AR067645A1 - Combinaciones de principios activos insecticidas (genesteina + insecticidas ) - Google Patents
Combinaciones de principios activos insecticidas (genesteina + insecticidas )Info
- Publication number
- AR067645A1 AR067645A1 ARP080103171A AR067645A1 AR 067645 A1 AR067645 A1 AR 067645A1 AR P080103171 A ARP080103171 A AR P080103171A AR 067645 A1 AR067645 A1 AR 067645A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- inhibitors
- active ingredients
- combinations
- agents
- Prior art date
Links
- 239000002917 insecticide Substances 0.000 title 1
- 239000004480 active ingredient Substances 0.000 abstract 8
- 239000003112 inhibitor Substances 0.000 abstract 8
- 239000003795 chemical substances by application Substances 0.000 abstract 3
- 102000012440 Acetylcholinesterase Human genes 0.000 abstract 2
- 108010022752 Acetylcholinesterase Proteins 0.000 abstract 2
- 229940022698 acetylcholinesterase Drugs 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 239000000556 agonist Substances 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- 230000010627 oxidative phosphorylation Effects 0.000 abstract 2
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 abstract 1
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 abstract 1
- ATROHALUCMTWTB-WYMLVPIESA-N (z)-n-diethoxyphosphinothioyloxybenzenecarboximidoyl cyanide Chemical compound CCOP(=S)(OCC)O\N=C(/C#N)C1=CC=CC=C1 ATROHALUCMTWTB-WYMLVPIESA-N 0.000 abstract 1
- MHKBMNACOMRIAW-UHFFFAOYSA-N 2,3-dinitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O MHKBMNACOMRIAW-UHFFFAOYSA-N 0.000 abstract 1
- -1 2,5-dimethylphenyl Chemical group 0.000 abstract 1
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 abstract 1
- 108091006112 ATPases Proteins 0.000 abstract 1
- 102000057290 Adenosine Triphosphatases Human genes 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
- 229920002101 Chitin Polymers 0.000 abstract 1
- 229940127437 Chloride Channel Antagonists Drugs 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 108010009685 Cholinergic Receptors Proteins 0.000 abstract 1
- 239000005892 Deltamethrin Substances 0.000 abstract 1
- UPEZCKBFRMILAV-JNEQICEOSA-N Ecdysone Natural products O=C1[C@H]2[C@@](C)([C@@H]3C([C@@]4(O)[C@@](C)([C@H]([C@H]([C@@H](O)CCC(O)(C)C)C)CC4)CC3)=C1)C[C@H](O)[C@H](O)C2 UPEZCKBFRMILAV-JNEQICEOSA-N 0.000 abstract 1
- FNELVJVBIYMIMC-UHFFFAOYSA-N Ethiprole Chemical compound N1=C(C#N)C(S(=O)CC)=C(N)N1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl FNELVJVBIYMIMC-UHFFFAOYSA-N 0.000 abstract 1
- 239000004606 Fillers/Extenders Substances 0.000 abstract 1
- 239000005899 Fipronil Substances 0.000 abstract 1
- 239000005901 Flubendiamide Substances 0.000 abstract 1
- 241000238631 Hexapoda Species 0.000 abstract 1
- 239000005907 Indoxacarb Substances 0.000 abstract 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 abstract 1
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 abstract 1
- 108010052164 Sodium Channels Proteins 0.000 abstract 1
- 102000018674 Sodium Channels Human genes 0.000 abstract 1
- 239000005930 Spinosad Substances 0.000 abstract 1
- 239000005664 Spirodiclofen Substances 0.000 abstract 1
- 229920002359 Tetronic® Polymers 0.000 abstract 1
- 239000005941 Thiamethoxam Substances 0.000 abstract 1
- WCXDHFDTOYPNIE-UHFFFAOYSA-N acetamiprid Chemical compound N#CN=C(C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-UHFFFAOYSA-N 0.000 abstract 1
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 abstract 1
- 229960004373 acetylcholine Drugs 0.000 abstract 1
- 102000034337 acetylcholine receptors Human genes 0.000 abstract 1
- QGLZXHRNAYXIBU-WEVVVXLNSA-N aldicarb Chemical compound CNC(=O)O\N=C\C(C)(C)SC QGLZXHRNAYXIBU-WEVVVXLNSA-N 0.000 abstract 1
- UPEZCKBFRMILAV-UHFFFAOYSA-N alpha-Ecdysone Natural products C1C(O)C(O)CC2(C)C(CCC3(C(C(C(O)CCC(C)(C)O)C)CCC33O)C)C3=CC(=O)C21 UPEZCKBFRMILAV-UHFFFAOYSA-N 0.000 abstract 1
- QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 abstract 1
- 229960002587 amitraz Drugs 0.000 abstract 1
- 244000000054 animal parasite Species 0.000 abstract 1
- 230000000433 anti-nutritional effect Effects 0.000 abstract 1
- 150000008047 benzoylureas Chemical class 0.000 abstract 1
- 239000003124 biologic agent Substances 0.000 abstract 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 abstract 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 abstract 1
- 150000003857 carboxamides Chemical class 0.000 abstract 1
- 239000003467 chloride channel stimulating agent Substances 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 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
- 230000001419 dependent effect Effects 0.000 abstract 1
- 150000008037 diacylhydrazines Chemical class 0.000 abstract 1
- YKBZOVFACRVRJN-UHFFFAOYSA-N dinotefuran Chemical compound [O-][N+](=O)\N=C(/NC)NCC1CCOC1 YKBZOVFACRVRJN-UHFFFAOYSA-N 0.000 abstract 1
- GCKZANITAMOIAR-XWVCPFKXSA-N dsstox_cid_14566 Chemical compound [O-]C(=O)C1=CC=CC=C1.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]([NH2+]C)[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 GCKZANITAMOIAR-XWVCPFKXSA-N 0.000 abstract 1
- UPEZCKBFRMILAV-JMZLNJERSA-N ecdysone Chemical compound C1[C@@H](O)[C@@H](O)C[C@]2(C)[C@@H](CC[C@@]3([C@@H]([C@@H]([C@H](O)CCC(C)(C)O)C)CC[C@]33O)C)C3=CC(=O)[C@@H]21 UPEZCKBFRMILAV-JMZLNJERSA-N 0.000 abstract 1
- 229940013764 fipronil Drugs 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
- 229960003692 gamma aminobutyric acid Drugs 0.000 abstract 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 abstract 1
- 238000002309 gasification Methods 0.000 abstract 1
- TZBJGXHYKVUXJN-UHFFFAOYSA-N genistein Chemical compound C1=CC(O)=CC=C1C1=COC2=CC(O)=CC(O)=C2C1=O TZBJGXHYKVUXJN-UHFFFAOYSA-N 0.000 abstract 1
- 239000003966 growth inhibitor Substances 0.000 abstract 1
- 239000005556 hormone Substances 0.000 abstract 1
- 229940088597 hormone Drugs 0.000 abstract 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 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
- 230000000968 intestinal effect Effects 0.000 abstract 1
- 229930014550 juvenile hormone Natural products 0.000 abstract 1
- 239000002949 juvenile hormone Substances 0.000 abstract 1
- 150000003633 juvenile hormone derivatives Chemical class 0.000 abstract 1
- 150000002632 lipids Chemical class 0.000 abstract 1
- 239000011777 magnesium Substances 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- 230000007246 mechanism Effects 0.000 abstract 1
- 239000012528 membrane Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- QCAWEPFNJXQPAN-UHFFFAOYSA-N methoxyfenozide Chemical compound COC1=CC=CC(C(=O)NN(C(=O)C=2C=C(C)C=C(C)C=2)C(C)(C)C)=C1C QCAWEPFNJXQPAN-UHFFFAOYSA-N 0.000 abstract 1
- 230000000813 microbial effect Effects 0.000 abstract 1
- DSOOGBGKEWZRIH-UHFFFAOYSA-N nereistoxin Chemical class CN(C)C1CSSC1 DSOOGBGKEWZRIH-UHFFFAOYSA-N 0.000 abstract 1
- 229940079888 nitenpyram Drugs 0.000 abstract 1
- 150000005063 oxadiazines Chemical class 0.000 abstract 1
- 239000003016 pheromone Substances 0.000 abstract 1
- NAYYNDKKHOIIOD-UHFFFAOYSA-N phthalamide Chemical class NC(=O)C1=CC=CC=C1C(N)=O NAYYNDKKHOIIOD-UHFFFAOYSA-N 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 abstract 1
- 150000003233 pyrroles Chemical class 0.000 abstract 1
- 239000000018 receptor agonist Substances 0.000 abstract 1
- 229940044601 receptor agonist Drugs 0.000 abstract 1
- 239000002464 receptor antagonist Substances 0.000 abstract 1
- 229940044551 receptor antagonist Drugs 0.000 abstract 1
- 229940080817 rotenone Drugs 0.000 abstract 1
- JUVIOZPCNVVQFO-UHFFFAOYSA-N rotenone Natural products O1C2=C3CC(C(C)=C)OC3=CC=C2C(=O)C2C1COC1=C2C=C(OC)C(OC)=C1 JUVIOZPCNVVQFO-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000003195 sodium channel blocking agent Substances 0.000 abstract 1
- 229940014213 spinosad Drugs 0.000 abstract 1
- 229930185156 spinosyn Natural products 0.000 abstract 1
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 239000005936 tau-Fluvalinate Substances 0.000 abstract 1
- 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 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 abstract 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
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)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Reivindicacion 1: Combinaciones de principios activos que comprenden genesteína de la formula (1) o sus sales y al menos un principio activo que está seleccionado de los siguientes grupos (2) a (25): Grupo (2) agonistas/antagonistas del receptor de acetilcolina (con preferencia, nicotinilos de cloro/ neonicotinoides); Grupo (3) inhibidores de la acetilcolinesterasa (AChE) (con preferencia, carbamatos y organofosfatos); Grupo (4) moduladores del canal de sodio/bloqueantes del canal de sodio dependientes de tension (con preferencia, piretroides y oxadiazinas); Grupo (5) moduladores del receptor de acetilcolina (con preferencia, espinosinas); Grupo (6) antagonistas del canal de cloruro controlado por GABA (con preferencia, organocloros ciclodiénicos y fiproles); Grupo (7) activadores del canal de cloruro (con preferencia, mectina); Grupo (8) miméticos de la hormona juvenil; Grupo (9) agonistas de ecdisona/disruptores (con preferencia, diacilhidrazinas); Grupo (10) inhibidores de la biosíntesis de quitina (con preferencia, benzoilureas); Grupo (11) inhibidores de la fosforilacion oxidativa, disruptores de ATP (con preferencia, organotinas); Grupo (12) desacopladores de la fosforilacion oxidativa por interrupcion del gradiente de protones H (con preferencia, pirroles y dinitrofenoles); Grupo (13) inhibidores del transporte de electrones de sitio 1 (con preferencia, METI); Grupo (14) inhibidores del transporte de electrones de sitio II; Grupo (15) inhibidores del transporte de electrones de sitio III; Grupo (16) disruptores microbianos de la membrana intestinal de insectos; Grupo (17) inhibidores de la síntesis de lípidos (con preferencia, ácidos tetronicos y ácidos tetrámicos); Grupo (18) carboxamidas; Grupo (19) agonistas octopaminérgicos; Grupo (20) inhibidores de la ATPasa estimulada con magnesio; Grupo (21) ftalamidas; Grupo (22) análogos de nereistoxina; Grupo (23) agentes biologicos, hormonas o feromonas; Grupo (24) principios activos con mecanismos de accion desconocidos o no específicos (con preferencia, agentes de gasificacion, agentes antinutritivos selectivos y inhibidores del crecimiento de ácaros), Grupo (25) Grupo (25). Reivindicacion 3: Combinaciones de principios activos de acuerdo con la reivindicacion 1, 2 o 3, en donde los principios activos de los grupos 2) a (25) están seleccionados de la siguiente lista: (2.1.1) clotianidina, (2.1.2) imidacloprida, (2.1.3) tiacloprida, (2.1.4) tiametoxam, (2.1.5) acetamiprida, (2.1.6) dinotefurano, (2.1.7) nitenpiram, (3.1.1) metiocarb, (3.1.2) tiodicarb, (3.1.4) Aldicarb, (3.1.5) propoxur, (3.2.3) foxima, (4.1.1) beta-ciflutrina, (4.1.2) ciflutrina, (4.1.3) deltametrina, (4.1.4) tau-fluvalinato, (4.1.5) eflusilanato, (4.2.1) indoxacarb, (5.1.1) espinosad, (5.1.2) XDE-175 de la formula (2), (6.2.1) fipronilo, (6.2.2) etiprol, (7.1.1)benzoato de emamectina, (8.1.1) piriproxifeno, (9.1.1) metoxifenozida, (10.1.1) triflumurona, (10.1.2) flufenoxurona, (13.1.1) tebufenpirad, (13.2.1) hidrametilona, (14.1.1) rotenona, (17.1.1) espirodiclofeno, (17.1.2) espiromesifeno, (17.2.1) carbonato de 3-(2,5-dimetilfenil)-8-metoxi-2-oxo-1-azaespiro[4.5]dec-3-en-4-iletilo, (18.1.1) flonicamida, (19.1.1) amitraz, (20.1.1) propargita, (21.1.1) flubendiamida, (21.1.2) rinaxipir, Grupo (25) Reivindicacion 11: Uso de combinaciones de principios activos de acuerdo con una de las reivindicaciones 1 a 9 para el combate de parásitos animales no deseados. Reivindicacion 13: Procedimiento para preparar agentes fitopatogenos, caracterizado porque se mezcla una combinacion de principios activos de acuerdo con una de las reivindicaciones 1 a 9 con agentes tensioactivos y/o extensores. Reivindicacion 17: Simiente que se trato con una combinacion de principios activos de acuerdo con una de las reivindicaciones 1 a 9.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07112965 | 2007-07-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR067645A1 true AR067645A1 (es) | 2009-10-21 |
Family
ID=39864822
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080103171 AR067645A1 (es) | 2007-07-23 | 2008-07-22 | Combinaciones de principios activos insecticidas (genesteina + insecticidas ) |
Country Status (2)
| Country | Link |
|---|---|
| AR (1) | AR067645A1 (es) |
| WO (1) | WO2009012909A2 (es) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2011037760A (ja) * | 2009-08-11 | 2011-02-24 | Sumitomo Chemical Co Ltd | 有害生物防除組成物 |
| CN102165958B (zh) * | 2011-03-10 | 2013-08-14 | 陕西汤普森生物科技有限公司 | 一种含有联苯肼酯与三唑磷的农药组合物 |
| CN103651456A (zh) * | 2012-09-04 | 2014-03-26 | 南京华洲药业有限公司 | 一种含乙虫腈和速灭威的复合杀虫组合物及其用途 |
| CN103404525B (zh) * | 2013-08-16 | 2014-11-05 | 利尔化学股份有限公司 | 一种农用杀虫组合物及其应用 |
| CN103651546A (zh) * | 2013-12-10 | 2014-03-26 | 济南凯因生物科技有限公司 | 用于防治水稻螟蛾类害虫的组合物 |
| CN110612983B (zh) * | 2019-10-29 | 2021-03-09 | 江苏扬农化工股份有限公司 | 一种含有噁虫酮和啶虫脒的杀虫组合物及其应用 |
| CN115299453B (zh) * | 2021-06-25 | 2023-04-18 | 华南农业大学 | Fatostatin作为昆虫生长调节剂的增效剂在制备杀虫剂中的应用 |
| CN116406673A (zh) * | 2021-12-29 | 2023-07-11 | 江苏扬农化工股份有限公司 | 一种含有噁虫威和拟除虫菊酯的卫生杀虫组合物 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6534099B1 (en) * | 1993-05-21 | 2003-03-18 | Ecosmart Technologies, Inc. | Pesticidal compositions containing menthyl salicylate |
| PL1755392T3 (pl) * | 2004-03-18 | 2016-08-31 | Novozymes Bioag As | Związki izoflawonoidowe i ich zastosowanie |
| JP5502493B2 (ja) * | 2007-01-16 | 2014-05-28 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | 農薬の組合せ剤 |
-
2008
- 2008-07-15 WO PCT/EP2008/005750 patent/WO2009012909A2/de not_active Ceased
- 2008-07-22 AR ARP080103171 patent/AR067645A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2009012909A2 (de) | 2009-01-29 |
| WO2009012909A3 (de) | 2009-05-07 |
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