ES2262854T3 - Mezcla fungicida que continen derivados de arilamidina. - Google Patents
Mezcla fungicida que continen derivados de arilamidina.Info
- Publication number
- ES2262854T3 ES2262854T3 ES02777410T ES02777410T ES2262854T3 ES 2262854 T3 ES2262854 T3 ES 2262854T3 ES 02777410 T ES02777410 T ES 02777410T ES 02777410 T ES02777410 T ES 02777410T ES 2262854 T3 ES2262854 T3 ES 2262854T3
- Authority
- ES
- Spain
- Prior art keywords
- group
- alkyl
- alkoxy
- optionally substituted
- alkylthiol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 96
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 52
- 239000000417 fungicide Substances 0.000 title description 12
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 48
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 25
- 150000002367 halogens Chemical class 0.000 claims abstract description 25
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 19
- 125000002252 acyl group Chemical group 0.000 claims abstract description 18
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 17
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 17
- 125000002837 carbocyclic group Chemical group 0.000 claims abstract description 15
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 15
- 239000001257 hydrogen Substances 0.000 claims abstract description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 13
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 9
- 150000004982 aromatic amines Chemical class 0.000 claims abstract description 4
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims abstract description 3
- OMOZGSRMZAYUCI-UHFFFAOYSA-N amino cyanate Chemical group NOC#N OMOZGSRMZAYUCI-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 claims abstract description 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 88
- -1 triazolinones Chemical class 0.000 claims description 49
- 125000003545 alkoxy group Chemical group 0.000 claims description 34
- 201000010099 disease Diseases 0.000 claims description 30
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 30
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 28
- 150000001356 alkyl thiols Chemical class 0.000 claims description 27
- 235000013311 vegetables Nutrition 0.000 claims description 27
- 235000013339 cereals Nutrition 0.000 claims description 20
- 125000001188 haloalkyl group Chemical group 0.000 claims description 20
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 18
- 241000896238 Oidium Species 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 17
- 241000196324 Embryophyta Species 0.000 claims description 15
- 235000021307 Triticum Nutrition 0.000 claims description 15
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 12
- 239000005785 Fluquinconazole Substances 0.000 claims description 11
- 239000002253 acid Substances 0.000 claims description 11
- 239000002585 base Substances 0.000 claims description 10
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 claims description 10
- 239000005778 Fenpropimorph Substances 0.000 claims description 8
- 240000005979 Hordeum vulgare Species 0.000 claims description 8
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 230000003449 preventive effect Effects 0.000 claims description 8
- RYAUSSKQMZRMAI-ALOPSCKCSA-N (2S,6R)-4-[3-(4-tert-butylphenyl)-2-methylpropyl]-2,6-dimethylmorpholine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1C[C@H](C)O[C@H](C)C1 RYAUSSKQMZRMAI-ALOPSCKCSA-N 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 235000013399 edible fruits Nutrition 0.000 claims description 6
- 230000008029 eradication Effects 0.000 claims description 6
- UKWHYYKOEPRTIC-UHFFFAOYSA-N mercury(ii) oxide Chemical compound [Hg]=O UKWHYYKOEPRTIC-UHFFFAOYSA-N 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 5
- 244000025254 Cannabis sativa Species 0.000 claims description 5
- 241000223221 Fusarium oxysporum Species 0.000 claims description 5
- 235000010469 Glycine max Nutrition 0.000 claims description 5
- 235000007688 Lycopersicon esculentum Nutrition 0.000 claims description 5
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 claims description 5
- 240000007594 Oryza sativa Species 0.000 claims description 5
- 235000007164 Oryza sativa Nutrition 0.000 claims description 5
- 235000010582 Pisum sativum Nutrition 0.000 claims description 5
- 240000004713 Pisum sativum Species 0.000 claims description 5
- 240000003768 Solanum lycopersicum Species 0.000 claims description 5
- 235000002595 Solanum tuberosum Nutrition 0.000 claims description 5
- 244000061456 Solanum tuberosum Species 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 235000009566 rice Nutrition 0.000 claims description 5
- 235000016068 Berberis vulgaris Nutrition 0.000 claims description 4
- 241000335053 Beta vulgaris Species 0.000 claims description 4
- 240000007124 Brassica oleracea Species 0.000 claims description 4
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 claims description 4
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 claims description 4
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 claims description 4
- 239000002169 Metam Substances 0.000 claims description 4
- LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 claims description 4
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 4
- 244000061176 Nicotiana tabacum Species 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 4
- 240000001987 Pyrus communis Species 0.000 claims description 4
- 235000014443 Pyrus communis Nutrition 0.000 claims description 4
- 239000005857 Trifloxystrobin Substances 0.000 claims description 4
- 240000008042 Zea mays Species 0.000 claims description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 4
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 claims description 4
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical compound OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 claims description 4
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 4
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims description 4
- 239000000194 fatty acid Substances 0.000 claims description 4
- 229930195729 fatty acid Natural products 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 230000003287 optical effect Effects 0.000 claims description 4
- 239000002420 orchard Substances 0.000 claims description 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 4
- 150000003852 triazoles Chemical class 0.000 claims description 4
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 claims description 4
- 239000002023 wood Substances 0.000 claims description 4
- 244000291564 Allium cepa Species 0.000 claims description 3
- 235000002732 Allium cepa var. cepa Nutrition 0.000 claims description 3
- 239000005730 Azoxystrobin Substances 0.000 claims description 3
- 240000006740 Cichorium endivia Species 0.000 claims description 3
- 235000013162 Cocos nucifera Nutrition 0.000 claims description 3
- 244000060011 Cocos nucifera Species 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 3
- 241000219104 Cucurbitaceae Species 0.000 claims description 3
- 239000005767 Epoxiconazole Substances 0.000 claims description 3
- 244000020551 Helianthus annuus Species 0.000 claims description 3
- 235000003222 Helianthus annuus Nutrition 0.000 claims description 3
- 239000005796 Ipconazole Substances 0.000 claims description 3
- 239000005797 Iprovalicarb Substances 0.000 claims description 3
- NWUWYYSKZYIQAE-ZBFHGGJFSA-N L-(R)-iprovalicarb Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)N[C@H](C)C1=CC=C(C)C=C1 NWUWYYSKZYIQAE-ZBFHGGJFSA-N 0.000 claims description 3
- 235000003228 Lactuca sativa Nutrition 0.000 claims description 3
- 240000008415 Lactuca sativa Species 0.000 claims description 3
- 235000011430 Malus pumila Nutrition 0.000 claims description 3
- 244000070406 Malus silvestris Species 0.000 claims description 3
- 235000015103 Malus silvestris Nutrition 0.000 claims description 3
- 239000005807 Metalaxyl Substances 0.000 claims description 3
- 239000005868 Metconazole Substances 0.000 claims description 3
- 240000005561 Musa balbisiana Species 0.000 claims description 3
- 235000018290 Musa x paradisiaca Nutrition 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 235000003733 chicria Nutrition 0.000 claims description 3
- 239000010949 copper Substances 0.000 claims description 3
- 229910052802 copper Inorganic materials 0.000 claims description 3
- 235000005822 corn Nutrition 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 claims description 3
- 229960002523 mercuric chloride Drugs 0.000 claims description 3
- 229940101209 mercuric oxide Drugs 0.000 claims description 3
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 claims description 3
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 claims description 3
- VBGJXKJKVVAVSJ-UHFFFAOYSA-N n'-[4-[2-chloro-3-(trifluoromethyl)phenoxy]-2,5-dimethylphenyl]-n-ethyl-n-methylmethanimidamide Chemical compound C1=C(C)C(N=CN(C)CC)=CC(C)=C1OC1=CC=CC(C(F)(F)F)=C1Cl VBGJXKJKVVAVSJ-UHFFFAOYSA-N 0.000 claims description 3
- 239000011593 sulfur Substances 0.000 claims description 3
- MKNJWAXSYGAMGJ-UHFFFAOYSA-N (2,3,4,5,6-pentachlorophenyl) dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl MKNJWAXSYGAMGJ-UHFFFAOYSA-N 0.000 claims description 2
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 claims description 2
- SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 claims description 2
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 claims description 2
- XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical class CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 claims description 2
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 claims description 2
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 claims description 2
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 claims description 2
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 claims description 2
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 claims description 2
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 claims description 2
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 claims description 2
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 claims description 2
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 claims description 2
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 claims description 2
- HILAYQUKKYWPJW-UHFFFAOYSA-N 1-dodecylguanidine Chemical compound CCCCCCCCCCCCN=C(N)N HILAYQUKKYWPJW-UHFFFAOYSA-N 0.000 claims description 2
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 claims description 2
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 claims description 2
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 claims description 2
- DNBMPXLFKQCOBV-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OCCOCCOCC)=NC2=C1 DNBMPXLFKQCOBV-UHFFFAOYSA-N 0.000 claims description 2
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 claims description 2
- YABFPHSQTSFWQB-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-(1,2,4-triazol-1-yl)-3-(trimethylsilyl)propan-2-ol Chemical compound C=1C=C(F)C=CC=1C(O)(C[Si](C)(C)C)CN1C=NC=N1 YABFPHSQTSFWQB-UHFFFAOYSA-N 0.000 claims description 2
- 229940061334 2-phenylphenol Drugs 0.000 claims description 2
- SOUGWDPPRBKJEX-UHFFFAOYSA-N 3,5-dichloro-N-(1-chloro-3-methyl-2-oxopentan-3-yl)-4-methylbenzamide Chemical compound ClCC(=O)C(C)(CC)NC(=O)C1=CC(Cl)=C(C)C(Cl)=C1 SOUGWDPPRBKJEX-UHFFFAOYSA-N 0.000 claims description 2
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 claims description 2
- HNNQYHFROJDYHQ-UHFFFAOYSA-N 3-(4-ethylcyclohexyl)propanoic acid 3-(3-ethylcyclopentyl)propanoic acid Chemical compound CCC1CCC(CCC(O)=O)C1.CCC1CCC(CCC(O)=O)CC1 HNNQYHFROJDYHQ-UHFFFAOYSA-N 0.000 claims description 2
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 claims description 2
- NEKULYKCZPJMMJ-UHFFFAOYSA-N 5-chloro-N-{1-[4-(difluoromethoxy)phenyl]propyl}-6-methylpyrimidin-4-amine Chemical compound C=1C=C(OC(F)F)C=CC=1C(CC)NC1=NC=NC(C)=C1Cl NEKULYKCZPJMMJ-UHFFFAOYSA-N 0.000 claims description 2
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 claims description 2
- 239000005964 Acibenzolar-S-methyl Substances 0.000 claims description 2
- 241000501812 Ampelomyces Species 0.000 claims description 2
- 240000007087 Apium graveolens Species 0.000 claims description 2
- 235000015849 Apium graveolens Dulce Group Nutrition 0.000 claims description 2
- 235000010591 Appio Nutrition 0.000 claims description 2
- 244000063299 Bacillus subtilis Species 0.000 claims description 2
- 235000014469 Bacillus subtilis Nutrition 0.000 claims description 2
- 239000005734 Benalaxyl Substances 0.000 claims description 2
- 241000167854 Bourreria succulenta Species 0.000 claims description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- 240000004160 Capsicum annuum Species 0.000 claims description 2
- 235000008534 Capsicum annuum var annuum Nutrition 0.000 claims description 2
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims description 2
- 235000005979 Citrus limon Nutrition 0.000 claims description 2
- 244000248349 Citrus limon Species 0.000 claims description 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 claims description 2
- 239000005750 Copper hydroxide Substances 0.000 claims description 2
- 239000005752 Copper oxychloride Substances 0.000 claims description 2
- 239000005757 Cyproconazole Substances 0.000 claims description 2
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 claims description 2
- 239000005762 Dimoxystrobin Substances 0.000 claims description 2
- 239000005766 Dodine Substances 0.000 claims description 2
- 239000005772 Famoxadone Substances 0.000 claims description 2
- 239000005774 Fenamidone Substances 0.000 claims description 2
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- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 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
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000004554 water soluble tablet Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0111685 | 2001-09-10 | ||
| FR0111685A FR2829362B1 (fr) | 2001-09-10 | 2001-09-10 | Composition fongicide a base de derives d'arylamidine et de composes fongicides connus |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2262854T3 true ES2262854T3 (es) | 2006-12-01 |
Family
ID=8867131
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES02777410T Expired - Lifetime ES2262854T3 (es) | 2001-09-10 | 2002-09-09 | Mezcla fungicida que continen derivados de arilamidina. |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US20040241098A1 (show.php) |
| EP (1) | EP1424893B1 (show.php) |
| JP (1) | JP2005502713A (show.php) |
| KR (1) | KR20040031072A (show.php) |
| CN (1) | CN1553770A (show.php) |
| AR (1) | AR037144A1 (show.php) |
| AT (1) | ATE323410T1 (show.php) |
| AU (1) | AU2002339023B2 (show.php) |
| BR (1) | BR0212689A (show.php) |
| CA (1) | CA2459098A1 (show.php) |
| CO (1) | CO5570633A2 (show.php) |
| DE (1) | DE60210785T2 (show.php) |
| DK (1) | DK1424893T3 (show.php) |
| ES (1) | ES2262854T3 (show.php) |
| FR (1) | FR2829362B1 (show.php) |
| GT (1) | GT200200179A (show.php) |
| HU (1) | HUP0401717A3 (show.php) |
| IL (1) | IL160756A0 (show.php) |
| IN (1) | IN2004DE00550A (show.php) |
| MX (1) | MX255195B (show.php) |
| PA (1) | PA8554501A1 (show.php) |
| PL (1) | PL368740A1 (show.php) |
| PT (1) | PT1424893E (show.php) |
| RU (1) | RU2304388C2 (show.php) |
| WO (1) | WO2003024219A1 (show.php) |
| ZA (1) | ZA200401920B (show.php) |
Families Citing this family (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2005211189A1 (en) * | 2004-02-05 | 2005-08-18 | Dsm Ip Assets B.V. | Polyene antibiotic for controlling fungal growth in banana crops |
| EP1570738A1 (en) * | 2004-02-12 | 2005-09-07 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the spores germination or mycelium growth by acting on different metabolic routes |
| EP1570736A1 (en) * | 2004-03-05 | 2005-09-07 | Bayer CropScience S.A. | Fungicide composition comprising an arylamidine derivative and known fungicide compounds |
| ES2288739T3 (es) * | 2004-03-22 | 2008-01-16 | Basf Aktiengesellschaft | Mezclas fungicidas. |
| JP5261181B2 (ja) * | 2005-09-13 | 2013-08-14 | バイエル・クロップサイエンス・アーゲー | 殺虫剤フェニルオキシ置換フェニルアミジン誘導体 |
| BRPI0615987A2 (pt) * | 2005-09-13 | 2012-04-10 | Bayer Cropscience Ag | composição fungicida e método de controle curativo ou preventivo dos fungos fitopatogênicos de plantas ou safras |
| BRPI0615849B1 (pt) * | 2005-09-13 | 2015-12-01 | Basf Se | método de proteção de uma planta contra um fitopatógeno, uso de um composto, e, composição para tratar semente de uma planta para protegê-la contra um fitopatógeno |
| RU2417590C3 (ru) * | 2006-02-09 | 2022-01-27 | Синджента Партисипейшнс Аг | Фунгицидная композиция |
| ES2376130T3 (es) * | 2006-10-06 | 2012-03-09 | Toyama Chemical Co., Ltd. | Composición farmacéutica que contiene un derivado de fenilamidina y método de utilización de la composición farmacéutica en combinación con un agente antifúngico. |
| WO2008110279A1 (de) * | 2007-03-12 | 2008-09-18 | Bayer Cropscience Ag | Dihalogenphenoxyphenylamidine und deren verwendung als fungizide |
| EP1969933A1 (de) * | 2007-03-12 | 2008-09-17 | Bayer CropScience AG | Dihalogenphenoxyphenylamidine und deren Verwendung als Fungizide |
| EP1969934A1 (de) * | 2007-03-12 | 2008-09-17 | Bayer CropScience AG | 4-Cycloalkyl-oder 4-arylsubstituierte Phenoxyphenylamidine und deren Verwendung als Fungizide |
| EP1969935A1 (de) * | 2007-03-12 | 2008-09-17 | Bayer CropScience AG | 3,4-Disubstituierte Phenoxyphenylamidine und deren Verwendung als Fungizide |
| JP2010520900A (ja) * | 2007-03-12 | 2010-06-17 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | フェノキシ置換されたフェニルアミジン誘導体及び殺真菌剤としてのその使用 |
| EP1969932A1 (de) * | 2007-03-12 | 2008-09-17 | Bayer CropScience AG | Phenoxyphenylamidine und deren Verwendung als Fungizide |
| EP1969929A1 (de) | 2007-03-12 | 2008-09-17 | Bayer CropScience AG | Substituierte Phenylamidine und deren Verwendung als Fungizide |
| EP1969931A1 (de) | 2007-03-12 | 2008-09-17 | Bayer CropScience Aktiengesellschaft | Fluoalkylphenylamidine und deren Verwendung als Fungizide |
| EP1969930A1 (de) * | 2007-03-12 | 2008-09-17 | Bayer CropScience AG | Phenoxyphenylamidine und deren Verwendung als Fungizide |
| BRPI0808798A2 (pt) | 2007-03-12 | 2014-10-07 | Bayer Cropscience Ag | Fenoxifenilamidinas 3,5-dissubstituídas e seu uso como fungicidas |
| US8168567B2 (en) | 2007-04-19 | 2012-05-01 | Bayer Cropscience Ag | Thiadiazolyl oxyphenyl amidines and the use thereof as a fungicide |
| EP2072506A1 (de) | 2007-12-21 | 2009-06-24 | Bayer CropScience AG | Thiazolyloxyphenylamidine oder Thiadiazolyloxyphenylamidine und deren Verwendung als Fungizide |
| JP5502354B2 (ja) | 2008-03-28 | 2014-05-28 | 石原産業株式会社 | 農園芸用殺菌剤組成物及び植物病害の防除方法 |
| WO2009156074A2 (de) | 2008-06-27 | 2009-12-30 | Bayer Cropscience Ag | Thiadiazolyloxyphenylamidine und deren verwendung als fungizide |
| BRPI0914536A8 (pt) | 2008-06-27 | 2017-05-16 | Bayer Cropscience Ag | Tiadiazoliloxifenilamidinas, processo para sua preparação e seus usos, composição e processo para combater microorganismos indesejáveis, e semente resistente a microorganismos indesejáveis |
| RU2371920C1 (ru) * | 2008-07-15 | 2009-11-10 | Николай Николаевич Леонов | Способ защиты персика от курчавости листьев |
| EP2223917A1 (de) | 2009-02-02 | 2010-09-01 | Bayer CropScience AG | Isothiazolyloxyphenylamidine und deren Verwendung als Fungizide |
| KR101992087B1 (ko) * | 2009-05-06 | 2019-06-21 | 바이엘 크롭사이언스 엘피 | 본질적으로 병원체 압력의 비-존재 하에서 농업 식물의 활기 및/또는 작물 수확량을 증가시키는 방법 |
| EP2264011A1 (de) | 2009-06-03 | 2010-12-22 | Bayer CropScience AG | Heteroarylamidine und deren Verwendung als Fungizide |
| EP2264012A1 (de) | 2009-06-03 | 2010-12-22 | Bayer CropScience AG | Heteroarylamidine und deren Verwendung als Fungizide |
| WO2011006604A1 (de) | 2009-07-17 | 2011-01-20 | Bayer Cropscience Ag | Substituierte aminothiazole und deren verwendung als fungizide |
| RU2409951C1 (ru) * | 2009-11-27 | 2011-01-27 | Мосин Владимир Александрович | Средство для защиты растений |
| WO2011080044A2 (en) | 2009-12-16 | 2011-07-07 | Bayer Cropscience Ag | Active compound combinations |
| WO2011082941A1 (de) | 2009-12-16 | 2011-07-14 | Bayer Cropscience Ag | Benzylsubstituierte thiadiazolyloxyphenylamidiniumsalze als fungizide |
| WO2012019998A1 (de) | 2010-08-10 | 2012-02-16 | Bayer Cropscience Ag | Herstellung von n'-(4-{[3-(4-chlorbenzyl)-1,2,4-thiadiazol-5-yl]oxy}-2,5-dimethylphenyl)-n-ethyl-n-methylimidoformamid |
| US20130045968A1 (en) * | 2011-08-15 | 2013-02-21 | Norman Helie | Plant treatment |
| EP2606726A1 (de) * | 2011-12-21 | 2013-06-26 | Bayer CropScience AG | N-Arylamidine-substituierte trifluoroethylsulfid-Derivate als Akarizide und Insektizide |
| ITMI20120405A1 (it) | 2012-03-15 | 2013-09-16 | Chemtura Corp | "composizioni sinergiche ad attivita' fungicida e relativo uso" |
| US10568327B1 (en) * | 2012-04-12 | 2020-02-25 | Syngenta Participations Ag | Method of controlling phytopathogenic diseases on turfgrass |
| US10524474B1 (en) * | 2012-04-12 | 2020-01-07 | Syngenta Participations Ag | Method of controlling phytopathogenic diseases on turfgrass |
| US10517298B1 (en) * | 2012-04-13 | 2019-12-31 | Syngenta Participations Ag | Method of controlling phytopathogenic diseases on turfgrass |
| CN102763648A (zh) * | 2012-06-30 | 2012-11-07 | 广东中迅农科股份有限公司 | 肟菌酯水分散粒剂及其制备方法 |
| CA2883801A1 (en) | 2012-09-07 | 2014-03-13 | Bayer Cropscience Ag | Active compound combinations |
| BR112015004938B1 (pt) | 2012-09-07 | 2020-07-28 | Bayer Cropscience Ag | combinações fungicidas sinérgicas compreendendo um composto amidina e um inibidor da biossíntese do ergosterol, suas utilizações e métodos para o controle de fungos fitopatogênicos |
| CN103688950A (zh) * | 2013-12-10 | 2014-04-02 | 济南凯因生物科技有限公司 | 防治番茄晚疫病的组合物 |
| WO2015121231A1 (en) * | 2014-02-13 | 2015-08-20 | Bayer Cropscience Ag | Active compound combinations comprising phenylamidine compounds and further fungicides |
| EP2865267A1 (en) | 2014-02-13 | 2015-04-29 | Bayer CropScience AG | Active compound combinations comprising phenylamidine compounds and biological control agents |
| EP2865265A1 (en) | 2014-02-13 | 2015-04-29 | Bayer CropScience AG | Active compound combinations comprising phenylamidine compounds and biological control agents |
| MX387554B (es) | 2014-12-29 | 2025-03-18 | Fmc Corp | Composiciones microbianas y metodos de uso para favorecer el crecimiento de las plantas y tratar las enfermedades de las plantas. |
| EP3011832A1 (en) | 2015-06-15 | 2016-04-27 | Bayer CropScience AG | Fungicidal combination comprising phenoxyphenylamidines and further fungicide |
| EP3307706B1 (en) | 2015-06-15 | 2019-07-24 | Bayer CropScience AG | Halogen-substituted phenoxyphenylamidines and the use thereof as fungicides |
| DK3307707T3 (da) | 2015-06-15 | 2020-12-21 | Syngenta Crop Protection Ag | Halogensubstituerede phenoxyphenylamidiner og anvendelsen deraf som fungicider |
| CA2991436A1 (en) | 2015-07-08 | 2017-01-12 | Bayer Cropscience Aktiengesellschaft | Phenoxyhalogenphenylamidines and the use thereof as fungicides |
| CN105145640B (zh) * | 2015-10-26 | 2018-01-19 | 广西南宁益土生物科技有限责任公司 | 一种含哈茨木霉菌的杀菌组合物 |
| JP2019532107A (ja) | 2016-10-14 | 2019-11-07 | ピーアイ インダストリーズ リミテッドＰｉ Ｉｎｄｕｓｔｒｉｅｓ Ｌｔｄ | 望ましくない植物病原性微生物と戦うことで作物を保護するための４−アミノ置換フェニルアミジン誘導体およびその使用 |
| US11155517B2 (en) | 2016-10-14 | 2021-10-26 | Pi Industries Ltd. | 4-substituted phenylamine derivatives and their use to protect crops by fighting undesired phytopathogenic micoorganisms |
| CN110213965A (zh) | 2016-12-14 | 2019-09-06 | 拜耳作物科学股份公司 | 苯氧基苯基脒及其作为杀真菌剂的用途 |
| WO2018109002A1 (en) | 2016-12-14 | 2018-06-21 | Bayer Cropscience Aktiengesellschaft | Active compound combinations |
| EP3335559A1 (en) | 2016-12-14 | 2018-06-20 | Bayer CropScience Aktiengesellschaft | Active compound combinations |
| BR112019012272A2 (pt) | 2016-12-14 | 2019-12-03 | Bayer Ag | fenilamidinas e seu uso como fungicidas |
| CN110740644B (zh) * | 2017-06-14 | 2021-09-28 | 先正达参股股份有限公司 | 杀真菌组合物 |
| UY38540A (es) | 2019-01-14 | 2020-08-31 | Pi Industries Ltd | Compuestos de fenilamidina 3-sustituida, preparación y uso |
| RU2718046C1 (ru) * | 2019-06-04 | 2020-03-30 | Евгений Михайлович Родимин | Способ индуцированного мутагенеза при селекции винограда на устойчивость к грибным заболеваниям |
| AR120427A1 (es) | 2019-11-12 | 2022-02-16 | Pi Industries Ltd | Composición agroquímica que comprende compuestos de fenilamidina 4-sustituidos |
| EP3708565A1 (en) | 2020-03-04 | 2020-09-16 | Bayer AG | Pyrimidinyloxyphenylamidines and the use thereof as fungicides |
| CN116801720A (zh) | 2020-11-30 | 2023-09-22 | 皮埃企业有限公司 | 包含3-取代苯甲脒的化合物的新颖农业化学组成物及其用途 |
| EP3915971A1 (en) | 2020-12-16 | 2021-12-01 | Bayer Aktiengesellschaft | Phenyl-s(o)n-phenylamidines and the use thereof as fungicides |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0683980B1 (de) * | 1990-11-02 | 1999-03-24 | Novartis AG | Fungizide Mittel |
| US5330984A (en) * | 1990-11-02 | 1994-07-19 | Ciba-Geigy Corporation | Fungicidal compositions |
| GB9902592D0 (en) * | 1999-02-06 | 1999-03-24 | Hoechst Schering Agrevo Gmbh | Fungicides |
-
2001
- 2001-09-10 FR FR0111685A patent/FR2829362B1/fr not_active Expired - Fee Related
-
2002
- 2002-09-05 GT GT200200179A patent/GT200200179A/es unknown
- 2002-09-09 PT PT02777410T patent/PT1424893E/pt unknown
- 2002-09-09 PL PL02368740A patent/PL368740A1/xx not_active Application Discontinuation
- 2002-09-09 EP EP02777410A patent/EP1424893B1/fr not_active Expired - Lifetime
- 2002-09-09 CN CNA028175719A patent/CN1553770A/zh active Pending
- 2002-09-09 MX MXPA04002170 patent/MX255195B/es active IP Right Grant
- 2002-09-09 IL IL16075602A patent/IL160756A0/xx unknown
- 2002-09-09 US US10/489,151 patent/US20040241098A1/en not_active Abandoned
- 2002-09-09 RU RU2004110931/04A patent/RU2304388C2/ru not_active IP Right Cessation
- 2002-09-09 HU HU0401717A patent/HUP0401717A3/hu unknown
- 2002-09-09 AT AT02777410T patent/ATE323410T1/de not_active IP Right Cessation
- 2002-09-09 BR BR0212689-3A patent/BR0212689A/pt not_active IP Right Cessation
- 2002-09-09 AR ARP020103406A patent/AR037144A1/es unknown
- 2002-09-09 KR KR10-2004-7003546A patent/KR20040031072A/ko not_active Ceased
- 2002-09-09 ES ES02777410T patent/ES2262854T3/es not_active Expired - Lifetime
- 2002-09-09 DE DE60210785T patent/DE60210785T2/de not_active Expired - Fee Related
- 2002-09-09 AU AU2002339023A patent/AU2002339023B2/en not_active Ceased
- 2002-09-09 DK DK02777410T patent/DK1424893T3/da active
- 2002-09-09 WO PCT/FR2002/003049 patent/WO2003024219A1/fr not_active Ceased
- 2002-09-09 JP JP2003528123A patent/JP2005502713A/ja active Pending
- 2002-09-09 CA CA002459098A patent/CA2459098A1/en not_active Abandoned
- 2002-09-09 PA PA20028554501A patent/PA8554501A1/es unknown
-
2004
- 2004-03-05 IN IN550DE2004 patent/IN2004DE00550A/en unknown
- 2004-03-09 ZA ZA200401920A patent/ZA200401920B/en unknown
- 2004-04-07 CO CO04032970A patent/CO5570633A2/es not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| IN2004DE00550A (show.php) | 2007-03-16 |
| DK1424893T3 (da) | 2006-08-14 |
| MX255195B (es) | 2008-03-10 |
| DE60210785D1 (de) | 2006-05-24 |
| FR2829362B1 (fr) | 2003-11-07 |
| ZA200401920B (en) | 2005-04-25 |
| RU2004110931A (ru) | 2005-08-20 |
| DE60210785T2 (de) | 2007-01-18 |
| AU2002339023B2 (en) | 2007-05-24 |
| GT200200179A (es) | 2003-10-09 |
| PT1424893E (pt) | 2006-08-31 |
| EP1424893A1 (fr) | 2004-06-09 |
| WO2003024219A1 (fr) | 2003-03-27 |
| IL160756A0 (en) | 2004-08-31 |
| JP2005502713A (ja) | 2005-01-27 |
| US20040241098A1 (en) | 2004-12-02 |
| HUP0401717A2 (hu) | 2004-12-28 |
| PL368740A1 (en) | 2005-04-04 |
| RU2304388C2 (ru) | 2007-08-20 |
| CO5570633A2 (es) | 2005-10-31 |
| KR20040031072A (ko) | 2004-04-09 |
| CN1553770A (zh) | 2004-12-08 |
| HUP0401717A3 (en) | 2005-10-28 |
| ATE323410T1 (de) | 2006-05-15 |
| MXPA04002170A (es) | 2004-07-23 |
| FR2829362A1 (fr) | 2003-03-14 |
| CA2459098A1 (en) | 2003-03-27 |
| BR0212689A (pt) | 2004-10-19 |
| AR037144A1 (es) | 2004-10-27 |
| EP1424893B1 (fr) | 2006-04-19 |
| PA8554501A1 (es) | 2003-05-14 |
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