AR127133A1 - Mezclas novedosas para protección de cultivos - Google Patents
Mezclas novedosas para protección de cultivosInfo
- Publication number
- AR127133A1 AR127133A1 ARP220102565A ARP220102565A AR127133A1 AR 127133 A1 AR127133 A1 AR 127133A1 AR P220102565 A ARP220102565 A AR P220102565A AR P220102565 A ARP220102565 A AR P220102565A AR 127133 A1 AR127133 A1 AR 127133A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- modulator
- inhibitor
- insecticide
- channel
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 4
- 239000002917 insecticide Substances 0.000 abstract 4
- 241000238631 Hexapoda Species 0.000 abstract 3
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 abstract 3
- -1 tetranortriterpenoid limonoid Chemical class 0.000 abstract 3
- 101001018064 Homo sapiens Lysosomal-trafficking regulator Proteins 0.000 abstract 2
- 101000667110 Homo sapiens Vacuolar protein sorting-associated protein 13B Proteins 0.000 abstract 2
- 102100033472 Lysosomal-trafficking regulator Human genes 0.000 abstract 2
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 abstract 2
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 abstract 2
- 239000003630 growth substance Substances 0.000 abstract 2
- 239000003112 inhibitor Substances 0.000 abstract 2
- 210000000056 organ Anatomy 0.000 abstract 2
- 239000005936 tau-Fluvalinate Substances 0.000 abstract 2
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 abstract 2
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 abstract 1
- XGWIJUOSCAQSSV-XHDPSFHLSA-N (S,S)-hexythiazox Chemical compound S([C@H]([C@@H]1C)C=2C=CC(Cl)=CC=2)C(=O)N1C(=O)NC1CCCCC1 XGWIJUOSCAQSSV-XHDPSFHLSA-N 0.000 abstract 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-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
- PTQBEFQWTBZMED-UHFFFAOYSA-N 2-(3-ethylsulfonylpyridin-2-yl)-5-(trifluoromethylsulfonyl)-1,3-benzoxazole Chemical group CCS(=O)(=O)C1=CC=CN=C1C1=NC2=CC(S(=O)(=O)C(F)(F)F)=CC=C2O1 PTQBEFQWTBZMED-UHFFFAOYSA-N 0.000 abstract 1
- LHZOTJOOBRODLL-UHFFFAOYSA-N 4-oxo-1-(pyrimidin-5-ylmethyl)-3-[3-(trifluoromethyl)phenyl]pyrido[1,2-a]pyrimidin-5-ium-2-olate Chemical compound O=C1[N+]2=CC=CC=C2N(CC=2C=NC=NC=2)C([O-])=C1C1=CC=CC(C(F)(F)F)=C1 LHZOTJOOBRODLL-UHFFFAOYSA-N 0.000 abstract 1
- 229940126565 ATP-synthase inhibitor Drugs 0.000 abstract 1
- 239000005875 Acetamiprid Substances 0.000 abstract 1
- 240000005343 Azadirachta indica Species 0.000 abstract 1
- 239000005730 Azoxystrobin Substances 0.000 abstract 1
- 241000193388 Bacillus thuringiensis Species 0.000 abstract 1
- 239000005653 Bifenazate Substances 0.000 abstract 1
- 239000005874 Bifenthrin Substances 0.000 abstract 1
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 abstract 1
- 108091006146 Channels Proteins 0.000 abstract 1
- 229920002101 Chitin Polymers 0.000 abstract 1
- 239000005886 Chlorantraniliprole Substances 0.000 abstract 1
- 108010062745 Chloride Channels Proteins 0.000 abstract 1
- 102000011045 Chloride Channels Human genes 0.000 abstract 1
- 239000005654 Clofentezine Substances 0.000 abstract 1
- 239000005889 Cyantraniliprole Substances 0.000 abstract 1
- 239000005946 Cypermethrin Substances 0.000 abstract 1
- 239000005891 Cyromazine Substances 0.000 abstract 1
- 239000005892 Deltamethrin Substances 0.000 abstract 1
- 239000005760 Difenoconazole Substances 0.000 abstract 1
- 239000005894 Emamectin Substances 0.000 abstract 1
- 239000005897 Etoxazole Substances 0.000 abstract 1
- 239000005657 Fenpyroximate Substances 0.000 abstract 1
- 239000005900 Flonicamid Substances 0.000 abstract 1
- 239000005901 Flubendiamide Substances 0.000 abstract 1
- 239000005781 Fludioxonil Substances 0.000 abstract 1
- 239000005788 Fluxapyroxad Substances 0.000 abstract 1
- 239000005661 Hexythiazox Substances 0.000 abstract 1
- 239000005907 Indoxacarb Substances 0.000 abstract 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 abstract 1
- 239000005802 Mancozeb Substances 0.000 abstract 1
- 235000013500 Melia azadirachta Nutrition 0.000 abstract 1
- 102000013379 Mitochondrial Proton-Translocating ATPases Human genes 0.000 abstract 1
- 108010026155 Mitochondrial Proton-Translocating ATPases Proteins 0.000 abstract 1
- 239000005925 Pymetrozine Substances 0.000 abstract 1
- 239000005926 Pyridalyl Substances 0.000 abstract 1
- 239000005927 Pyriproxyfen Substances 0.000 abstract 1
- 239000005929 Spinetoram Substances 0.000 abstract 1
- GOENIMGKWNZVDA-OAMCMWGQSA-N Spinetoram Chemical compound CO[C@@H]1[C@H](OCC)[C@@H](OC)[C@H](C)O[C@H]1OC1C[C@H]2[C@@H]3C=C4C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@H](CC5)N(C)C)CCC[C@H](CC)OC(=O)CC4[C@@H]3CC[C@@H]2C1 GOENIMGKWNZVDA-OAMCMWGQSA-N 0.000 abstract 1
- 239000005930 Spinosad Substances 0.000 abstract 1
- 239000005931 Spirotetramat Substances 0.000 abstract 1
- 239000005934 Sulfoxaflor Substances 0.000 abstract 1
- 102000003563 TRPV Human genes 0.000 abstract 1
- 108060008564 TRPV Proteins 0.000 abstract 1
- 239000005839 Tebuconazole Substances 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 abstract 1
- 229940121373 acetyl-coa carboxylase inhibitor Drugs 0.000 abstract 1
- LRZWFURXIMFONG-HRSIRGMGSA-N afidopyropen Chemical compound C([C@@]1(C)[C@H]2[C@]([C@H]3[C@@H](O)C=4C(=O)OC(=CC=4O[C@]3(C)[C@@H](O)C2)C=2C=NC=CC=2)(C)CC[C@@H]1OC(=O)C1CC1)OC(=O)C1CC1 LRZWFURXIMFONG-HRSIRGMGSA-N 0.000 abstract 1
- 229940125516 allosteric modulator Drugs 0.000 abstract 1
- 229930184024 azadirachitin Natural products 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
- 229940097012 bacillus thuringiensis Drugs 0.000 abstract 1
- ZYXYTGQFPZEUFX-UHFFFAOYSA-N benzpyrimoxan Chemical compound O1C(OCCC1)C=1C(=NC=NC=1)OCC1=CC=C(C=C1)C(F)(F)F ZYXYTGQFPZEUFX-UHFFFAOYSA-N 0.000 abstract 1
- VHLKTXFWDRXILV-UHFFFAOYSA-N bifenazate Chemical compound C1=C(NNC(=O)OC(C)C)C(OC)=CC=C1C1=CC=CC=C1 VHLKTXFWDRXILV-UHFFFAOYSA-N 0.000 abstract 1
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- QSLZKWPYTWEWHC-UHFFFAOYSA-N broflanilide Chemical compound C=1C=CC(C(=O)NC=2C(=CC(=CC=2Br)C(F)(C(F)(F)F)C(F)(F)F)C(F)(F)F)=C(F)C=1N(C)C(=O)C1=CC=CC=C1 QSLZKWPYTWEWHC-UHFFFAOYSA-N 0.000 abstract 1
- PSOVNZZNOMJUBI-UHFFFAOYSA-N chlorantraniliprole Chemical compound CNC(=O)C1=CC(Cl)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl PSOVNZZNOMJUBI-UHFFFAOYSA-N 0.000 abstract 1
- UXADOQPNKNTIHB-UHFFFAOYSA-N clofentezine Chemical compound ClC1=CC=CC=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 UXADOQPNKNTIHB-UHFFFAOYSA-N 0.000 abstract 1
- 230000002860 competitive effect Effects 0.000 abstract 1
- DVBUIBGJRQBEDP-UHFFFAOYSA-N cyantraniliprole Chemical compound CNC(=O)C1=CC(C#N)=CC(C)=C1NC(=O)C1=CC(Br)=NN1C1=NC=CC=C1Cl DVBUIBGJRQBEDP-UHFFFAOYSA-N 0.000 abstract 1
- 229960005424 cypermethrin Drugs 0.000 abstract 1
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 abstract 1
- LVQDKIWDGQRHTE-UHFFFAOYSA-N cyromazine Chemical compound NC1=NC(N)=NC(NC2CC2)=N1 LVQDKIWDGQRHTE-UHFFFAOYSA-N 0.000 abstract 1
- 229950000775 cyromazine Drugs 0.000 abstract 1
- 229960002483 decamethrin Drugs 0.000 abstract 1
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 abstract 1
- WOWBFOBYOAGEEA-UHFFFAOYSA-N diafenthiuron Chemical compound CC(C)C1=C(NC(=S)NC(C)(C)C)C(C(C)C)=CC(OC=2C=CC=CC=2)=C1 WOWBFOBYOAGEEA-UHFFFAOYSA-N 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
- CXEGAUYXQAKHKJ-NSBHKLITSA-N emamectin B1a Chemical compound C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](NC)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 CXEGAUYXQAKHKJ-NSBHKLITSA-N 0.000 abstract 1
- IXSZQYVWNJNRAL-UHFFFAOYSA-N etoxazole Chemical compound CCOC1=CC(C(C)(C)C)=CC=C1C1N=C(C=2C(=CC=CC=2F)F)OC1 IXSZQYVWNJNRAL-UHFFFAOYSA-N 0.000 abstract 1
- YYJNOYZRYGDPNH-MFKUBSTISA-N fenpyroximate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1CO/N=C/C=1C(C)=NN(C)C=1OC1=CC=CC=C1 YYJNOYZRYGDPNH-MFKUBSTISA-N 0.000 abstract 1
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 abstract 1
- ZGNITFSDLCMLGI-UHFFFAOYSA-N flubendiamide Chemical compound CC1=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C1NC(=O)C1=CC=CC(I)=C1C(=O)NC(C)(C)CS(C)(=O)=O ZGNITFSDLCMLGI-UHFFFAOYSA-N 0.000 abstract 1
- MUJOIMFVNIBMKC-UHFFFAOYSA-N fludioxonil Chemical compound C=12OC(F)(F)OC2=CC=CC=1C1=CNC=C1C#N MUJOIMFVNIBMKC-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
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 229930195712 glutamate Natural products 0.000 abstract 1
- 239000003966 growth inhibitor Substances 0.000 abstract 1
- VBCVPMMZEGZULK-NRFANRHFSA-N indoxacarb Chemical compound C([C@@]1(OC2)C(=O)OC)C3=CC(Cl)=CC=C3C1=NN2C(=O)N(C(=O)OC)C1=CC=C(OC(F)(F)F)C=C1 VBCVPMMZEGZULK-NRFANRHFSA-N 0.000 abstract 1
- 239000012528 membrane Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 230000000813 microbial effect Effects 0.000 abstract 1
- 230000002438 mitochondrial effect Effects 0.000 abstract 1
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 abstract 1
- 239000003992 organochlorine insecticide Substances 0.000 abstract 1
- 229960000490 permethrin Drugs 0.000 abstract 1
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 abstract 1
- QHMTXANCGGJZRX-WUXMJOGZSA-N pymetrozine Chemical compound C1C(C)=NNC(=O)N1\N=C\C1=CC=CN=C1 QHMTXANCGGJZRX-WUXMJOGZSA-N 0.000 abstract 1
- 239000002728 pyrethroid Substances 0.000 abstract 1
- AEHJMNVBLRLZKK-UHFFFAOYSA-N pyridalyl Chemical group N1=CC(C(F)(F)F)=CC=C1OCCCOC1=C(Cl)C=C(OCC=C(Cl)Cl)C=C1Cl AEHJMNVBLRLZKK-UHFFFAOYSA-N 0.000 abstract 1
- MIOBBYRMXGNORL-UHFFFAOYSA-N pyrifluquinazon Chemical compound C1C2=CC(C(F)(C(F)(F)F)C(F)(F)F)=CC=C2N(C(=O)C)C(=O)N1NCC1=CC=CN=C1 MIOBBYRMXGNORL-UHFFFAOYSA-N 0.000 abstract 1
- 150000003230 pyrimidines Chemical class 0.000 abstract 1
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 abstract 1
- 229940075993 receptor modulator Drugs 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- 102000042094 ryanodine receptor (TC 1.A.3.1) family Human genes 0.000 abstract 1
- 108091052345 ryanodine receptor (TC 1.A.3.1) family Proteins 0.000 abstract 1
- 229940014213 spinosad Drugs 0.000 abstract 1
- WOPFPAIGRGHWAQ-UHFFFAOYSA-N spiropidion Chemical compound CCOC(=O)OC1=C(C=2C(=CC(Cl)=CC=2C)C)C(=O)N(C)C11CCN(OC)CC1 WOPFPAIGRGHWAQ-UHFFFAOYSA-N 0.000 abstract 1
- CLSVJBIHYWPGQY-GGYDESQDSA-N spirotetramat Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)N[C@@]11CC[C@H](OC)CC1 CLSVJBIHYWPGQY-GGYDESQDSA-N 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 abstract 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 abstract 1
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-UHFFFAOYSA-N 0.000 abstract 1
- 239000003053 toxin Substances 0.000 abstract 1
- 231100000765 toxin Toxicity 0.000 abstract 1
- 239000000664 voltage gated sodium channel blocking agent Substances 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
-
- 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
- A01N37/38—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 having at least one oxygen or sulfur atom attached to an aromatic ring system
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
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)
Abstract
La presente invención se refiere a combinaciones novedosas de compuestos activos que comprenden tau-fluvalinato y al menos un compuesto activo adicional, y a métodos de control de plagas mediante la aplicación de dichas combinaciones. Reivindicación 1: Una combinación de mezclas de compuestos activos que comprende: i) tau-fluvalinato y ii) al menos un compuesto químico II para la protección de cultivos seleccionado del grupo que comprende (a) a (x): (a) un piretroide sintético seleccionado de un grupo que consiste en l-cialotrina, bifentrina, cipermetrina, deltametrina, fenvalerato, permetrina, (b) un modulador competitivo del receptor nicotínico de acetilcolina (nAChR) seleccionado del grupo que comprende acetamiprid, espinetoram, espinosad y sulfoxaflor, (c) un bloqueante del canal del receptor nicotínico de acetilcolina seleccionado del grupo que comprende tiociclam, (d) un modulador del canal TRPV del órgano cordotonal seleccionado del grupo que comprende afidopiropeno, pimetrozina y pirifluquinazon, (e) un modulador del órgano cordotonal con sitio diana indefinido, seleccionado del grupo que comprende flonicamid, (f) un limonoide tetranortriterpenoide complejo de las semillas de neem, seleccionado del grupo que comprende azadiraquitina, (g) un inhibidor de la ATP sintasa mitocondrial, seleccionado del grupo que comprende azociclotina, diafentiurón, óxido de fenbutatina y tetradifón, (h) un derivado de pirimidina seleccionado del grupo que comprende benzpirimoxán, (i) un Inhibidor del transporte de electrones del complejo mitocondrial (METI) seleccionado del grupo que comprende bifenazato, fenpiroximato, tolfenpirad y piromita, (j) un insecticida meta-diamida seleccionado del grupo que comprende broflanilida, (k) un inhibidor del crecimiento de ácaros que afectan a la CHS1, seleccionado del grupo que comprende clofentezina, diflovidazina, etoxazol y hexitiazox, (l) un modulador del receptor de rianodina seleccionado del grupo que comprende clorantraniliprol, ciclaniliprol, ciantraniliprol y flubendiamida, (m) un regulador de crecimiento de insectos triazina seleccionado del grupo que comprende ciromazina, (n) un regulador del crecimiento de insectos de amplio espectro seleccionado del grupo que comprende piriproxifeno, (o) un modulador alostérico del canal de cloruro regulado por glutamato (GluCl) seleccionado del grupo que comprende emamectina, (p) un insecticida nicotínico quimiotipo seleccionado del grupo que comprende flupirimina, (q) un bloqueante del canal de sodio dependiente de voltaje seleccionado del grupo que comprende indoxacarb, (r) un inhibidor de la síntesis de quitina que afectan a la CHS1, seleccionado del grupo que comprende novalurón, (s) una clase de insecticida sulfilo seleccionado del grupo que comprende oxazosulfilo, (t) un insecticida organoclorado seleccionado del grupo que comprende piridalilo, (u) un inhibidor de la acetil CoA carboxilasa seleccionado del grupo que comprende espiropidión y espirotetramat, (v) un disruptor microbiano de las membranas del intestino medio de los insectos, seleccionado del grupo que comprende toxina de Bacillus thuringiensis, (w) un fungicida seleccionado del grupo que comprende pidiflumetofén, fluxapiroxad, difenoconazol, tebuconazol, fludioxonil, azoxistrobina y mancozeb, y (x) un insecticida mesoiónico seleccionado del grupo que comprende triflumezopirim.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN202111043563 | 2021-09-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR127133A1 true AR127133A1 (es) | 2023-12-20 |
Family
ID=83689981
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP220102565A AR127133A1 (es) | 2021-09-25 | 2022-09-23 | Mezclas novedosas para protección de cultivos |
Country Status (5)
| Country | Link |
|---|---|
| AR (1) | AR127133A1 (es) |
| AU (1) | AU2022353246A1 (es) |
| CA (1) | CA3232990A1 (es) |
| TW (1) | TW202312872A (es) |
| WO (1) | WO2023047406A1 (es) |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR097362A1 (es) * | 2013-08-16 | 2016-03-09 | Cheminova As | Combinación de 2-metilbifenil-3-ilmetil (z)-(1r)-cis-3-(2-cloro-3,3,3-trifluorprop-1-enil)-2, 2-dimetilciclopropanocarboxilato con por lo menos un insecticida, acaricida, nematicida y/o fungicida |
| KR20220162860A (ko) * | 2016-04-06 | 2022-12-08 | 에프엠씨 코포레이션 | 거미강 종의 번식을 제어하기 위한 조성물 및 방법 |
-
2022
- 2022-09-23 AR ARP220102565A patent/AR127133A1/es unknown
- 2022-09-25 WO PCT/IL2022/051023 patent/WO2023047406A1/en active Application Filing
- 2022-09-25 CA CA3232990A patent/CA3232990A1/en active Pending
- 2022-09-25 AU AU2022353246A patent/AU2022353246A1/en active Pending
- 2022-09-26 TW TW111136379A patent/TW202312872A/zh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA3232990A1 (en) | 2023-03-30 |
| WO2023047406A1 (en) | 2023-03-30 |
| TW202312872A (zh) | 2023-04-01 |
| AU2022353246A1 (en) | 2024-04-11 |
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