MA19672A1 - Procede de preparation de nouveaux derives d'acides amines bicycliques - Google Patents

Procede de preparation de nouveaux derives d'acides amines bicycliques

Info

Publication number
MA19672A1
MA19672A1 MA19890A MA19890A MA19672A1 MA 19672 A1 MA19672 A1 MA 19672A1 MA 19890 A MA19890 A MA 19890A MA 19890 A MA19890 A MA 19890A MA 19672 A1 MA19672 A1 MA 19672A1
Authority
MA
Morocco
Prior art keywords
preparation
amino acid
acid derivatives
bicyclic amino
new bicyclic
Prior art date
Application number
MA19890A
Other languages
English (en)
Original Assignee
Hoechst Ag
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=25798350&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA19672(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from DE19813151690 external-priority patent/DE3151690A1/de
Priority claimed from DE19823210701 external-priority patent/DE3210701A1/de
Application filed by Hoechst Ag filed Critical Hoechst Ag
Publication of MA19672A1 publication Critical patent/MA19672A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02—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
    • 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
    • C07D215/20—Oxygen atoms
    • C07D215/22—Oxygen atoms attached in position 2 or 4
    • C07D215/227—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 2
    • 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
    • A61P7/10—Antioedematous agents; Diuretics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/08—Indoles; Hydrogenated indoles with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to carbon atoms of the hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32—Oxygen atoms
    • C07D209/34—Oxygen atoms in position 2
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
    • C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/52—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/02—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link
    • C07K5/022—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -X-C(=O)-(C)n-N-C-C(=O)-Y-; X and Y being heteroatoms; n being 1 or 2
    • C07K5/0222—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing at least one abnormal peptide link containing the structure -X-C(=O)-(C)n-N-C-C(=O)-Y-; X and Y being heteroatoms; n being 1 or 2 with the first amino acid being heterocyclic, e.g. Pro, Trp
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Cardiology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Hematology (AREA)
  • Diabetes (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Peptides Or Proteins (AREA)
  • Indole Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
MA19890A 1981-12-29 1982-12-27 Procede de preparation de nouveaux derives d'acides amines bicycliques MA19672A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19813151690 DE3151690A1 (de) 1981-12-29 1981-12-29 "neue derivate bicyclischer aminosaeuren, verfahren zu ihrer herstellung, diese enthaltende mittel und deren verwendung sowie neue bicyclische aminosaeuren als zwischenstufen und verfahren zu deren herstellung"
DE19823210701 DE3210701A1 (de) 1982-03-24 1982-03-24 2-azabicycloalkan-3-carbonsaeuren und verfahren zu ihrer herstellung

Publications (1)

Publication Number Publication Date
MA19672A1 true MA19672A1 (fr) 1983-07-01

Family

ID=25798350

Family Applications (1)

Application Number Title Priority Date Filing Date
MA19890A MA19672A1 (fr) 1981-12-29 1982-12-27 Procede de preparation de nouveaux derives d'acides amines bicycliques

Country Status (27)

Country Link
US (3) US5008400A (fr)
EP (1) EP0084164B1 (fr)
JP (3) JPS58118569A (fr)
KR (1) KR890003424B1 (fr)
AR (1) AR247571A1 (fr)
AU (1) AU559140B2 (fr)
BG (1) BG60936B2 (fr)
CA (1) CA1341296C (fr)
CS (1) CS409591A3 (fr)
DE (2) DE3275293D1 (fr)
DK (2) DK170444B1 (fr)
DZ (1) DZ490A1 (fr)
ES (2) ES518574A0 (fr)
FI (1) FI80017C (fr)
GR (1) GR78413B (fr)
HK (1) HK74989A (fr)
HU (1) HU194167B (fr)
IE (1) IE55867B1 (fr)
IL (1) IL67572A (fr)
LU (1) LU88263I2 (fr)
MA (1) MA19672A1 (fr)
NL (1) NL930048I2 (fr)
NO (1) NO156786C (fr)
NZ (1) NZ202903A (fr)
PH (2) PH18918A (fr)
PT (1) PT76052B (fr)
SG (1) SG1389G (fr)

Families Citing this family (69)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LU88621I2 (fr) * 1980-10-23 1995-09-01 Schering Corp Sandopril
GR78413B (fr) * 1981-12-29 1984-09-27 Hoechst Ag
DE3246503A1 (de) * 1982-12-16 1984-06-20 Hoechst Ag, 6230 Frankfurt Derivate der cis, endo-2-azabicyclo-(5.3.0)-decan-3-carbonsaeure, verfahren zu ihrer herstellung, diese enthaltende mittel und deren verwendung
FI841052A (fi) * 1983-03-16 1984-09-17 Usv Pharma Corp Foereningar foer behandling av blodtryckssjukdomar.
DE3324263A1 (de) * 1983-07-06 1985-01-17 Hoechst Ag, 6230 Frankfurt Derivate der 2-azabicyclo(3.1.0)hexan-3-carbonsaeure, verfahren zu ihrer herstellung, diese enthaltende mittel und deren verwendung sowie 2-azabicyclo(3.1.0)hexan-derivate als zwischenprodukte und verfahren zu deren herstellung
DE3410732A1 (de) * 1984-03-23 1985-09-26 Hoechst Ag, 6230 Frankfurt Methode zur behandlung des glaukoms
DE3413710A1 (de) * 1984-04-12 1985-10-24 Hoechst Ag, 6230 Frankfurt Verfahren zur behandlung der herzinsuffizienz
US5684016A (en) * 1984-04-12 1997-11-04 Hoechst Aktiengesellschaft Method of treating cardiac insufficiency
EP0190224A1 (fr) * 1984-07-30 1986-08-13 Schering Corporation PROCEDE POUR LA PREPARATION DE CIS, ENDO-OCTAHYDROCYCLOPENTA [b] PYRROLE-2-CARBOXYLATE
GB8422165D0 (en) * 1984-09-01 1984-10-03 Wellcome Found Compounds
US5231084A (en) * 1986-03-27 1993-07-27 Hoechst Aktiengesellschaft Compounds having a cognition adjuvant action, agents containing them, and the use thereof for the treatment and prophylaxis of cognitive dysfuncitons
FR2605630B1 (fr) * 1986-10-22 1989-06-30 Roussel Uclaf Procede de preparation de derives de l'octahydroindole et intermediaires de preparation
DE3641451A1 (de) * 1986-12-04 1988-06-16 Hoechst Ag Derivate bicyclischer aminocarbonsaeuren, verfahren und zwischenprodukte zu deren herstellung sowie deren verwendung
DE3722007A1 (de) * 1987-07-03 1989-01-12 Hoechst Ag Verfahren zur herstellung bicyclischer aminocarbonsaeuren, zwischenprodukte dieses verfahrens und deren verwendung
TW197945B (fr) * 1990-11-27 1993-01-11 Hoechst Ag
DE4109134A1 (de) * 1991-03-20 1992-09-24 Knoll Ag Erzeugnisse, enthaltend verapamil und trandolapril
LT3872B (en) 1993-12-06 1996-04-25 Hoechst Ag Novel peptides and pharmaceutical compositions containing them
US5602167A (en) * 1995-05-17 1997-02-11 Ortho Pharmaceutical Corporation 4-arylcyclohepta[c] pyrrole analgesics
EP0796855B1 (fr) 1996-03-20 2002-02-06 Hoechst Aktiengesellschaft Inhibiteurs de la résorption osseuse et antagonistes du récepteur de la vitronectine
FR2746394B1 (fr) 1996-03-20 1998-05-29 Roussel Uclaf Nouveaux composes tricycliques, leur procede de preparation, et les intermediaires de ce procede, leur application a titre de medicaments et les compositions pharmaceutiques les renfermant
DE19653647A1 (de) 1996-12-20 1998-06-25 Hoechst Ag Vitronectin - Rezeptorantagonisten, deren Herstellung sowie deren Verwendung
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DE19741235A1 (de) 1997-09-18 1999-03-25 Hoechst Marion Roussel De Gmbh Neue Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate
DE19741873A1 (de) * 1997-09-23 1999-03-25 Hoechst Marion Roussel De Gmbh Neue 5-Ring-Heterocyclen, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate
DE19751251A1 (de) 1997-11-19 1999-05-20 Hoechst Marion Roussel De Gmbh Substituierte Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmezeutische Präparate
DE19821483A1 (de) 1998-05-14 1999-11-18 Hoechst Marion Roussel De Gmbh Imidazolidinderivate, ihre Herstellung, ihre Verwendung und sie enthaltende pharmazeutische Präparate
DE19900205A1 (de) * 1999-01-07 2000-07-13 Basf Ag Verfahren zur Herstellung von (2S,4R,9S)-Octahydro-1H-indol-2-carbonsäure und Zwischenprodukte dafür
CA2363658C (fr) * 2001-11-21 2005-12-13 Brantford Chemicals Inc. Methode amelioree de preparation du ramipril
WO2003074048A1 (fr) * 2002-03-01 2003-09-12 Warner-Lambert Company Llc Methode de traitement de l'osteoarthrite
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PT1403277E (pt) * 2003-02-28 2005-11-30 Servier Lab Novo processo de sintese de derivados do acido (2s, 3as, 7as)-1-((s)-alanil)-octa-hidro-1h-indole-2-carboxilico e aplicacao a sintese do perindopril
DK1319668T3 (da) * 2003-03-12 2005-02-14 Servier Lab Fremgangsmåde til syntese af (2S, 3aS, 7aS)-1-((S)-alanyl)-octahydro-1H-indol-2-carboxylsyrederivater og anvendelse heraf ved syntese af perindopril
ATE294814T1 (de) * 2003-03-12 2005-05-15 Servier Lab Verfahren für die synthese von perindopril und seiner pharmazeutischen annehmbaren salzen
EP1323729B1 (fr) * 2003-03-12 2004-11-03 Les Laboratoires Servier Nouveau procédé de synthèse de l'acide (2S, 3aS, 7aS)-perhydroindole-2-carboxylique et de ses esters, et application à la synthèse du perindopril
CL2004000544A1 (es) * 2003-03-18 2005-01-28 Pharmacia Corp Sa Organizada B Uso de una combinacion farmaceutica, de un antagonista del receptor de aldosterona y un inhibidor de endopeptidasa neutral, util para el tratamiento y prevencion de una condicion patologica relacionada con hipertension, disfuncion renal, insulinopati
US20050032784A1 (en) * 2003-04-01 2005-02-10 University Of Florida Research Foundation, Inc. Combination drug therapy for treating hypertension
WO2004092132A1 (fr) * 2003-04-15 2004-10-28 Warner-Lambert Company Llc Derives bicycliques [b]-fusionnes de proline et leur utilisation pour traiter des etats arthritiques
PT1354874E (pt) * 2003-04-15 2005-03-31 Servier Lab Novo processo de sintese do acido (2s,3as,7as)-per-hidroindole-2-carboxilico e dos seus esteres e aplicacao a sintese do processo perindopril
EP1354875B1 (fr) * 2003-05-19 2004-11-24 Les Laboratoires Servier Nouveau procédé de synthèse de l'acide (2S, 3aS, 7aS)-perhydroindole-2-carboxilique et de ses esters, et application à la synthèse du perindopril
EP1354876B1 (fr) * 2003-06-13 2005-04-27 Les Laboratoires Servier Nouveau procédé de synthèse de l'acide (2S, 3aS, 7aS)-perhydroindole-2-carboxylique et de ses esters, et application à la synthèse du perindopril
US20050037063A1 (en) * 2003-07-21 2005-02-17 Bolton Anthony E. Combined therapies
EP1687271A1 (fr) * 2003-11-25 2006-08-09 Texcontor Etablissement Procede de preparation de (2s, 3ar, 7as)-octahydro-1h-indole-2-acide carboxylique en tant qu'intermediaire dans la preparation de trandolapril par reaction d'un cyclohexyl aziridine avec un dialkyl malonate
WO2005051909A1 (fr) * 2003-11-28 2005-06-09 Azad Pharmaceuticals Ingredients Ag Procede pour produire des composes d'{acide n-[1-(s)-carbalcoxy-3-phenylpropyl]-s-alanyl-2s, 3ar, 7as-octahydroindol-2-carboxylique}
GB2413128A (en) * 2004-04-13 2005-10-19 Neopharma Ltd Process for the preparation of perindopril
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US20060079698A1 (en) * 2004-10-07 2006-04-13 Glenmark Pharmaceuticals Limited Process for the preparation of intermediates of trandolapril and use thereof for the preparation of trandolapril
AU2005327440A1 (en) * 2005-02-14 2006-08-17 Lupin Limited Improved process for preparation of highly pure trandolapril
ATE386718T1 (de) * 2005-05-06 2008-03-15 Sochinaz Sa Verfahren zur herstellung von (2s, 3ar, 7as)- octahydroindole-2-carbonsäure und umwandlung zum trandolapril
EP1899300A2 (fr) * 2005-07-05 2008-03-19 Cipla Limited Procede de synthese d'un inhibiteur de l'enzyme de conversion de l'angiotensine (eca)
WO2007026371A2 (fr) * 2005-09-01 2007-03-08 Wockhardt Limited Procede de preparation de trandolapril et de ses intermediaires
WO2007026372A2 (fr) * 2005-09-01 2007-03-08 Wockhardt Limited Nouveau polymorphe cristallin de trandolapril et un procede de sa preparation
US7741317B2 (en) 2005-10-21 2010-06-22 Bristol-Myers Squibb Company LXR modulators
US7888376B2 (en) 2005-11-23 2011-02-15 Bristol-Myers Squibb Company Heterocyclic CETP inhibitors
US7943655B2 (en) * 2006-04-05 2011-05-17 Universitat Zurich Polymorphic and pseudopolymorphic forms of trandolaprilat, pharmaceutical compositions and methods for production and use
CN101663262B (zh) 2006-12-01 2014-03-26 百时美施贵宝公司 用于治疗动脉粥样硬化和心血管疾病的作为cetp抑制剂的n-(3-苄基)-2,2-(二苯基)-丙-1胺衍生物
CN101302218B (zh) * 2007-05-08 2011-02-23 上海医药工业研究院 群多普利双酮的制备方法
CN101302185B (zh) * 2007-05-08 2010-09-01 上海医药工业研究院 群多普利拉的制备方法
WO2011009021A1 (fr) 2009-07-16 2011-01-20 Abbott Laboratories Procédés de synthèse d'acide (2s, 3ar, 7as)-octahydro-1h-indole carboxylique comme intermédiaire pour le trandolapril
CN104045593B (zh) * 2013-03-12 2016-11-02 上海交通大学 一种群多普利中间体的制备方法
CN105143203A (zh) 2013-04-17 2015-12-09 辉瑞大药厂 用于治疗心血管疾病的n-哌啶-3-基苯甲酰胺衍生物
CN103288710A (zh) * 2013-05-20 2013-09-11 大连海荣科技开发有限公司 群多普利中间体（2S，3aR，7aS）-八氢-1H-吲哚-2-羧酸的制备方法
CN104086623B (zh) * 2014-07-02 2017-05-24 牡丹江友搏药业有限责任公司 一种新的具有降压和细胞保护作用的化合物
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CN113574055B (zh) 2019-01-18 2024-07-23 阿斯利康(瑞典)有限公司 Pcsk9抑制剂及其使用方法

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US5101039A (en) 1992-03-31
DK119992D0 (da) 1992-09-28
NO824394L (no) 1983-06-30
JPS58118569A (ja) 1983-07-14
PH19771A (en) 1986-06-27
EP0084164B1 (fr) 1987-01-28
DE3280014D1 (en) 1989-12-14
IL67572A0 (en) 1983-05-15
CA1341296C (fr) 2001-09-25
PT76052A (de) 1983-01-01
ES8308850A1 (es) 1983-10-01
CS409591A3 (en) 1992-04-15
NO156786C (no) 1987-11-25
DK170444B1 (da) 1995-09-04
DZ490A1 (fr) 2004-09-13
FI824474A0 (fi) 1982-12-27
NL930048I2 (nl) 1994-01-03
JPH064586B2 (ja) 1994-01-19
IE55867B1 (en) 1991-02-14
GR78413B (fr) 1984-09-27
JPH0587504B2 (fr) 1993-12-16
DK576782A (da) 1983-06-30
FI80017C (fi) 1990-04-10
AU9193182A (en) 1983-07-07
DK119992A (da) 1992-09-28
JPH01301695A (ja) 1989-12-05
ES8402271A1 (es) 1984-01-16
JPH01301659A (ja) 1989-12-05
LU88263I2 (fr) 1994-02-03
FI824474L (fi) 1983-06-30
NL930048I1 (nl) 1993-09-01
BG60936B2 (bg) 1996-06-28
IE823065L (en) 1983-06-29
PT76052B (de) 1985-11-28
DK171232B1 (da) 1996-08-05
KR890003424B1 (ko) 1989-09-20
EP0084164A2 (fr) 1983-07-27
IL67572A (en) 1992-08-18
US4933361A (en) 1990-06-12
US5008400A (en) 1991-04-16
NO156786B (no) 1987-08-17
FI80017B (fi) 1989-12-29
HU194167B (en) 1988-01-28
ES518574A0 (es) 1983-10-01
ES521740A0 (es) 1984-01-16
NZ202903A (en) 1988-01-08
KR840002810A (ko) 1984-07-21
SG1389G (en) 1989-06-02
EP0084164A3 (en) 1983-10-12
DE3275293D1 (en) 1987-03-05
AU559140B2 (en) 1987-02-26
HK74989A (en) 1989-09-22
AR247571A1 (es) 1995-01-31
PH18918A (en) 1985-11-06

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