AR055192A1 - 2-quinolil-oxazoles sustituidos utiles como inhibidores de pde4, composicion farmaceutica en base al compuesto y el uso del compuesto para preparar medicamentos - Google Patents
2-quinolil-oxazoles sustituidos utiles como inhibidores de pde4, composicion farmaceutica en base al compuesto y el uso del compuesto para preparar medicamentosInfo
- Publication number
- AR055192A1 AR055192A1 ARP050102012A ARP050102012A AR055192A1 AR 055192 A1 AR055192 A1 AR 055192A1 AR P050102012 A ARP050102012 A AR P050102012A AR P050102012 A ARP050102012 A AR P050102012A AR 055192 A1 AR055192 A1 AR 055192A1
- Authority
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- Argentina
- Prior art keywords
- alkyl
- phenyl
- heteroaryl
- cycloalkyl
- nr18r19
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 229940123932 Phosphodiesterase 4 inhibitor Drugs 0.000 title 1
- 229940079593 drug Drugs 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 239000002587 phosphodiesterase IV inhibitor Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 56
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 17
- 229910052739 hydrogen Inorganic materials 0.000 abstract 16
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 16
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 13
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 12
- 125000003545 alkoxy group Chemical group 0.000 abstract 11
- 125000001424 substituent group Chemical group 0.000 abstract 11
- 125000001475 halogen functional group Chemical group 0.000 abstract 9
- 125000001188 haloalkyl group Chemical group 0.000 abstract 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 4
- 125000003709 fluoroalkyl group Chemical group 0.000 abstract 4
- -1 alkyl-NR18R19 Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004990 dihydroxyalkyl group Chemical group 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000002757 morpholinyl group Chemical group 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 208000026935 allergic disease Diseases 0.000 abstract 1
- 230000000172 allergic effect Effects 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 229910021386 carbon form Inorganic materials 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- 125000005358 mercaptoalkyl group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
Classifications
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- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/4709—Non-condensed quinolines and containing further heterocyclic rings
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- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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Abstract
Estos compuestos resultan utiles para tratar enfermedades alérgicas e inflamatorias, enfermedades del S.N.C. y diabetes. Reivindicacion 1: Un compuesto representado por la formula estructural (1) o una sal o solvato del mismo aceptable para uso farmacéutico, donde el anillo A es como los compuestos de formulas (2); R es H o alquilo, X es O o S; R1 es H, alquilo, cicloalquilo, cicloalquilC1-4alquilo-, - CH2F, -CHF2, -CF3, -C(O)alquilo o -C(O)NR18R19; R3 y R4 se seleccionan en forma independiente del grupo integrado por H, alquilo, hidroxialquilo y -C(O)Oalquilo; R5 y R6 se seleccionan en forma independiente del grupo integrado por H, alquilo, hidroxialquilo, alcoxialquilo, mercaptoalquilo, -CH2F, -CHF2, -CF3, -C(O)OH, - C(O)Oalquilo y -C(O)NR43R44; t es 1 o 2; R7 es H es H, alquilo, alquenilo, hidroxialquilo, cicloalquilo, alcoxialquilo, aminoalquilo, (R17-fenil)alquilo o -CH2-C(O)-O-alquilo; R8 es H, alquilo, alquenilo, alcoxi, alcoxialquilo, hidroxialquilo, dihidroxialquilo, alquil-NR18R19, cianoalquilo, haloalquilo, R23-heteroarilo, R23-heteroarilalquilo, R36-heterocicloalquilo, (R36-heterocicloalquiI) alquilo, R17-fenilo, (R17-fenil)alquilo, R17-naftilo, (R17-naftil)alquilo, R17-benciloxi, -alquil- C(O)-NR18R19, -alquil-C(O)-N(R30)-(R23- heteroarilo), -alquil-C(O)-(R17-fenilo), -alquiI-C(O)-(R36-heterocicloalquilo); -alquil-N(R30)-C(O)Oalquilo, -alquil-N(R30)-C(O)-NR18R19, -alquil- N(R30)-C(O)alquilo, -alquil-N(R30)-C(O)-(fluoroalquilo), -alquil- N(R30)-C(O)-(R39-cicloalquilo), -alquil-N(R30)-C(O)-(R17-fenilo), -alquil-N(R30)- C(O)-(R23-heteroarilo), -alquil-N(R30)-C(O)-alquilen-(R23-heteroarilo), -aIquil-NH-SO2-NR18R19, -alquil-N(R30)-(R17-fenilo), -alquil- N(R30)-(R23-heteroarilo), -alquil-O- (R17-fenilo), -alquil-O-(R23-heteroarilo), -alquil-N(R30)-SO2-alquilo, alquiltioalquilo-, alquil-SO2-alquilo-, (R35-fenilalquil)-S-alquilo-, (hidroxialquil)-S-alquilo-, (alcoxialquil)-S-alquilo-, -alquil-CO2-alquilo, R45-hidroxialquilo, dihidroxialquilo sustituido con R17-benciloxi, dihidroxialquilo sustituido con R17-fenilo, alcoxialquilo sustituido con R17-fenilo, (R17-fenil)alquilo sustituido con -CO2alquilo, (R17-fenil)alquilo sustituido con -C(O)N(R30)2, alquilo sustituido con (R23-heteroarilo) y -C(O)NR37R38, haloalquilo sustituido con CO2alquiIo, R12-cicloalquilo, (R12-cicloalquil)alquilo, el grupo de formulas (3) o R7 y R8 y el N al cual están unidos forman un sistema anular seleccionado del grupo integrado por las formulas (4) donde el resto (5) comprende un grupo heteroarilo de 5 o 6 miembros sustituido con R35 fusionado al anillo piperidinilo o pirrolidinilo; p es 0 o 1; q es 0 o 1; la línea de puntos representa un doble enlace opcional; R9 es H, halo, alquilo, cicloalquilo, -CH2F, -CHF2 o CF3, R10, R11 y R13 se seleccionan en forma independiente del grupo integrado por H y halo; R12 es 1-3 sustituyentes seleccionados en forma independiente del grupo integrado por H, alquilo, hidroxi, alcoxi, hidroxialquilo, alcoxialquilo, -C(O) Oalquilo, -(CH2)n-N(R30)-C(O)-cicloalquilo, -(CH2)n-N(R30)-C(O)alquilo, -(CH2)n-N(R30)-C(O)Oalquilo, -(CH2)n-N(R30)-(R23-heteroarilo), -(CH2)n-N(R30)-C(O)-NR18R19, -(CH2)n-C(O)-NR18R19, R17-fenilo, R35- heteroarilalquilo, R35-heteroariloxi, -C(O)-heterocicloalquilo, -O-C(O)- heterocicloalquilo, -O-C(O)-NR18R19, -NH-SO2-alquilo, -NH-C(=NH)NH2 y el resto de formula (6), o dos sustituyentes R12 sobre el mismo carbono forman =O, =NOR30 o =CH2; R14 es 1 o 2 sustituyentes seleccionados en forma independiente del grupo integrado por H, OH, halo, alquilo, alcoxi, hidroxialquilo, alcoxialquilo, -CF3, CN, R17-fenilo, (R17-fenil)alquilo, -NR18R19, alquil-NR18R19, -(CH2)n-C(O)OH, -(CH2)n-C(O) Oalquilo, - (CH2)n-C(O)aIquilo, -(CH2)n-C(O)(R35-feniIo), -(CH2)n-C(O)(R23-heteroarilo), -(CH2)n-C(O)NR18R19, -(CH2)n-C(O)N(R30)-(CH2) n-(R23-heteroarilo), -(CH2)n-N(R30)-C(O)alquilo, -(CH2)n-N(R30)-C(O)-(fluoroalquiIo), -(CH2)n-N(R30)-C(O)-(cicloalquilo), - (CH2)n-N(R30)- C(O)(R35-fenilo), -(CH2)n,-N(R30)-C(O)(R23-heteroarilo), -(CH2)n-N(R30)C(O)NR18R19, -(CH2)n-N(R30)-C(O)OaIquilo, -(CH2)n-N(R30) cicloalquilo, -(CH2)n-N(R30)(R17-fenilo), -(CH2)n-N(R30)(R23-heteroarilo), -(CH2)n-N(R18)SO2alquilo, -(CH2)n- N(R20)SO2-(R17-fenilo), -(CH2)n-N(R30)SO2-CF3, -CH2S(O)0-2(R35-fenilo), -(CH2)n-OC(O)N(R30)alquilo, R23-heteroarilo, (R23- heteroaril)alquilo, (R23-heteroaril)oxi, (R23-heteroaril)amino, -CH(OH)-(R17-fenilo), -CH(OH)-(R23-heteroarilo), -C(=NOR30)- (R17-fenilo), -C(=NOR30)-(R23-heteroarilo), morfolinilo, tiomorfolinilo, los restos de formulas (7); w es 0 o 1; o dos sustituyentes R14 y el C al que ambos están unidos forman -C(=NOR30)- o -C(O)-; cada n es en forma independiente 0, 1, 2 o 3; R15 es H, alquilo, cicloalquilo, (cicloalquil)alquilo, hidroxialquilo, alcoxialquilo, haloalquilo, -C(O) Oalquilo, C(O)O(R30-cicloaIquilo), -aIquil-C(O)Oalquilo, -C(O)O-alquilen-(R35-fenilo), R17-fenilo, (R17-fenil)alquilo, -CH-(R17-fenilo)2, R23- heteroarilo, -(CH2)nC(O)NR18R19, -SO2-alquilo, -SO2-cicloalquilo, -SO2-CF3, -SO2-(R35-fenilo), -SO2-NR18R19, -C(O)alquilo, - C(O)-(fluoroalquilo), -C(O)-C(CH3)(CF3)2, -C(O)-(R17-fenilo), -C(O)-(R23-heteroarilo), -C(O)-hidroxialquilo, -C(O)- alcoxialquilo, -C(O)-(R39- cicloalquilo), -C(O)-alquilen-(R17-fenilo), -C(O)-alquilen-(23-heteroarilo), -C(O)-alquilen-S-C(O)alquilo, -C(=S)-(R17-fenilo), hidroxialquilo sustituido con R17-fenilo, hidroxialquilo sustituido con R23-heteroarilo, alcoxialquilo sustituido con R17-fenilo, alcoxialquilo sustituido con R23- heteroarilo, los restos de formulas (8), donde z es 0, 1 o2; R16 es 1 a 4 sustituyentes seleccionados en forma independiente del grupo integrado por H, alquilo, R17-fenilo, (R17-fenil)alquilo, (R23-heteroaril)alquilo, hidroxialquilo, alcoxialquilo y -C(O)Oalquilo, o dos grupos R16 y el carbono al que ambos están unidos forman -C(O)-; R17 es 1 a 3 sustituyentes seleccionados en forma independiente del grupo integrado por H, halo, alquilo, cicloalquilo, -OH, hidroxialquilo, alcoxi, alcoxialquilo, -CN, -CF3, -OCF3, -OCHF2, -OCH2F, -C(O)OH, -C(O)Oalquilo, -C(O)O-(R35- fenilo), -C(O)alquilo, -C(O)-(R35-fenilo), -SOalquilo, -SO2alquilo, -SO2-CF3, alquiltio, -NR43R44, - alquil-NR43R44, R35-fenilo, R35-fenoxi, R35- heteroarilo, R35-heteroariloxi, R36-heterocicloalquilo, -C(O)-(R36-heterocicloalquilo), hidroxialquil-NH-, -C(O)N(R30)2, -N(R43)-(R35- cicloalquilo) y -C(=NOR30); o dos sustituyentes R17 sobre átomos de carbono adyacentes conjuntamente forman -O-CH2-O-, -O(CH2)2-O-, -(CH2)2-O- o -O-CH2-O-CH2-; R18 y R19 se seleccionan en forma independiente del grupo integrado por H, alquilo, hidroxialquilo, alcoxialquilo, haloalquilo, R17-fenilo, (R17- fenil)alquilo, naftilo y cicloalquilo; R20 es H, alquilo o cicloalquilo; R22 es 1 a 4 sustituyentes seleccionados en forma independiente del grupo integrado por H, alquilo, hidroxi, alcoxi, halo, -CF3, -NH2 y R35-feniIo; R23 es 1 a 4 sustituyentes seleccionados en forma independiente del grupo integrado por H, alquilo, hidroxi, alcoxi, halo, -CF3, -NR18R19, -CN, -C(O)Oalquilo, -SO2-alquilo, -NHSO2- alquilo, R35-fenilo, R35-heteroarilo, morfolinilo y -(CH2)n-C(O)-N(R30)2; R24 es H, OH o alcoxi; o cuando el doble enlace opcional está presente, R24 y el átomo de carbono adyacente forman el doble enlace; R25 es H o R35-fenilo; R27 es 1 a 3 sustituyentes seleccionados en forma independiente del grupo integrado por H, halo, OH, alquilo, alcoxi, hidroxialquilo, alcoxialquilo, haloalquilo, -CN, -C(O)OH, -C(O)Oalquilo, - C(O)N(R30)(R18), -C(O)-(R36-heterocicloalquilo), R17-fenilo, (R17-fenil)-alquilo, R23-heteroarilo, (R23-heteroaril)alquilo, (R23-heteroaril)oxi, (R23-heteroaril)amino, NR18R19, NR18R19-aIquilo, -(CH2)n-N(R30)-C(O)alquilo, -(CH2)n-N(R30)-C(O)-(fluoroalquilo), -(CH2)n-N(R30)-C(O) alcoxialquilo, -(CH2)n-N(R30)-C(O)(cicloalquilo), -(CH2)n-N(R30)-(R23-heteroarilo), -(CH2)n-N(R30)-C(O)-(R23-heteroarilo), -(CH2)n-N(R30)- C(O)O-alquilo, -(CH2)nN(R30)-C(O)O-(CF3-alquilo),-(CH2)n-N(R30)-C(O)O-(R39-cicloalquilo), -(CH2)n-N(R30)-C(O)O-alquilen-cicloalquilo, -(CH2)n-N(R30)-C(O)-N(R30)(R20), -(CH2)n-N(R30)-SO2alquilo, -(CH2)n-N(R30)-SO2CF3, (CH2)n-N(R30)-SO2-N(R30)2 y el resto de formula (9); o dos grupos R27 y el carbono al cual ambos están unidos forman -C(NOR30)- o -C(O)-; R28 es H, alquilo, R35-bencilo o -alquil-C(O)O- alquilo; R29 es alquilo, haloalquilo, -C(O)Oalquilo, -C(O)alquilo, -C(O)CF3, -C(O)-(R12- cicloalquilo), -C(O)-(R17-fenilo), -C(O)-(R23- heteroarilo), -C(O)-(R36-heterocicloalquilo), -SO2-alquilo, -SO2(R35-fenilo), -C(O)NR18R19, R35-fenilo, (R35-fenil)alquilo o R23-heteroarilo; R30 se selecciona en forma independiente del grupo integrado por H, alquilo, R35-bencilo y R35-fenilo; R31 es H, alquilo, R35-bencilo o fenoxialquilo; R33 es H, OH o alcoxi; R34 es H, alquilo, hidroxialquilo, alcoxialquilo o -C(O)Oalquilo; R35 es 1 a 3 sustituyentes seleccionados en forma independiente del grupo integrado por H, halo, alquilo, OH, -CF3, alcoxi, -CO2alquilo y -N(R43)(R44); R36 es 1 o 2 sustituyentes seleccionados en forma independiente del grupo integrado por H, alquilo, R17-fenilo, -OH, hidroxialquilo, alcoxialquilo, -C(O)Oalquilo y - NR18R19 o dos grupos R36 y el carbono al cual ambos están unidos forman -C(=NOR30)- o -C(O)-; R37 y R38 y se seleccionan en forma independiente del grupo integrado por H y alquilo, o R37 y R38 juntos son -(CH2)3- o -(CH24)-, y junto con el nitrogeno al cual están unidos, forman un anillo; R39 es H, OH, alquilo, alcoxi o CF3; R40 es -OR30 o -NHC(O)alquilo; R41 es H o -SO2alquilo; R42 es -(CH2)n-(R35-fenilo), -(CH2)n-(R23-heteroarilo), -C(O)Oalquilo o -C(O)alquilo; R43 y R44 se seleccionan en forma independiente del grupo integrado por H y alquilo; y R45 es 1 o 2 sustituyentes seleccionados en forma independiente del grupo integrado por halo, aIcoxialquilo, -CO2alquilo, R17-fenilo, R23- heteroarilo y cicloalquilo.
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| DE69738949D1 (de) * | 1996-05-20 | 2008-10-09 | Darwin Discovery Ltd | Chinolincarboxamide als tnf-inhibitoren und als pde-iv inhibitoren |
| US6069151A (en) * | 1996-11-06 | 2000-05-30 | Darwin Discovery, Ltd. | Quinolines and their therapeutic use |
| EP0946541B1 (en) * | 1996-11-06 | 2003-07-30 | Darwin Discovery Limited | Quinolines and their therapeutic use |
| WO1999032450A1 (en) * | 1997-12-22 | 1999-07-01 | Pharmacia & Upjohn Company | 4-hydroxyquinoline-3-carboxamides and hydrazides as antiviral agents |
| EP1165542B1 (en) * | 1999-03-29 | 2003-08-20 | Neurogen Corporation | 4-substituted quinoline derivatives as nk-3 and/or gaba(a) receptor ligands |
| US6569885B1 (en) * | 1999-12-23 | 2003-05-27 | Icos Corporation | Cyclic AMP-specific phosphodiesterase inhibitors |
| GB0003254D0 (en) * | 2000-02-11 | 2000-04-05 | Darwin Discovery Ltd | Heterocyclic compounds and their therapeutic use |
| ATE542805T1 (de) * | 2000-08-11 | 2012-02-15 | Nippon Chemiphar Co | Ppar-delta aktivatoren |
| WO2002076957A1 (en) * | 2001-03-23 | 2002-10-03 | Nippon Chemiphar Co.,Ltd. | Activator for peroxisome proliferator-activated receptor |
| DE10227269A1 (de) | 2002-06-19 | 2004-01-08 | Merck Patent Gmbh | Thiazolderivate |
| CA2657902A1 (en) * | 2006-07-11 | 2008-01-17 | Schering Corporation | Xinafoate salt of a substituted 5-oxazol-2-yl-quinoline compound |
-
2005
- 2005-05-16 WO PCT/US2005/017134 patent/WO2005116009A1/en not_active Ceased
- 2005-05-16 BR BRPI0511295-8A patent/BRPI0511295A/pt not_active IP Right Cessation
- 2005-05-16 AT AT05750076T patent/ATE531705T1/de active
- 2005-05-16 CA CA2565599A patent/CA2565599C/en not_active Expired - Fee Related
- 2005-05-16 RU RU2006144709/04A patent/RU2417993C9/ru not_active IP Right Cessation
- 2005-05-16 NZ NZ551017A patent/NZ551017A/en unknown
- 2005-05-16 MX MXPA06013414A patent/MXPA06013414A/es active IP Right Grant
- 2005-05-16 EP EP05750076A patent/EP1758883B1/en not_active Expired - Lifetime
- 2005-05-16 US US11/130,359 patent/US7511062B2/en not_active Expired - Fee Related
- 2005-05-16 PE PE2005000540A patent/PE20060241A1/es not_active Application Discontinuation
- 2005-05-16 KR KR1020067024186A patent/KR100907354B1/ko not_active Expired - Fee Related
- 2005-05-16 CN CN2005800236668A patent/CN1984901B/zh not_active Expired - Fee Related
- 2005-05-16 JP JP2007513471A patent/JP4584990B2/ja not_active Expired - Fee Related
- 2005-05-16 AU AU2005247906A patent/AU2005247906B2/en not_active Ceased
- 2005-05-17 AR ARP050102012A patent/AR055192A1/es not_active Application Discontinuation
- 2005-05-17 TW TW094115924A patent/TWI286475B/zh not_active IP Right Cessation
-
2006
- 2006-11-07 ZA ZA200609277A patent/ZA200609277B/en unknown
- 2006-11-14 IL IL179280A patent/IL179280A/en not_active IP Right Cessation
- 2006-11-17 EC EC2006007013A patent/ECSP067013A/es unknown
- 2006-12-15 NO NO20065830A patent/NO20065830L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| CA2565599A1 (en) | 2005-12-08 |
| BRPI0511295A (pt) | 2007-12-04 |
| EP1758883B1 (en) | 2011-11-02 |
| JP2007537300A (ja) | 2007-12-20 |
| WO2005116009A1 (en) | 2005-12-08 |
| NO20065830L (no) | 2007-02-16 |
| WO2005116009B1 (en) | 2006-01-26 |
| CA2565599C (en) | 2012-07-31 |
| TW200602056A (en) | 2006-01-16 |
| ZA200609277B (en) | 2008-06-25 |
| IL179280A (en) | 2011-07-31 |
| RU2006144709A (ru) | 2008-06-27 |
| AU2005247906A1 (en) | 2005-12-08 |
| RU2417993C9 (ru) | 2011-10-10 |
| CN1984901A (zh) | 2007-06-20 |
| RU2417993C2 (ru) | 2011-05-10 |
| KR100907354B1 (ko) | 2009-07-10 |
| MXPA06013414A (es) | 2007-01-23 |
| AU2005247906B2 (en) | 2011-08-25 |
| CN1984901B (zh) | 2011-02-09 |
| ATE531705T1 (de) | 2011-11-15 |
| TWI286475B (en) | 2007-09-11 |
| JP4584990B2 (ja) | 2010-11-24 |
| US20060106062A1 (en) | 2006-05-18 |
| ECSP067013A (es) | 2006-12-29 |
| PE20060241A1 (es) | 2006-04-01 |
| US7511062B2 (en) | 2009-03-31 |
| KR20070013306A (ko) | 2007-01-30 |
| NZ551017A (en) | 2010-11-26 |
| EP1758883A1 (en) | 2007-03-07 |
| IL179280A0 (en) | 2007-03-08 |
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