New! Search for patents from more than 100 countries including Australia, Brazil, Sweden and more

EP0584208A4 - - Google Patents

Info

Publication number
EP0584208A4
EP0584208A4 EP19920911583 EP92911583A EP0584208A4 EP 0584208 A4 EP0584208 A4 EP 0584208A4 EP 19920911583 EP19920911583 EP 19920911583 EP 92911583 A EP92911583 A EP 92911583A EP 0584208 A4 EP0584208 A4 EP 0584208A4
Authority
EP
EUROPEAN PATENT OFFICE
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP19920911583
Other versions
EP0584208A1 (en
Inventor
Paul Elliot Bender
Siegfried Benjamin Christensen, Iv
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
SmithKline Beecham Corp
Original Assignee
SmithKline Beecham Corp
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
Priority to US69462491A priority Critical
Priority to US694624 priority
Application filed by SmithKline Beecham Corp filed Critical SmithKline Beecham Corp
Publication of EP0584208A1 publication Critical patent/EP0584208A1/en
Publication of EP0584208A4 publication Critical patent/EP0584208A4/xx
Application status is Withdrawn legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/18Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D207/22Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D207/24Oxygen or sulfur atoms
    • C07D207/262-Pyrrolidones
EP19920911583 1991-05-02 1992-05-01 Withdrawn EP0584208A4 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US69462491A true 1991-05-02 1991-05-02
US694624 1991-05-02

Publications (2)

Publication Number Publication Date
EP0584208A1 EP0584208A1 (en) 1994-03-02
EP0584208A4 true EP0584208A4 (en) 1994-03-23

Family

ID=24789624

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19920911583 Withdrawn EP0584208A4 (en) 1991-05-02 1992-05-01

Country Status (11)

Country Link
EP (1) EP0584208A4 (en)
JP (1) JPH06507405A (en)
CN (1) CN1067244A (en)
AP (1) AP9200379A0 (en)
AU (1) AU1917092A (en)
CA (1) CA2102106A1 (en)
IE (1) IE921376A1 (en)
MX (1) MX9202090A (en)
PT (1) PT100441A (en)
WO (1) WO1992019594A1 (en)
ZA (1) ZA9203210B (en)

Families Citing this family (124)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5679696A (en) * 1992-07-28 1997-10-21 Rhone-Poulenc Rorer Limited Compounds containing phenyl linked to aryl or heteroaryl by an aliphatic-or heteroatom-containing linking group
US5698711A (en) 1991-01-28 1997-12-16 Rhone-Poulenc Rorer Limited Compounds containing phenyl linked to aryl or heteroaryl by an aliphatic- or heteroatom-containing linking group
GB9212673D0 (en) * 1992-06-15 1992-07-29 Celltech Ltd Chemical compounds
GB9222253D0 (en) * 1992-10-23 1992-12-09 Celltech Ltd Chemical compounds
ES2192192T3 (en) * 1992-12-02 2003-10-01 Pfizer Catechol diethers as selective PDE IV inhibitors.
US5814651A (en) * 1992-12-02 1998-09-29 Pfizer Inc. Catechol diethers as selective PDEIV inhibitors
TW263495B (en) * 1992-12-23 1995-11-21 Celltech Ltd
US5622977A (en) * 1992-12-23 1997-04-22 Celltech Therapeutics Limited Tri-substituted (aryl or heteroaryl) derivatives and pharmaceutical compositions containing the same
GB9226830D0 (en) * 1992-12-23 1993-02-17 Celltech Ltd Chemical compounds
GB9304920D0 (en) * 1993-03-10 1993-04-28 Celltech Ltd Chemical compounds
GB9304919D0 (en) * 1993-03-10 1993-04-28 Celltech Ltd Chemical compounds
GB9311281D0 (en) * 1993-06-01 1993-07-21 Rhone Poulenc Rorer Ltd Novel composition of matter
US5998428A (en) * 1995-05-31 1999-12-07 Smithkline Beecham Corporation Compounds and methods for treating PDE IV-related diseases
PT710109E (en) * 1993-06-18 2005-01-31 Smithkline Beecham Corp Method for identifying a PDE IV inhibitor
AU7267094A (en) 1993-07-28 1995-02-28 Rhone-Poulenc Rorer Limited Compounds as pde iv and tnf inhibitors
US5665754A (en) * 1993-09-20 1997-09-09 Glaxo Wellcome Inc. Substituted pyrrolidines
ES2104424T3 (en) * 1993-11-26 1997-10-01 Pfizer Isoxazoline compounds as antiinflammatory agents.
CA2177375A1 (en) * 1993-11-26 1995-06-01 Edward F. Kleinman 3-aryl-2-isoxazolines as antiinflammatory agents
WO1995017399A1 (en) * 1993-12-22 1995-06-29 Celltech Therapeutics Limited Trisubstituted phenyl derivatives, processes for their preparation and their use as phosphodiesterase (type iv) inhibitors
GB9326173D0 (en) * 1993-12-22 1994-02-23 Celltech Ltd Chemical compounds and process
CA2143143A1 (en) * 1994-03-08 1995-09-09 Toshihiko Tanaka 3-phenylpyrrolidine derivatives
DE69503769T2 (en) * 1994-03-09 1998-12-03 Pfizer Isoxazolines connection to inhibition tnf-release
JPH09505081A (en) * 1994-03-09 1997-05-20 ファイザー・インコーポレーテッド Isoxazoline compounds as 5-lipoxygenase inhibitors
DK0758233T3 (en) * 1994-04-21 2004-03-22 Schering Ag PDE IV inhibitors for treating multiple sclerosis
US5672622A (en) * 1994-04-21 1997-09-30 Berlex Laboratories, Inc. Treatment of multiple sclerosis
EP1380291A1 (en) * 1994-04-21 2004-01-14 Schering Aktiengesellschaft PDE IV inhibitors for treating multiple sclerosis
US6060501A (en) * 1994-06-02 2000-05-09 Schering Aktiengesellschaft Combined treatment of multiple sclerosis
US6245774B1 (en) 1994-06-21 2001-06-12 Celltech Therapeutics Limited Tri-substituted phenyl or pyridine derivatives
US5786354A (en) * 1994-06-21 1998-07-28 Celltech Therapeutics, Limited Tri-substituted phenyl derivatives and processes for their preparation
GB9412571D0 (en) 1994-06-22 1994-08-10 Celltech Ltd Chemical compounds
GB9412573D0 (en) * 1994-06-22 1994-08-10 Celltech Ltd Chemical compounds
GB9412672D0 (en) * 1994-06-23 1994-08-10 Celltech Ltd Chemical compounds
US5591776A (en) * 1994-06-24 1997-01-07 Euro-Celtique, S.A. Pheynl or benzyl-substituted rolipram-based compounds for and method of inhibiting phosphodiesterase IV
US5563143A (en) * 1994-09-21 1996-10-08 Pfizer Inc. Catechol diether compounds as inhibitors of TNF release
US5665737B1 (en) * 1994-10-12 1999-02-16 Euro Celtique Sa Substituted benzoxazoles
EP0814809B1 (en) * 1994-12-13 2003-08-13 Euroceltique S.A. Aryl thioxanthines
AU706159B2 (en) * 1995-02-10 1999-06-10 Schering Aktiengesellschaft Pharmaceutical preparations for TNF inhibition
US6268373B1 (en) 1995-06-07 2001-07-31 Euro-Celtique S.A. Trisubstituted thioxanthines
US5658940A (en) * 1995-10-06 1997-08-19 Celgene Corporation Succinimide and maleimide cytokine inhibitors
DE19540475A1 (en) * 1995-10-20 1997-04-24 Schering Ag chiral methylphenyloxazolidinones
GB9523675D0 (en) 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
GB9526245D0 (en) * 1995-12-21 1996-02-21 Celltech Therapeutics Ltd Chemical compounds
GB9526246D0 (en) * 1995-12-21 1996-02-21 Celltech Therapeutics Ltd Chemical compounds
GB9608435D0 (en) * 1996-04-24 1996-06-26 Celltech Therapeutics Ltd Chemical compounds
BR9712782A (en) * 1996-06-25 1999-12-07 Pfizer substituted indazole derivatives and their use as inhibitors fosfodiesterose (powder) and tumor necrosis factor (TNF)
US5744473A (en) * 1996-09-16 1998-04-28 Euro-Celtique, S.A. PDE IV inhibitors: "bis-compounds"
GB9619284D0 (en) * 1996-09-16 1996-10-30 Celltech Therapeutics Ltd Chemical compounds
GB9622363D0 (en) 1996-10-28 1997-01-08 Celltech Therapeutics Ltd Chemical compounds
GB9625184D0 (en) * 1996-12-04 1997-01-22 Celltech Therapeutics Ltd Chemical compounds
US6057329A (en) * 1996-12-23 2000-05-02 Celltech Therapeutics Limited Fused polycyclic 2-aminopyrimidine derivatives
GB9705361D0 (en) 1997-03-14 1997-04-30 Celltech Therapeutics Ltd Chemical compounds
AU6636598A (en) * 1997-03-21 1998-10-20 Dae Woong Pharmaceutical Co., Ltd. Novel 3,4-dialkoxyphenyl derivatives and the use thereof
GB9713087D0 (en) * 1997-06-20 1997-08-27 Celltech Therapeutics Ltd Chemical compounds
GB9914258D0 (en) 1999-06-18 1999-08-18 Celltech Therapeutics Ltd Chemical compounds
GB9924862D0 (en) 1999-10-20 1999-12-22 Celltech Therapeutics Ltd Chemical compounds
US6680336B2 (en) 1999-12-15 2004-01-20 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
US6372777B1 (en) 1999-12-23 2002-04-16 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
US6348602B1 (en) 1999-12-23 2002-02-19 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
US6376489B1 (en) 1999-12-23 2002-04-23 Icos Corporation Cyclic AMP-specific phosphodiesterase inhibitors
KR100755103B1 (en) * 2000-01-06 2007-09-04 사노피-아벤티스 Novel Tetrahydropyridines, Preparation Method and Pharmaceutical Compositions Containing Same
FR2803593B1 (en) * 2000-01-06 2002-02-15 Sanofi Synthelabo News tetrahydropyridine, process for their preparation and pharmaceutical compositions containing them
AU4215801A (en) 2000-03-16 2001-09-24 Inflazyme Pharm Ltd Benzylated pde4 inhibitors
IT1317049B1 (en) 2000-06-23 2003-05-26 Sigma Tau Ind Farmaceuti Compounds useful for the preparation of medicaments having phosphodiesterase attivita'inibitrice iv.
WO2002081446A1 (en) * 2001-04-06 2002-10-17 Daewoong Co., Ltd. 3-cyclopentyloxy-4-methoxyphenyl-isoindolinone derivatives and the use thereof
WO2002081447A1 (en) * 2001-04-06 2002-10-17 Daewoong Pharmaceutical Co., Ltd. 3-cyclopentyloxy-4-methoxyphenyl-isothiazolinone derivatives and the use thereof
FR2823748B1 (en) * 2001-04-20 2004-02-20 Sanofi Synthelabo Tetrahydropyridyl-alkyl benzodiazines, process for their preparation and pharmaceutical compositions containing them
EP1392662B1 (en) 2001-05-29 2009-01-07 Bayer Schering Pharma Aktiengesellschaft Cdk inhibiting pyrimidines, production thereof and their use as medicaments
DE60233884D1 (en) * 2001-10-16 2009-11-12 Memory Pharmaceutical Corp 4 (4-alkoxy-3-hydroxyphenyl) -2-pyrrolidone derivatives as PDE4 inhibitor for the treatment of neurological syndromes
AU2003252259A1 (en) * 2002-07-26 2004-02-16 Nihon Nohyaku Co., Ltd. Novel haloalkylsulfonanilide derivatives, herbicides and usage thereof
JP2004107323A (en) * 2002-07-26 2004-04-08 Nippon Nohyaku Co Ltd New haloalkylsulfone anilide derivative, herbicide and use thereof
UA83202C2 (en) 2002-11-26 2008-06-25 Пфайзер Продактс Инк. Phenyl substituted piperidine compounds for use as ppar activators
JP2006523710A (en) * 2003-04-16 2006-10-19 エフ.ホフマン ラ−ロシュ インコーポレイティド Phosphodiesterase 4 inhibitor
AU2004232973A1 (en) 2003-04-18 2004-11-04 Memory Pharmaceuticals Corporation Pyrazole derivatives as phosphodiesterase 4 inhibitors
GB0401334D0 (en) 2004-01-21 2004-02-25 Novartis Ag Organic compounds
JPWO2006041121A1 (en) * 2004-10-13 2008-05-15 協和醗酵工業株式会社 Of chronic skin diseases and / or prophylactic agent
WO2006041120A1 (en) * 2004-10-13 2006-04-20 Kyowa Hakko Kogyo Co., Ltd. Pharmaceutical composition
CN101166733A (en) 2004-10-15 2008-04-23 记忆药物公司 Pyrazole derivatives as phosphodiesterase 4 inhibitors
CN101166737A (en) 2004-10-20 2008-04-23 记忆药物公司 Phosphodiesterase 4 inhibitors
GT200500281A (en) 2004-10-22 2006-04-24 Novartis Ag organic compounds.
GB0424284D0 (en) 2004-11-02 2004-12-01 Novartis Ag Organic compounds
GB0426164D0 (en) 2004-11-29 2004-12-29 Novartis Ag Organic compounds
US7517870B2 (en) 2004-12-03 2009-04-14 Fondazione Telethon Use of compounds that interfere with the hedgehog signaling pathway for the manufacture of a medicament for preventing, inhibiting, and/or reversing ocular diseases related with ocular neovascularization
GB0507577D0 (en) 2005-04-14 2005-05-18 Novartis Ag Organic compounds
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
PL2532679T3 (en) 2005-10-21 2017-09-29 Novartis Ag Human antibodies against il13 and therapeutic uses
GB0526244D0 (en) 2005-12-22 2006-02-01 Novartis Ag Organic compounds
GB0601951D0 (en) 2006-01-31 2006-03-15 Novartis Ag Organic compounds
RU2457209C2 (en) 2006-04-21 2012-07-27 Новартис Аг Purine derivatives applicable as adenosine receptor a2a agonists
AU2007302263A1 (en) 2006-09-29 2008-04-03 Novartis Ag Pyrazolopyrimidines as P13K lipid kinase inhibitors
AU2007315234A1 (en) 2006-10-30 2008-05-08 Novartis Ag Heterocyclic compounds as antiinflammatory agents
DK2104535T3 (en) 2007-01-10 2011-04-04 Irm Llc Compounds and compositions as channel activating protease inhibitors
CN101687851B (en) 2007-05-07 2013-02-27 诺瓦提斯公司 Organic compounds
MX2010006421A (en) 2007-12-10 2010-06-25 Novartis Ag Organic compounds.
WO2009087224A1 (en) 2008-01-11 2009-07-16 Novartis Ag Pyrimidines as kinase inhibitors
ES2535736T3 (en) 2008-06-10 2015-05-14 Novartis Ag Pyrazine derivatives as blockers of epithelial sodium channels
JP2012516345A (en) 2009-01-29 2012-07-19 ノバルティス アーゲー Astrocytoma Therapeutic substituted benzimidazole
US8389526B2 (en) 2009-08-07 2013-03-05 Novartis Ag 3-heteroarylmethyl-imidazo[1,2-b]pyridazin-6-yl derivatives
KR20120089643A (en) 2009-08-12 2012-08-13 노파르티스 아게 Heterocyclic hydrazone compounds and their uses to treat cancer and inflammation
EA026693B1 (en) 2009-08-17 2017-05-31 Интелликайн ЭлЭлСи Benzoxazole and benzothiazole derivatives as pi3 kinase inhibitors
CA2771432A1 (en) 2009-08-20 2011-02-24 Novartis Ag Heterocyclic oxime compounds
WO2011050325A1 (en) 2009-10-22 2011-04-28 Vertex Pharmaceuticals Incorporated Compositions for treatment of cystic fibrosis and other chronic diseases
US8247436B2 (en) 2010-03-19 2012-08-21 Novartis Ag Pyridine and pyrazine derivative for the treatment of CF
US8637516B2 (en) 2010-09-09 2014-01-28 Irm Llc Compounds and compositions as TRK inhibitors
WO2012034095A1 (en) 2010-09-09 2012-03-15 Irm Llc Compounds and compositions as trk inhibitors
US8372845B2 (en) 2010-09-17 2013-02-12 Novartis Ag Pyrazine derivatives as enac blockers
US20130324526A1 (en) 2011-02-10 2013-12-05 Novartis Ag [1,2,4] triazolo [4,3-b] pyridazine compounds as inhibitors of the c-met tyrosine kinase
US9127000B2 (en) 2011-02-23 2015-09-08 Intellikine, LLC. Heterocyclic compounds and uses thereof
BR112013021638A2 (en) 2011-02-25 2016-08-02 Irm Llc "Trk inhibitor compounds, their use and compositions comprising"
UY34305A (en) 2011-09-01 2013-04-30 Novartis Ag Derivatives bicyclic heterocycles for treating pulmonary arterial hypertension
BR112014006223A8 (en) 2011-09-15 2018-01-09 Novartis Ag 3- (quinolin-6-ylthio) - [1,2,4-triazolo [4,3-a] piradinas 6-substituted, their uses, pharmaceutical compositions, and combination
WO2013038381A1 (en) 2011-09-16 2013-03-21 Novartis Ag Pyridine/pyrazine amide derivatives
WO2013038390A1 (en) 2011-09-16 2013-03-21 Novartis Ag N-substituted heterocyclyl carboxamides
US9034879B2 (en) 2011-09-16 2015-05-19 Novartis Ag Heterocyclic compounds for the treatment of CF
WO2013038378A1 (en) 2011-09-16 2013-03-21 Novartis Ag Pyridine amide derivatives
WO2013038373A1 (en) 2011-09-16 2013-03-21 Novartis Ag Pyridine amide derivatives
CA2856803A1 (en) 2011-11-23 2013-05-30 Intellikine, Llc Enhanced treatment regimens using mtor inhibitors
US8809340B2 (en) 2012-03-19 2014-08-19 Novartis Ag Crystalline form
KR20150001782A (en) 2012-04-03 2015-01-06 노파르티스 아게 Combination products with tyrosine kinase inhibitors and their use
US9073921B2 (en) 2013-03-01 2015-07-07 Novartis Ag Salt forms of bicyclic heterocyclic derivatives
WO2015084804A1 (en) 2013-12-03 2015-06-11 Novartis Ag Combination of mdm2 inhibitor and braf inhibitor and their use
JP6404944B2 (en) 2014-04-24 2018-10-17 ノバルティス アーゲー Pyrazine derivatives as phosphatidylinositol 3-kinase inhibitor
KR20160141855A (en) 2014-04-24 2016-12-09 노파르티스 아게 Amino pyrazine derivatives as phosphatidylinositol 3-kinase inhibitors
JP6454727B2 (en) 2014-04-24 2019-01-16 ノバルティス アーゲー Aminopyridine derivatives as phosphatidylinositol 3-kinase inhibitor
RU2017105827A (en) 2014-07-31 2018-08-30 Новартис Аг Combined therapy

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4916872A (en) * 1972-04-21 1974-02-14
JPS4916870A (en) * 1972-06-14 1974-02-14
JPS4916871A (en) * 1972-06-14 1974-02-14
JPS5182258A (en) * 1974-04-25 1976-07-19 Yoshitomi Pharmaceutical Pirorijinonjudotaino seizoho
US4476311A (en) * 1980-03-12 1984-10-09 The Purdue Frederick Company Analgesic 4-carboxy-pyrrolidin-2-one compound
EP0350437A1 (en) * 1988-07-07 1990-01-10 Schering Aktiengesellschaft 3,4-Disubstituted phenyl-heterocycles and their use

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1350582A (en) * 1970-07-24 1974-04-18 Ucb Sa Cerivatives of 2-pyrrolidinone

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4916872A (en) * 1972-04-21 1974-02-14
JPS4916870A (en) * 1972-06-14 1974-02-14
JPS4916871A (en) * 1972-06-14 1974-02-14
JPS5182258A (en) * 1974-04-25 1976-07-19 Yoshitomi Pharmaceutical Pirorijinonjudotaino seizoho
US4476311A (en) * 1980-03-12 1984-10-09 The Purdue Frederick Company Analgesic 4-carboxy-pyrrolidin-2-one compound
EP0350437A1 (en) * 1988-07-07 1990-01-10 Schering Aktiengesellschaft 3,4-Disubstituted phenyl-heterocycles and their use

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
CHEMICAL ABSTRACTS, vol. 82, no. 19, 1974, Columbus, Ohio, US; abstract no. 125269 *
CHEMICAL ABSTRACTS, vol. 82, no. 21, 1974, Columbus, Ohio, US; abstract no. 139948 *
CHEMICAL ABSTRACTS, vol. 82, no. 21, 1974, Columbus, Ohio, US; abstract no. 139964 *
CHEMICAL ABSTRACTS, vol. 86, no. 11, 1977, Columbus, Ohio, US; abstract no. 72427 *
M. C. MARIVET ET. AL.: "Inhibition of Cyclic Adenosine-3',5'-monophosphate Phosphodiesterase from Vascular Smooth Muscle by Rolipram Analogues.", JOURNAL OF MEDICINAL CHEMISTRY., vol. 32, 1989, WASHINGTON US, pages 1450 - 1457 *
See also references of WO9219594A1 *

Also Published As

Publication number Publication date
AP9200379A0 (en) 1992-04-30
MX9202090A (en) 1992-11-01
EP0584208A1 (en) 1994-03-02
CN1067244A (en) 1992-12-23
PT100441A (en) 1993-09-30
WO1992019594A1 (en) 1992-11-12
AU1917092A (en) 1992-12-21
IE921376A1 (en) 1992-11-04
ZA9203210B (en) 1993-03-31
JPH06507405A (en) 1994-08-25
CA2102106A1 (en) 1992-11-03

Similar Documents

Publication Publication Date Title
DE9105350U1 (en)
DE9105651U1 (en)
DE9102829U1 (en)
DE9103001U1 (en)
DE9101923U1 (en)
DE9102599U1 (en)
DE9108392U1 (en)
DE9103346U1 (en)
DE9101981U1 (en)
DE9106479U1 (en)
DE9108229U1 (en)
DE9108420U1 (en)
DE9103322U1 (en)
DE9100174U1 (en)
DE9104115U1 (en)
DE9104661U1 (en)
DE9105750U1 (en)
DE9102048U1 (en)
DE9100983U1 (en)
DE9108662U1 (en)
DE9105370U1 (en)
DE9106861U1 (en)
DE9107456U1 (en)
DE9104544U1 (en)
DE9103044U1 (en)

Legal Events

Date Code Title Description
AK Designated contracting states:

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU MC NL SE

17P Request for examination filed

Effective date: 19931028

A4 Despatch of supplementary search report

Effective date: 19940203

AK Designated contracting states:

Kind code of ref document: A4

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU MC NL SE

17Q First examination report

Effective date: 19970611

18D Deemed to be withdrawn

Effective date: 19991019