JP2008518068A5 - - Google Patents
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- JP2008518068A5 JP2008518068A5 JP2007538385A JP2007538385A JP2008518068A5 JP 2008518068 A5 JP2008518068 A5 JP 2008518068A5 JP 2007538385 A JP2007538385 A JP 2007538385A JP 2007538385 A JP2007538385 A JP 2007538385A JP 2008518068 A5 JP2008518068 A5 JP 2008518068A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- hydroxyalkyl
- aryl
- acid
- nhc
- Prior art date
- 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.)
- Pending
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- 150000001413 amino acids Chemical class 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical group 0.000 claims description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 2
- 150000001342 alkaline earth metals Chemical group 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- -1 morpholino, piperidino Chemical group 0.000 claims description 2
- 230000003287 optical effect Effects 0.000 claims description 2
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 2
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 235000001014 amino acid Nutrition 0.000 description 7
- 229940024606 amino acid Drugs 0.000 description 7
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 4
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 3
- 239000004471 Glycine Substances 0.000 description 2
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 2
- ROHFNLRQFUQHCH-YFKPBYRVSA-N L-leucine Chemical compound CC(C)C[C@H](N)C(O)=O ROHFNLRQFUQHCH-YFKPBYRVSA-N 0.000 description 2
- OUYCCCASQSFEME-QMMMGPOBSA-N L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-QMMMGPOBSA-N 0.000 description 2
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 description 2
- AHLPHDHHMVZTML-UHFFFAOYSA-N Orn-delta-NH2 Natural products NCCCC(N)C(O)=O AHLPHDHHMVZTML-UHFFFAOYSA-N 0.000 description 2
- 235000004279 alanine Nutrition 0.000 description 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- MYFWUKZYURBPHI-BYPYZUCNSA-N (2s)-2-amino-3-(1h-imidazol-2-yl)propanoic acid Chemical compound OC(=O)[C@@H](N)CC1=NC=CN1 MYFWUKZYURBPHI-BYPYZUCNSA-N 0.000 description 1
- NYPYHUZRZVSYKL-UHFFFAOYSA-N -3,5-Diiodotyrosine Natural products OC(=O)C(N)CC1=CC(I)=C(O)C(I)=C1 NYPYHUZRZVSYKL-UHFFFAOYSA-N 0.000 description 1
- QWCKQJZIFLGMSD-UHFFFAOYSA-N 2-Aminobutanoic acid Natural products CCC(N)C(O)=O QWCKQJZIFLGMSD-UHFFFAOYSA-N 0.000 description 1
- UQZLXZWXCZGLSW-UHFFFAOYSA-N 2-[2-[2-sulfo-4-(triazin-4-ylamino)phenyl]ethenyl]-5-(triazin-4-ylamino)benzenesulfonic acid Chemical class C=1C=C(C=CC=2C(=CC(NC=3N=NN=CC=3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC1=CC=NN=N1 UQZLXZWXCZGLSW-UHFFFAOYSA-N 0.000 description 1
- XDDMZVMWZMSAMX-FHAQVOQBSA-N 2-amino-3-methylpentanoic acid;(2s,3s)-2-amino-3-methylpentanoic acid Chemical compound CCC(C)C(N)C(O)=O.CC[C@H](C)[C@H](N)C(O)=O XDDMZVMWZMSAMX-FHAQVOQBSA-N 0.000 description 1
- HOZBSSWDEKVXNO-DKWTVANSSA-N 2-aminobutanedioic acid;(2s)-2-aminobutanedioic acid Chemical compound OC(=O)C(N)CC(O)=O.OC(=O)[C@@H](N)CC(O)=O HOZBSSWDEKVXNO-DKWTVANSSA-N 0.000 description 1
- NYPYHUZRZVSYKL-ZETCQYMHSA-N 3,5-diiodo-L-tyrosine Chemical compound OC(=O)[C@@H](N)CC1=CC(I)=C(O)C(I)=C1 NYPYHUZRZVSYKL-ZETCQYMHSA-N 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- QWCKQJZIFLGMSD-GSVOUGTGSA-N D-alpha-aminobutyric acid Chemical compound CC[C@@H](N)C(O)=O QWCKQJZIFLGMSD-GSVOUGTGSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- NNIVFXCKHNRSRL-VKHMYHEASA-N Hydroxyglutamic acid Chemical compound ON[C@H](C(O)=O)CCC(O)=O NNIVFXCKHNRSRL-VKHMYHEASA-N 0.000 description 1
- SNDPXSYFESPGGJ-BYPYZUCNSA-N L-2-aminopentanoic acid Chemical compound CCC[C@H](N)C(O)=O SNDPXSYFESPGGJ-BYPYZUCNSA-N 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- AHLPHDHHMVZTML-BYPYZUCNSA-N L-Ornithine Chemical compound NCCC[C@H](N)C(O)=O AHLPHDHHMVZTML-BYPYZUCNSA-N 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- ODKSFYDXXFIFQN-BYPYZUCNSA-P L-argininium(2+) Chemical compound NC(=[NH2+])NCCC[C@H]([NH3+])C(O)=O ODKSFYDXXFIFQN-BYPYZUCNSA-P 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- FFEARJCKVFRZRR-BYPYZUCNSA-N L-methionine Chemical compound CSCC[C@H](N)C(O)=O FFEARJCKVFRZRR-BYPYZUCNSA-N 0.000 description 1
- SNDPXSYFESPGGJ-UHFFFAOYSA-N L-norVal-OH Natural products CCCC(N)C(O)=O SNDPXSYFESPGGJ-UHFFFAOYSA-N 0.000 description 1
- LRQKBLKVPFOOQJ-YFKPBYRVSA-N L-norleucine Chemical compound CCCC[C@H]([NH3+])C([O-])=O LRQKBLKVPFOOQJ-YFKPBYRVSA-N 0.000 description 1
- AHLPHDHHMVZTML-BYPYZUCNSA-O L-ornithinium(1+) Chemical compound [NH3+]CCC[C@H]([NH3+])C([O-])=O AHLPHDHHMVZTML-BYPYZUCNSA-O 0.000 description 1
- COLNVLDHVKWLRT-QMMMGPOBSA-N L-phenylalanine Chemical compound OC(=O)[C@@H](N)CC1=CC=CC=C1 COLNVLDHVKWLRT-QMMMGPOBSA-N 0.000 description 1
- AYFVYJQAPQTCCC-GBXIJSLDSA-N L-threonine Chemical compound C[C@@H](O)[C@H](N)C(O)=O AYFVYJQAPQTCCC-GBXIJSLDSA-N 0.000 description 1
- QIVBCDIJIAJPQS-VIFPVBQESA-N L-tryptophane Chemical compound C1=CC=C2C(C[C@H](N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-VIFPVBQESA-N 0.000 description 1
- ROHFNLRQFUQHCH-UHFFFAOYSA-N Leucine Natural products CC(C)CC(N)C(O)=O ROHFNLRQFUQHCH-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- XTRXBOSGRMJASM-UHFFFAOYSA-N N1=NN=C(C=C1)NC(=C(C1=C(C(=CC=C1)S(=O)(=O)O)S(=O)(=O)O)NC1=NN=NC=C1)C1=CC=CC=C1 Chemical class N1=NN=C(C=C1)NC(=C(C1=C(C(=CC=C1)S(=O)(=O)O)S(=O)(=O)O)NC1=NN=NC=C1)C1=CC=CC=C1 XTRXBOSGRMJASM-UHFFFAOYSA-N 0.000 description 1
- UTJLXEIPEHZYQJ-UHFFFAOYSA-N Ornithine Natural products OC(=O)C(C)CCCN UTJLXEIPEHZYQJ-UHFFFAOYSA-N 0.000 description 1
- MTCFGRXMJLQNBG-UHFFFAOYSA-N Serine Natural products OCC(N)C(O)=O MTCFGRXMJLQNBG-UHFFFAOYSA-N 0.000 description 1
- AYFVYJQAPQTCCC-UHFFFAOYSA-N Threonine Natural products CC(O)C(N)C(O)=O AYFVYJQAPQTCCC-UHFFFAOYSA-N 0.000 description 1
- 239000004473 Threonine Substances 0.000 description 1
- QIVBCDIJIAJPQS-UHFFFAOYSA-N Tryptophan Natural products C1=CC=C2C(CC(N)C(O)=O)=CNC2=C1 QIVBCDIJIAJPQS-UHFFFAOYSA-N 0.000 description 1
- KZSNJWFQEVHDMF-UHFFFAOYSA-N Valine Natural products CC(C)C(N)C(O)=O KZSNJWFQEVHDMF-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000000539 amino acid group Chemical group 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- 229960000415 diiodotyrosine Drugs 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- NBZBKCUXIYYUSX-UHFFFAOYSA-N iminodiacetic acid Chemical compound OC(=O)CNCC(O)=O NBZBKCUXIYYUSX-UHFFFAOYSA-N 0.000 description 1
- 229930182817 methionine Natural products 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- UGOWMXKRKUKFFW-UHFFFAOYSA-N n'-(2-hydroxyethyl)propanehydrazide Chemical group CCC(=O)NNCCO UGOWMXKRKUKFFW-UHFFFAOYSA-N 0.000 description 1
- 229960003104 ornithine Drugs 0.000 description 1
- COLNVLDHVKWLRT-UHFFFAOYSA-N phenylalanine Natural products OC(=O)C(N)CC1=CC=CC=C1 COLNVLDHVKWLRT-UHFFFAOYSA-N 0.000 description 1
- 235000008729 phenylalanine Nutrition 0.000 description 1
- 235000004400 serine Nutrition 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 235000002374 tyrosine Nutrition 0.000 description 1
- 239000004474 valine Substances 0.000 description 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04105343 | 2004-10-27 | ||
| PCT/EP2005/055301 WO2006045714A1 (en) | 2004-10-27 | 2005-10-17 | Compositions of fluorescent whitening agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008518068A JP2008518068A (ja) | 2008-05-29 |
| JP2008518068A5 true JP2008518068A5 (cg-RX-API-DMAC10.html) | 2011-04-14 |
Family
ID=34929769
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007538385A Pending JP2008518068A (ja) | 2004-10-27 | 2005-10-17 | 蛍光増白剤の組成物 |
Country Status (15)
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007135003A1 (en) | 2006-05-23 | 2007-11-29 | Ciba Holding Inc. | A detergent composition for textile fibre materials |
| SE530020C2 (sv) * | 2006-06-15 | 2008-02-12 | Holmen Ab | Förfarande för stabilisering av vitheten hos i ytbehandlingslim/smet för papper ingående fluroescerande vitmedel (FWA) och hos av detta/dessa formade ytbehandlingsskikt |
| FR2911884B1 (fr) * | 2007-01-31 | 2010-02-26 | Arjowiggins Licensing Sas | Feuille couchee blanche imprimable par offset et ayant un haut pouvoir de fluorescence et son procede de fabrication |
| CA2682924A1 (en) | 2007-04-05 | 2008-10-16 | Akzo Nobel N.V. | Process for improving optical properties of paper |
| US8227808B2 (en) * | 2007-12-06 | 2012-07-24 | Chimei Innolux Corporation | Method for manufacturing thin film transistor (TFT) and OLED display having TFTS manufactured by the same |
| BR112012001857A2 (pt) * | 2009-07-24 | 2016-03-15 | Clariant Finance Bvi Ltd | soluções aquosas de tinturas ácidas para o sombreado em aplicações de impressão dimensionada |
| ES2394545T3 (es) * | 2009-09-17 | 2013-02-01 | Blankophor Gmbh & Co. Kg | Agente blanqueador fluorescente de tipo disulfo |
| KR20130096218A (ko) * | 2010-06-14 | 2013-08-29 | 바스프 에스이 | 개선된 색 안정성을 갖는 수분-흡수 중합체 입자 |
| TW201217610A (en) * | 2010-07-23 | 2012-05-01 | Clariant Int Ltd | Method for preparing white paper |
| EP2412870B1 (en) * | 2010-07-30 | 2013-04-17 | Blankophor GmbH & Co. KG | Composition and process for whitening paper |
| PT2431519E (pt) | 2010-09-17 | 2013-10-28 | Blankophor Gmbh & Co Kg | Composições de agente de branqueamento fluorescente |
| UA110221C2 (uk) | 2010-09-28 | 2015-12-10 | Tetra Laval Holdings & Finance | Спосіб одержання пакувального матеріалу для упаковки, що стерилізується, пакувальний матеріал та упаковка |
| FR2966467B1 (fr) * | 2010-10-26 | 2014-11-07 | Berkem Sa | Composition pour le traitement du bois |
| PL2799618T3 (pl) * | 2013-04-29 | 2016-12-30 | Zastosowanie mikronizowanej celulozy oraz fluorescencyjnego środka bielącego do powierzchniowej obróbki celulozowych materiałów | |
| US9181656B2 (en) * | 2013-11-06 | 2015-11-10 | Meng Jun Li | FWA formulation used for the papermaking process |
| EP3118811B1 (en) | 2014-03-13 | 2023-05-03 | Nec Corporation | Detecting device, detecting method, and recording medium |
| CN106087384A (zh) * | 2016-06-21 | 2016-11-09 | 太仓市东明化工有限公司 | 一种织物用耐水型荧光增白剂 |
| CN107602492A (zh) * | 2017-10-12 | 2018-01-19 | 贺州学院 | 一种两性丙烯酸酯季铵盐荧光增白剂的合成与应用 |
| EP3623392B1 (en) * | 2018-09-14 | 2023-07-19 | Archroma IP GmbH | Optically brightened latexes |
| CN112888310A (zh) * | 2018-10-17 | 2021-06-01 | 巴斯夫欧洲公司 | 在高剪切条件下稳定聚丙烯酰胺共聚物溶液的添加剂 |
| WO2020251532A1 (en) * | 2019-06-10 | 2020-12-17 | Hewlett-Packard Development Company, L.P. | Three-dimensional printing |
| CN116296703B (zh) * | 2023-05-17 | 2023-07-28 | 广州盛安医学检验有限公司 | 一种荧光染色液在制备阴道炎检测试剂中的应用 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2928052A1 (de) * | 1978-07-17 | 1980-01-31 | Ciba Geigy Ag | Stabile stilbenaufhellerloesungen |
| JPS5725365A (en) * | 1980-07-22 | 1982-02-10 | Showa Kagaku Kogyo Kk | Dyestuff salt-containing fluorescent brightener composition |
| JPS608371A (ja) * | 1983-06-27 | 1985-01-17 | Sumitomo Chem Co Ltd | 螢光増白剤水性組成物 |
| GB8330404D0 (en) * | 1983-11-15 | 1983-12-21 | Dow Chemical Europ | Activation of fluorescent whitening agents |
| JPS6131468A (ja) * | 1984-07-23 | 1986-02-13 | Nippon Kayaku Co Ltd | 水性液状螢光増白染料組成物 |
| DE3502038A1 (de) * | 1985-01-23 | 1986-07-24 | Sandoz-Patent-GmbH, 7850 Lörrach | Waessrige aufhellerpraeparate und deren verwendung im papierstrich |
| GB9422280D0 (en) * | 1994-11-04 | 1994-12-21 | Ciba Geigy Ag | Fluorescent whitening agent formulation |
| GB2294708B (en) * | 1994-11-04 | 1998-08-05 | Ciba Geigy Ag | Fluorescent whitening agent formulation |
| RU2241703C2 (ru) * | 1998-02-20 | 2004-12-10 | Циба Спешиалти Кемикалз Холдинг Инк. | Способ получения жидкой композиции, содержащей соединения стильбена |
| US6202294B1 (en) * | 1998-09-25 | 2001-03-20 | Lucent Technologies Inc. | EMI/RFI shield assembly cover removal tool |
| JP4340995B2 (ja) * | 1999-07-09 | 2009-10-07 | 星光Ｐｍｃ株式会社 | 紙塗工用組成物、並びにそれを塗工したクリアコート紙及びピグメントコート紙 |
| GB9917508D0 (en) * | 1999-07-27 | 1999-09-29 | Ciba Spec Chem Water Treat Ltd | Coating colour |
| IL147292A0 (en) * | 1999-08-05 | 2002-08-14 | Ciba Sc Holding Ag | Use of whitening pigments for whitening paper coating compositions |
| ATE318954T1 (de) | 1999-08-13 | 2006-03-15 | Ciba Sc Holding Ag | Formulierungen fluoreszierender optischer aufheller |
| CN1373758A (zh) * | 1999-09-10 | 2002-10-09 | 西巴特殊化学品控股有限公司 | 用作荧光增白剂的三嗪基氨基1,2－二苯乙烯衍生物 |
| DE10055592A1 (de) * | 2000-11-09 | 2002-05-23 | Basf Ag | Papierstreichmassen |
| GB0100610D0 (en) * | 2001-01-10 | 2001-02-21 | Clariant Int Ltd | Improvements in or relating to organic compounds |
| US20040238791A1 (en) * | 2001-09-03 | 2004-12-02 | Simon Champ | Reinforcement of the effect of optical brighteners by means of polymers |
| EP1438197B1 (de) * | 2001-09-03 | 2008-10-15 | Basf Se | Verfahren zur erhöhung der weisse von papier mit hilfe von kationischen polyelektrolyten |
| GB0125177D0 (en) * | 2001-10-19 | 2001-12-12 | Clariant Int Ltd | Improvements in or relating to organic compounds |
| DE10162052A1 (de) * | 2001-12-17 | 2003-06-26 | Basf Ag | Verfahren zur Herstellung von Papier, Pappe und Karton |
| DE10217677A1 (de) * | 2002-04-19 | 2003-11-06 | Bayer Ag | Verwendung von Aufhellern zur Herstellung von Streichmassen |
| ES2290473T3 (es) * | 2002-06-11 | 2008-02-16 | Ciba Specialty Chemicals Holding Inc. | Pigmentos de blanqueo. |
| JP2004145254A (ja) * | 2002-08-28 | 2004-05-20 | Fuji Photo Film Co Ltd | 記録材料用支持体及びその製造方法 |
| US20060260509A1 (en) * | 2005-04-22 | 2006-11-23 | Evers Glenn R | Compositions for enhanced paper brightness and whiteness |
-
2005
- 2005-10-17 WO PCT/EP2005/055301 patent/WO2006045714A1/en not_active Ceased
- 2005-10-17 RU RU2007119642/02A patent/RU2418904C2/ru not_active IP Right Cessation
- 2005-10-17 US US11/665,886 patent/US7731820B2/en not_active Expired - Fee Related
- 2005-10-17 AU AU2005298779A patent/AU2005298779B2/en not_active Ceased
- 2005-10-17 EP EP05796932A patent/EP1805361B1/en not_active Expired - Lifetime
- 2005-10-17 AT AT05796932T patent/ATE441000T1/de active
- 2005-10-17 ES ES05796932T patent/ES2329699T3/es not_active Expired - Lifetime
- 2005-10-17 DE DE602005016291T patent/DE602005016291D1/de not_active Expired - Lifetime
- 2005-10-17 JP JP2007538385A patent/JP2008518068A/ja active Pending
- 2005-10-17 CN CN2005800364454A patent/CN101048551B/zh not_active Expired - Fee Related
- 2005-10-17 BR BRPI0516966-6A patent/BRPI0516966A/pt not_active IP Right Cessation
- 2005-10-17 KR KR1020077011774A patent/KR20070085440A/ko not_active Ceased
- 2005-10-17 PL PL05796932T patent/PL1805361T3/pl unknown
- 2005-10-17 PT PT05796932T patent/PT1805361E/pt unknown
-
2007
- 2007-04-03 ZA ZA200702771A patent/ZA200702771B/xx unknown
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