http://rdf.ncbi.nlm.nih.gov/pubchem/patent/AR-094829-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8e0bf0928b608797b70bbc2b91c7e52e |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N2300-00 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N25-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N47-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-88 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-32 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N43-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N37-50 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A01N63-22 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N61-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N63-22 |
| filingDate | 2013-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2015-09-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | AR-094829-A1 |
| titleOfInvention | PESTICIDED BLENDS |
| abstract | Claim 1: Synergistic mixtures, comprising as active components: 1) A fungicidal compound lA selected from the group consisting of A) Breathing inhibitors: inhibitors of complex III at the Qₒ site: azoxystrobin, coumetoxistrobin, coumoxystrobin, dimoxystrobin, enestroburin, fenaminstrobin, phenoxy-strobin / flufenoxystrobin, fluoxastrobin, kresoximmethyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, trifloxystrobin, 2- [2- (2,5-dimethyl-phenoxy) methyl ester -acrylic and 2- (2- (3- (2,6-di-chlorophenyl) -1-methyl-allylidenaminooxymethyl) -phenyl) -2-methoxyimino-N-methyl-acetamide, pyribencarb, triclopyricarb / chlorodincarb, famoxadone, fenamidone ; complex III inhibitors at the Qⁱ site: cyazofamid, amisulbrom, 2-methylpropanoate [(3S, 6S, 7R, 8R) -8-benzyl-3 - [(3-acetoxy-4-methoxy-pyridin-2-carbonyl) amino ] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl], [(3S, 6S, 7R, 8R) -2-benzyl-3 - [[3- ( acetoxymethoxy) -4-methoxy-pyridin-2-carbonyl] amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl], [(3S, 6S, 7R, 8R-2-methylpropanoate] ) -8-benzyl-3 - [(3-isobutoxycarbonyloxy-4-methoxy-pyridin-2-carbonyl) amino] -6-methyl-4,9-dioxo-1,5-dioxonan-7-yl], -2 [(3S, 6S, 7R, 8R) -8-benzyl-3 - [[3- (1,3-benzodioxol-5-ylmethoxy) -4-methoxy-pyridin-2-carbonyl] amino] -6-methylpropanoate -methyl-4,9-dioxo-1,5-dioxonan-7-yl]; (3S, 6S, 7R, 8R) -3 - [[(3-hydroxy-4-methoxy-2-pyridinyl) carbonyl] amino] -6-methyl-4,9-dioxo-8- (phenylmethyl) 2-methylpropanoate ) -1,5-dioxonan-7-yl; complex II inhibitors: benodanil, bixafen, boscalid, carboxin, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, isopyrazam, mepronil, oxycarboxin, penflufen, pentiopyrad, sedaxane, tecloftalam, thifluzomet-i-trifl-thio-imidomethyl-trifluorideamide -3-difluoromethyl-1-methyl-1H-pyrazol-4-carboxamide, N- (2- (1,3,3-trimethyl-butyl) -phenyl) -1,3-dimethyl-5-fluoro-1H-pyrazole -4-carboxamide, benzovindiflupyr, 3- (difluoromethyl) -1-methyl-N- (1,1,3-trimethylindan-4-yl) pyrazol-4-carboxamide, 3- (trifluoromethyl) -1-methyl-N- (1,1,3-trimethylindan-4-iI) pyrazol-4-carboxamide, 1,3-dimethyl-N- (1,1,3-trimethylindan-4-yl) pyrazol-4-carboxamide, 3- (trifluoromethyl ) -1,5-dimethyl-N- (1,1,3-trimethylindan-4-yl) pyrazol-4-carboxamide, 3- (difluoromethyl) -1,5-dimethyl-N- (1,1,3- trimethylindan-4-iI) pyrazol-4-carboxamide, 1,3,5-trimethyl-N- (1,1,3-trimethylindan-4-yl) pyrazol-4-carboxamide; other respiration inhibitors: diflumetorim, (5,8-difluoro-quinazolin-4-iI) - {2- [2-fluoro-4- (4-trifluoromethylpyridin-2-yloxy) -phenyl] -ethyl} -amine; nitrophenyl derivatives: binapacryl, dinobuton, dinocap, fluazinam; ferimzone; organometal compounds: fentin salts, such as fentin-acetate, fentin chloride or fentin hydroxide; ametoctradin; and siltiofam; B) inhibitors sterol biosynthesis inhibitors, demethylase C₁₄: triazoles: azaconazole, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazole, paclobutrazole, penconazole, propiconazole, protioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, uniconazole, 1- [rel- (2S; 3R) -3- (2-(chlorophenyl) 4-difluorophenyl) -oxyranylmethyl] -5-thiocyanate-1H- [1,2,4] triazole, 2- [rel- (2S; 3R) -3- (2-chlorophenyl) -2- (2,4-difluorophenyl ) -oxyranylmethyl] -2H- [1,2,4] triazol-3-thiol; imidazoles: imazalil, pefurazoate, prochloraz, triflumizol; pyrimidines, pyridines and piperazines: fenarimol, nuarimol, pyrifenox, triforine; d14-reductase inhibitors: aldimorph, dodemorph, dodemorphacetate, fenpropimorph, tridemorph, fenpropidin, piperalin, spiroxamine; 3-keto reductase inhibitors: fenhexamid; C) Nucleic acid synthesis inhibitors: acylamino acid or phenylamide fungicides: benalaxyl, benalaxyl-M, kiralaxyl, metalaxyl, ofurace, oxadixyl; others: hymexazole, octhilinone, oxolinic acid, bupirimate, 5-fluorocytosine, 5-fluoro-2- (p-tolylmethoxy) pyrimidin-4-amine, 5-fluoro-2- (4-fluorophenylmethoxy) pyrimidin-4-amine; D) Cell division and cytoskeleton inhibitors: tubulin inhibitors: benomyl, carbendazim, fuberidazole, thiabendazole, thiophanate-methyl, 5-chloro-7- (4-methylpiperidin-1-yl) -6- (2,4,6 -trifluorophenyl) - [1,2,4] triazolo [1,5-a] pyrimidine; other cell division inhibitors: diethofencarb, ethaboxam, pencycuron, fluopicolide, zoxamide, metrafenone, pyriofenone; E) Inhibitors of amino acid and protein synthesis: inhibitors of methionine synthesis: cyprodinil, mepanipyrim, pyrimethanil; protein synthesis inhibitors: blasticidin-S, kasugamycin, kasugamycin hydrochloride-hydrate, mildiomycin, streptomycin, oxytetracyclin, polyoxine, validamycin A; F) Signal transduction inhibitors: MAP / histidine kinase inhibitors: fluoroimid, iprodione, procymidone, vinclozolin, fenpiclonil, fludioxonil; G protein inhibitors: quinoxyfen; G) Inhibitors of lipid and membrane synthesis: phospholipid biosynthesis inhibitors: edifenphos, iprobenfos, pyrazophos, isoprothiolane; lipid peroxidation: dichloran, fifthzene, tecnazene, tolclofosmethyl, biphenyl, chloroneb, etridiazole; phospholipid biosynthesis and cell wall deposition: dimethomorph, flumorph, mandipropamid, pyrimorph, benthiavalicarb, iprovalicarb, valifenalate, (4-fluorophenyl) N- (1- (1- (1- (4-cyano-phenyl)) -ethanesulfonyl acid ester) ) -but-2-yl) carbamic; compounds that affect the permeability of the cell membrane and fatty acids: propamocarb, propamocarb hydrochloride; fatty acid amide hydrolase inhibitors: 1- [4- [4- [5- (2,6-Difluorophenyl) -4,5-dihydro-3-isoxazolyl] -2-thiazolyl] -1-piperidinyl] -2- [5-methyl-3- (trifluoromethyl) -1 H -pyrazol-1-yl] ethanone; H) Inhibitors with action at multiple sites: inorganic active substances: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur; thio- and dithiocarbamates: ferbam, mancozeb, maneb, metam, metiram, propineb, thiram, zineb, ziram; organochlorine compounds: anilazine, chlorothalonil, captafol, captan, folpet, dichlofluanid, dichlorophen, hexachlorobenzene, pentachlorphenole and its salts, phthalide, tolylfluanid, N- (4-chloro-2-nitro-phenyl) -N-ethyl-4-methyl-4-methyl-4-methyl -benzenesulfonamide; guanidines and others: guanidine, dodine, dodine-free base, guazatine, guazatine-acetate, iminoctadine, iminoctadine-triacetate, iminoctadinetris (albesilate), dithianon, 2,6-dimethyl-1H, 5H- [1,4] dithiino [2 , 3-c: 5,6-c] dipyrrol-1,3,5,7 (2H, 6H) -tetraone; I) Inhibitors of cell wall synthesis: inhibitors of glucan synthesis: validamycin, polyoxin B; Melanin synthesis inhibitors: pyroquilon, tricyclazole, carpropamid, dicyclomet, phenoxyanil; J) Plant defense inducers: acibenzolar-S-methyl, probenazole, isothianyl, thiadinyl, prohexadione-calcium, 4-cyclopropyl-N- (2,4-dimethoxyphenyl) thiadiazol-5-carboxamide; phosphonates: fosetyl, fosetyl-aluminum, phosphorous acid and its salts; K) mode unknown action: bronopol, chinomethionat, cyflufenamid, cymoxanil, dazomet, debacarb, diclomezine, difenzoquat, difenzoquat-methylsulfate, difenilamin, fenpyrazamina, flumetover, flusulfamide, flutianil, methasulfocarb, nitrapyrin, nitrothal-isopropyl, oxine-copper, picarbutrazox , proquinazid, tebufloquin, tecloftalam, triazoxide, 2-butoxy-6-iodo-3-propylchromen-4-one, N- (cyclopropylmethoxyimino- (6-difluoro-methoxy-2,3-difluoro-phenyl) -methyl) -2 -phenyl-acetamide, N- (4- (4-chloro-3-trifluoromethyl-phenoxy) -2,5-dimethyl-phenyl) -N-ethyl-N-methyl formamidine, N- (4- (4-fluoro- 3-Trifluoromethyl-phenoxy) -2,5-dimethyl-phenyl) -N-ethyl-N-methyl formamidine, N- (2-methyl-5-trifluoromethyl-4- (3-trimethylsilanyl-propoxy) -phenyl) -N -ethyl-N-methyl formamidine, N- (5-difluoromethyl-2-methyl-4- (3-tri-methylsilanyl-propoxy) -phenyl) -N-ethyl-N-methyl formamidine, 6-tert-butyl-8 2-methoxy-acetic acid, -fluoro-2,3-dimethyl-quinolin-4-yl ester, 3- [5- (4-methylphenyl) -2,3-dimethyl-isoxazolidin-3yl] -pyridine, 3- [5 - (4-chloro-phenyl) -2 , 3-dimethyl-isoxazolidin-3-yl] -pyridine (pyrisoxazole), N- (6-methoxy-pyridin-3-yl) cyclopropancarboxylic acid, 5-chloro-1- (4,6-dimethoxy-pyrimidin-) 2-yl) -2-methyl-1H-benzoimidazole, 2- (4-chloro-phenyl) -N- [4- (3,4-dimethoxy-phenyl) -isoxazol-5-yl] -2-prop-2 -ynyloxy-acetamide, 4,4-difluoro-3,3-dimethyl-1- (3-quinolyl) isoquinoline; L) Antifungal biological control agents: Ampelomyces quisqualis, Aspergillus flavus, Aureobasidium pullulans, Bacillus pumilus, Bacillus pumilus NRRL B-30087, Bacillus subtilis, Bacillus subtilis NRRL B-21661, Bacillus subtilis var. amylolique-faciens FZB24, Candida oleophila I-82, Candida saitoana, chitosan, Clonostachys rosea f. catenulate, Clonostachys rosea f. catenulate J1446, Coniothyrium minitans, Cryphonectria parasitica, Endothia parasitica, Cryptococcus albidus, Fusarium oxysporum, Metschnikowia fructicola, Microdochium dimerum, Phlebiopsis gigantea, flocculosa Pseudozyma, Pythium oligandrum DV74, Reynoutria sachlinensis, Talaromyces flavus V117b, Trichoderma asperellum SKT-1, T. atroviride LC52, T. harzianum T-22, T. harzianum TH 35, T. harzianum T-39, T. harzianum and T. viride, T. harzianum ICC012 and T. viride ICC080, T. polysporum and T. harzianum, T. stromaticum, T. virens GL21, T. viride, T. viride TV1, Ulocladium oudemansii HRU3; or 2) An insecticidal compound IB selected from the group consisting of M-1.A) Acetylcholine esterase inhibitors of the class of carbamates: aldicarb, alanycarb, bendiocarb, benfuracarb, butocarboxim, butoxycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, fenobucarb , formetanate, furathiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pyrimicarb, propoxur, thiodicarb, thiofanox, trimethacarb, XMC, xylylcarb and triazamate; M-1.B) Acetylcholine esterase inhibitors of the organophosphate class: acephate, azamethiphos, azinphos-ethyl, azinphosmethyl, cadusafos, chlorethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, |
| priorityDate | 2012-11-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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