AR054364A1 - Compuestos con estructura de 1- (imidazolin -2-il-) amino -1,2-difeniletano para combatir plagas animales - Google Patents
Compuestos con estructura de 1- (imidazolin -2-il-) amino -1,2-difeniletano para combatir plagas animalesInfo
- Publication number
- AR054364A1 AR054364A1 ARP060102176A ARP060102176A AR054364A1 AR 054364 A1 AR054364 A1 AR 054364A1 AR P060102176 A ARP060102176 A AR P060102176A AR P060102176 A ARP060102176 A AR P060102176A AR 054364 A1 AR054364 A1 AR 054364A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- radicals
- alkoxy
- alkylthio
- carbonyl
- Prior art date
Links
- -1 AMINO Chemical class 0.000 title abstract 13
- 150000001875 compounds Chemical class 0.000 title abstract 2
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 title 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 15
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 15
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 12
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 12
- 229910052736 halogen Inorganic materials 0.000 abstract 12
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 10
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 10
- 150000002367 halogens Chemical class 0.000 abstract 9
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 8
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group 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
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 abstract 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 3
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 3
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 229910003827 NRaRb Inorganic materials 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004414 alkyl thio group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 2
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 abstract 1
- DYXWASYPBSFSKL-UHFFFAOYSA-N 1-(4,5-dihydro-1h-imidazol-2-yl)-1,2-diphenylethanamine Chemical compound N=1CCNC=1C(C=1C=CC=CC=1)(N)CC1=CC=CC=C1 DYXWASYPBSFSKL-UHFFFAOYSA-N 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 125000006323 alkenyl amino group Chemical group 0.000 abstract 1
- 125000005137 alkenylsulfonyl group Chemical group 0.000 abstract 1
- 125000005108 alkenylthio group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005109 alkynylthio group Chemical group 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/44—Nitrogen atoms not forming part of a nitro radical
- C07D233/48—Nitrogen atoms not forming part of a nitro radical with acyclic hydrocarbon or substituted acyclic hydrocarbon radicals, attached to said nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/44—Nitrogen atoms not forming part of a nitro radical
- C07D233/50—Nitrogen atoms not forming part of a nitro radical with carbocyclic radicals directly attached to said nitrogen atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Compuestos con estructura de 1-(imidazolin-2-il)amino-1,2-difeniletano caracterizados porque tienen la formula (1) donde A es un radical de la formula (2) o (3), m es 0, 1, 2, 3, 4 o 5; n es 0, 1, 2, 3, 4 o 5; R1, R2 son cada uno en forma independiente: halogeno, OH, SH, NH2, SO3H, COOH, ciano, nitro, formilo, alquilo C1-6, alcoxi C1-6, alquilamino C1-6, di(C1-6 alquil)amino, alquiltio C1-8, alquenilo C2-6, alqueniloxi C2-6, alquenilamino C2-6, alqueniltio C2-6, alquinilo C2-6, alquiniloxi C2-6, alquilamino C2-6, alquiniltio C2-6, alquilsulfonil C2-6, alquilsulfoxilo C1-6, alquenilsulfonilo C2-6, alquinilsulfonilo C2-6, (alquil C1-6)carbonilo, (alquenil C2-6)carbonilo, (alquinil C2-6)carbonilo, (alcoxi C1-6)carbonilo, (alqueniloxi C2-6)carbonilo, (alquiniloxi C2-6)carbonilo, (alquil C1-6)carboniloxi, (alquenil C2-6)carboniloxi o (alquinil C2-6) carboniloxi, donde los átomos de C en los radicales alifáticos de los grupos mencionados con anterioridad pueden portar cualquier combinacion de 1, 2 o 3 radicales, seleccionados independientemente entre sí del grupo que consiste en halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6; C(O)NRaRb, (SO2)NRaRb, un radical Y-Ar o un radical Y-Cy, donde Y es un enlace simple, O, S, alcandiilo C1-6 o alcandiiloxi C1-6; Ar es fenilo, naftilo o un anillo heteroaromático mono o bicíclico de 5 a 10 miembros, que contiene 1, 2, 3 o 4 heteroátomos seleccionados de 2 átomos de O, 2 de S y 3 de N como miembros anulares, donde Ar no se sustituye o puede portar cualquier combinacion de 1 a 5 radicales, seleccionados independientemente entre sí del grupo que consiste en halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6; y Cy es cicloalquilo C3-12, que es no sustituido o se sustituye con 1 a 5 radicales, seleccionados independientemente entre sí del grupo que consiste en halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, C1-6- haloalcoxi C1-6 y alquiltio C1-6; y donde dos radicales R1 o dos radicales R2 que están unidos a átomos de C contiguos de los anillos fenilo pueden formar, junto con dichos átomos de C, un anillo bencénico fusionado, un carbociclo fusionado saturado o parcialmente no saturado de 5, 6 o 7 miembros o un heterociclo fusionado de 5, 6, o 7 miembros, que contiene 1, 2, 3 o 4 heteroátomos seleccionados de 2 átomos de O, 2 de S y 3 de N como miembros anulares, y donde el anillo fusionado es no sustituido o puede portar 1, 2, 3 o 4 radicales, seleccionados independientemente entre sí del grupo que consiste en halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6; R3, R4 son cada uno en forma independiente H, alquilo C1-6, haloalquilo C1-6 o cicloalquilo C3-6, donde los átomos de C en los ultimos grupos pueden portar cualquier combinacion de 1, 2 o 3 radicales, seleccionados independientemente entre sí del grupo que consiste en halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6, o fenilo o bencilo, cada uno no sustituido o sustituido con 1 a 5 radicales, seleccionados independientemente entre sí del grupo que consiste en 5 radicales halogeno, 3 radicales alquilo C1-6, 3 haloalquilo C1-6, 3 alquiltio C1-6, 3 haloalquiltio C1-6, 3 alcoxi C1-6 y 3 haloalcoxi C1-6; R5, R6 son cada uno de forma independiente H, ciano, nitro, formilo, alquilo C1-6, (alquil C1-6)carbonilo, (alcoxi C1-6)carbonilo, (alquiltio C1-6)carbonilo o (alcoxi C1-6)metileno, donde los átomos de C en los radicales alifáticos de los grupos mencionados con anterioridad pueden portar cualquier combinacion de 1, 2 o 3 radicales, seleccionados independientemente entre sí del grupo que consiste en halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alcoxi C1- 6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6, o C(O)NRcRd, (SO2)NRcRd, fenilo, feniloxi o bencilo, cada uno de los 3 ultimos grupos mencionados puede ser no sustituido o sustituirse con 1 a 5 radicales, seleccionados independientemente entre sí del grupo que consiste en 5 radicales halogeno, 3 radicales alquilo C1-6, 3 haloalquilo C1-6, 3 alquiltio C1-6, 3 haloalquiltio C1-6, 3 alcoxi C1-6 y 3 haloalcoxi C1-6; R7 es H, ciano, nitro, formilo, alquilo C1-6, (alquil C1-6)carbonilo, (alcoxi C1-6)carbonilo, (alquiltio C1-6)carbonilo o (alcoxi C1-6)metileno, donde los átomos de C en los radicales alifáticos de los grupos mencionados con anterioridad pueden portar cualquier combinacion de 1, 2 o 3 radicales, seleccionados independientemente entre sí del grupo que consiste en halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alcoxi C1-6, alqueniloxi C2-6, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6, o R7 es C(O)NReRf, (SO2)NReRf, fenilo, feniloxi o bencilo, cada uno de los 3 ultimos grupos mencionados puede ser no sustituido o sustituirse con 1 a 5 radicales, seleccionados independientemente entre sí del grupo que consiste en 5 radicales halogeno, 3 radicales alquilo C1-6, 3 haloalquilo C1-6, 3 alquiltio C1-6, 3 haloalquiltio C1-6, 3 alcoxi C1-6 y 3 haloalcoxi C1-6; R8, R9, R10, R11 son cada uno en forma independiente H, alquilo C1-6, haloalquilo C1-6, alquilamino C1-6, alcoxi C1-6 o cicloalquilo C3-6, donde los átomos de C e os ultimos 5 grupos puede portar cualquier combinacion de 1, 2 o 3radicales, seleccionados independientemente entre sí del grupo que consiste en halogeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, alquilo C1-6, alcoxi C1-6, alqueniloxi C26, alquiniloxi C2-6, haloalcoxi C1-6 y alquiltio C1-6, Ra, Rb, Rc, Rd, Re, Rf son cada uno en forma independiente entre sí H, alquilo C1-6, haloalquilo C1-6, alquenilo C2-6 o alquinilo C2-6, y las sales aceptables para uso en agricultura del mismo.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US68412205P | 2005-05-24 | 2005-05-24 | |
US73671405P | 2005-11-15 | 2005-11-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR054364A1 true AR054364A1 (es) | 2007-06-20 |
Family
ID=36778208
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060102176A AR054364A1 (es) | 2005-05-24 | 2006-05-24 | Compuestos con estructura de 1- (imidazolin -2-il-) amino -1,2-difeniletano para combatir plagas animales |
Country Status (21)
Country | Link |
---|---|
US (1) | US7871960B2 (es) |
EP (1) | EP1888533B1 (es) |
JP (1) | JP2008542234A (es) |
KR (1) | KR20080031199A (es) |
AR (1) | AR054364A1 (es) |
AT (1) | ATE491692T1 (es) |
AU (1) | AU2006251187A1 (es) |
BR (1) | BRPI0611499A2 (es) |
CA (1) | CA2610010A1 (es) |
CR (1) | CR9532A (es) |
DE (1) | DE602006018910D1 (es) |
EC (1) | ECSP078048A (es) |
GT (1) | GT200600219A (es) |
IL (1) | IL187194A0 (es) |
MA (1) | MA29905B1 (es) |
MX (1) | MX2007014138A (es) |
PE (1) | PE20070050A1 (es) |
RU (1) | RU2007147431A (es) |
TW (1) | TW200716562A (es) |
UY (1) | UY29560A1 (es) |
WO (1) | WO2006125748A1 (es) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2063711A1 (en) * | 2007-03-01 | 2009-06-03 | Basf Se | Pesticidal active mixtures comprising aminothiazoline compounds |
WO2008123821A1 (en) * | 2007-03-01 | 2008-10-16 | Albireo Ab | 4, 5-dihydro-lh-imidazol-2-amine derivatives for use in the treatment of respiratory, cardiovascular, neurological or gastrointestinal disorders |
WO2008115141A1 (en) * | 2007-03-19 | 2008-09-25 | Albireo Ab | 4, 5-dihydro-1,3-thiazol-2-amine derivatives and their use in the treatment of respiratory, cardiovascular, neurological or gastrointestinal disorders |
RU2010103325A (ru) * | 2007-07-03 | 2011-08-10 | Басф Се (De) | 1-(азолин-2-ил)амино-1, 2-дифенилэтановые соединения для подавления вредителей-животных |
WO2009059603A1 (en) | 2007-11-05 | 2009-05-14 | Vestergaard Frandsen Sa | Room with two counter-resistant insecticidal objects |
BRPI0915917A2 (pt) * | 2008-07-17 | 2019-09-24 | Basf Se | compostos de azolin-2-ilamino, processo para a preparação de compostos, composição veterinária ou agrícola, métodos para controlar pestes animais, para proteger um material de propagação de planta ou de plantas que crescem a partir do mesmo, e para tratar, controlar, prevenir ou proteger animais contra infestação ou infecção por parasitas, semente, e, uso de composto |
BRPI0918298A2 (pt) | 2008-09-09 | 2015-08-11 | Basf Se | Compostos de pirrolin-2-ilamino, método para controlar pragas de animais, material de propagação vegetal, método para tratar ou proteger um animal da infestação ou infecção pelos parasitas, e, uso dos compostos de pirrolin-2-ilamino. |
US8695707B2 (en) * | 2009-06-16 | 2014-04-15 | Schlumberger Technology Corporation | Asphaltene removal composition and methods |
CN104237191A (zh) * | 2014-10-09 | 2014-12-24 | 南京林业大学 | 一种快速判定植株光强和温度适应范围的方法及其装置 |
US20180360040A1 (en) * | 2015-12-03 | 2018-12-20 | Syngenta Participations Ag | Pesticidal compounds and their uses |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3264474D1 (en) | 1981-02-09 | 1985-08-08 | Ciba Geigy Ag | Substituted 2-anilinomethyl-2 imidazolin derivatives, process for their preparation, agents containing them and their pesticidal application |
US4379147A (en) * | 1981-02-09 | 1983-04-05 | Ciba-Geigy Corporation | Substituted 2-(anilinomethyl)-2-imidazoline derivatives, compositions containing these derivatives, and the use thereof for combating pests |
DE59002510D1 (de) * | 1989-03-17 | 1993-10-07 | Bayer Ag | Mittel gegen Keratinschädlinge. |
DE3908814A1 (de) | 1989-03-17 | 1990-09-20 | Bayer Ag | Mittel gegen keratinschaedlinge |
JP4614968B2 (ja) * | 2003-12-23 | 2011-01-19 | ビーエーエスエフ ソシエタス・ヨーロピア | 昆虫、蛛形類および線虫を駆除するための1−(アゾリン−2−イル)アミノ−1,2−ジフェニルエタン化合物 |
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2006
- 2006-05-18 KR KR1020077029894A patent/KR20080031199A/ko not_active Application Discontinuation
- 2006-05-18 DE DE602006018910T patent/DE602006018910D1/de active Active
- 2006-05-18 EP EP06777225A patent/EP1888533B1/en active Active
- 2006-05-18 JP JP2008512811A patent/JP2008542234A/ja not_active Ceased
- 2006-05-18 CA CA002610010A patent/CA2610010A1/en not_active Abandoned
- 2006-05-18 RU RU2007147431/04A patent/RU2007147431A/ru not_active Application Discontinuation
- 2006-05-18 WO PCT/EP2006/062419 patent/WO2006125748A1/en active Application Filing
- 2006-05-18 BR BRPI0611499-7A patent/BRPI0611499A2/pt not_active IP Right Cessation
- 2006-05-18 MX MX2007014138A patent/MX2007014138A/es not_active Application Discontinuation
- 2006-05-18 AU AU2006251187A patent/AU2006251187A1/en not_active Abandoned
- 2006-05-18 US US11/914,992 patent/US7871960B2/en not_active Expired - Fee Related
- 2006-05-18 AT AT06777225T patent/ATE491692T1/de not_active IP Right Cessation
- 2006-05-23 PE PE2006000542A patent/PE20070050A1/es not_active Application Discontinuation
- 2006-05-24 UY UY29560A patent/UY29560A1/es unknown
- 2006-05-24 GT GT200600219A patent/GT200600219A/es unknown
- 2006-05-24 TW TW095118463A patent/TW200716562A/zh unknown
- 2006-05-24 AR ARP060102176A patent/AR054364A1/es unknown
-
2007
- 2007-11-06 IL IL187194A patent/IL187194A0/en unknown
- 2007-11-16 CR CR9532A patent/CR9532A/es not_active Application Discontinuation
- 2007-12-21 EC EC2007008048A patent/ECSP078048A/es unknown
- 2007-12-24 MA MA30493A patent/MA29905B1/fr unknown
Also Published As
Publication number | Publication date |
---|---|
PE20070050A1 (es) | 2007-02-06 |
JP2008542234A (ja) | 2008-11-27 |
ECSP078048A (es) | 2008-01-23 |
CR9532A (es) | 2008-02-21 |
WO2006125748A1 (en) | 2006-11-30 |
RU2007147431A (ru) | 2009-06-27 |
UY29560A1 (es) | 2006-12-29 |
BRPI0611499A2 (pt) | 2011-02-22 |
EP1888533A1 (en) | 2008-02-20 |
CA2610010A1 (en) | 2006-11-30 |
TW200716562A (en) | 2007-05-01 |
GT200600219A (es) | 2006-12-19 |
MA29905B1 (fr) | 2008-11-03 |
US7871960B2 (en) | 2011-01-18 |
MX2007014138A (es) | 2008-01-11 |
US20080200335A1 (en) | 2008-08-21 |
ATE491692T1 (de) | 2011-01-15 |
AU2006251187A1 (en) | 2006-11-30 |
IL187194A0 (en) | 2008-02-09 |
EP1888533B1 (en) | 2010-12-15 |
DE602006018910D1 (de) | 2011-01-27 |
KR20080031199A (ko) | 2008-04-08 |
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