SK279102B6 - Tolunitrily substituované heterocyklickým zvyškom - Google Patents

Tolunitrily substituované heterocyklickým zvyškom Download PDF

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Publication number
SK279102B6
SK279102B6 SK7367-87A SK736787A SK279102B6 SK 279102 B6 SK279102 B6 SK 279102B6 SK 736787 A SK736787 A SK 736787A SK 279102 B6 SK279102 B6 SK 279102B6
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SK
Slovakia
Prior art keywords
compounds
formula
group
compound
benzonitrile
Prior art date
Application number
SK7367-87A
Other languages
English (en)
Slovak (sk)
Other versions
SK736787A3 (en
Inventor
Robert M. Bowman
Ronald E. Steele
Leslie J. Browne
Original Assignee
Novartis 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=25274596&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SK279102(B6) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of SK736787A3 publication Critical patent/SK736787A3/sk
Publication of SK279102B6 publication Critical patent/SK279102B6/sk

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/02Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/24Heterocyclic 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 with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/57Nitriles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Reproductive Health (AREA)
  • Urology & Nephrology (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Fats And Perfumes (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Saccharide Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
  • Steroid Compounds (AREA)
  • Indole Compounds (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
SK7367-87A 1986-03-07 1987-03-06 Tolunitrily substituované heterocyklickým zvyškom SK279102B6 (sk)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/837,489 US4749713A (en) 1986-03-07 1986-03-07 Alpha-heterocycle substituted tolunitriles

Publications (2)

Publication Number Publication Date
SK736787A3 SK736787A3 (en) 1998-06-03
SK279102B6 true SK279102B6 (sk) 1998-06-03

Family

ID=25274596

Family Applications (3)

Application Number Title Priority Date Filing Date
SK7367-87A SK279102B6 (sk) 1986-03-07 1987-03-06 Tolunitrily substituované heterocyklickým zvyškom
SK7368-87A SK279103B6 (sk) 1986-03-07 1987-03-06 Substituované imidazolyl- alebo 1,2,4-triazolylmet
SK1512-87A SK151287A3 (en) 1986-03-07 1987-03-06 Process for producing tolunitriles substituted by a heterocyclic residue

Family Applications After (2)

Application Number Title Priority Date Filing Date
SK7368-87A SK279103B6 (sk) 1986-03-07 1987-03-06 Substituované imidazolyl- alebo 1,2,4-triazolylmet
SK1512-87A SK151287A3 (en) 1986-03-07 1987-03-06 Process for producing tolunitriles substituted by a heterocyclic residue

Country Status (36)

Country Link
US (1) US4749713A (cs)
EP (1) EP0236940B3 (cs)
JP (1) JPH0755930B2 (cs)
KR (1) KR910000482B1 (cs)
AT (1) ATE94873T1 (cs)
BG (4) BG45701A3 (cs)
CA (1) CA1316928C (cs)
CY (1) CY1905A (cs)
CZ (3) CZ279027B6 (cs)
DD (1) DD264432A5 (cs)
DE (2) DE19775016I2 (cs)
DK (1) DK172190B1 (cs)
DZ (1) DZ1055A1 (cs)
ES (1) ES2059317T3 (cs)
FI (1) FI91857C (cs)
HK (1) HK50296A (cs)
HU (1) HU202843B (cs)
IE (1) IE61101B1 (cs)
IL (1) IL81746A (cs)
LU (1) LU90128I2 (cs)
LV (1) LV5769B4 (cs)
MA (1) MA20888A1 (cs)
MC (1) MC1805A1 (cs)
MT (1) MTP998B (cs)
MX (1) MX5496A (cs)
MY (1) MY102428A (cs)
NL (1) NL970011I2 (cs)
NO (2) NO170277C (cs)
PH (1) PH24159A (cs)
PL (2) PL151490B1 (cs)
PT (1) PT84410B (cs)
RO (2) RO101532B1 (cs)
SK (3) SK279102B6 (cs)
SU (3) SU1470184A3 (cs)
TN (1) TNSN87033A1 (cs)
ZA (1) ZA871637B (cs)

Families Citing this family (49)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5112845A (en) * 1986-03-07 1992-05-12 Ciba-Geigy Corporation Alpha-heterocycle substituted tolunitriles
US5352795A (en) * 1986-03-07 1994-10-04 Ciba-Geigy Corporation Alpha-heterocycle substituted tolunitriles
GB8714013D0 (en) * 1987-06-16 1987-07-22 Ici Plc (substituted-aralkyl)heterocyclic compounds
DE3811574A1 (de) * 1988-03-31 1989-10-19 Schering Ag N-substituierte imidazole, verfahren zu ihrer herstellung sowie ihre verwendung in arzneimitteln
ES2084687T3 (es) * 1989-07-14 1996-05-16 Ciba Geigy Ag Benzonitrilos substituidos.
DE3926365A1 (de) * 1989-08-04 1991-02-07 Schering Ag Cycloalkylenazole, verfahren zu deren herstellung, pharmazeutische praeparate, die diese enthalten sowie ihre verwendung zur herstellung von arzneimitteln
JP2602456B2 (ja) * 1990-04-12 1997-04-23 雪印乳業株式会社 子宮内膜症治療剤
EP0457716A1 (de) * 1990-04-20 1991-11-21 Ciba-Geigy Ag Naphthalinderivate
DE4039559A1 (de) * 1990-12-07 1992-06-11 Schering Ag Funktionalisierte vinylazole, verfahren zu deren herstellung, pharmazeutische praeparate die diese vinylazole enthalten sowie deren verwendung zur herstellung von arzneimitteln
TW210334B (cs) * 1990-12-12 1993-08-01 Ciba Geigy Ag
CH683151A5 (de) * 1991-04-24 1994-01-31 Ciba Geigy Ag Antikonzeption bei weiblichen Primaten ohne Beeinflussung des menstruellen Zyklus.
DE4120107A1 (de) * 1991-06-14 1992-12-17 Schering Ag Bicyclisch substituierte vinylimidazole, -triazole und -tetrazole
TW225526B (cs) 1991-09-02 1994-06-21 Yamanouchi Pharma Co Ltd
US5223539A (en) * 1991-11-22 1993-06-29 G. D. Searle & Co. N,n-di-alkyl(phenoxy)benzamide derivatives
AU5285593A (en) * 1992-10-21 1994-05-09 Sankyo Company Limited Azole compound
GB2273704B (en) * 1992-12-16 1997-01-22 Orion Yhtymae Oy Triazolyl diaryl selective aromatase inhibiting compounds
US5426196A (en) * 1993-12-22 1995-06-20 Glaxo Inc. Synthesis of diaryl methanes
WO1997027852A1 (en) * 1996-01-30 1997-08-07 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
WO1997027853A1 (en) * 1996-01-30 1997-08-07 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
US6080870A (en) * 1996-04-03 2000-06-27 Merck & Co., Inc. Biaryl substituted imidazole compounds useful as farnesyl-protein transferase inhibitors
US6063930A (en) * 1996-04-03 2000-05-16 Merck & Co., Inc. Substituted imidazole compounds useful as farnesyl-protein transferase inhibitors
AU715658B2 (en) * 1996-04-03 2000-02-10 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
CA2250353A1 (en) * 1996-04-03 1997-10-09 Christopher J. Dinsmore Inhibitors of farnesyl-protein transferase
US6833373B1 (en) 1998-12-23 2004-12-21 G.D. Searle & Co. Method of using an integrin antagonist and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia
US6858598B1 (en) 1998-12-23 2005-02-22 G. D. Searle & Co. Method of using a matrix metalloproteinase inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia
JP4477303B2 (ja) 2001-05-16 2010-06-09 ノバルティス アーゲー N−{5−[4−(4−メチル−ピペラジノ−メチル)−ベンゾイルアミド]−2−メチルフェニル}−4−(3−ピリジル)−2−ピリミジン−アミンおよび化学療法剤を含んでなる併用剤
WO2003050093A1 (en) * 2001-12-11 2003-06-19 Emory University Bis(cyanophenyl)methyl-triazole for use in prevention of breast cancer
BR0313081A (pt) * 2002-07-30 2005-07-12 Novartis Ag Combinação de um inibidor de aromatase com um bisfosfanato
GB0217636D0 (en) * 2002-07-30 2002-09-11 Novartis Ag Organic compounds
JP2004196795A (ja) * 2002-12-16 2004-07-15 Wyeth 外部寄生虫駆除剤としてのn−フェニル−3−シクロプロピルピラゾール−4−カルボニトリル
AU2003282380A1 (en) * 2003-11-14 2004-06-06 ADIBHATLA, KALI,SATYA, Bhujanga,rao A method for the separation of the letrozole precursor 4-1-(1,2,4-triazolyl) methyl benzonitrile from its 1,3,4-triazolyl isomer
JP4834557B2 (ja) * 2003-12-15 2011-12-14 ラボラトワール テラメックス 1−n−フェニルアミノ−1h−イミダゾール誘導体及びこれを含む医薬組成物
US7705159B2 (en) * 2005-07-06 2010-04-27 Sicor, Inc. Process for the preparation of letrozole
GT200600381A (es) 2005-08-25 2007-03-28 Compuestos organicos
US20090082413A1 (en) * 2007-09-26 2009-03-26 Protia, Llc Deuterium-enriched letrozole
RU2425038C2 (ru) * 2009-11-27 2011-07-27 Федеральное государственное унитарное предприятие "Государственный научный центр "Научно-исследовательский институт органических полупродуктов и красителей" (ФГУП "ГНЦ "НИОПИК") Способ получения 1-[ди(4-цианфенил)метил]-1,2,4-триазола
EP2558098A2 (en) 2010-04-16 2013-02-20 Novartis AG Treatment of endocrine resistant breast cancer
WO2012025762A2 (en) 2010-08-27 2012-03-01 Generics [Uk] Limited Pure intermediate
MX360315B (es) * 2011-09-08 2018-10-29 Novartis Ag Composiciones farmaceuticas que comprenden un inhibidor de aromatasa.
RU2665949C2 (ru) 2012-06-08 2018-09-05 Ф.Хоффманн-Ля Рош Аг Селективность в отношении мутантных форм и комбинации соединения, представляющего собой ингибитор фосфоинозитид-3-киназы, и химиотерапевтических агентов для лечения рака
HUE057061T2 (hu) 2013-08-14 2022-04-28 Novartis Ag Kombinációs terápia rák kezelésére
AR104068A1 (es) 2015-03-26 2017-06-21 Hoffmann La Roche Combinaciones de un compuesto inhibidor de fosfoinosítido 3-cinasa y un compuesto inhibidor de cdk4/6 para el tratamiento del cáncer
GB201614179D0 (en) 2016-08-19 2016-10-05 Mereo Biopharma 2 Ltd Dosage regimen for the treatment of endometriosis
EP3826622A1 (en) 2018-07-23 2021-06-02 F. Hoffmann-La Roche AG Methods of treating cancer with pi3k inhibitor, gdc-0077
EP3863618A1 (en) 2018-10-08 2021-08-18 F. Hoffmann-La Roche AG Methods of treating cancer with pi3k alpha inhibitors and metformin
CA3156205A1 (en) 2019-12-03 2021-06-10 Jennifer O'hara Lauchle Combination therapies for treatment of breast cancer
TW202237136A (zh) 2020-12-11 2022-10-01 美商建南德克公司 用於治療her2癌症的組合療法
CN116925001B (zh) * 2023-07-26 2025-09-30 陕西师范大学 一种抗乳腺癌药物来曲唑类似物的合成方法
WO2025122745A1 (en) 2023-12-05 2025-06-12 Genentech, Inc. Combination therapies for treatment of her2 cancer

Family Cites Families (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3290281A (en) * 1963-07-18 1966-12-06 Weinstein Julius Photochromic nitrobenzylpyridines
US3397273A (en) * 1966-02-18 1968-08-13 Lilly Co Eli Controlling phytopathogenic fungi on plants with 3-pyridyl methane derivatives
GB1170188A (en) * 1967-09-15 1969-11-12 Bayer Ag N-trityl-imidazoles and salts and uses thereof
DE1670976B2 (de) * 1968-01-29 1976-07-22 N-trityl-imidazole
DE1908991B2 (de) * 1969-02-22 1977-05-26 Bayer Ag, 5090 Leverkusen Alpha, alpha-disubstituierte n- benzylimidazole und deren salze
BR6915465D0 (pt) * 1969-03-07 1973-01-04 Bayer Ag Processo para preparar n-benzimidazois substituidos na posicao alfa por heterociclos penta-membrados com atividade antimicotica
DE2007794A1 (de) * 1970-02-20 1971-09-02 Farbenfabriken Bayer Aktiengesell schaft, 5090 Leverkusen Fungizide Mittel
DE2009020C3 (de) * 1970-02-26 1979-09-13 Bayer Ag, 5090 Leverkusen Verfahren zur Herstellung von N-(l,l,l-trisubstituierten)-Methylazolen
US3764690A (en) * 1972-03-03 1973-10-09 Bayer Ag Substituted n-benzylimidazoles as antimycotic agents
US3927017A (en) * 1974-06-27 1975-12-16 Janssen Pharmaceutica Nv 1-({62 -Aryl-{62 -R-ethyl)imidazoles
DE2628152C2 (de) * 1976-06-23 1985-03-28 Bayer Ag, 5090 Leverkusen Fungizide und nematizide Mittel
DE2732531A1 (de) * 1977-07-19 1979-02-01 Hoechst Ag Imidazolcarbonsaeuren und deren derivate
DE2735314A1 (de) * 1977-08-05 1979-02-22 Basf Ag Alpha-azolylsulfide und deren derivate
US4431815A (en) * 1977-08-26 1984-02-14 Burroughs Wellcome Co. 1-[3-(2,4-Dichlorophenyl)propyl]imidazole and salts thereof
DE2862340D1 (en) * 1978-02-01 1983-11-24 Wellcome Found Imidazole derivatives and salts thereof, their synthesis, and pharmaceutical formulations thereof
DE2808086A1 (de) * 1978-02-24 1979-08-30 Bayer Ag Substituierte diphenyl-imidazolyl- methane, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
DE2821829A1 (de) * 1978-05-19 1979-11-22 Basf Ag Mittel zur regulierung des pflanzenwachstums
JPS55313A (en) * 1978-06-13 1980-01-05 Kissei Pharmaceut Co Ltd Imidazole derivative
DE2847441A1 (de) 1978-11-02 1980-05-22 Basf Ag Imidazol-kupferkomplexverbindungen
DK157860C (da) * 1979-06-07 1990-07-30 Shionogi & Co Analogifremgangsmaade til fremstilling af benzylimidazolderivater samt farmaceutisk acceptable syreadditionssalte deraf
US4281141A (en) * 1980-05-30 1981-07-28 Eli Lilly And Company 3-(Imidazol-4-yl)-2-phenylpropanenitriles
US4617307A (en) * 1984-06-20 1986-10-14 Ciba-Geigy Corporation Substituted imidazo[1,5-A]pyridine derivatives as aromatase inhibitors
US4562199A (en) * 1983-08-11 1985-12-31 Thorogood Peter B Imidazole derivatives, compositions and use
EP0149976A3 (de) * 1983-12-30 1986-12-10 Ciba-Geigy Ag Substituierte Imidazole
US4605661A (en) * 1984-06-18 1986-08-12 Eli Lilly And Company Aromastase inhibiting α,α-diarylimidazole-4(5)-propionitriles, α,α-diarylimidazole-4(5)-propionamides, and 4(5)-(2,2-diarylethyl)imidazoles
US4801594A (en) * 1984-06-18 1989-01-31 Eli Lilly And Company Aromatase inhibitors
US4755526A (en) * 1984-06-18 1988-07-05 Eli Lilly And Company Method of inhibiting aromatase
US4766140A (en) * 1984-06-18 1988-08-23 Eli Lilly And Company Method of inhibiting aromatase
US4602025A (en) * 1984-06-18 1986-07-22 Eli Lilly And Company Aromatase inhibitors

Also Published As

Publication number Publication date
SU1577695A3 (ru) 1990-07-07
PL152025B1 (en) 1990-10-31
SK736787A3 (en) 1998-06-03
MC1805A1 (fr) 1987-12-22
KR910000482B1 (ko) 1991-01-25
AU6976887A (en) 1987-09-10
CZ279027B6 (en) 1994-11-16
LV5769A4 (lv) 1996-12-20
SK736887A3 (en) 1998-06-03
BG46598A3 (bg) 1990-01-15
FI91857B (fi) 1994-05-13
LU90128I2 (fr) 1997-10-06
PT84410A (en) 1987-04-01
IE61101B1 (en) 1994-10-05
DK117687A (da) 1987-09-08
DK117687D0 (da) 1987-03-06
SK279101B6 (sk) 1998-06-03
SK279103B6 (sk) 1998-06-03
SK151287A3 (en) 1998-06-03
SU1549478A3 (ru) 1990-03-07
EP0236940B3 (en) 2011-03-23
FI91857C (fi) 1994-08-25
BG61204B2 (bg) 1997-02-28
CA1316928C (en) 1993-04-27
CS8707368A2 (en) 1991-02-12
MY102428A (en) 1992-06-30
LV5769B4 (lv) 1997-04-20
ES2059317T3 (es) 1994-11-16
NO870937L (no) 1987-09-08
NO1998010I1 (no) 1998-03-04
EP0236940A2 (en) 1987-09-16
RO101533B1 (en) 1992-06-25
DE19775016I2 (de) 2002-02-21
JPS62212369A (ja) 1987-09-18
NO870937D0 (no) 1987-03-06
SU1470184A3 (ru) 1989-03-30
RO101532B1 (en) 1992-11-03
HU202843B (en) 1991-04-29
HUT43822A (en) 1987-12-28
CZ279028B6 (en) 1994-11-16
PT84410B (pt) 1989-10-04
BG45700A3 (bg) 1989-07-14
ZA871637B (en) 1987-10-28
US4749713A (en) 1988-06-07
JPH0755930B2 (ja) 1995-06-14
HK50296A (en) 1996-03-29
IL81746A0 (en) 1987-10-20
CS8701512A2 (en) 1991-02-12
EP0236940B1 (en) 1993-09-22
NO170277B (no) 1992-06-22
ATE94873T1 (de) 1993-10-15
EP0236940A3 (en) 1989-10-18
IL81746A (en) 1992-02-16
CZ279026B6 (en) 1994-11-16
DE3787480D1 (de) 1993-10-28
PL151490B1 (en) 1990-09-28
TNSN87033A1 (fr) 1990-01-01
AU604011B2 (en) 1990-12-06
FI870903L (fi) 1987-09-08
DD264432A5 (de) 1989-02-01
NL970011I2 (nl) 1997-09-01
PL264460A1 (en) 1988-07-21
DK172190B1 (da) 1997-12-22
PH24159A (en) 1990-03-22
BG45701A3 (bg) 1989-07-14
MTP998B (en) 1987-08-21
DE3787480T2 (de) 1994-02-24
NL970011I1 (nl) 1997-05-01
IE870575L (en) 1987-09-07
MX5496A (es) 1993-12-01
CS8707367A2 (en) 1991-02-12
MA20888A1 (fr) 1987-10-01
NO170277C (no) 1992-09-30
KR870008851A (ko) 1987-10-21
DZ1055A1 (fr) 2004-09-13
FI870903A0 (fi) 1987-03-02
CY1905A (en) 1987-03-05

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