AR050516A1 - Bifeniltiazolcarboxamidas. composiciones antimicrobianas - Google Patents
Bifeniltiazolcarboxamidas. composiciones antimicrobianasInfo
- Publication number
- AR050516A1 AR050516A1 ARP050103215A ARP050103215A AR050516A1 AR 050516 A1 AR050516 A1 AR 050516A1 AR P050103215 A ARP050103215 A AR P050103215A AR P050103215 A ARP050103215 A AR P050103215A AR 050516 A1 AR050516 A1 AR 050516A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- carbonyl
- halogen
- alkoxy
- halogenoalkyl
- Prior art date
Links
- 230000000845 anti-microbial effect Effects 0.000 title abstract 2
- 239000000203 mixture Substances 0.000 title abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 13
- 125000000217 alkyl group Chemical group 0.000 abstract 10
- 125000001188 haloalkyl group Chemical group 0.000 abstract 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 8
- 229910052801 chlorine Inorganic materials 0.000 abstract 8
- 239000000460 chlorine Substances 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 7
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 150000002367 halogens Chemical class 0.000 abstract 7
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 6
- 229910052731 fluorine Inorganic materials 0.000 abstract 6
- 239000011737 fluorine Substances 0.000 abstract 6
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 5
- 125000001246 bromo group Chemical group Br* 0.000 abstract 5
- 150000002431 hydrogen Chemical class 0.000 abstract 5
- -1 formyl C1-3alkyl Chemical group 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000004414 alkyl thio group Chemical group 0.000 abstract 3
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 3
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 2
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 125000005842 heteroatom Chemical group 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
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 125000006413 ring segment Chemical group 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000004983 dialkoxyalkyl group Chemical group 0.000 abstract 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 125000005188 oxoalkyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
-
- 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
- A01N43/74—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 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Composiciones antimicrobianas y compuestos intermediarios. Reivindicacion 1: Bifeniltiazolcarboxamidas de la formula (1), en la que: R1 significa hidrogeno, halogeno, amino, alquilamino C1-4, di-(alquilo C1-4)amino, ciano, alquilo C1-4 o halogenoalquilo C1-4 con 1 hasta 5 átomos de halogeno; R2 significa halogeno, alquilo C1-4 o halogenoalquilo C1-4 con 1 hasta 5 átomos de halogeno; R3 significa hidrogeno, alquilo C1-8, alquilsulfinilo C1-6, alquilsulfonilo C1-6, alcoxiC1-4- alquiloC1-4, cicloalquilo C3-8; halogenoalquilo C1-6, halogenoalquiltio C1-4, halogenoalquilsulfinilo C1-4, halogenoalquilsulfonilo C1-4, halogeno-alcoxiC1-4-alquiloC1-4, halogenocicloalquilo C3-8 con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; formilo, formil-alquiloC1-3, (alquilo C1-3)carbonil-alquiloC1-3, (alcoxi C1-3)carbonil-alquiloC1-3; halogeno-(alquilo C1-3)carbonil-alquiloC1-3, halogeno-(alcoxi C1-3)carbonil-alquiloC1-3 con, respectivamente, 1 hasta 13 átomos de fluor, de cloro y/o de bromo; (alquilo C1-8)carbonilo, (alcoxi C1-8)carbonilo, (alcoxiC1-4-alquiloC1-4)carbonilo, (cicloalquilo C3-8)carbonilo; (halogenoalquilo C1-6)carbonilo, (halogenoalcoxi C1-6)carbonilo, (halogeno-alcoxiC1-4-alquiloC1- 4)carbonilo, (halogenocicloalquilo C3-8)carbonilo con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; o -C(=O)C(=O)R6, -CONR7R8 o -CH2NR9R10; R4 significa halogeno, alquilo C1-4, alcoxi C1-4, alquiltio C1-4 o halogenoalquilo C1-4 con 1 hasta 9 átomos de fluor, de cloro y/o de bromo; m significa 1 o 2, pudiendo ser iguales o diferentes los restos R4, cuando m signifique 2; R5 significa halogeno, ciano, nitro, amino, hidroxi, formilo, carboxi, carbamoilo, tiocarbamoilo, alquilo C1-8, alquenilo C2-6, alcoxi C1-8, alqueniloxi C2-6, alquiltio C1-8, alquilsulfinilo C1-8, alquilsulfonilo C1-8, hidroxialquilo C1-8, oxoalquilo C1-8, alcoxialquilo C1-8, alquiltioalquilo C1-8, dialcoxialquilo C1-8, alquilamino C1-6, di(alquilo C1-6)amino, (alquilo C1-6)carbonilo, (alquilo C1-6)carboniloxi, (alcoxi C1-6)carbonilo, (alquilo C1-6)aminocarbonilo, di(alquilo C1-6)aminocarbonilo, (alquilo C1-6)carbonilamino, (alquilo C1-6)carbonil(alquilo C1-6)amino, (alquenilo C2- 6)carbonilo, (alquinilo C2-6)carbonilo, cicloalquilo C3-6, cicloalquiloxi C3-6, o significa halogenoalquilo C1-6, halogenoalcoxi C1-6, halogenoalquiltio C1-6, halogenoalquilsulfinilo C1-6 o halogenoalquilsulfonilo C1-6 con, respectivamente, 1 hasta 13 átomos de halogeno, halogenoalquenilo C2-6, halogenoalqueniloxi C2-6 con, respectivamente, 1 hasta 11 átomos de halogeno iguales o diferentes; R6 significa hidrogeno, alquilo C1-8, alcoxi C1-8, alcoxiC1-4-alquiloC1-4, cicloalquilo C3-8; halogenoalquilo C1-6, halogenoalcoxi C1-6, halogeno-alcoxiC1-4-alquiloC1-4, halogenocicloalquilo C3-8 con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; R7 y R8 significan, independientemente entre sí, hidrogeno, alquilo C1-8, alcoxiC1-4-alquiloC1-4, cicloalquilo C3-8; halogenoalquilo C1-8, halogeno-alcoxiC1-4-alquiloC1-4, halogenocicloalquilo C3-8 con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; R7 y R8 además significan, junto con el átomo de nitrogeno, con el que están enlazados, un heterociclo saturado, con hasta 5 hasta 8 átomos en el anillo, sustituido, en caso dado, una o varias veces, de forma igual o de formas diferentes por halogeno o por alquilo C1-4, pudiendo contener el heterociclo 1 o 2 heteroátomos más, no contiguos, de la serie formada por oxígeno, azufre o NR11; R9 y R10 significan, independientemente entre sí, hidrogeno, alquilo C1-8, cicloalquilo C3-8; halogenoalquilo C1-8, halogenocicloalquilo C3-8 con, respectivamente, 1 hasta 9 átomos de fluor, de cloro y/o de bromo; R9 y R10 además significan, junto con el átomo de nitrogeno, con el que están enlazados, un heterociclo saturado, con 5 hasta 8 átomos en el anillo, sustituido, en caso dado, una o varias veces, de forma igual o de formas diferentes por halogeno o por alquilo C1-4, pudiendo contener el heterociclo 1 o 2 heteroátomos más, no contiguos, de la serie formada por oxígeno, azufre o NR11; R11 significa hidrogeno o alquilo C1-6, quedando excluidos los compuestos de la formula (1), en la que: R1 significa hidrogeno o metilo; R2 significa cloro, metilo, difluormetilo o trifluormetilo; R5 significa halogeno, alquilo C1-4, trifluormetilo, alcoxi C1-4 o alquiltio C1-4, cuando R3 signifique hidrogeno y R4 signifique fluor y m signifique 1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004041532A DE102004041532A1 (de) | 2004-08-27 | 2004-08-27 | Biphenylthiazolcarboxamide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR050516A1 true AR050516A1 (es) | 2006-11-01 |
Family
ID=35745600
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP050103215A AR050516A1 (es) | 2004-08-27 | 2005-08-02 | Bifeniltiazolcarboxamidas. composiciones antimicrobianas |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20090105316A1 (es) |
| EP (1) | EP1786795A2 (es) |
| JP (1) | JP2008510746A (es) |
| KR (1) | KR20070050958A (es) |
| CN (1) | CN101044128B (es) |
| AR (1) | AR050516A1 (es) |
| BR (1) | BRPI0514439A (es) |
| CA (1) | CA2577997A1 (es) |
| CR (1) | CR8879A (es) |
| DE (1) | DE102004041532A1 (es) |
| MX (1) | MX2007002243A (es) |
| WO (1) | WO2006024389A2 (es) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10246959A1 (de) * | 2002-10-09 | 2004-04-22 | Bayer Cropscience Ag | Thiazolylbiphenylamide |
| DE102004005786A1 (de) * | 2004-02-06 | 2005-08-25 | Bayer Cropscience Ag | Haloalkylcarboxamide |
| DE102004041530A1 (de) * | 2004-08-27 | 2006-03-02 | Bayer Cropscience Ag | Biphenylthiazolcarboxamide |
| DE102005022147A1 (de) * | 2005-04-28 | 2006-11-02 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| BRPI0710774A2 (pt) * | 2006-05-03 | 2011-06-21 | Basf Se | método para proteger plantas após germinação contra o ataque de fungos fitopatogênicos foliares, formulação para tratamento de semente, semente, e, uso de pelo menos um composto |
| JO3598B1 (ar) | 2006-10-10 | 2020-07-05 | Infinity Discovery Inc | الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني |
| PE20091838A1 (es) | 2008-04-09 | 2009-12-18 | Infinity Pharmaceuticals Inc | Inhibidores de amida hidrolasa de acido graso |
| ES2386940T3 (es) | 2008-05-02 | 2012-09-06 | Basf Se | Método para la preparación de ésteres halosustituidos de ácido 2-(aminometiliden)-3-oxobutírico |
| BRPI0911898A2 (pt) | 2008-05-02 | 2015-10-13 | Basf Se | processo para preparar compostos, e, composto. |
| ES2525807T3 (es) * | 2008-05-05 | 2014-12-30 | Basf Se | Procedimiento de preparación de compuestos de pirazol sustituidos en las posiciones 1, 3, 4 |
| CN102099343B (zh) | 2008-07-21 | 2014-06-04 | 巴斯夫欧洲公司 | 制备1,3-二取代的吡唑羧酸酯的方法 |
| CA2757679A1 (en) | 2009-04-07 | 2010-10-14 | Infinity Pharmaceuticals, Inc. | Inhibitors of fatty acid amide hydrolase |
| JP2012523425A (ja) | 2009-04-07 | 2012-10-04 | インフイニトイ プハルマセウトイカルス インコーポレイテッド | 脂肪酸アミドヒドロラーゼの阻害薬 |
| BR112012010486A2 (pt) | 2009-11-05 | 2016-03-15 | Basf Se | processo para preparação de compostos 1-3 pirazol, processo para preparação de um acido pirazolcarboxilico da formula ia e processo para preparação de um composto da formula v |
| JP2013510112A (ja) | 2009-11-05 | 2013-03-21 | ビーエーエスエフ ソシエタス・ヨーロピア | アミナールの調製方法及び１，３−二置換ピラゾール化合物を調製するためのその使用 |
| RU2569061C2 (ru) | 2010-02-03 | 2015-11-20 | Инфинити Фармасьютикалз, Инк. | Ингибиторы амид-гидролазы жирных кислот |
| CN102344578A (zh) * | 2011-09-09 | 2012-02-08 | 深圳市金钒能源科技有限公司 | 一种离子膜的生产方法 |
| EP3178813A1 (en) | 2015-12-09 | 2017-06-14 | Basf Se | Method for preparing halogenated 3-oxocarboxylates carrying a 2-alkoxymethylidene or a 2-dialkylaminomethylidene group |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5045554A (en) * | 1988-11-29 | 1991-09-03 | Monsanto Company | Substituted thiazoles and their use as fungicides |
| AU6049590A (en) * | 1989-07-25 | 1991-02-22 | Monsanto Company | Substituted carboxanilidothiazoles and their use as fungicides |
| DE19531813A1 (de) * | 1995-08-30 | 1997-03-06 | Basf Ag | Bisphenylamide |
| AU7200300A (en) * | 1999-12-16 | 2001-06-21 | Rohm And Haas Company | 5-carboxanilido-haloalkylthiazoles as antimicrobial and marine antifouling agents |
| AU774001B2 (en) * | 1999-12-16 | 2004-06-10 | Nissan Chemical Industries, Ltd. | 5-carboxanilido-2,4-bis-trifluoromethylthiazoles and their use to control rice blast |
| GB0101996D0 (en) * | 2001-01-25 | 2001-03-14 | Syngenta Participations Ag | Organtic compounds |
| DE10204391A1 (de) * | 2002-02-04 | 2003-08-14 | Bayer Cropscience Ag | Difluormethylthiazolylcarboxanilide |
| DE10246959A1 (de) * | 2002-10-09 | 2004-04-22 | Bayer Cropscience Ag | Thiazolylbiphenylamide |
| DE10347090A1 (de) * | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE10349501A1 (de) * | 2003-10-23 | 2005-05-25 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE102004041530A1 (de) * | 2004-08-27 | 2006-03-02 | Bayer Cropscience Ag | Biphenylthiazolcarboxamide |
| DE102005060462A1 (de) * | 2005-12-17 | 2007-06-28 | Bayer Cropscience Ag | Biphenylcarboxamide |
-
2004
- 2004-08-27 DE DE102004041532A patent/DE102004041532A1/de not_active Withdrawn
-
2005
- 2005-08-02 AR ARP050103215A patent/AR050516A1/es not_active Application Discontinuation
- 2005-08-13 KR KR1020077005773A patent/KR20070050958A/ko not_active Ceased
- 2005-08-13 JP JP2007528686A patent/JP2008510746A/ja not_active Withdrawn
- 2005-08-13 BR BRPI0514439-6A patent/BRPI0514439A/pt not_active IP Right Cessation
- 2005-08-13 MX MX2007002243A patent/MX2007002243A/es not_active Application Discontinuation
- 2005-08-13 CA CA002577997A patent/CA2577997A1/en not_active Abandoned
- 2005-08-13 WO PCT/EP2005/008839 patent/WO2006024389A2/de not_active Ceased
- 2005-08-13 EP EP05771671A patent/EP1786795A2/de not_active Withdrawn
- 2005-08-13 CN CN2005800361352A patent/CN101044128B/zh not_active Expired - Fee Related
- 2005-08-13 US US11/661,092 patent/US20090105316A1/en not_active Abandoned
-
2007
- 2007-01-26 CR CR8879A patent/CR8879A/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1786795A2 (de) | 2007-05-23 |
| WO2006024389A2 (de) | 2006-03-09 |
| JP2008510746A (ja) | 2008-04-10 |
| KR20070050958A (ko) | 2007-05-16 |
| CN101044128B (zh) | 2012-04-18 |
| BRPI0514439A (pt) | 2008-06-10 |
| CR8879A (es) | 2007-08-28 |
| DE102004041532A1 (de) | 2006-03-02 |
| US20090105316A1 (en) | 2009-04-23 |
| MX2007002243A (es) | 2007-04-20 |
| CA2577997A1 (en) | 2006-03-09 |
| CN101044128A (zh) | 2007-09-26 |
| WO2006024389A3 (de) | 2006-05-18 |
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