PE20070534A1 - Derivados de 3-feniluracilo para controlar malezas o cultivos resistentes a glifosato o su habitat - Google Patents
Derivados de 3-feniluracilo para controlar malezas o cultivos resistentes a glifosato o su habitatInfo
- Publication number
- PE20070534A1 PE20070534A1 PE2006000924A PE2006000924A PE20070534A1 PE 20070534 A1 PE20070534 A1 PE 20070534A1 PE 2006000924 A PE2006000924 A PE 2006000924A PE 2006000924 A PE2006000924 A PE 2006000924A PE 20070534 A1 PE20070534 A1 PE 20070534A1
- Authority
- PE
- Peru
- Prior art keywords
- inhibitors
- herbicides
- glyphosate
- derivatives
- flamprop
- Prior art date
Links
- 239000005562 Glyphosate Substances 0.000 title abstract 2
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 title abstract 2
- 229940097068 glyphosate Drugs 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 11
- 239000004009 herbicide Substances 0.000 abstract 3
- -1 CARBOXYL GROUP Chemical group 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 2
- PSOZMUMWCXLRKX-UHFFFAOYSA-N 2,4-dinitro-6-pentan-2-ylphenol Chemical compound CCCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O PSOZMUMWCXLRKX-UHFFFAOYSA-N 0.000 abstract 1
- KGKGSIUWJCAFPX-UHFFFAOYSA-N 2,6-dichlorothiobenzamide Chemical compound NC(=S)C1=C(Cl)C=CC=C1Cl KGKGSIUWJCAFPX-UHFFFAOYSA-N 0.000 abstract 1
- OWZPCEFYPSAJFR-UHFFFAOYSA-N 2-(butan-2-yl)-4,6-dinitrophenol Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O OWZPCEFYPSAJFR-UHFFFAOYSA-N 0.000 abstract 1
- SVGBNTOHFITEDI-UHFFFAOYSA-N 2-[4-(3,5-dichloropyridin-2-yl)oxyphenoxy]propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1Cl SVGBNTOHFITEDI-UHFFFAOYSA-N 0.000 abstract 1
- SVOAUHHKPGKPQK-UHFFFAOYSA-N 2-chloro-9-hydroxyfluorene-9-carboxylic acid Chemical compound C1=C(Cl)C=C2C(C(=O)O)(O)C3=CC=CC=C3C2=C1 SVOAUHHKPGKPQK-UHFFFAOYSA-N 0.000 abstract 1
- ABOOPXYCKNFDNJ-UHFFFAOYSA-N 2-{4-[(6-chloroquinoxalin-2-yl)oxy]phenoxy}propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-UHFFFAOYSA-N 0.000 abstract 1
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical class [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 abstract 1
- SOPHXJOERHTMIL-UHFFFAOYSA-N 3-methyl-4,6-dinitro-2-propan-2-ylphenol Chemical compound CC(C)C1=C(C)C([N+]([O-])=O)=CC([N+]([O-])=O)=C1O SOPHXJOERHTMIL-UHFFFAOYSA-N 0.000 abstract 1
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 abstract 1
- PVSGXWMWNRGTKE-UHFFFAOYSA-N 5-methyl-2-[4-methyl-5-oxo-4-(propan-2-yl)-4,5-dihydro-1H-imidazol-2-yl]pyridine-3-carboxylic acid Chemical compound N1C(=O)C(C(C)C)(C)N=C1C1=NC=C(C)C=C1C(O)=O PVSGXWMWNRGTKE-UHFFFAOYSA-N 0.000 abstract 1
- LJGZUMNXGLDTFF-UHFFFAOYSA-N 6-tert-butyl-3-methyl-2,4-dinitrophenol Chemical compound CC1=C([N+]([O-])=O)C=C(C(C)(C)C)C(O)=C1[N+]([O-])=O LJGZUMNXGLDTFF-UHFFFAOYSA-N 0.000 abstract 1
- WBFYVDCHGVNRBH-UHFFFAOYSA-N 7,8-dihydropteroic acid Chemical compound N=1C=2C(=O)NC(N)=NC=2NCC=1CNC1=CC=C(C(O)=O)C=C1 WBFYVDCHGVNRBH-UHFFFAOYSA-N 0.000 abstract 1
- 108010000700 Acetolactate synthase Proteins 0.000 abstract 1
- 229930192334 Auxin Natural products 0.000 abstract 1
- 239000005484 Bifenox Substances 0.000 abstract 1
- 239000005490 Carbetamide Substances 0.000 abstract 1
- 239000005498 Clodinafop Substances 0.000 abstract 1
- 239000005644 Dazomet Substances 0.000 abstract 1
- QNXAVFXEJCPCJO-UHFFFAOYSA-N Diclosulam Chemical compound N=1N2C(OCC)=NC(F)=CC2=NC=1S(=O)(=O)NC1=C(Cl)C=CC=C1Cl QNXAVFXEJCPCJO-UHFFFAOYSA-N 0.000 abstract 1
- IIPZYDQGBIWLBU-UHFFFAOYSA-N Dinoterb Chemical compound CC(C)(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O IIPZYDQGBIWLBU-UHFFFAOYSA-N 0.000 abstract 1
- ICWUMLXQKFTJMH-UHFFFAOYSA-N Etobenzanid Chemical compound C1=CC(OCOCC)=CC=C1C(=O)NC1=CC=CC(Cl)=C1Cl ICWUMLXQKFTJMH-UHFFFAOYSA-N 0.000 abstract 1
- YQVMVCCFZCMYQB-UHFFFAOYSA-N Flamprop Chemical compound C=1C=C(F)C(Cl)=CC=1N(C(C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-UHFFFAOYSA-N 0.000 abstract 1
- YQVMVCCFZCMYQB-SNVBAGLBSA-N Flamprop-M Chemical compound C=1C=C(F)C(Cl)=CC=1N([C@H](C)C(O)=O)C(=O)C1=CC=CC=C1 YQVMVCCFZCMYQB-SNVBAGLBSA-N 0.000 abstract 1
- AOQMRUTZEYVDIL-UHFFFAOYSA-N Flupoxam Chemical compound C=1C=C(Cl)C(COCC(F)(F)C(F)(F)F)=CC=1N1N=C(C(=O)N)N=C1C1=CC=CC=C1 AOQMRUTZEYVDIL-UHFFFAOYSA-N 0.000 abstract 1
- UCHDFLNGIZUADY-UHFFFAOYSA-N Fosamine Chemical compound CCOP(O)(=O)C(N)=O UCHDFLNGIZUADY-UHFFFAOYSA-N 0.000 abstract 1
- 239000005570 Isoxaben Substances 0.000 abstract 1
- 102000003960 Ligases Human genes 0.000 abstract 1
- 108090000364 Ligases Proteins 0.000 abstract 1
- SUSRORUBZHMPCO-UHFFFAOYSA-N MC-4379 Chemical compound C1=C([N+]([O-])=O)C(C(=O)OC)=CC(OC=2C(=CC(Cl)=CC=2)Cl)=C1 SUSRORUBZHMPCO-UHFFFAOYSA-N 0.000 abstract 1
- 239000002169 Metam Substances 0.000 abstract 1
- 108020001991 Protoporphyrinogen Oxidase Proteins 0.000 abstract 1
- 102000005135 Protoporphyrinogen oxidase Human genes 0.000 abstract 1
- AMRQXHFXNZFDCH-SECBINFHSA-N [(2r)-1-(ethylamino)-1-oxopropan-2-yl] n-phenylcarbamate Chemical compound CCNC(=O)[C@@H](C)OC(=O)NC1=CC=CC=C1 AMRQXHFXNZFDCH-SECBINFHSA-N 0.000 abstract 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 abstract 1
- RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 abstract 1
- VGPYEHKOIGNJKV-UHFFFAOYSA-N asulam Chemical compound COC(=O)NS(=O)(=O)C1=CC=C(N)C=C1 VGPYEHKOIGNJKV-UHFFFAOYSA-N 0.000 abstract 1
- PXWUKZGIHQRDHL-UHFFFAOYSA-N atraton Chemical compound CCNC1=NC(NC(C)C)=NC(OC)=N1 PXWUKZGIHQRDHL-UHFFFAOYSA-N 0.000 abstract 1
- 239000002363 auxin Substances 0.000 abstract 1
- LVKBXDHACCFCTA-UHFFFAOYSA-N bencarbazone Chemical compound C1=C(C(N)=S)C(NS(=O)(=O)CC)=CC(N2C(N(C)C(=N2)C(F)(F)F)=O)=C1F LVKBXDHACCFCTA-UHFFFAOYSA-N 0.000 abstract 1
- GINJFDRNADDBIN-FXQIFTODSA-N bilanafos Chemical compound OC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@@H](N)CCP(C)(O)=O GINJFDRNADDBIN-FXQIFTODSA-N 0.000 abstract 1
- WZDDLAZXUYIVMU-UHFFFAOYSA-N bromobutide Chemical compound CC(C)(C)C(Br)C(=O)NC(C)(C)C1=CC=CC=C1 WZDDLAZXUYIVMU-UHFFFAOYSA-N 0.000 abstract 1
- 230000008166 cellulose biosynthesis Effects 0.000 abstract 1
- YUIKUTLBPMDDNQ-MRVPVSSYSA-N clodinafop Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=NC=C(Cl)C=C1F YUIKUTLBPMDDNQ-MRVPVSSYSA-N 0.000 abstract 1
- QAYICIQNSGETAS-UHFFFAOYSA-N dazomet Chemical compound CN1CSC(=S)N(C)C1 QAYICIQNSGETAS-UHFFFAOYSA-N 0.000 abstract 1
- ZDXPYRJPNDTMRX-UHFFFAOYSA-N glutamine Natural products OC(=O)C(N)CCC(N)=O ZDXPYRJPNDTMRX-UHFFFAOYSA-N 0.000 abstract 1
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 abstract 1
- PMHURSZHKKJGBM-UHFFFAOYSA-N isoxaben Chemical compound O1N=C(C(C)(CC)CC)C=C1NC(=O)C1=C(OC)C=CC=C1OC PMHURSZHKKJGBM-UHFFFAOYSA-N 0.000 abstract 1
- 150000002632 lipids Chemical class 0.000 abstract 1
- 150000004668 long chain fatty acids Chemical class 0.000 abstract 1
- HYVVJDQGXFXBRZ-UHFFFAOYSA-N metam Chemical compound CNC(S)=S HYVVJDQGXFXBRZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000011278 mitosis Effects 0.000 abstract 1
- DEDOPGXGGQYYMW-UHFFFAOYSA-N molinate Chemical compound CCSC(=O)N1CCCCCC1 DEDOPGXGGQYYMW-UHFFFAOYSA-N 0.000 abstract 1
- JXTHEWSKYLZVJC-UHFFFAOYSA-N naptalam Chemical compound OC(=O)C1=CC=CC=C1C(=O)NC1=CC=CC2=CC=CC=C12 JXTHEWSKYLZVJC-UHFFFAOYSA-N 0.000 abstract 1
- 230000029553 photosynthesis Effects 0.000 abstract 1
- 238000010672 photosynthesis Methods 0.000 abstract 1
- VTRWMTJQBQJKQH-UHFFFAOYSA-N pyributicarb Chemical compound COC1=CC=CC(N(C)C(=S)OC=2C=C(C=CC=2)C(C)(C)C)=N1 VTRWMTJQBQJKQH-UHFFFAOYSA-N 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 230000002087 whitening effect Effects 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
- A01N43/48—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
DE FORMULA (I) DONDE: R1 ES METILO o NH2;R2 ES HALOALQUILO C1-C2;R3 ES H o HALOGENO;R4 ES HALOGENO o CIANO;R5 ES H o ALQUILO C1-C6; R6 Y R7 SON H, ALQUILO C1-C6,ALCOXI C1-C6,ALQUENILO C3-C6,ALQUINILO C3-C6,CICLOALQUILO C3-C7, CICLOALQUENILO C3-C7,FENILO o BENCILO. DICHOS DERIVADOS SE USAN EN COMBINACION CON UNO O VARIOS HERBICIDAS B,TENIENDO UN GRUPO CARBOXILO, TALES COMO: INHIBIDORES DE BIOSINTESIS DE LIPIDOS: CLORAZIFOP,CLODINAFOP,FLUAZIPOP,QUIZALOFOP Y MOLINATO; INHIBIDORES DE ACETOLACTATO SINTETASA: AMIDOSULFURONA, IMAZAPIC, DICLOSULAM, BISPIRIBAC Y PIRIMISULFANO; INHIBIDORES DE LA FOTOSINTESIS: ATRATONA, AMETRINA Y METOMENONA; INHIBIDORES DE LA PROTOPORFIRINOGEN-IX OXIDASA: BIFENOX, FLUFENPIR Y BENCARBAZONA; HERBICIDAS BLANQUEADORES; INHIBIDORES DE LA ENOLPIRUVIL SHIKIMATO 3-FOSFATO SINTETASA: GLIFOSATO; INHIBIDORES DE LA GLUTAMINA SINTETASA: GLUFOSINATO Y BILANAFOS; INHIBIDORES DE 7,8-DIHIDROPTEROATO SINTETASA: ASULAM; INHIBIDORES DE LA MITOSIS:CARBETAMIDA;INHIBIDORES DE LA SINTESIS DE ACIDOS GRASOS DE CADENA LARGA; INHIBIDORES DE LA BIOSINTESIS DE CELULOSA: DICLOBENILO,CLORTIAMIDA,ISOXABENO Y FLUPOXAM; HERBICIDAS DESACOPLADORES: DINOFENATO,DINOPROP,DINOSAM, DINOSEB,DINOTERB,DNOC,ETINOFENO Y MEDINOTERB; INHIBIDORES DEL TRANSPORTE DE AUXINA: NAPTALAM,DIFLUFENZOPIR; Y OTROS COMO BENZOILPROP,FLAMPROP,FLAMPROP-M,BROMOBUTIDA,CLOROFLURENOL,CINMETILINA, METILDIMURONA,ETOBENZANIDA,FOSAMINA,METAM,PIRIBUTICARB, OXAZICLOMEFONA,DAZOMET,TRIAZIFLAM Y BROMURO DE METILO; ENTRE OTROS
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US70387505P | 2005-08-01 | 2005-08-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PE20070534A1 true PE20070534A1 (es) | 2007-06-11 |
Family
ID=37039383
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PE2006000924A PE20070534A1 (es) | 2005-08-01 | 2006-07-31 | Derivados de 3-feniluracilo para controlar malezas o cultivos resistentes a glifosato o su habitat |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20080227637A1 (es) |
| EP (1) | EP1926374A1 (es) |
| JP (1) | JP2009503004A (es) |
| KR (1) | KR20080058323A (es) |
| CN (1) | CN101232813A (es) |
| AR (1) | AR056436A1 (es) |
| AU (1) | AU2006275053A1 (es) |
| BR (1) | BRPI0614194A2 (es) |
| CA (1) | CA2617247A1 (es) |
| EA (1) | EA200800390A1 (es) |
| MX (1) | MX2008001097A (es) |
| PE (1) | PE20070534A1 (es) |
| TW (1) | TW200738138A (es) |
| WO (1) | WO2007014758A1 (es) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE602006009704D1 (de) | 2005-12-23 | 2009-11-19 | Basf Se | Verfahren zur bekämpfung des wasserunkrauts hydrilla verticillata |
| US9060516B2 (en) | 2005-12-23 | 2015-06-23 | Basf Se | Method for controlling aquatic weeds |
| US9210930B2 (en) | 2005-12-23 | 2015-12-15 | Basf Se | Control of submerged aquatic vegetation |
| WO2010046420A2 (en) * | 2008-10-22 | 2010-04-29 | Basf Se | Use of protoporphyrinogen oxidase inhibitors on cultivated plants |
| MX2012001732A (es) | 2009-08-27 | 2012-04-02 | Basf Se | Formulaciones concentradas en suspension acuosa que contienen saflufenacilo. |
| US8778838B2 (en) | 2009-08-27 | 2014-07-15 | Basf Se | Aqueous concentrate formulations containing saflufenacil and glyphosate |
| TW201113377A (en) * | 2009-09-01 | 2011-04-16 | Basf Agrochemical Products Bv | Herbicide-tolerant plants |
| AU2010329964B2 (en) | 2009-12-09 | 2015-08-20 | Basf Se | Liquid suspension concentrate formulations containing saflufenacil and glyphosate |
| US8703650B2 (en) | 2009-12-09 | 2014-04-22 | Basf Se | Liquid suspension concentrate formulations containing saflufenacil |
| UY33860A (es) | 2011-01-07 | 2012-08-31 | Dow Agrosciences Llc | Tolerancia aumentada de plantas habilitadas por dht a herbicidas auxínicos resultante de diferencias de porciones en estructuras moleculares del herbicida |
| RU2601057C2 (ru) * | 2011-01-18 | 2016-10-27 | ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи | Синергическая гербицидная смесь, содержащая пеноксулам, триклопир и имазетапир или имазамокс, композиция на основе смеси и способ борьбы с нежелательной растительностью |
| TR201902463T4 (tr) * | 2012-04-12 | 2019-03-21 | Dongbu Farm Hannong Co Ltd | Etken madde olarak bir urasil bileşiği içeren herbisidal bileşim. |
| CN105454240A (zh) * | 2015-12-28 | 2016-04-06 | 南京华洲药业有限公司 | 一种含苯嘧磺草胺与炔草酯的混合除草剂 |
| US10863743B2 (en) | 2016-07-29 | 2020-12-15 | Basf Se | Method for controlling PPO resistant weeds |
| CA3030354A1 (en) * | 2016-07-29 | 2018-02-01 | Basf Se | Method for controlling ppo resistant weeds |
| JP2017019840A (ja) | 2016-07-29 | 2017-01-26 | 住友化学株式会社 | 農作物における有害生物の防除方法 |
| IL274683B (en) * | 2017-11-29 | 2022-09-01 | Basf Se | Plants having increased tolerance to herbicides |
| US20190254277A1 (en) * | 2018-02-21 | 2019-08-22 | Sumitomo Chemical Company, Limited | Method of controlling herbicide resistant weeds |
| US10772329B2 (en) | 2018-12-26 | 2020-09-15 | Sumitomo Chemical Company, Limited | Method of controlling weeds |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2734842B1 (fr) * | 1995-06-02 | 1998-02-27 | Rhone Poulenc Agrochimie | Sequence adn d'un gene de l'hydroxy-phenyl pyruvate dioxygenase et obtention de plantes contenant un gene de l'hydroxy-phenyl pyruvate dioxygenase, tolerantes a certains herbicides |
| US6245968B1 (en) * | 1997-11-07 | 2001-06-12 | Aventis Cropscience S.A. | Mutated hydroxyphenylpyruvate dioxygenase, DNA sequence and isolation of plants which contain such a gene and which are tolerant to herbicides |
| DE19846792A1 (de) * | 1998-10-10 | 2000-04-13 | Hoechst Schering Agrevo Gmbh | Benzoylcyclohexandione, Verfahren zur ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
| DK1226127T3 (da) * | 2000-05-04 | 2009-10-19 | Basf Se | Substituerede phenylsulfamoylcarboxamider |
| JP4237622B2 (ja) * | 2001-09-14 | 2009-03-11 | ビーエーエスエフ ソシエタス・ヨーロピア | ３−フェニルウラシルをベースとする除草性混合物 |
| EP1605758B1 (en) * | 2003-03-13 | 2008-09-10 | Basf Se | Herbicidal mixtures based on 3-phenyluracils |
-
2006
- 2006-07-31 AR ARP060103331A patent/AR056436A1/es not_active Application Discontinuation
- 2006-07-31 PE PE2006000924A patent/PE20070534A1/es not_active Application Discontinuation
- 2006-08-01 CA CA002617247A patent/CA2617247A1/en not_active Abandoned
- 2006-08-01 MX MX2008001097A patent/MX2008001097A/es unknown
- 2006-08-01 KR KR1020087002610A patent/KR20080058323A/ko not_active Withdrawn
- 2006-08-01 TW TW095128150A patent/TW200738138A/zh unknown
- 2006-08-01 EP EP06762937A patent/EP1926374A1/en not_active Withdrawn
- 2006-08-01 JP JP2008524425A patent/JP2009503004A/ja not_active Withdrawn
- 2006-08-01 CN CNA200680028370XA patent/CN101232813A/zh active Pending
- 2006-08-01 BR BRPI0614194A patent/BRPI0614194A2/pt not_active IP Right Cessation
- 2006-08-01 WO PCT/EP2006/007614 patent/WO2007014758A1/en active Application Filing
- 2006-08-01 AU AU2006275053A patent/AU2006275053A1/en not_active Abandoned
- 2006-08-01 EA EA200800390A patent/EA200800390A1/ru unknown
- 2006-08-01 US US11/997,165 patent/US20080227637A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| AU2006275053A1 (en) | 2007-02-08 |
| MX2008001097A (es) | 2008-03-11 |
| TW200738138A (en) | 2007-10-16 |
| JP2009503004A (ja) | 2009-01-29 |
| WO2007014758A8 (en) | 2008-03-27 |
| EP1926374A1 (en) | 2008-06-04 |
| KR20080058323A (ko) | 2008-06-25 |
| EA200800390A1 (ru) | 2008-08-29 |
| CA2617247A1 (en) | 2007-02-08 |
| WO2007014758A1 (en) | 2007-02-08 |
| US20080227637A1 (en) | 2008-09-18 |
| BRPI0614194A2 (pt) | 2016-11-22 |
| AR056436A1 (es) | 2007-10-10 |
| CN101232813A (zh) | 2008-07-30 |
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