AR043596A1 - Mezclas herbicidas basados en 3-feniluracilos - Google Patents
Mezclas herbicidas basados en 3-feniluracilosInfo
- Publication number
- AR043596A1 AR043596A1 ARP040100834A ARP040100834A AR043596A1 AR 043596 A1 AR043596 A1 AR 043596A1 AR P040100834 A ARP040100834 A AR P040100834A AR P040100834 A ARP040100834 A AR P040100834A AR 043596 A1 AR043596 A1 AR 043596A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- agriculture
- alkoxy
- hydroxy
- acceptable
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title abstract 3
- 239000004009 herbicide Substances 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 3
- QWWHRELOCZEQNZ-UHFFFAOYSA-N 2,2-dichloro-1-(1-oxa-4-azaspiro[4.5]decan-4-yl)ethanone Chemical compound ClC(Cl)C(=O)N1CCOC11CCCCC1 QWWHRELOCZEQNZ-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- -1 amino, formyl Chemical group 0.000 abstract 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 3
- 229910052736 halogen Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- KMDUXADUKNTNFV-UHFFFAOYSA-N 2,2-dichloro-1-(1,3-oxazolidin-2-yl)ethanone Chemical compound ClC(Cl)C(=O)C1NCCO1 KMDUXADUKNTNFV-UHFFFAOYSA-N 0.000 abstract 1
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 abstract 1
- DJPNGLRIBDVWAR-UHFFFAOYSA-N CC1=NC(C(F)(F)F)=CC=C1C(=O)C(C1=O)=C(O)C2CC1CC2 Chemical compound CC1=NC(C(F)(F)F)=CC=C1C(=O)C(C1=O)=C(O)C2CC1CC2 DJPNGLRIBDVWAR-UHFFFAOYSA-N 0.000 abstract 1
- HUYBEDCQLAEVPD-UHFFFAOYSA-N COCCOCC1=NC(C(F)(F)F)=CC=C1C(=O)C(C1=O)=C(O)C2CC1CC2 Chemical compound COCCOCC1=NC(C(F)(F)F)=CC=C1C(=O)C(C1=O)=C(O)C2CC1CC2 HUYBEDCQLAEVPD-UHFFFAOYSA-N 0.000 abstract 1
- NRFQZTCQAYEXEE-UHFFFAOYSA-N Fenclorim Chemical compound ClC1=CC(Cl)=NC(C=2C=CC=CC=2)=N1 NRFQZTCQAYEXEE-UHFFFAOYSA-N 0.000 abstract 1
- GRSMWKLPSNHDHA-UHFFFAOYSA-N Naphthalic anhydride Chemical compound C1=CC(C(=O)OC2=O)=C3C2=CC=CC3=C1 GRSMWKLPSNHDHA-UHFFFAOYSA-N 0.000 abstract 1
- 239000005597 Pinoxaden Substances 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- MKQSWTQPLLCSOB-UHFFFAOYSA-N benzyl 2-chloro-4-(trifluoromethyl)-1,3-thiazole-5-carboxylate Chemical compound N1=C(Cl)SC(C(=O)OCC=2C=CC=CC=2)=C1C(F)(F)F MKQSWTQPLLCSOB-UHFFFAOYSA-N 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- ICJSJAJWTWPSBD-UHFFFAOYSA-N cloquintocet Chemical compound C1=CN=C2C(OCC(=O)O)=CC=C(Cl)C2=C1 ICJSJAJWTWPSBD-UHFFFAOYSA-N 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- ITGSCCPVERXFGN-UHFFFAOYSA-N isoxadifen Chemical compound C1C(C(=O)O)=NOC1(C=1C=CC=CC=1)C1=CC=CC=C1 ITGSCCPVERXFGN-UHFFFAOYSA-N 0.000 abstract 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group 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
- 239000001301 oxygen Chemical group 0.000 abstract 1
- MGOHCFMYLBAPRN-UHFFFAOYSA-N pinoxaden Chemical compound CCC1=CC(C)=CC(CC)=C1C(C1=O)=C(OC(=O)C(C)(C)C)N2N1CCOCC2 MGOHCFMYLBAPRN-UHFFFAOYSA-N 0.000 abstract 1
- YWZBGRYDSPLRHR-UHFFFAOYSA-N pinoxaden acid Chemical compound CCC1=CC(C)=CC(CC)=C1C(C1=O)=C(O)N2N1CCOCC2 YWZBGRYDSPLRHR-UHFFFAOYSA-N 0.000 abstract 1
- 230000001012 protector Effects 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229910052717 sulfur Chemical group 0.000 abstract 1
- 239000011593 sulfur Chemical group 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Reivindicación 1: Una composición con efecto herbicida que comprende 3-feniluracilos de la fórmula (1), caracterizada porque las variables R1-R7 se definen en lo que sigue: R1 es metilo o NH2; R2 es haloalquilo C1-2; R3 es hidrógeno o halógeno; R4 es halógeno o ciano; R5 es hidrógeno, ciano, alquilo C1-6, alcoxi C1-6, alcoxi(C1-4)-alquilo(C1-4), cicloalquilo C3-7, alquenilo C3-6, alquinilo C3-6 o bencilo que es no sustituido o sustituido por halógeno o alquilo C1-6; R6, R7 son, independientemente el uno del otro, hidrógeno, alquilo C1-6, alcoxi C1-6, alquenilo C3-6, alquinilo C3-6, cicloalquilo C3-7, cicloalquenilo C3-7, fenilo o bencilo, donde cada uno de los 8 sustituyentes arriba mencionados está no sustituido o está sustituido por 1 a 6 átomos de halógeno y/o por uno, dos o tres grupos seleccionados de: OH, NH2, CN, CONH2, alcoxi C1-4, haloalcoxi C1-4, alquil(C1-4)-tio, haloalquil(C1-4)-tio, alquil(C1-4)-sulfonilo, haloalquil(C1-4)-sulfonilo, alquil(C1-4)-amino, di(alquil C1-4)amino, formilo, alquil(C1-4)-carbonilo, alcoxi(C1-4)-carbonilo, alquil(C1-4)-aminocarbonilo, di(alquil C1-4)aminocarbonilo, cicloalquilo C3-7, fenilo o bencilo; o R6, R7 juntamente con el átomo de nitrógeno al cual están unidos forman un heterociclo de nitrógeno saturado o no saturado de 3, 4, 5, 6 ó 7 miembros, que puede estar sustituido por 1 a 6 grupos metilo y que puede contener 1 ó 2 heteroátomos adicionales seleccionados del grupo consistente en nitrógeno, oxígeno y azufre, como miembros del anillo, incluyendo sus sales aceptables en agricultura; y por lo menos otro herbicida B, seleccionado de grupo compuesto por aminopiralida y sus derivados aceptables en agricultura, 4-hidroxi-3-{[2-metil-6-(trifluorometil)-3-piridinil]carbonil}biciclo[3.2.1]oct-3-en-2-ona, 4-hidroxi-3-{[2-(2-metoxietoxi)metil-6-(trifluorometil)-3-piridinil]carbonil}biciclo[3.2.1]oct-3-en-2-ona, 4-hidroxi-3-[4-(metilsulfonil)-3-nitrobenzoil]biciclo[3.2.1]oct-3-en-2-ona, 8-(2,6-dietil-4-metilfenil)-1,2,4,5-tetrahidro-9-hidroxi-7H-pirazolo[1,2-d][1,4,5]oxadiazepin-7-ona, y éster[8-(2,6-dietil-4-metilfenil)-1,2,4,5-tetrahidro-7-oxo-7H-pirazolo[1,2-d][1,4,5]oxadiazepin-9-ílico] de ácido piválico (pinoxaden) y [N-(5,7-dimetoxi[1,2,4]triazolo[1,5-a]pirimidin-2-il)-2-metoxi-4-(trifluorometil)-3-piridinsulfonamida, incluyendo sus respectivas sales aceptables en agricultura; y opcionalmente por lo menos un protector C, seleccionado de grupo compuesto por benoxacor, cloquintocet, ciometrinilo, diclormida, diciclonona, dietolate, fenclorazol, fenclorim, flurazol, fuxofemin, flurilazol, isoxadifen, mefenpry, mefenato, anhídrido naftálico, 2,2,5-trimetil-3-(dicloroacetil-1,3-oxazolidina (R-29148), 4-(dicloroacetil)-1-oxa-4-azaspiro [4.5] decano (AD-67, MON 4660) y oxabetrinilo, incluyendo sus sales aceptables en agricultura y, siempre que tengan un grupo carboxilo, sus derivados aceptables en agricultura.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45395903P | 2003-03-13 | 2003-03-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR043596A1 true AR043596A1 (es) | 2005-08-03 |
Family
ID=32990845
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040100834A AR043596A1 (es) | 2003-03-13 | 2004-03-12 | Mezclas herbicidas basados en 3-feniluracilos |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US20060293187A1 (es) |
| EP (1) | EP1605758B1 (es) |
| JP (1) | JP4879732B2 (es) |
| KR (1) | KR101202886B1 (es) |
| CN (1) | CN100405908C (es) |
| AR (1) | AR043596A1 (es) |
| AT (1) | ATE407559T1 (es) |
| BR (1) | BRPI0407949A (es) |
| CA (1) | CA2518042C (es) |
| CL (1) | CL2004000519A1 (es) |
| DE (1) | DE602004016471D1 (es) |
| EA (1) | EA007949B1 (es) |
| ES (1) | ES2310720T3 (es) |
| GE (1) | GEP20084404B (es) |
| IL (1) | IL170203A (es) |
| MX (1) | MXPA05008647A (es) |
| NZ (1) | NZ542275A (es) |
| PL (1) | PL1605758T3 (es) |
| UA (1) | UA82509C2 (es) |
| WO (1) | WO2004080183A1 (es) |
| ZA (1) | ZA200508236B (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10163079A1 (de) | 2001-12-20 | 2003-07-03 | Basf Ag | Verfahren zur Verbesserung des Pflanzenwachstums durch Applikation einer Mischung aus Schwefel und Komplexbildner |
| MY144905A (en) * | 2005-03-17 | 2011-11-30 | Basf Ag | Herbicidal compositions based on 3-phenyluracils and 3-sulfonylisoxazolines |
| AR056437A1 (es) * | 2005-08-01 | 2007-10-10 | Basf Ag | Un metodo para desecar y/o desfoliar cultivos resistentes a glifosfato |
| AR055593A1 (es) * | 2005-08-01 | 2007-08-29 | Basf Ag | Un metodo para controlar malezas |
| AR056436A1 (es) * | 2005-08-01 | 2007-10-10 | Basf Ag | Un metodo para controlar malezas |
| UA90757C2 (ru) | 2005-10-12 | 2010-05-25 | Басф Се | Гербицидная композиция, способ борьбы с нежелательной растительностью и способ защиты посевов от фитотоксичного действия 3-фенилурацилов |
| SA06270491B1 (ar) * | 2005-12-27 | 2010-10-20 | سينجنتا بارتيسبيشنز ايه جي | تركيبة مبيدة للأعشاب تشتمل على حمض 2، 2- ثنائي ميثيل بروبيونيك 8- (2، 6- ثنائي إيثيل –4- ميثيل – فينيل) –9- أوكسو –1، 2، 4، 5- تتراهيدرو –9h- بيرازولو[2.1-دي][ 5.4.1] أوكسادايازيبين –7- يل إستر وكحول |
| GB0920891D0 (en) | 2009-11-27 | 2010-01-13 | Syngenta Participations Ag | Herbicidal compositions |
| AR090661A1 (es) | 2012-04-12 | 2014-11-26 | Dongbu Farm Hannong Co Ltd | Composicion herbicida que contiene un compuesto de uracilo como ingrediente activo |
| CN103766372A (zh) * | 2013-12-09 | 2014-05-07 | 广东中迅农科股份有限公司 | 一种含有氟唑磺隆和苯嘧磺草胺的除草组合物 |
| CN106135226B (zh) * | 2015-04-24 | 2021-05-18 | 江苏龙灯化学有限公司 | 一种除草组合物 |
| CN106135215A (zh) * | 2015-04-24 | 2016-11-23 | 江苏龙灯化学有限公司 | 除草组合物 |
| CN109232442B (zh) * | 2018-09-13 | 2021-11-02 | 深圳大学 | 芳基尿嘧啶类化合物或其农药学上可接受的盐、其制备方法、除草剂组合物 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4431219A1 (de) * | 1994-09-02 | 1996-03-07 | Bayer Ag | Selektive Herbizide auf Basis von Aryluracilen |
| DE19504188A1 (de) * | 1995-02-09 | 1996-08-14 | Basf Ag | Neue 3-(4-Cyanophenyl)uracile |
| DE19617532A1 (de) * | 1996-05-02 | 1997-11-06 | Bayer Ag | Substituierte Phenyluracile |
| CA2332348A1 (en) * | 1998-06-26 | 2000-01-06 | Novartis Ag | Herbicidal composition |
| DE19830694A1 (de) * | 1998-07-09 | 2000-01-13 | Bayer Ag | Substituierte Acylaminophenyl-uracile |
| BR9913745B1 (pt) * | 1998-09-15 | 2011-05-31 | cetonas de piridina, composição herbicida e inibidora do crescimento de plantas, seu uso, método para controle de crescimento de plantas indesejáveis, bem como método para inibir o crescimento de plantas. | |
| AU2623399A (en) * | 1999-02-11 | 2000-08-29 | Novartis Ag | 3-hydroxy-4-aryl-5-pyrazoline derivatives as herbicides |
| US6297197B1 (en) * | 2000-01-14 | 2001-10-02 | Dow Agrosciences Llc | 4-aminopicolinates and their use as herbicides |
| IL148464A0 (en) * | 2000-05-04 | 2002-09-12 | Basf Ag | Uracil substituted phenyl sulfamoyl carboxamides |
| AR035209A1 (es) * | 2000-11-03 | 2004-05-05 | Dow Agrosciences Llc | Compuestos de n-(5,7-dimetoxi(1,2,4)triazol(1,5-a)pirimidin-2-il)arilsulfonamida y composiciones herbicidas formuladas con dichos compuestos como agente activo; proceso para prepararlos y metodo para controlar vegetacion indeseable utilizando dichos compuestos |
| MEP7108A (en) * | 2001-09-14 | 2010-06-10 | Basf Se | Herbicidal mixtures based on 3-phenyluracils |
| AU2003213473A1 (en) * | 2002-08-07 | 2004-02-26 | Syngenta Participations Ag | Herbicidal composition |
| MXPA05008782A (es) * | 2003-03-13 | 2005-10-18 | Basf Ag | Mezclas herbicidas con accion sinergica. |
-
2004
- 2004-03-05 CN CNB2004800063289A patent/CN100405908C/zh not_active Expired - Lifetime
- 2004-03-05 CA CA2518042A patent/CA2518042C/en not_active Expired - Lifetime
- 2004-03-05 NZ NZ542275A patent/NZ542275A/en not_active IP Right Cessation
- 2004-03-05 WO PCT/EP2004/002239 patent/WO2004080183A1/en active IP Right Grant
- 2004-03-05 KR KR1020057016976A patent/KR101202886B1/ko not_active IP Right Cessation
- 2004-03-05 MX MXPA05008647A patent/MXPA05008647A/es active IP Right Grant
- 2004-03-05 EA EA200501355A patent/EA007949B1/ru not_active IP Right Cessation
- 2004-03-05 US US10/548,815 patent/US20060293187A1/en not_active Abandoned
- 2004-03-05 AT AT04717572T patent/ATE407559T1/de not_active IP Right Cessation
- 2004-03-05 DE DE602004016471T patent/DE602004016471D1/de not_active Expired - Lifetime
- 2004-03-05 EP EP04717572A patent/EP1605758B1/en not_active Expired - Lifetime
- 2004-03-05 PL PL04717572T patent/PL1605758T3/pl unknown
- 2004-03-05 ES ES04717572T patent/ES2310720T3/es not_active Expired - Lifetime
- 2004-03-05 BR BRPI0407949-3A patent/BRPI0407949A/pt not_active Application Discontinuation
- 2004-03-05 JP JP2006504547A patent/JP4879732B2/ja not_active Expired - Fee Related
- 2004-03-05 GE GEAP20049019A patent/GEP20084404B/en unknown
- 2004-03-12 AR ARP040100834A patent/AR043596A1/es not_active Application Discontinuation
- 2004-03-12 CL CL200400519A patent/CL2004000519A1/es unknown
- 2004-05-03 UA UAA200509522A patent/UA82509C2/uk unknown
-
2005
- 2005-08-10 IL IL170203A patent/IL170203A/en not_active IP Right Cessation
- 2005-10-12 ZA ZA2005/08236A patent/ZA200508236B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE602004016471D1 (de) | 2008-10-23 |
| CN1758851A (zh) | 2006-04-12 |
| AU2004218836A1 (en) | 2004-09-23 |
| EP1605758B1 (en) | 2008-09-10 |
| CL2004000519A1 (es) | 2005-05-06 |
| MXPA05008647A (es) | 2005-10-18 |
| ATE407559T1 (de) | 2008-09-15 |
| PL1605758T3 (pl) | 2009-03-31 |
| GEP20084404B (en) | 2008-06-25 |
| KR20050114650A (ko) | 2005-12-06 |
| KR101202886B1 (ko) | 2012-11-19 |
| WO2004080183A1 (en) | 2004-09-23 |
| UA82509C2 (uk) | 2008-04-25 |
| JP4879732B2 (ja) | 2012-02-22 |
| EA007949B1 (ru) | 2007-02-27 |
| EA200501355A1 (ru) | 2006-02-24 |
| BRPI0407949A (pt) | 2006-03-07 |
| US20060293187A1 (en) | 2006-12-28 |
| ZA200508236B (en) | 2007-03-25 |
| EP1605758A1 (en) | 2005-12-21 |
| IL170203A (en) | 2010-02-17 |
| NZ542275A (en) | 2008-12-24 |
| CN100405908C (zh) | 2008-07-30 |
| CA2518042C (en) | 2012-05-22 |
| CA2518042A1 (en) | 2004-09-23 |
| JP2006519801A (ja) | 2006-08-31 |
| ES2310720T3 (es) | 2009-01-16 |
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