UA78528C2 - Fungicidal composition containing pyrimethanil and phocetyl-aluminium, method to treat plants and using phocetyl-aluminium as agent to improve stability of pyrimethanil activity - Google Patents
Fungicidal composition containing pyrimethanil and phocetyl-aluminium, method to treat plants and using phocetyl-aluminium as agent to improve stability of pyrimethanil activity Download PDFInfo
- Publication number
- UA78528C2 UA78528C2 UA20040503389A UA20040503389A UA78528C2 UA 78528 C2 UA78528 C2 UA 78528C2 UA 20040503389 A UA20040503389 A UA 20040503389A UA 20040503389 A UA20040503389 A UA 20040503389A UA 78528 C2 UA78528 C2 UA 78528C2
- Authority
- UA
- Ukraine
- Prior art keywords
- pyrimethanil
- sipegea
- fosetyl
- plants
- akegpagia
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 50
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 title claims abstract description 26
- 239000005828 Pyrimethanil Substances 0.000 title claims abstract description 25
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 25
- 238000000034 method Methods 0.000 title claims description 24
- 239000003795 chemical substances by application Substances 0.000 title claims description 4
- 230000000694 effects Effects 0.000 title abstract description 7
- 229910052782 aluminium Inorganic materials 0.000 title description 3
- 239000004411 aluminium Substances 0.000 title 2
- 201000010099 disease Diseases 0.000 claims abstract description 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 14
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- 235000013399 edible fruits Nutrition 0.000 claims description 13
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- 239000004480 active ingredient Substances 0.000 claims description 6
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- 235000003805 Musa ABB Group Nutrition 0.000 claims description 4
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
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- 230000000749 insecticidal effect Effects 0.000 description 3
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- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 description 2
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
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- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
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- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- NCXMLFZGDNKEPB-FFPOYIOWSA-N natamycin Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]2O[C@@H]2C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 NCXMLFZGDNKEPB-FFPOYIOWSA-N 0.000 description 1
- 235000010298 natamycin Nutrition 0.000 description 1
- 239000004311 natamycin Substances 0.000 description 1
- 229960003255 natamycin Drugs 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 1
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 description 1
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- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
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- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- JPFWJDMDPLEUBD-ITJAGOAWSA-N polyoxorim Polymers O[C@@H]1[C@H](O)[C@@H]([C@H](NC(=O)[C@H]([C@H](O)[C@@H](O)COC(N)=O)N)C(O)=O)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 JPFWJDMDPLEUBD-ITJAGOAWSA-N 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229940050982 potassium hydroxyquinoline sulfate Drugs 0.000 description 1
- DWBSXHMYTSZXQL-UHFFFAOYSA-M potassium;quinolin-8-yl sulfate Chemical compound [K+].C1=CN=C2C(OS(=O)(=O)[O-])=CC=CC2=C1 DWBSXHMYTSZXQL-UHFFFAOYSA-M 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 description 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 description 1
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- 239000008262 pumice Substances 0.000 description 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 description 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
- MRUMAIRJPMUAPZ-UHFFFAOYSA-N quinolin-8-ol;sulfuric acid Chemical compound OS(O)(=O)=O.C1=CN=C2C(O)=CC=CC2=C1 MRUMAIRJPMUAPZ-UHFFFAOYSA-N 0.000 description 1
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
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- BHRZNVHARXXAHW-UHFFFAOYSA-N sec-butylamine Chemical compound CCC(C)N BHRZNVHARXXAHW-UHFFFAOYSA-N 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
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- 229960004029 silicic acid Drugs 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229960001866 silicon dioxide Drugs 0.000 description 1
- 239000004504 smoke candle Substances 0.000 description 1
- 239000004509 smoke generator Substances 0.000 description 1
- HCJLVWUMMKIQIM-UHFFFAOYSA-M sodium;2,3,4,5,6-pentachlorophenolate Chemical compound [Na+].[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl HCJLVWUMMKIQIM-UHFFFAOYSA-M 0.000 description 1
- WSFQLUVWDKCYSW-UHFFFAOYSA-M sodium;2-hydroxy-3-morpholin-4-ylpropane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(O)CN1CCOCC1 WSFQLUVWDKCYSW-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000004553 water soluble powder for seed treatment Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 230000003442 weekly effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0114439A FR2831768B1 (fr) | 2001-11-08 | 2001-11-08 | Composition fongicide comprenant au moins un compose fongici de de la famille des anilinopyrimidines et au moins un derive de l'acide phosphoreux et utilisation de cette composition pour la lutte contre les maladies des plantes |
| PCT/FR2002/003832 WO2003039257A1 (fr) | 2001-11-08 | 2002-11-08 | Composition fongicide comprenant du pyrimethanil et au moins un derive de l'acide phosphoreux et son utilisation pour la lutte contre les maladies de plantes |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA78528C2 true UA78528C2 (en) | 2007-04-10 |
Family
ID=8869173
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA20040503389A UA78528C2 (en) | 2001-11-08 | 2002-08-11 | Fungicidal composition containing pyrimethanil and phocetyl-aluminium, method to treat plants and using phocetyl-aluminium as agent to improve stability of pyrimethanil activity |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US20050019420A1 (pl) |
| EP (1) | EP1441590B1 (pl) |
| JP (1) | JP2005507430A (pl) |
| KR (1) | KR20050044356A (pl) |
| CN (1) | CN1264406C (pl) |
| AR (1) | AR037334A1 (pl) |
| AT (1) | ATE394032T1 (pl) |
| AU (1) | AU2002358878B2 (pl) |
| BR (1) | BR0213918B1 (pl) |
| CA (1) | CA2463707C (pl) |
| CO (1) | CO5590859A2 (pl) |
| DE (1) | DE60226477D1 (pl) |
| ES (1) | ES2305332T3 (pl) |
| FR (1) | FR2831768B1 (pl) |
| HK (1) | HK1071035A1 (pl) |
| HU (1) | HUP0402032A3 (pl) |
| IL (2) | IL161637A0 (pl) |
| MA (1) | MA27148A1 (pl) |
| MX (1) | MXPA04004316A (pl) |
| NZ (1) | NZ532342A (pl) |
| PL (1) | PL209101B1 (pl) |
| PT (1) | PT1441590E (pl) |
| RU (1) | RU2278516C2 (pl) |
| TW (1) | TWI336242B (pl) |
| UA (1) | UA78528C2 (pl) |
| WO (1) | WO2003039257A1 (pl) |
| ZA (1) | ZA200402967B (pl) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1810571A4 (en) | 2004-10-22 | 2009-03-25 | Ishihara Sangyo Kaisha | AGRICULTURAL OR HORTICULTURAL BACTERICIDE COMPOSITION AND METHOD FOR COMBATING PLANT DISEASES |
| JP4769921B2 (ja) * | 2005-04-25 | 2011-09-07 | 丸善製薬株式会社 | 植物病害防除剤及び農薬 |
| EP2320742B1 (en) | 2008-07-17 | 2016-12-21 | Bioworks, Inc. | Control of plant diseases using a combination of a trichoderma virens species and a rhizosphere competent trichoderma harzianum species |
| NZ592226A (en) * | 2008-10-15 | 2012-12-21 | Bayer Cropscience Ag | Use of dithiin tetracarboximides for treating phytopathogenic fungi for protecting plants |
| AR077956A1 (es) * | 2009-09-14 | 2011-10-05 | Bayer Cropscience Ag | Combinaciones de compuestos activos |
| UA125792C2 (uk) * | 2015-06-08 | 2022-06-08 | Вм Аґритек Лімітед | Антимікробні й агрохімічні композиції |
| JP7361696B2 (ja) * | 2017-12-20 | 2023-10-16 | バイエル アクチェンゲゼルシャフト | リンゴのモザイク黒星病を防除するための殺真菌剤の使用 |
| CN111269844B (zh) * | 2020-04-02 | 2021-05-25 | 山东省科学院生态研究所 | 一株防治韭菜灰霉病的哈茨木霉tw21990及其应用 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2254276B1 (pl) * | 1973-12-14 | 1977-03-04 | Philagro Sa | |
| DD133148A5 (de) * | 1976-11-16 | 1978-12-13 | Philagro Sa | Verfahren zur herstellung von aluminiumaethylphosphit |
| JP3086746B2 (ja) * | 1991-03-20 | 2000-09-11 | クミアイ化学工業株式会社 | 農園芸用殺菌剤組成物 |
| FR2722652B1 (fr) * | 1994-07-22 | 1997-12-19 | Rhone Poulenc Agrochimie | Composition fongicide comprenant une 2-imidazoline-5-one |
| FR2737086B1 (fr) * | 1995-07-24 | 1997-08-22 | Rhone Poulenc Agrochimie | Composition fongicide comprenant un compose analogue de la strobilurine |
| DE19739982A1 (de) * | 1996-12-10 | 1998-06-18 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| FR2771898B1 (fr) * | 1997-12-04 | 2000-01-07 | Rhone Poulenc Agrochimie | Composition fongicide et/ou bactericide synergique |
| WO1999053761A1 (fr) * | 1998-04-16 | 1999-10-28 | Aventis Cropscience S.A. | Nouvelle utilisation de composes antifongiques et/ou antibacteriens et/ou antiviraux |
| FR2787295A1 (fr) * | 1998-12-22 | 2000-06-23 | Rhone Poulenc Agrochimie | Composition fongicide synergique comprenant un compose analogue de la strobilurine |
-
2001
- 2001-11-08 FR FR0114439A patent/FR2831768B1/fr not_active Expired - Fee Related
-
2002
- 2002-08-11 UA UA20040503389A patent/UA78528C2/uk unknown
- 2002-11-07 AR ARP020104278A patent/AR037334A1/es unknown
- 2002-11-08 EP EP02793216A patent/EP1441590B1/fr not_active Expired - Lifetime
- 2002-11-08 TW TW091132919A patent/TWI336242B/zh not_active IP Right Cessation
- 2002-11-08 US US10/494,868 patent/US20050019420A1/en not_active Abandoned
- 2002-11-08 KR KR1020047006921A patent/KR20050044356A/ko active Search and Examination
- 2002-11-08 PT PT02793216T patent/PT1441590E/pt unknown
- 2002-11-08 NZ NZ532342A patent/NZ532342A/en not_active IP Right Cessation
- 2002-11-08 AT AT02793216T patent/ATE394032T1/de active
- 2002-11-08 RU RU2004117214/04A patent/RU2278516C2/ru not_active IP Right Cessation
- 2002-11-08 CA CA2463707A patent/CA2463707C/fr not_active Expired - Fee Related
- 2002-11-08 AU AU2002358878A patent/AU2002358878B2/en not_active Ceased
- 2002-11-08 BR BRPI0213918-9A patent/BR0213918B1/pt not_active IP Right Cessation
- 2002-11-08 WO PCT/FR2002/003832 patent/WO2003039257A1/fr active IP Right Grant
- 2002-11-08 JP JP2003541363A patent/JP2005507430A/ja active Pending
- 2002-11-08 CN CNB028221265A patent/CN1264406C/zh not_active Expired - Fee Related
- 2002-11-08 ES ES02793216T patent/ES2305332T3/es not_active Expired - Lifetime
- 2002-11-08 HU HU0402032A patent/HUP0402032A3/hu unknown
- 2002-11-08 MX MXPA04004316A patent/MXPA04004316A/es active IP Right Grant
- 2002-11-08 IL IL16163702A patent/IL161637A0/xx unknown
- 2002-11-08 DE DE60226477T patent/DE60226477D1/de not_active Expired - Lifetime
- 2002-11-08 PL PL368232A patent/PL209101B1/pl not_active IP Right Cessation
-
2004
- 2004-04-19 ZA ZA2004/02967A patent/ZA200402967B/en unknown
- 2004-04-26 IL IL161637A patent/IL161637A/en not_active IP Right Cessation
- 2004-05-28 MA MA27702A patent/MA27148A1/fr unknown
- 2004-06-07 CO CO04053193A patent/CO5590859A2/es not_active Application Discontinuation
-
2005
- 2005-05-06 HK HK05103816A patent/HK1071035A1/xx not_active IP Right Cessation
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