousses pour la mise en oeuvre de ces methodes
US6013654A (en) * 1997-08-14 2000-01-11 Pharmacia & Upjohn Company Imidazo[1,2-A]pyridines for the treatment of CNS and cardiac diseases
EP0976404A3 (fr) * 1998-07-30 2001-06-27 Pfizer Products Inc. Compositions pharmaceutiques pour la prévention et la therapie de troubles cognitifes chez les mammifères
CN1572299A (zh) 1998-09-30 2005-02-02 武田药品工业株式会社 改善膀胱排泄能力的药物
US6951873B1 (en) 1999-04-27 2005-10-04 Pfizer Inc. Methods for treating age-related behavioral disorders in companion animals
EP1050303A3 (fr) * 1999-04-27 2003-01-15 Pfizer Products Inc. Methodes et compositions pour le traitement des troubles du comportement liées à l'age des animaux de compagnie
EP1048302A3 (fr) * 1999-04-30 2002-07-17 Pfizer Products Inc. Traceurs radioactifs pour étude de l'acétylcholinesterase et la maladie de Alzheimer
GB9914486D0 (en) 1999-06-21 1999-08-18 Smithkline Beecham Plc Medicaments
GB9917406D0 (en) 1999-07-23 1999-09-22 Smithkline Beecham Plc Compounds
GB9917408D0 (en) 1999-07-23 1999-09-22 Smithkline Beecham Plc Compounds
CA2382117C (fr) 1999-09-01 2009-11-10 Eisai Co., Ltd. Compose de piperidine 4-substituee
EP1300395B1 (fr) 2000-06-21 2009-09-02 Eisai R&D Management Co., Ltd. Compose piperidine 4-substitue
EP1609783A1 (fr) * 2004-06-17 2005-12-28 Neuropharma S.A.U. Composes marines bloquant les canaux calciques pur le traitement de la maladie de alzheimer
DE102005038947A1 (de) * 2005-05-18 2006-11-30 Grünenthal GmbH Substituierte Benzo[d]isoxazol-3-yl-amin-Verbindungen und deren Verwendung in Arzneimitteln
EP1907384A2 (fr) * 2005-06-30 2008-04-09 Prosidion Limited Agonistes de gpcr
GB0519879D0 (en) 2005-09-30 2005-11-09 Astrazeneca Ab Chemical process
JPWO2007126041A1 (ja) 2006-04-28 2009-09-10 エーザイ・アール・アンド・ディー・マネジメント株式会社 ベンゾイソオキサゾール化合物
AU2008263206A1 (en) 2007-06-01 2008-12-18 Schering Corporation Gamma secretase modulators
US8008327B2 (en) 2008-04-29 2011-08-30 Boehringer Ingelheim International Gmbh Indazole compounds as CCR1 receptor antagonists
CA2722811C (fr) 2008-05-06 2016-07-05 Boehringer Ingelheim International Gmbh Composes de pyrazole comme antagonistes de ccr1
CN102227425A (zh) 2008-09-26 2011-10-26 贝林格尔·英格海姆国际有限公司 作为ccr1受体拮抗剂的氮杂吲唑化合物
MX2011005905A (es) * 2008-12-12 2011-06-20 Actelion Pharmaceuticals Ltd Derivados de 5-amino-2-(1-hidroxi-etil)-tetrahidropirano.
RS53130B (en) 2009-10-21 2014-06-30 Boehringer Ingelheim International Gmbh INDASOL AND PYRAZOLOPYRIDINE COMPOUNDS AS CCR1 RECEPTOR ANTAGONISTS
EP2493875B1 (fr) 2009-10-27 2014-08-06 Boehringer Ingelheim International GmbH Composés hétérocycliques utilisés en tant qu'antagonistes des récepteurs ccr1
EP2533645B1 (fr) 2010-02-09 2016-07-27 The Johns Hopkins University Procédés et compositions pour améliorer la fonction cognitive
US8871786B2 (en) 2010-04-30 2014-10-28 Boehringer Ingelheim International Gmbh Azaindazole amide compounds as CCR1 receptor antagonists
WO2012087782A1 (fr) 2010-12-23 2012-06-28 Boehringer Ingelheim International Gmbh Composés de pyrazolopipéridine en tant qu'antagonistes de récepteur ccr1
EP2919788A4 (fr) 2012-11-14 2016-05-25 Univ Johns Hopkins Méthodes et compositions pour le traitement de la schizophrénie
CA2890861C (fr) 2012-11-21 2021-03-30 Raqualia Pharma Inc. Formes polymorphiques de 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazole -3-yl]oxy}methyl)piperidin-1-yl]methyl}-tetrahydro-2h-pyran-4-acide_carboxylique
EP2968237A4 (fr) 2013-03-15 2016-08-31 Univ Johns Hopkins Procédés et compositions pour améliorer la fonction cognitive
DK2968220T3 (da) 2013-03-15 2021-06-14 Agenebio Inc Fremgangsmåder og sammensætninger til forbedring af kognitiv funktion
BR112017025031B1 (pt) 2015-05-22 2023-03-21 Agenebio, Inc Composições farmacêuticas de liberação prolongada de levetiracetam
RU2638155C1 (ru) * 2016-02-29 2017-12-12 Общество С Ограниченной Ответственностью "Сай Фарма" Производные бензо[d]изоксазола и их применение
AU2022325367A1 (en) * 2021-08-10 2024-02-08 Jiangsu Hengrui Pharmaceuticals Co., Ltd. Sulfonamide derivative, preparation method therefor and medical use thereof

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JPS63234065A (ja) * 1987-03-23 1988-09-29 Mitsubishi Rayon Co Ltd 包接能を有する高分子組成物
JPH0657707B2 (ja) * 1987-05-25 1994-08-03 吉富製薬株式会社 ピペリジン化合物
FI95572C (fi) * 1987-06-22 1996-02-26 Eisai Co Ltd Menetelmä lääkeaineena käyttökelpoisen piperidiinijohdannaisten tai sen farmaseuttisen suolan valmistamiseksi
US4980365A (en) * 1987-07-13 1990-12-25 Hoechst-Roussel Pharmaceuticals Inc. N-substituted-5,6-dimethoxy-1,2-benzisoxazole-3-propanamine and related compounds as analgesic and hypotensive agents
ZA891113B (en) * 1988-02-19 1990-10-31 Lilly Co Eli Tetrazole excitatory amino acid receptor antagonists
JPH0283375A (ja) * 1988-09-21 1990-03-23 Dainippon Pharmaceut Co Ltd ２−置換ピペラジニル−２−（１，２−ベンズイソキサゾール−３−イル）酢酸誘導体
FR2654104B1 (fr) * 1989-11-07 1992-01-03 Adir Nouveaux derives du 1,2-benzisoxazole, leurs procedes de preparation et les compositions pharmaceutiques qui les contiennent.
CA2105666C (fr) * 1991-04-17 2006-02-14 Kjell Anders Ivan Svensson Nouveaux phenylazacycloalcanes substitues, a action centrale

Also Published As

Publication number Publication date
JP3051076B2 (ja) 2000-06-12
WO1992017475A1 (fr) 1992-10-15
CN1044242C (zh) 1999-07-21
PL171915B1 (pl) 1997-06-30
CA2107105C (fr) 2003-10-07
CZ289756B6 (cs) 2002-04-17
ES2188584T3 (es) 2003-07-01
IE920980A1 (en) 1992-10-07
CZ395892A3 (en) 1994-04-13
IL101327A (en) 1998-06-15
IL116122A0 (en) 1996-01-31
HU225047B1 (en) 2006-05-29
PL170567B1 (pl) 1997-01-31
JP2000154185A (ja) 2000-06-06
IL101327A0 (en) 1992-11-15
DE69232907T2 (de) 2003-05-15
YU31392A (sh) 1994-12-28
AU1878292A (en) 1992-11-02
BR9205811A (pt) 1994-06-28
CA2195129C (fr) 2002-09-10
EP0646115B1 (fr) 2003-01-22
PT100300A (pt) 1993-08-31
PT100300B (pt) 1999-09-30
HU9302733D0 (en) 1993-12-28
NZ250987A (en) 1997-06-24
RU2119920C1 (ru) 1998-10-10
JP2659107B2 (ja) 1997-09-30
DK0646115T3 (da) 2003-04-22
PL171914B1 (pl) 1997-06-30
DE69232907D1 (de) 2003-02-27
ATE231505T1 (de) 2003-02-15
AU674477B2 (en) 1996-12-19
ZA922239B (en) 1993-09-27
EP0646115A1 (fr) 1995-04-05
MY108885A (en) 1996-11-30
HUT68357A (en) 1995-06-28
NZ248946A (en) 1995-04-27
FI934223A0 (fi) 1993-09-27
JPH10158264A (ja) 1998-06-16
NO933445D0 (no) 1993-09-27
CN1065267A (zh) 1992-10-14
UA45944C2 (uk) 2002-05-15
MX9201419A (es) 1992-10-01
JPH06500794A (ja) 1994-01-27
CA2195129A1 (fr) 1992-09-29
NO933445L (no) 1993-09-27
NZ242151A (en) 1994-10-26
AU658194B2 (en) 1995-04-06
CA2107105A1 (fr) 1992-09-29
FI934223A (fi) 1993-09-27
AU2178895A (en) 1995-09-07
KR0179054B1 (en) 1999-03-20
EG20281A (en) 1998-07-30
NO304071B1 (no) 1998-10-19
SG49055A1 (en) 1998-05-18

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