JP2009514801A5 - - Google Patents
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- Publication number
- JP2009514801A5 JP2009514801A5 JP2008534911A JP2008534911A JP2009514801A5 JP 2009514801 A5 JP2009514801 A5 JP 2009514801A5 JP 2008534911 A JP2008534911 A JP 2008534911A JP 2008534911 A JP2008534911 A JP 2008534911A JP 2009514801 A5 JP2009514801 A5 JP 2009514801A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- phenyl
- oxy
- fluorophenyl
- disease
- 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.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 claims 27
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 26
- 201000010099 disease Diseases 0.000 claims 19
- 125000000217 alkyl group Chemical group 0.000 claims 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 10
- 150000003839 salts Chemical class 0.000 claims 8
- 208000035475 disorder Diseases 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- 239000012453 solvate Substances 0.000 claims 7
- -1 4-{[(2-fluorophenyl) methyl] oxy} phenyl Chemical group 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 125000004438 haloalkoxy group Chemical group 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 238000000034 method Methods 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims 4
- 208000020925 Bipolar disease Diseases 0.000 claims 3
- 206010065390 Inflammatory pain Diseases 0.000 claims 3
- 125000003545 alkoxy group Chemical group 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 206010015037 epilepsy Diseases 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 125000005843 halogen group Chemical group 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 3
- 230000001404 mediated effect Effects 0.000 claims 3
- 208000004296 neuralgia Diseases 0.000 claims 3
- 208000021722 neuropathic pain Diseases 0.000 claims 3
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims 2
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 2
- 208000032841 Bulimia Diseases 0.000 claims 2
- 206010006550 Bulimia nervosa Diseases 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 208000022497 Cocaine-Related disease Diseases 0.000 claims 2
- 208000030814 Eating disease Diseases 0.000 claims 2
- ITKLEASWWYEUPP-UHFFFAOYSA-N FC1=C(C=CC=C1)COC1=CC=C(C=C1)N1CCCC11C(N(CC1)C)=O Chemical compound FC1=C(C=CC=C1)COC1=CC=C(C=C1)N1CCCC11C(N(CC1)C)=O ITKLEASWWYEUPP-UHFFFAOYSA-N 0.000 claims 2
- 208000019454 Feeding and Eating disease Diseases 0.000 claims 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 208000019022 Mood disease Diseases 0.000 claims 2
- 108010052164 Sodium Channels Proteins 0.000 claims 2
- 102000018674 Sodium Channels Human genes 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 2
- 208000028505 alcohol-related disease Diseases 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 230000001419 dependent effect Effects 0.000 claims 2
- 235000014632 disordered eating Nutrition 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 229960002715 nicotine Drugs 0.000 claims 2
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 claims 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 208000011117 substance-related disease Diseases 0.000 claims 2
- 239000011593 sulfur Substances 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 238000002560 therapeutic procedure Methods 0.000 claims 2
- JSJWYHYFOUBEOG-UYAOXDASSA-N (2r,5r)-2-[3-[(2-fluorophenyl)methoxy]phenyl]-1,7-diazaspiro[4.4]nonan-6-one Chemical compound FC1=CC=CC=C1COC1=CC=CC([C@@H]2N[C@]3(C(NCC3)=O)CC2)=C1 JSJWYHYFOUBEOG-UYAOXDASSA-N 0.000 claims 1
- FDIJVQHOCKBDLC-TZIWHRDSSA-N (2r,5r)-2-[3-[(2-fluorophenyl)methoxy]phenyl]-7-methyl-1,7-diazaspiro[4.4]nonan-6-one Chemical compound O=C1N(C)CC[C@@]11N[C@@H](C=2C=C(OCC=3C(=CC=CC=3)F)C=CC=2)CC1 FDIJVQHOCKBDLC-TZIWHRDSSA-N 0.000 claims 1
- VPZIEOMVSIQMAR-IRLDBZIGSA-N (2r,5r)-2-[4-[(2-fluorophenyl)methoxy]phenyl]-1,10-diazaspiro[4.6]undec-7-en-11-one Chemical compound FC1=CC=CC=C1COC1=CC=C([C@@H]2N[C@]3(C(NCC=CC3)=O)CC2)C=C1 VPZIEOMVSIQMAR-IRLDBZIGSA-N 0.000 claims 1
- OQVGCOLDYHIXTP-UYAOXDASSA-N (2r,5r)-2-[4-[(2-fluorophenyl)methoxy]phenyl]-1,7-diazaspiro[4.4]nonan-6-one Chemical compound FC1=CC=CC=C1COC1=CC=C([C@@H]2N[C@]3(C(NCC3)=O)CC2)C=C1 OQVGCOLDYHIXTP-UYAOXDASSA-N 0.000 claims 1
- BRANALMHLZEEND-TZIWHRDSSA-N (2r,5r)-2-[4-[(2-fluorophenyl)methoxy]phenyl]-7-methyl-1,7-diazaspiro[4.4]nonan-6-one Chemical compound O=C1N(C)CC[C@@]11N[C@@H](C=2C=CC(OCC=3C(=CC=CC=3)F)=CC=2)CC1 BRANALMHLZEEND-TZIWHRDSSA-N 0.000 claims 1
- AJYGGNUGQMYSRP-CTNGQTDRSA-N (2r,5s)-2-[4-[(2-fluorophenyl)methoxy]phenyl]-1,9-diazaspiro[4.5]decan-10-one Chemical compound FC1=CC=CC=C1COC1=CC=C([C@@H]2N[C@]3(C(NCCC3)=O)CC2)C=C1 AJYGGNUGQMYSRP-CTNGQTDRSA-N 0.000 claims 1
- FLDNUZQZRDKZTB-PKOBYXMFSA-N (2r,5s)-2-methyl-5-(4-phenylmethoxyphenyl)pyrrolidine-2-carboxamide Chemical compound N1[C@@](C)(C(N)=O)CC[C@H]1C(C=C1)=CC=C1OCC1=CC=CC=C1 FLDNUZQZRDKZTB-PKOBYXMFSA-N 0.000 claims 1
- KQYOVKQPWIEUHR-PKOBYXMFSA-N (2r,5s)-5-[4-[(2-fluorophenyl)methoxy]phenyl]-2-methylpyrrolidine-2-carboxamide Chemical compound N1[C@@](C)(C(N)=O)CC[C@H]1C(C=C1)=CC=C1OCC1=CC=CC=C1F KQYOVKQPWIEUHR-PKOBYXMFSA-N 0.000 claims 1
- OQVGCOLDYHIXTP-ICSRJNTNSA-N (2s,5s)-2-[4-[(2-fluorophenyl)methoxy]phenyl]-1,7-diazaspiro[4.4]nonan-6-one Chemical compound FC1=CC=CC=C1COC1=CC=C([C@H]2N[C@@]3(C(NCC3)=O)CC2)C=C1 OQVGCOLDYHIXTP-ICSRJNTNSA-N 0.000 claims 1
- AJYGGNUGQMYSRP-FPOVZHCZSA-N (2s,5s)-2-[4-[(2-fluorophenyl)methoxy]phenyl]-1,9-diazaspiro[4.5]decan-10-one Chemical compound FC1=CC=CC=C1COC1=CC=C([C@H]2N[C@]3(C(NCCC3)=O)CC2)C=C1 AJYGGNUGQMYSRP-FPOVZHCZSA-N 0.000 claims 1
- SMPXCHFZGCEVTB-TZIWHRDSSA-N (5r,7r)-7-[4-[(2-fluorophenyl)methoxy]phenyl]-2,6-diazaspiro[4.5]decan-1-one Chemical compound FC1=CC=CC=C1COC1=CC=C([C@@H]2N[C@]3(C(NCC3)=O)CCC2)C=C1 SMPXCHFZGCEVTB-TZIWHRDSSA-N 0.000 claims 1
- SMPXCHFZGCEVTB-FPOVZHCZSA-N (5s,7s)-7-[4-[(2-fluorophenyl)methoxy]phenyl]-2,6-diazaspiro[4.5]decan-1-one Chemical compound FC1=CC=CC=C1COC1=CC=C([C@H]2N[C@@]3(C(NCC3)=O)CCC2)C=C1 SMPXCHFZGCEVTB-FPOVZHCZSA-N 0.000 claims 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 1
- SBHXOKHTYAXNBT-YLJYHZDGSA-N 2-[4-[(2r,5r)-6-oxo-1,7-diazaspiro[4.4]nonan-2-yl]phenoxy]benzonitrile Chemical compound O=C1NCC[C@@]11N[C@@H](C=2C=CC(OC=3C(=CC=CC=3)C#N)=CC=2)CC1 SBHXOKHTYAXNBT-YLJYHZDGSA-N 0.000 claims 1
- KYRYDOSGFVANRO-TZIWHRDSSA-N 2-[[4-[(2r,5r)-6-oxo-1,7-diazaspiro[4.4]nonan-2-yl]phenoxy]methyl]benzonitrile Chemical compound O=C1NCC[C@@]11N[C@@H](C=2C=CC(OCC=3C(=CC=CC=3)C#N)=CC=2)CC1 KYRYDOSGFVANRO-TZIWHRDSSA-N 0.000 claims 1
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 235000011114 ammonium hydroxide Nutrition 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical group O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 1
- 0 CC1CC(C(CC(*)C2)N(CC(OC(C)(C)C)=O)C2(CCN*)C(O*)=O)=*C(*)C(*)C1 Chemical compound CC1CC(C(CC(*)C2)N(CC(OC(C)(C)C)=O)C2(CCN*)C(O*)=O)=*C(*)C(*)C1 0.000 description 1
Applications Claiming Priority (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0520578A GB0520578D0 (en) | 2005-10-10 | 2005-10-10 | Novel compounds |
| GB0520578.6 | 2005-10-10 | ||
| GB0523030.5 | 2005-11-11 | ||
| GB0523030A GB0523030D0 (en) | 2005-11-11 | 2005-11-11 | Novel compounds |
| GB0603897.0 | 2006-02-27 | ||
| GB0603897A GB0603897D0 (en) | 2006-02-27 | 2006-02-27 | Novel compounds |
| GB0609159A GB0609159D0 (en) | 2006-05-09 | 2006-05-09 | Novel Compounds |
| GB0609159.9 | 2006-05-09 | ||
| GB0618511.0 | 2006-09-20 | ||
| GB0618511A GB0618511D0 (en) | 2006-09-20 | 2006-09-20 | Novel compounds |
| PCT/EP2006/009732 WO2007042240A1 (en) | 2005-10-10 | 2006-10-06 | Quaternary alpha-aminocarboxamide derivatives as modulators of voltage-gated sodium channels |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2009514801A JP2009514801A (ja) | 2009-04-09 |
| JP2009514801A5 true JP2009514801A5 (enExample) | 2009-11-26 |
| JP5139306B2 JP5139306B2 (ja) | 2013-02-06 |
Family
ID=37762326
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008534911A Expired - Fee Related JP5139306B2 (ja) | 2005-10-10 | 2006-10-06 | 電位依存性ナトリウムチャネルの調節因子としての第四級α−アミノカルボキサミド誘導体 |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US7803833B2 (enExample) |
| EP (1) | EP1934176B1 (enExample) |
| JP (1) | JP5139306B2 (enExample) |
| KR (1) | KR20080059297A (enExample) |
| AR (1) | AR057869A1 (enExample) |
| AT (1) | ATE543797T1 (enExample) |
| AU (1) | AU2006301471A1 (enExample) |
| BR (1) | BRPI0617189A2 (enExample) |
| CA (1) | CA2625763A1 (enExample) |
| CR (1) | CR9926A (enExample) |
| EA (1) | EA200801068A1 (enExample) |
| ES (1) | ES2381686T3 (enExample) |
| IL (1) | IL190544A (enExample) |
| NO (1) | NO20082122L (enExample) |
| NZ (1) | NZ567030A (enExample) |
| PE (1) | PE20070495A1 (enExample) |
| TW (1) | TW200728258A (enExample) |
| WO (1) | WO2007042240A1 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200730494A (en) * | 2005-10-10 | 2007-08-16 | Glaxo Group Ltd | Novel compounds |
| ATE472529T1 (de) * | 2005-10-10 | 2010-07-15 | Glaxo Group Ltd | Prolinamidderivate als natriumkanalmodulatoren |
| GB0701365D0 (en) * | 2007-01-24 | 2007-03-07 | Glaxo Group Ltd | Novel pharmaceutical compositions |
| GB0701366D0 (en) * | 2007-01-24 | 2007-03-07 | Glaxo Group Ltd | Novel pharmaceutical compositions |
| GB0706630D0 (en) * | 2007-04-04 | 2007-05-16 | Glaxo Group Ltd | Novel compounds |
| PL2477964T3 (pl) * | 2009-09-14 | 2015-08-31 | Convergence Pharmaceuticals | Proces wytwarzania pochodnych alfa-karboksyamidu |
| JP2011232320A (ja) * | 2009-10-01 | 2011-11-17 | Sony Corp | 生体内物質検出用プローブ、および該生体内物質検出用プローブを用いた生体内物質検出装置 |
| EP2681200A4 (en) | 2011-03-03 | 2015-05-27 | Zalicus Pharmaceuticals Ltd | INHIBITORS OF BENZIMIDAZOLE TYPE OF SODIUM CHANNEL |
| GB201122113D0 (en) | 2011-12-22 | 2012-02-01 | Convergence Pharmaceuticals | Novel compounds |
| GB201209015D0 (en) | 2012-05-22 | 2012-07-04 | Convergence Pharmaceuticals | Novel compounds |
| GB201209670D0 (en) * | 2012-05-31 | 2012-07-18 | Convergence Pharmaceuticals | Novel compounds |
| ES2912881T3 (es) | 2014-12-23 | 2022-05-30 | Convergence Pharmaceuticals | Procedimiento para preparar derivados de alfa-carboxamida pirrolidina |
| WO2016160574A2 (en) * | 2015-03-27 | 2016-10-06 | Scifluor Life Sciences, Inc. | Aryl- and heteroaryl-pyrrolidine-2-carboxamide compounds |
| CN112153968A (zh) | 2017-10-05 | 2020-12-29 | 生物基因公司 | 制备α-羧酰胺吡咯烷衍生物的工艺 |
| JP2020536898A (ja) | 2017-10-10 | 2020-12-17 | バイオジェン インコーポレイテッド | スピロ誘導体を調製するためのプロセス |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL94466A (en) | 1989-05-25 | 1995-01-24 | Erba Carlo Spa | Pharmaceutical preparations containing the history of A-amino carboxamide N-phenylalkyl are converted into such new compounds and their preparation |
| US6201016B1 (en) | 1994-06-27 | 2001-03-13 | Cytomed Incorporated | Compounds and methods for the treatment of cardiovascular, inflammatory and immune disorders |
| GB9727523D0 (en) | 1997-12-31 | 1998-02-25 | Pharmacia & Upjohn Spa | Alpha-aminoamide derivatives useful as analgesic agents |
| ES2345921T3 (es) | 1999-03-26 | 2010-10-06 | Euro-Celtique S.A. | Pirazoles, imidazoles, oxazoles, tiazoles y pirroles sustituidos con arilo y su uso. |
| AR037233A1 (es) * | 2001-09-07 | 2004-11-03 | Euro Celtique Sa | Piridinas aril sustituidas, composiciones farmaceuticas y el uso de dichos compuestos para la elaboracion de un medicamento |
| TW200404796A (en) * | 2002-08-19 | 2004-04-01 | Ono Pharmaceutical Co | Nitrogen-containing compound |
| TWI286132B (en) | 2002-09-20 | 2007-09-01 | Hoffmann La Roche | 4-pyrrolidino-phenyl-benzyl ether derivatives |
| MY142651A (en) | 2003-03-18 | 2010-12-15 | Merck Sharp & Dohme | Biaryl substituted triazoles as sodium channel blockers |
| CA2520804A1 (en) | 2003-04-03 | 2004-10-28 | Merck & Co., Inc. | Biaryl substituted pyrazoles as sodium channel blockers |
| US20070060584A1 (en) | 2003-04-18 | 2007-03-15 | Chakravarty Prasun K | Biaryl substituted thiazoles, oxazoles and imidazoles as sodium channel blockers |
| WO2005000309A2 (en) | 2003-06-27 | 2005-01-06 | Ionix Pharmaceuticals Limited | Chemical compounds |
| US20060217365A1 (en) * | 2003-07-02 | 2006-09-28 | Astrazeneca Ab | Method of treating mood disorders |
| EP1524265A1 (en) * | 2003-10-15 | 2005-04-20 | Newron Pharmaceuticals S.p.A. | Prolinamide derivatives as sodium and/or calcium channel blockers or selective MAO-B inhibitors |
| WO2006119390A1 (en) | 2005-05-04 | 2006-11-09 | Vertex Pharmaceuticals Incorporated | Pyridines useful as modulators of ion channels |
| JP2008540443A (ja) | 2005-05-04 | 2008-11-20 | バーテックス ファーマシューティカルズ インコーポレイテッド | イオンチャネルのモジュレーターとして有用なピリミジンおよびピラジン |
| WO2006124865A2 (en) | 2005-05-19 | 2006-11-23 | Vertex Pharmaceuticals Incorporated | Biaryls derivatives useful as modulators of ion channels |
| GB0701365D0 (en) | 2007-01-24 | 2007-03-07 | Glaxo Group Ltd | Novel pharmaceutical compositions |
| JP2010516731A (ja) | 2007-01-24 | 2010-05-20 | グラクソ グループ リミテッド | ２−メトキシ−５−（５−トリフルオロメチル−テトラゾール−１−イル）−ベンジル］−（２ｓ−フェニル−ピペリジン−３ｓ−イル）−アミンを含む医薬組成物 |
| GB0701366D0 (en) | 2007-01-24 | 2007-03-07 | Glaxo Group Ltd | Novel pharmaceutical compositions |
| GB0706630D0 (en) | 2007-04-04 | 2007-05-16 | Glaxo Group Ltd | Novel compounds |
-
2006
- 2006-10-05 TW TW095136996A patent/TW200728258A/zh unknown
- 2006-10-06 CA CA002625763A patent/CA2625763A1/en not_active Abandoned
- 2006-10-06 BR BRPI0617189-3A patent/BRPI0617189A2/pt not_active IP Right Cessation
- 2006-10-06 PE PE2006001224A patent/PE20070495A1/es not_active Application Discontinuation
- 2006-10-06 JP JP2008534911A patent/JP5139306B2/ja not_active Expired - Fee Related
- 2006-10-06 EA EA200801068A patent/EA200801068A1/ru unknown
- 2006-10-06 EP EP06806111A patent/EP1934176B1/en active Active
- 2006-10-06 US US11/570,564 patent/US7803833B2/en active Active
- 2006-10-06 NZ NZ567030A patent/NZ567030A/en unknown
- 2006-10-06 WO PCT/EP2006/009732 patent/WO2007042240A1/en not_active Ceased
- 2006-10-06 ES ES06806111T patent/ES2381686T3/es active Active
- 2006-10-06 KR KR1020087011273A patent/KR20080059297A/ko not_active Withdrawn
- 2006-10-06 AU AU2006301471A patent/AU2006301471A1/en not_active Abandoned
- 2006-10-06 AT AT06806111T patent/ATE543797T1/de active
- 2006-10-09 AR ARP060104440A patent/AR057869A1/es active IP Right Grant
-
2008
- 2008-03-31 IL IL190544A patent/IL190544A/en active IP Right Grant
- 2008-04-25 CR CR9926A patent/CR9926A/es not_active Application Discontinuation
- 2008-05-06 NO NO20082122A patent/NO20082122L/no not_active Application Discontinuation
-
2010
- 2010-08-04 US US12/850,330 patent/US8153623B2/en not_active Expired - Fee Related
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