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PL356766A1 - Stabilne sole nowoczesnych pochodnych 3,3-difenylopropyloamin - Google Patents

Stabilne sole nowoczesnych pochodnych 3,3-difenylopropyloamin

Info

Publication number
PL356766A1
PL356766A1 PL00356766A PL35676600A PL356766A1 PL 356766 A1 PL356766 A1 PL 356766A1 PL 00356766 A PL00356766 A PL 00356766A PL 35676600 A PL35676600 A PL 35676600A PL 356766 A1 PL356766 A1 PL 356766A1
Authority
PL
Poland
Prior art keywords
new
diphenylpropylamines
novel derivatives
stable salts
salts
Prior art date
Application number
PL00356766A
Other languages
English (en)
Other versions
PL201422B1 (pl
Inventor
Claus Meese
Original Assignee
Schwarz Pharma 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=7929277&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PL356766(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Schwarz Pharma Ag filed Critical Schwarz Pharma Ag
Publication of PL356766A1 publication Critical patent/PL356766A1/pl
Publication of PL201422B1 publication Critical patent/PL201422B1/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C219/00Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C219/26Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C215/00Compounds containing amino and hydroxy groups bound to the same carbon skeleton
    • C07C215/46Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C215/48Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups
    • C07C215/54Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by hydroxy groups linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • 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
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/06Anti-spasmodics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/10Drugs for disorders of the urinary system of the bladder
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C219/00Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton
    • C07C219/26Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C219/28Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton having amino groups bound to acyclic carbon atoms of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/38Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to acyclic carbon atoms and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Urology & Nephrology (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Detergent Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Luminescent Compositions (AREA)
PL356766A 1999-11-16 2000-11-15 Stabilna sól izomaślanu R-(+)-2-(3-(diizopropyloamino-1-fenylopropylo)-4-hydroksymetylofenylowego PL201422B1 (pl)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19955190A DE19955190A1 (de) 1999-11-16 1999-11-16 Stabile Salze neuartiger Derivate von 3,3-Diphenylpropylaminen
PCT/EP2000/011309 WO2001035957A1 (de) 1999-11-16 2000-11-15 Stabile salze neuartiger derivate von 3,3-diphenylpropylaminen

Publications (2)

Publication Number Publication Date
PL356766A1 true PL356766A1 (pl) 2004-07-12
PL201422B1 PL201422B1 (pl) 2009-04-30

Family

ID=7929277

Family Applications (1)

Application Number Title Priority Date Filing Date
PL356766A PL201422B1 (pl) 1999-11-16 2000-11-15 Stabilna sól izomaślanu R-(+)-2-(3-(diizopropyloamino-1-fenylopropylo)-4-hydroksymetylofenylowego

Country Status (30)

Country Link
US (1) US6858650B1 (pl)
EP (3) EP1230209B3 (pl)
JP (6) JP4083431B2 (pl)
KR (2) KR100563149B1 (pl)
CN (1) CN1215045C (pl)
AT (3) ATE286872T1 (pl)
AU (1) AU778132B2 (pl)
BR (1) BRPI0015610C1 (pl)
CA (1) CA2389749C (pl)
CY (2) CY1106204T1 (pl)
CZ (2) CZ302497B6 (pl)
DE (5) DE29923134U1 (pl)
DK (3) DK1481964T3 (pl)
EA (1) EA005588B1 (pl)
ES (3) ES2236032T7 (pl)
GE (1) GEP20084430B (pl)
HK (3) HK1067114A1 (pl)
HU (2) HU228197B1 (pl)
IL (2) IL149567A0 (pl)
IS (2) IS2124B (pl)
MX (1) MXPA02004603A (pl)
NO (2) NO323920B1 (pl)
NZ (1) NZ519230A (pl)
PL (1) PL201422B1 (pl)
PT (3) PT1481964E (pl)
SI (3) SI1481964T1 (pl)
SK (3) SK287430B6 (pl)
UA (2) UA73324C2 (pl)
WO (1) WO2001035957A1 (pl)
ZA (1) ZA200203315B (pl)

Families Citing this family (48)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0957073A1 (en) * 1998-05-12 1999-11-17 Schwarz Pharma Ag Novel derivatives of 3,3-diphenylpropylamines
DE29923134U1 (de) * 1999-11-16 2000-06-29 Schwarz Pharma Ag, 40789 Monheim Stabile Salze neuartiger Derviate von 3,3-Diphenylpropylaminen
DE10028443C1 (de) * 2000-06-14 2002-05-29 Sanol Arznei Schwarz Gmbh Verfahren zur Herstellung von 3,3-Diarylpropylaminen, (R,S)- und (R)-4-Phenyl-2-chromanon-6-carbonsäure sowie (R)-4-Phenyl-2-chromanon-carbonsäure-cinchonidinsalz und deren Verwendung zur Herstellung eines rechtsdrehenden Hydroxybenzylalkohols und von pharmazeutischen Zusammensetzungen
DE10315917A1 (de) * 2003-04-08 2004-11-18 Schwarz Pharma Ag Hochreine Basen von 3,3-Diphenylpropylaminmonoestern
DE10315878B4 (de) 2003-04-08 2009-06-04 Schwarz Pharma Ag Vorrichtung zur transdermalen Verabreichung von Fesoterodin und Verwendung
WO2005012227A2 (en) * 2003-08-05 2005-02-10 Ranbaxy Laboratories Limited Process for preparation of 2-(3-diisopropylamino-1-phenylpropyl)-4-hydroxymethyl-phenol, a metabolite of tolterodine
ES2235648B1 (es) * 2003-12-22 2006-11-01 Ragactives, S.L. Procedimiento para la obtencion de tolterodina.
US8034823B2 (en) * 2005-02-22 2011-10-11 Savvipharm Inc Method of increasing drug oral bioavailability and compositions of less toxic orotate salts
KR100647068B1 (ko) 2005-09-15 2006-11-23 하나제약 주식회사 라세믹n,n-디이소프로필-3-(2-히드록시-5-메틸페닐)-3-페닐프로판아민의 제조방법
ATE480531T1 (de) * 2006-05-24 2010-09-15 Pfizer Ltd Verfahren zur herstellung von benzopyran-2- olderivaten
BRPI0711881B1 (pt) 2006-05-31 2016-09-27 Schwarz Pharma Ltd síntese de hidroximetil fenóis substituídos
EP1862449A1 (en) * 2006-05-31 2007-12-05 Schwarz Pharma Ltd. A shortened synthesis of substituted hydroxymethyl phenols
IES20060424A2 (en) * 2006-06-08 2007-10-31 Schwarz Pharma Ltd Accelerated synthesis of (3-Diisopropylamino-1-phenylpropyl)-4-(hydroxymethyl)phenol and its phenolic monoesters
PE20080331A1 (es) * 2006-06-09 2008-06-19 Sanol Arznei Schwarz Gmbh Composiciones farmaceuticas estabilizadas que comprenden fesoterodina
CA2648333C (en) * 2006-06-09 2014-04-29 Schwarz Pharma Ltd Synthesis of phenolic esters of hydroxymethyl phenols
US7807715B2 (en) 2006-06-09 2010-10-05 Ucb Pharma Gmbh Pharmaceutical compositions comprising fesoterodine
IES20060435A2 (en) * 2006-06-12 2007-12-12 Schwarz Pharma Ltd Shortened synthesis using paraformaldehyde or trioxane
KR20140010198A (ko) 2006-06-12 2014-01-23 유씨비 파마 게엠베하 새로운 키랄 중간체, 그 키랄 중간체의 제조방법 및 톨테로딘, 페소테로딘 또는 그 활성대사물질의 제조에서 그 키랄 중간체의 사용
US20100217034A1 (en) * 2007-09-21 2010-08-26 Actavis Group Ptc Ehf Process for the Preparation of Fesoterodine
US20100297241A1 (en) * 2007-10-01 2010-11-25 Actavis Group Ptc Ehf Amorphous Fesoterodine Fumarate
WO2009122303A2 (en) * 2008-04-04 2009-10-08 Actavis Group Ptc Ehf Novel mandelate salt of fesoterodine
WO2010010464A2 (en) * 2008-07-21 2010-01-28 Actavis Group Ptc Ehf Fesoterodine substantially free of dehydroxy impurity
IT1392082B1 (it) * 2008-12-10 2012-02-09 Chemi Spa Nuove forme solide della fesoterodina fumarato
US9085507B2 (en) 2009-05-11 2015-07-21 Ratiopharm Gmbh Desfesoterodine in the form of a tartaric acid salt
IT1394217B1 (it) * 2009-05-15 2012-06-01 Chemi Spa Metodo di preparazione di fesoterodina e/o fesoterodina fumarato.
IT1394219B1 (it) 2009-05-15 2012-06-01 Chemi Spa Metodo di preparazione di fesoterodina fumarato di elevata purezza.
WO2011029005A1 (en) 2009-09-03 2011-03-10 Teva Gyogyszergyar Zartkoruen Mukodo Reszvenytarsasag Crystalline forms of fesoterodine fumarate and fesoterodine base
IT1396373B1 (it) * 2009-10-29 2012-11-19 Dipharma Francis Srl Procedimento per la preparazione di fesoterodina.
EP2316432A1 (de) 2009-10-30 2011-05-04 ratiopharm GmbH Zusammensetzung enthaltend Fesoterodin und Ballaststoffe
US20110124903A1 (en) * 2009-11-20 2011-05-26 Actavis Group Ptc Ehf Solid state forms of fesoterodine intermediates
IT1397521B1 (it) * 2009-12-21 2013-01-16 Dipharma Francis Srl Procedimento per la preparazione di fesoterodina con un basso contenuto di impurezze.
IT1397920B1 (it) * 2010-02-08 2013-02-04 Dipharma Francis Srl Forma cristallina di fesoterodina fumarato e procedimento per la sua preparazione
EP2549985A1 (en) 2010-03-22 2013-01-30 Cadila Healthcare Limited Stable pharmaceutical compositions comprising fesoterodine
CA2796877A1 (en) 2010-04-30 2011-11-03 Merck Sharp & Dohme Corp. Novel beta 3 adrenergic receptor agonists
WO2011141932A2 (en) 2010-05-11 2011-11-17 Intas Pharmaceuticals Limited Process for preparation of phenolic monoesters of hydroxymethyl phenols
WO2011145019A1 (en) * 2010-05-17 2011-11-24 Orchid Chemicals And Pharmaceuticals Limited Improved process for diphenylpropylamine derivatives
IT1401451B1 (it) 2010-06-10 2013-07-26 Chemi Spa Nuovo processo di preparazione di 2-idrossi-4-fenil-3,4-diidro-2h-cromen-6-il-metanolo e (r)-2-[3-(diisopropilammino)-1-fenilpropil]-4-(idrossimetil)fenolo.
WO2011158257A1 (en) 2010-06-18 2011-12-22 Panacea Biotec Ltd Preparation process of fesoterodine and intermediates
US9012678B2 (en) * 2010-08-25 2015-04-21 Cadila Healthcare Limited Processes for the preparation of fesoterodine
IT1403094B1 (it) 2010-12-09 2013-10-04 Dipharma Francis Srl Procedimento per la preparazione di fesoterodina o un suo sale
WO2012098560A2 (en) * 2011-01-17 2012-07-26 Msn Laboratories Limited Process for the preparation of muscarinic receptor antagonist
TWI590821B (zh) 2011-01-18 2017-07-11 輝瑞有限公司 固體分子分散液
EP2508175A1 (en) 2011-04-08 2012-10-10 LEK Pharmaceuticals d.d. Pharmaceutical composition comprising fesoterodine or a salt or a solvate thereof
EP2508173A1 (en) 2011-04-08 2012-10-10 LEK Pharmaceuticals d.d. Stabilized pharmaceutical composition comprising fesoterodine
US9422228B2 (en) 2012-05-04 2016-08-23 Crystal Pharma, S.A.U. Process for the preparation of optically pure fesoterodine derivatives
ITMI20121232A1 (it) 2012-07-16 2014-01-17 Cambrex Profarmaco Milano Srl Procedimento per la preparazione di 2-(3-n,n-diisopropilamino-1-fenilpropil)-4-idrossimetil-fenolo e suoi derivati
TR201721437A2 (tr) 2017-12-25 2019-07-22 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Fesoterodi̇ni̇n modi̇fi̇ye salim sağlayan formülasyonlari
EP4237405A1 (en) * 2020-10-27 2023-09-06 Wella Germany GmbH 2-methoxymethyl-p-phenylenediamine in cosmetic grade quality

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GR75395B (pl) * 1980-11-14 1984-07-13 Lilly Co Eli
IL66831A0 (en) * 1981-10-05 1982-12-31 Kefalas As Indane derivatives
SE8800207D0 (sv) * 1988-01-22 1988-01-22 Kabivitrum Ab Nya aminer, deras anvendning och framstellning
IE910752A1 (en) * 1990-03-08 1991-09-11 Fujisawa Pharmaceutical Co A novel substituted-amine compound and a process for the¹preparation thereof
JPH0483431A (ja) * 1990-07-26 1992-03-17 Seiko Epson Corp 選択呼出受信機
SE9203318D0 (sv) * 1992-11-06 1992-11-06 Kabi Pharmacia Ab Novel 3,3-diphenylpropylamines, their use and preparation
SE9701144D0 (sv) * 1997-03-27 1997-03-27 Pharmacia & Upjohn Ab Novel compounds, their use and preparation
EP0957073A1 (en) * 1998-05-12 1999-11-17 Schwarz Pharma Ag Novel derivatives of 3,3-diphenylpropylamines
DE29923134U1 (de) * 1999-11-16 2000-06-29 Schwarz Pharma Ag, 40789 Monheim Stabile Salze neuartiger Derviate von 3,3-Diphenylpropylaminen

Also Published As

Publication number Publication date
SK287430B6 (sk) 2010-09-07
HK1095736A1 (en) 2007-05-18
EP1230209A2 (de) 2002-08-14
DK1481964T3 (da) 2006-11-27
PL201422B1 (pl) 2009-04-30
EA200200511A1 (ru) 2002-10-31
KR20050100711A (ko) 2005-10-19
JP2014111589A (ja) 2014-06-19
DK1230209T3 (da) 2005-05-30
CA2389749A1 (en) 2001-05-25
SK288384B6 (sk) 2016-08-01
SI1481964T1 (sl) 2006-12-31
EP1230209B3 (de) 2011-10-05
WO2001035957A3 (de) 2001-12-27
EP1230209B1 (de) 2005-01-12
HK1045148B (zh) 2005-05-06
BR0015610B8 (pt) 2017-10-31
DE19955190A1 (de) 2001-06-21
JP2003514018A (ja) 2003-04-15
HK1045148A1 (en) 2002-11-15
JP2011148824A (ja) 2011-08-04
JP5650924B2 (ja) 2015-01-07
WO2001035957A1 (de) 2001-05-25
ATE337293T1 (de) 2006-09-15
CY1110389T1 (el) 2015-04-29
US6858650B1 (en) 2005-02-22
JP2010180243A (ja) 2010-08-19
HU227608B1 (en) 2011-09-28
IL149567A (en) 2007-08-19
EP1481964A1 (de) 2004-12-01
ATE286872T1 (de) 2005-01-15
IS2124B (is) 2006-07-14
ES2236032T7 (es) 2012-06-14
ATE395056T1 (de) 2008-05-15
NZ519230A (en) 2004-11-26
DK1690536T3 (da) 2008-09-01
KR100563149B1 (ko) 2006-03-21
EP1481964B1 (de) 2006-08-23
ZA200203315B (en) 2003-09-23
NO20022314L (no) 2002-05-15
HK1067114A1 (en) 2005-04-01
JP5290351B2 (ja) 2013-09-18
ES2303708T3 (es) 2008-08-16
KR20020059744A (ko) 2002-07-13
EA005588B1 (ru) 2005-04-28
NO332637B1 (no) 2012-11-26
KR100536095B1 (ko) 2005-12-12
CN1390194A (zh) 2003-01-08
UA77322C2 (en) 2006-11-15
ES2236032T3 (es) 2005-07-16
GEP20084430B (pl) 2008-07-25
HU228197B1 (en) 2013-01-28
JP2007137895A (ja) 2007-06-07
DE29923134U1 (de) 2000-06-29
ES2270240T3 (es) 2007-04-01
JP5503393B2 (ja) 2014-05-28
CZ20021343A3 (cs) 2002-09-11
UA73324C2 (uk) 2005-07-15
NO20022314D0 (no) 2002-05-15
IS6351A (is) 2002-04-19
HUP0204034A3 (en) 2004-12-28
SK288185B6 (sk) 2014-04-02
JP5717824B2 (ja) 2015-05-13
PT1481964E (pt) 2006-12-29
SK6572002A3 (en) 2002-12-03
BR0015610A (pt) 2002-07-30
JP4083431B2 (ja) 2008-04-30
CZ302497B6 (cs) 2011-06-15
WO2001035957A8 (de) 2001-06-21
JP2010180242A (ja) 2010-08-19
PT1230209E (pt) 2005-05-31
DE50013365D1 (de) 2006-10-05
BRPI0015610C1 (pt) 2021-05-25
DE50015163D1 (de) 2008-06-26
AU778132B2 (en) 2004-11-18
NO20065380L (no) 2002-05-15
IL149567A0 (en) 2002-11-10
CA2389749C (en) 2009-03-31
NO323920B1 (no) 2007-07-23
EP1690536A2 (de) 2006-08-16
HUP0204034A2 (hu) 2003-03-28
IS2673B (is) 2010-09-15
HU0900587D0 (en) 2009-11-30
EP1690536B1 (de) 2008-05-14
CN1215045C (zh) 2005-08-17
SI1690536T1 (sl) 2008-08-31
MXPA02004603A (es) 2004-09-10
BRPI0015610B1 (pt) 2016-04-19
DE50009239D1 (de) 2005-02-17
PT1690536E (pt) 2008-07-14
CY1106204T1 (el) 2011-06-08
AU2666701A (en) 2001-05-30
CZ302967B6 (cs) 2012-01-25
HUP0900587A3 (en) 2010-04-28
SI1230209T1 (en) 2005-06-30
EP1690536A3 (de) 2006-08-23
IS8382A (is) 2006-03-29

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