AR059891A1 - Metodo para inducir la tolerancia de plantas contra bacteriosis - Google Patents
Metodo para inducir la tolerancia de plantas contra bacteriosisInfo
- Publication number
- AR059891A1 AR059891A1 ARP070101020A ARP070101020A AR059891A1 AR 059891 A1 AR059891 A1 AR 059891A1 AR P070101020 A ARP070101020 A AR P070101020A AR P070101020 A ARP070101020 A AR P070101020A AR 059891 A1 AR059891 A1 AR 059891A1
- Authority
- AR
- Argentina
- Prior art keywords
- membered
- radicals
- alkyl
- alkylamino
- alkylaminocarbonyl
- Prior art date
Links
- -1 cyano, nitro, amino, aminocarbonyl Chemical group 0.000 abstract 11
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 5
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 5
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical group 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 4
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 abstract 4
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 2
- 125000003320 C2-C6 alkenyloxy group Chemical group 0.000 abstract 2
- 239000004215 Carbon black (E152) Substances 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 abstract 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 abstract 2
- XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 abstract 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- FSKNXCHJIFBRBT-UHFFFAOYSA-N 2-[2-[2-(dodecylamino)ethylamino]ethylamino]acetic acid Chemical compound CCCCCCCCCCCCNCCNCCNCC(O)=O FSKNXCHJIFBRBT-UHFFFAOYSA-N 0.000 abstract 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 abstract 1
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- 239000005752 Copper oxychloride Substances 0.000 abstract 1
- 239000005756 Cymoxanil Substances 0.000 abstract 1
- MDNWOSOZYLHTCG-UHFFFAOYSA-N Dichlorophen Chemical compound OC1=CC=C(Cl)C=C1CC1=CC(Cl)=CC=C1O MDNWOSOZYLHTCG-UHFFFAOYSA-N 0.000 abstract 1
- IIUZTXTZRGLYTI-UHFFFAOYSA-N Dihydrogriseofulvin Natural products COC1CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 IIUZTXTZRGLYTI-UHFFFAOYSA-N 0.000 abstract 1
- 239000005772 Famoxadone Substances 0.000 abstract 1
- IWDQPCIQCXRBQP-UHFFFAOYSA-M Fenaminosulf Chemical compound [Na+].CN(C)C1=CC=C(N=NS([O-])(=O)=O)C=C1 IWDQPCIQCXRBQP-UHFFFAOYSA-M 0.000 abstract 1
- UXWOXTQWVMFRSE-UHFFFAOYSA-N Griseoviridin Natural products O=C1OC(C)CC=C(C(NCC=CC=CC(O)CC(O)C2)=O)SCC1NC(=O)C1=COC2=N1 UXWOXTQWVMFRSE-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- DDUHZTYCFQRHIY-UHFFFAOYSA-N Negwer: 6874 Natural products COC1=CC(=O)CC(C)C11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-UHFFFAOYSA-N 0.000 abstract 1
- KYGZCKSPAKDVKC-UHFFFAOYSA-N Oxolinic acid Chemical compound C1=C2N(CC)C=C(C(O)=O)C(=O)C2=CC2=C1OCO2 KYGZCKSPAKDVKC-UHFFFAOYSA-N 0.000 abstract 1
- 239000004100 Oxytetracycline Substances 0.000 abstract 1
- 229930182764 Polyoxin Natural products 0.000 abstract 1
- YTLSJDFAYCIPMN-UHFFFAOYSA-N S(=O)(=O)(O)O.OC1=C2C=CC=NC2=CC=C1 Chemical compound S(=O)(=O)(O)O.OC1=C2C=CC=NC2=CC=C1 YTLSJDFAYCIPMN-UHFFFAOYSA-N 0.000 abstract 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract 1
- 229930182692 Strobilurin Natural products 0.000 abstract 1
- 125000005090 alkenylcarbonyl group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000005087 alkynylcarbonyl group Chemical group 0.000 abstract 1
- 239000003242 anti bacterial agent Substances 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- 229940088710 antibiotic agent Drugs 0.000 abstract 1
- 239000003899 bactericide agent Substances 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 229960003168 bronopol Drugs 0.000 abstract 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 abstract 1
- 229940013361 cresol Drugs 0.000 abstract 1
- 229930003836 cresol Natural products 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 229960003887 dichlorophen Drugs 0.000 abstract 1
- ZHDBTKPXEJDTTQ-UHFFFAOYSA-N dipyrithione Chemical compound [O-][N+]1=CC=CC=C1SSC1=CC=CC=[N+]1[O-] ZHDBTKPXEJDTTQ-UHFFFAOYSA-N 0.000 abstract 1
- 229940044165 dodicin Drugs 0.000 abstract 1
- 229960002867 griseofulvin Drugs 0.000 abstract 1
- DDUHZTYCFQRHIY-RBHXEPJQSA-N griseofulvin Chemical compound COC1=CC(=O)C[C@@H](C)[C@@]11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-RBHXEPJQSA-N 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000005844 heterocyclyloxy group Chemical group 0.000 abstract 1
- 230000001939 inductive effect Effects 0.000 abstract 1
- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 abstract 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 229960003255 natamycin Drugs 0.000 abstract 1
- 239000004311 natamycin Substances 0.000 abstract 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 abstract 1
- 235000010298 natamycin Nutrition 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229960000321 oxolinic acid Drugs 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 229960000625 oxytetracycline Drugs 0.000 abstract 1
- IWVCMVBTMGNXQD-PXOLEDIWSA-N oxytetracycline Chemical compound C1=CC=C2[C@](O)(C)[C@H]3[C@H](O)[C@H]4[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-PXOLEDIWSA-N 0.000 abstract 1
- 235000019366 oxytetracycline Nutrition 0.000 abstract 1
- KDNVJBRRDKAHDA-UHFFFAOYSA-L phenyl-[3-[[3-(phenylmercuriooxysulfonyl)naphthalen-2-yl]methyl]naphthalen-2-yl]sulfonyloxymercury Chemical compound C=1C2=CC=CC=C2C=C(CC=2C(=CC3=CC=CC=C3C=2)S(=O)(=O)O[Hg]C=2C=CC=CC=2)C=1S(=O)(=O)O[Hg]C1=CC=CC=C1 KDNVJBRRDKAHDA-UHFFFAOYSA-L 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 abstract 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 abstract 1
- 229960003811 pyrithione disulfide Drugs 0.000 abstract 1
- 229910052709 silver Inorganic materials 0.000 abstract 1
- 239000004332 silver Substances 0.000 abstract 1
- 239000002689 soil Substances 0.000 abstract 1
- 229960005322 streptomycin Drugs 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- ROZUQUDEWZIBHV-UHFFFAOYSA-N tecloftalam Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C(=O)NC1=CC=CC(Cl)=C1Cl ROZUQUDEWZIBHV-UHFFFAOYSA-N 0.000 abstract 1
- IWVCMVBTMGNXQD-UHFFFAOYSA-N terramycin dehydrate Natural products C1=CC=C2C(O)(C)C3C(O)C4C(N(C)C)C(O)=C(C(N)=O)C(=O)C4(O)C(O)=C3C(=O)C2=C1O IWVCMVBTMGNXQD-UHFFFAOYSA-N 0.000 abstract 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 abstract 1
- RTKIYNMVFMVABJ-UHFFFAOYSA-L thimerosal Chemical compound [Na+].CC[Hg]SC1=CC=CC=C1C([O-])=O RTKIYNMVFMVABJ-UHFFFAOYSA-L 0.000 abstract 1
- 229960004906 thiomersal Drugs 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
- 150000003751 zinc Chemical class 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
- A01N37/44—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 nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—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 nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- 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
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- A01N47/14—Di-thio analogues thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Immunology (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Abstract
Un método de inducir la tolerancia de plantas contra basteriosis, caracterizada porque comprende tratar las plantas, el suelo o las semillas con una cantidad efectiva de una combinacion de 1) un compuesto de estrobilurina de la formula 1 en la que X es halogeno, alquilo C1-4 o trifluorometilo; m es 0 o 1; Q es C(=CH-CH3)-COOCH3, C(=CH-OCH3)-COOCH3, C(=N-OCH3)-CONHCH3, C(=N-OCH3)-COOCH3, N(-OCH3)-COOCH3, o un grupo Q1 de formula (2) en donde representa el enlace con el anillo fenilo; A es -O- B, -CH2O-B, -OCH2-B, -CH=CH-B, C:::C-B, -CH2O-N=C(R1)-B, -CH2O-N=C(R1)-CH=CH-B, o -CH2O-N=C(R1)-C(R2)=N-OR3, donde B es fenilo, naftilo, hetarilo de cinco o seis miembros heterociclilo de cinco o seis miembros, que contiene uno a tres átomos de N y/o un átomo de O o de S o uno o dos átomos de O y/o de S, estando los sistemas de anillo sin sustituir o sustituidos por uno a tres radicales Ra; Ra es ciano, nitro, amino, aminocarbonilo, aminotiocarbonilo, halogeno, alquilo C1-6, haloalquilo C1- 6, alquilcarbonilo C1-6, alquilsulfonilo C1-6, alquilsulfinilo C1-6, cicloalquilo C3-6, alcoxi C1-6, haloalcoxi C1-6, alquiloxicarbonilo C1-6, alquiltio C1-6, alquilamino C1-6, di-C1-6alquilamino, alquilaminocarbonilo C1-6, di-C1-6- alquilaminocarbonilo, alquilaminotiocarbonilo C1-6, di-C1-6-alquilaminotiocarbonilo, alquenilo C2-6, aIqueniloxi C2-6, fenilo, fenoxi, bencilo, benciloxi, heterociclilo de cinco o seis miembros, hetarilo de cinco o seis miembros, hetariloxi de cinco o seis miembros, C(=NORa)-Rb o OC(Ra)2-C(Rb)=NORb, estando los radicales cíclicos a su vez no sustituidos o sustituidos por uno a tres radicales Rb, Rb es ciano, nitro, halogeno, amino, aminocarbonilo, aminotiocarbonilo, alquilo C1-6, haloalquilo C1- 6, alquilsulfonilo C1-6, alquilsulfinilo C1-6, cicloalquilo C3-6, alcoxi C1-6, haloalcoxi C1-6, alcoxicarbonilo C1-6, alquiltio C1-6, alquilamino C1-6, di-C1-6-alquilamino, alquilaminocarbonilo C1-6, di-C1-6-alquilaminocarbonilo, alquilaminotiocarbonilo C1-6, di-C1-6-alquil-aminotiocarbonilo, alquenilo C2-6, alqueniloxi C2-6, cicloalquilo C3-6, cicloalquenilo C3-6, fenilo, fenoxi, feniltio, bencilo, benciloxi, heterociclilo de cinco o seis miembros, hetarilo de cinco o seis miembros, hetariloxi de cinco o seis miembros o C(=NORA)-RB; RA, RB significan hidrogeno o alquilo C1-6; R1 es hidrogeno, ciano, alquilo C1-4, haloalquilo C1-4, cicloalquilo C3-6, alcoxi C1-4; R2 es fenilo, fenilcarbonilo, fenilsulfonilo, hetarilo de cinco o seis miembros, hetarilcarbonilo de cinco o seis miembros o hetarilsulfonilo de cinco o seis miembros, estando los sistemas de anillo sin sustituir o sustituidos por uno a tres radicales Ra, alquilo C1-10, cicloalquilo C3-6, aIquenilo C2- 10, alquinilo C2-10, alquilcarbonilo C1-10, alquenilcarbonilo C2-10, alquinilcarbonilo C3-10, alquilsulfonilo C1-10, o C(=NORa)-Rb, estando los radicales hidrocarburo de estos grupos sin sustituir o sustituidos por uno a tres radicales Rc: Rc es ciano, nitro, amino, aminocarbonilo, aminotiocarbonilo, halogeno, alquilo C1-6, haloalquilo C1-6, alquilsulfonilo C1-6, alquilsulfinilo C1-6, alcoxi C1-6, haloalcoxi C1-6, alcoxicarbonilo C1-6, alquiltio C1-6, alquilamino C1-6, di-C1-6-alquilamino, alquilaminocarbonilo C1-6, di-C1-6-alquilaminocarbonilo, alquilaminotiocarbonilo C1-6, di-C1-6-alquilaminotiocarbonilo, alquenilo C2-6, aIqueniloxi C2-6, cicloalquilo C3-6, cicloalquiloxi C3-6, heterociclilo de cinco o seis miembros, heterocicliloxi de cinco o seis miembros, bencilo, benciloxi, fenilo, fenoxi, feniltio, hetarilo de cinco o seis miembros, hetariloxi de cinco o seis miembros y hetariltio, siendo posible que los grupos cíclicos a su vez, sean parcial o completamente halogenado o que lleven enlazados uno a tres radicales Ra; y R3 es hidrogeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, estando los radicales hidrocarburo de estos grupos sin sustituir o sustituidos por uno a tres radicales Rc; y 2) un compuesto seleccionado entre los grupos A) a D): A) antibioticos: cicloheximida, griseofulvina, kasugamicina, natamicina, polioxina y estreptomicina, B) bactericidas: bronopol, cresol, diclorofeno, dipiritiona, dodicina, fenaminosulf, formaldehido, hidrargafeno, sulfato de 5-hidroxiquinolina, nitrapirina, octilinona, oxolinic acid, oxitetraciclina, probenazol, tecloftalam, tiomersal; C) famoxadona y cimoxanilo, y D) sales de cobre, plata y de cinc, como p.ej. Caldo de Burdeos, acetato de cobre, oxicloruro de cobre, sulfato de cobre básico; en cantidades sinergéticamente efectivas, cuyos compuestos activos 1) y 2) son absorbidos por las plantas o semillas.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US78218406P | 2006-03-14 | 2006-03-14 |
Publications (1)
| Publication Number | Publication Date |
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| AR059891A1 true AR059891A1 (es) | 2008-05-07 |
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| Application Number | Title | Priority Date | Filing Date |
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| ARP070101020A AR059891A1 (es) | 2006-03-14 | 2007-03-13 | Metodo para inducir la tolerancia de plantas contra bacteriosis |
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| Country | Link |
|---|---|
| US (1) | US20090143416A1 (es) |
| EP (1) | EP1996019A1 (es) |
| JP (1) | JP2009529568A (es) |
| KR (1) | KR20080106346A (es) |
| CN (1) | CN101400260A (es) |
| AR (1) | AR059891A1 (es) |
| AU (1) | AU2007224503A1 (es) |
| BR (1) | BRPI0708896A2 (es) |
| CA (1) | CA2640518A1 (es) |
| CR (1) | CR10257A (es) |
| EA (1) | EA200801901A1 (es) |
| PE (1) | PE20071284A1 (es) |
| TW (1) | TW200803733A (es) |
| WO (1) | WO2007104677A1 (es) |
| ZA (1) | ZA200808668B (es) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090011935A1 (en) * | 2006-03-14 | 2009-01-08 | Basf Se | Method of Inducing Tolerance of Plants Against Bacterioses |
| NZ570075A (en) | 2006-03-24 | 2010-11-26 | Basf Se | Method for combating phytopathogenic fungi |
| JP2011201852A (ja) * | 2010-03-03 | 2011-10-13 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
| TWI548343B (zh) * | 2010-07-23 | 2016-09-11 | 石原產業股份有限公司 | 軟腐病之防除劑及防除方法 |
| CN102067851B (zh) * | 2011-01-20 | 2014-03-05 | 陕西美邦农药有限公司 | 一种含多抗霉素与甲氧基丙烯酸酯类的杀菌组合物 |
| WO2012117055A1 (en) | 2011-03-03 | 2012-09-07 | Dsm Ip Assets B.V. | New antifungal compositions |
| US9034792B2 (en) | 2011-03-03 | 2015-05-19 | Dsm Ip Assets B.V. | Antifungal compositions |
| CN102204536A (zh) * | 2011-04-15 | 2011-10-05 | 陕西汤普森生物科技有限公司 | 一种含有啶氧菌酯与抗生素类化合物的杀菌组合物 |
| CN102550580A (zh) * | 2011-12-10 | 2012-07-11 | 陕西美邦农药有限公司 | 一种含啶氧菌酯和霜脲氰的杀菌组合物 |
| GB2519982B (en) * | 2013-11-04 | 2016-04-27 | Rotam Agrochem Int Co Ltd | Fungicidal composition and the use thereof |
| EP4014738B1 (en) * | 2013-11-26 | 2024-10-30 | UPL Ltd | A method for controlling rust |
| CN104351208B (zh) * | 2014-11-10 | 2016-08-10 | 江苏丰登作物保护股份有限公司 | 一种含啶氧菌酯和噁唑菌酮的杀菌组合物及其应用 |
| CN107787986A (zh) * | 2016-08-29 | 2018-03-13 | 南京华洲药业有限公司 | 一种含啶氧菌酯和噁唑菌酮的杀菌组合物及其应用 |
| PE20211981A1 (es) | 2017-03-07 | 2021-10-05 | Upl Ltd | Combinaciones fungicidas |
| BR112022025002A2 (pt) * | 2020-06-10 | 2022-12-27 | Basf Se | Compostos, composição agroquímica, uso de composto e método de combate a fungos fitopatogênicos |
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| GB1193954A (en) * | 1966-08-12 | 1970-06-03 | Boots Pure Drug Co Ltd | Control of Micro-Organisms |
| NZ534978A (en) * | 2002-03-11 | 2006-03-31 | Basf Ag | Method for immunizing plants against bacterioses |
| WO2006094127A1 (en) * | 2005-03-02 | 2006-09-08 | Osmose, Inc. | Wood preservative formulations comprising dichlorophen |
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2007
- 2007-03-06 KR KR1020087024923A patent/KR20080106346A/ko not_active Withdrawn
- 2007-03-06 BR BRPI0708896-5A patent/BRPI0708896A2/pt not_active IP Right Cessation
- 2007-03-06 US US12/223,029 patent/US20090143416A1/en not_active Abandoned
- 2007-03-06 WO PCT/EP2007/052101 patent/WO2007104677A1/en not_active Ceased
- 2007-03-06 JP JP2008558779A patent/JP2009529568A/ja not_active Withdrawn
- 2007-03-06 EP EP07726659A patent/EP1996019A1/en not_active Withdrawn
- 2007-03-06 CA CA002640518A patent/CA2640518A1/en not_active Abandoned
- 2007-03-06 CN CNA2007800090928A patent/CN101400260A/zh active Pending
- 2007-03-06 EA EA200801901A patent/EA200801901A1/ru unknown
- 2007-03-06 AU AU2007224503A patent/AU2007224503A1/en not_active Abandoned
- 2007-03-13 TW TW096108573A patent/TW200803733A/zh unknown
- 2007-03-13 AR ARP070101020A patent/AR059891A1/es not_active Application Discontinuation
- 2007-03-13 PE PE2007000269A patent/PE20071284A1/es not_active Application Discontinuation
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2008
- 2008-08-28 CR CR10257A patent/CR10257A/es not_active Application Discontinuation
- 2008-10-10 ZA ZA200808668A patent/ZA200808668B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2640518A1 (en) | 2007-09-20 |
| CN101400260A (zh) | 2009-04-01 |
| BRPI0708896A2 (pt) | 2011-06-14 |
| EP1996019A1 (en) | 2008-12-03 |
| TW200803733A (en) | 2008-01-16 |
| WO2007104677A1 (en) | 2007-09-20 |
| KR20080106346A (ko) | 2008-12-04 |
| AU2007224503A1 (en) | 2007-09-20 |
| ZA200808668B (en) | 2009-12-30 |
| CR10257A (es) | 2008-10-29 |
| US20090143416A1 (en) | 2009-06-04 |
| PE20071284A1 (es) | 2008-03-02 |
| JP2009529568A (ja) | 2009-08-20 |
| EA200801901A1 (ru) | 2009-02-27 |
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