AR130577A1 - Métodos agrícolas - Google Patents
Métodos agrícolasInfo
- Publication number
- AR130577A1 AR130577A1 ARP230102554A ARP230102554A AR130577A1 AR 130577 A1 AR130577 A1 AR 130577A1 AR P230102554 A ARP230102554 A AR P230102554A AR P230102554 A ARP230102554 A AR P230102554A AR 130577 A1 AR130577 A1 AR 130577A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- compound
- prop
- phenoxy
- methoxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 abstract 6
- 230000003032 phytopathogenic effect Effects 0.000 abstract 4
- 241000233866 Fungi Species 0.000 abstract 3
- -1 (Z)-2-(5-cyclopropyl-2-methyl-phenoxy)-3-methoxy-prop-2-enoate Chemical compound 0.000 abstract 2
- 102100025287 Cytochrome b Human genes 0.000 abstract 2
- 108010075028 Cytochromes b Proteins 0.000 abstract 2
- 206010061217 Infestation Diseases 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 230000002438 mitochondrial effect Effects 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 230000035772 mutation Effects 0.000 abstract 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- 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 abstract 1
- MNHVNIJQQRJYDH-UHFFFAOYSA-N 2-[2-(1-chlorocyclopropyl)-3-(2-chlorophenyl)-2-hydroxypropyl]-1,2-dihydro-1,2,4-triazole-3-thione Chemical compound N1=CNC(=S)N1CC(C1(Cl)CC1)(O)CC1=CC=CC=C1Cl MNHVNIJQQRJYDH-UHFFFAOYSA-N 0.000 abstract 1
- JERZEQUMJNCPRJ-UHFFFAOYSA-N 2-[4-(4-chlorophenoxy)-2-(trifluoromethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=C(C(F)(F)F)C=1C(O)(C)CN1C=NC=N1 JERZEQUMJNCPRJ-UHFFFAOYSA-N 0.000 abstract 1
- XCGBHLLWJZOLEM-UHFFFAOYSA-N 3-(difluoromethyl)-N-(7-fluoro-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1-methyl-1H-pyrazole-4-carboxamide Chemical compound CC1CC(C)(C)C(C(=CC=2)F)=C1C=2NC(=O)C1=CN(C)N=C1C(F)F XCGBHLLWJZOLEM-UHFFFAOYSA-N 0.000 abstract 1
- XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 abstract 1
- 239000005964 Acibenzolar-S-methyl Substances 0.000 abstract 1
- 239000005730 Azoxystrobin Substances 0.000 abstract 1
- 239000005737 Benzovindiflupyr Substances 0.000 abstract 1
- 239000005738 Bixafen Substances 0.000 abstract 1
- 239000005740 Boscalid Substances 0.000 abstract 1
- COHXKDBBCILNGN-WJDWOHSUSA-N CC(C=CC(C1CCCCC1)=C1)=C1O/C(\C(O)=O)=C\OC Chemical compound CC(C=CC(C1CCCCC1)=C1)=C1O/C(\C(O)=O)=C\OC COHXKDBBCILNGN-WJDWOHSUSA-N 0.000 abstract 1
- 239000005747 Chlorothalonil Substances 0.000 abstract 1
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 abstract 1
- 239000005750 Copper hydroxide Substances 0.000 abstract 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005751 Copper oxide Substances 0.000 abstract 1
- 239000005752 Copper oxychloride Substances 0.000 abstract 1
- 239000005757 Cyproconazole Substances 0.000 abstract 1
- 239000005760 Difenoconazole Substances 0.000 abstract 1
- 239000005762 Dimoxystrobin Substances 0.000 abstract 1
- 239000005767 Epoxiconazole Substances 0.000 abstract 1
- 239000005777 Fenpropidin Substances 0.000 abstract 1
- 239000005778 Fenpropimorph Substances 0.000 abstract 1
- 239000005780 Fluazinam Substances 0.000 abstract 1
- 239000005788 Fluxapyroxad Substances 0.000 abstract 1
- 239000005799 Isopyrazam Substances 0.000 abstract 1
- 239000005802 Mancozeb Substances 0.000 abstract 1
- IEKSGOPPBDNFFP-UHFFFAOYSA-N N-(2-fluorophenyl)-4-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzamide Chemical compound FC1=C(C=CC=C1)NC(C1=CC=C(C=C1)C1=NOC(=N1)C(F)(F)F)=O IEKSGOPPBDNFFP-UHFFFAOYSA-N 0.000 abstract 1
- CCCGEKHKTPTUHJ-UHFFFAOYSA-N N-[9-(dichloromethylene)-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-3-(difluoromethyl)-1-methylpyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC2=C1C1CCC2C1=C(Cl)Cl CCCGEKHKTPTUHJ-UHFFFAOYSA-N 0.000 abstract 1
- XQJQCBDIXRIYRP-UHFFFAOYSA-N N-{2-[1,1'-bi(cyclopropyl)-2-yl]phenyl}-3-(difluoromethyl)-1-methyl-1pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1C(C2CC2)C1 XQJQCBDIXRIYRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005818 Picoxystrobin Substances 0.000 abstract 1
- 239000005822 Propiconazole Substances 0.000 abstract 1
- 239000005825 Prothioconazole Substances 0.000 abstract 1
- 239000005869 Pyraclostrobin Substances 0.000 abstract 1
- 239000005834 Sedaxane Substances 0.000 abstract 1
- 239000005839 Tebuconazole Substances 0.000 abstract 1
- 239000005857 Trifloxystrobin Substances 0.000 abstract 1
- CGIHPACLZJDCBQ-UHFFFAOYSA-N acibenzolar Chemical compound SC(=O)C1=CC=CC2=C1SN=N2 CGIHPACLZJDCBQ-UHFFFAOYSA-N 0.000 abstract 1
- UELITFHSCLAHKR-UHFFFAOYSA-N acibenzolar-S-methyl Chemical group CSC(=O)C1=CC=CC2=C1SN=N2 UELITFHSCLAHKR-UHFFFAOYSA-N 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 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 abstract 1
- LDLMOOXUCMHBMZ-UHFFFAOYSA-N bixafen Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=C(F)C=C1C1=CC=C(Cl)C(Cl)=C1 LDLMOOXUCMHBMZ-UHFFFAOYSA-N 0.000 abstract 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 abstract 1
- 229940118790 boscalid Drugs 0.000 abstract 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 abstract 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 abstract 1
- 229910001956 copper hydroxide Inorganic materials 0.000 abstract 1
- 229910000431 copper oxide Inorganic materials 0.000 abstract 1
- 229910000365 copper sulfate Inorganic materials 0.000 abstract 1
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 abstract 1
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 abstract 1
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 abstract 1
- ATZHVIVDMUCBEY-HOTGVXAUSA-N florylpicoxamid Chemical compound C(C)(=O)OC=1C(=NC=CC=1OC)C(=O)N[C@H](C(=O)O[C@H](C(C1=CC=C(C=C1)F)C1=CC=C(C=C1)F)C)C ATZHVIVDMUCBEY-HOTGVXAUSA-N 0.000 abstract 1
- UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 abstract 1
- SXSGXWCSHSVPGB-UHFFFAOYSA-N fluxapyroxad Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1=CC(F)=C(F)C(F)=C1 SXSGXWCSHSVPGB-UHFFFAOYSA-N 0.000 abstract 1
- 230000002538 fungal effect Effects 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- CAUHWGTUUBORAX-IKGGRYGDSA-N metarylpicoxamid Chemical compound CCC(=O)Oc1c(OC)ccnc1C(=O)N[C@@H](C)C(=O)O[C@@H](C)[C@@H](C)c1ccccc1C CAUHWGTUUBORAX-IKGGRYGDSA-N 0.000 abstract 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 abstract 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 abstract 1
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 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 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P3/00—Fungicides
-
- 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
- A01N37/36—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Microbiology (AREA)
- Mycology (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
La presente invención se refiere a un método de control o prevención de la infestación por hongos fitopatogénicos en una planta, en el que los hongos fitopatogénicos comprenden una mutación F129L en el citocromo b mitocondrial que confiere resistencia a los inhibidores de Qₒ. Reivindicación 1: Un método para controlar o prevenir la infestación por hongos fitopatogénicos en una planta, en el que los hongos fitopatogénicos comprenden una mutación F129L en el citocromo b mitocondrial que confiere resistencia a los inhibidores de Qₒ, el método comprende aplicar a la planta, a partes de la misma o al sitio de la misma, una composición fungicida que comprende una mezcla de componentes (A) y (B) como ingredientes activos, en la que el componente (A) es un compuesto seleccionado entre: (Z)-2-(5-ciclobutil-2-metil-fenoxi)-3-metoxi-prop-2-enoato de metilo (compuesto X.01), (Z)-2-(5-ciclopentil-2-metil-fenoxi)-3-metoxi-prop-2-enoato de metilo (compuesto X.02), (Z)-2-(5-ciclopropil-2-metil-fenoxi)-3-metoxi-prop-2-enoato de metilo (compuesto X.03), o (Z)-2-(5-ciclohexil-2-metil-fenoxi)-3-metoxi-prop-2-enoato de metilo (compuesto X.04); o una sal agronómicamente aceptable del mismo; y el componente (B) es un compuesto seleccionado del grupo que consiste en: bixafeno, acibenzolar, acibenzolar-S-metilo, sulfato de cobre, hidróxido de cobre, oxicloruro de cobre, óxido de cobre, ciproconazol, difenoconazol, hexaconazol, protioconazol, propiconazol, tebuconazol, epoxiconazol, fenpropidina, fenpropimorf, azoxistrobina, dimoxistrobina, trifloxistrobina, picoxistrobina, piraclostrobina, mancozeb, clorotalonil, fluazinam, fluxapiroxad, isopirazam, sedaxano, boscalid, flufenoxadiazam, benzovindiflupir, pidiflumetofeno, isoflucipram, fluindapir, inpirfluxam, mefentrifluconazol, florilpicoxamid, metarilpicoxamid y metiltetraprol.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB2214202.0A GB202214202D0 (en) | 2022-09-28 | 2022-09-28 | Agricultural methods |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR130577A1 true AR130577A1 (es) | 2024-12-18 |
Family
ID=83978695
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP230102554A AR130577A1 (es) | 2022-09-28 | 2023-09-26 | Métodos agrícolas |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP4593603A1 (es) |
| AR (1) | AR130577A1 (es) |
| AU (1) | AU2023348186A1 (es) |
| GB (1) | GB202214202D0 (es) |
| UY (1) | UY40450A (es) |
| WO (1) | WO2024068837A1 (es) |
Family Cites Families (72)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8805394D0 (en) | 1988-03-07 | 1988-04-07 | Agricultural Genetics Co | Antibiotic |
| IL132533A0 (en) | 1997-05-09 | 2001-03-19 | Agraquest Inc | A novel strain of bacillus for controlling plant diseases and corn rootworm |
| JP3691265B2 (ja) | 1997-11-13 | 2005-09-07 | クミアイ化学工業株式会社 | イネの育苗時病害防除剤 |
| US6245551B1 (en) | 1999-03-30 | 2001-06-12 | Agraquest, Inc. | Strain of Bacillus pumilus for controlling plant diseases caused by fungi |
| US6569425B2 (en) | 2001-06-22 | 2003-05-27 | David Joseph Drahos | Bacillus licheniformis biofungicide |
| JP4071036B2 (ja) | 2001-11-26 | 2008-04-02 | クミアイ化学工業株式会社 | バシルスｓｐ．Ｄ７４７菌株およびそれを用いた植物病害防除剤および害虫防除剤 |
| JP5256020B2 (ja) | 2005-04-08 | 2013-08-07 | バイエル・クロップサイエンス・エヌ・ヴェー | エリートイベントａ２７０４−１２、ならびに生物サンプル中の該イベントを同定するための方法およびキット |
| CA2603949C (en) | 2005-04-11 | 2014-12-09 | Bayer Bioscience N.V. | Elite event a5547-127 and methods and kits for identifying such event in biological samples |
| DE102005016939A1 (de) | 2005-04-12 | 2006-10-19 | Vekörrer, Franz | Verfahren zur Herstellung von Dentalformteilen |
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| CA2976174C (en) | 2006-05-25 | 2019-12-03 | Monsanto Technology Llc | A method to identify disease resistant quantitative trait loci in soybean and compositions thereof |
| US7951995B2 (en) | 2006-06-28 | 2011-05-31 | Pioneer Hi-Bred International, Inc. | Soybean event 3560.4.3.5 and compositions and methods for the identification and detection thereof |
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| AU2023348186A1 (en) | 2025-03-27 |
| EP4593603A1 (en) | 2025-08-06 |
| GB202214202D0 (en) | 2022-11-09 |
| UY40450A (es) | 2024-04-30 |
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