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Combinaisons pesticides de substances actives
专利权人:
BAYER CROPSCIENCE AG
发明人:
SUTY-HEINZE, ANNE,HUNGENBERG, HEIKE,THIELERT, WOLFGANG,ELBE, HANS-LUDWIG
申请号:
EP10161262.0
公开号:
EP2213168B1
申请日:
2006.04.15
申请国别(地区):
EP
年份:
2013
代理人:
摘要:
Active agent combination (A) with very good fungicide-, insecticide- and/or acaricide- characteristics, comprises a carboxyamide compound (I) and/or at least an active agent e.g. acetylcholine-receptor-agonist/antagonist, preferably chloronicotinyl/neonicotinoide; and acetylchloline esterase inhibitor, preferably carbamate and organophosphate. Active agent combination (A) with very good fungicide-, insecticide- and/or acaricide- characteristics, comprises a carboxyamide compound of formula (I) and/or at least one acetylcholine-receptor-agonist/antagonist, preferably chloronicotinyl/neonicotinoide; acetylchloline esterase inhibitor, preferably carbamate and organophosphate; sodium-channel-modulator/stress dependent sodium-channel-blocker, preferably pyrethroid and oxadiazine; acetylcholine-receptor-modulator, preferably sphingosine; gamma-amminobutyric acid-chloride-channel-antagonist, preferably organochlorine and fiprole; chloride-channel-activator, preferably mectine; juvenile hormone-mimetic; ecdysone agonist/disruptor, preferably diacylhydrazine; chitin biosynthase inhibitor, preferably benzoylurea material; oxidative phosphoryl inhibitor, ATP-disruptor, preferably organotin; oxidative phosphoryl coupler by interruption of hydrogen-proton-gradient, preferably pyrrole and dinitrophenol; site-I-electrontransport inhibitor, preferably myto chondrial electron transport; site-II-electrontransport inhibitor; site-III-electrontransport inhibitor; microbial disruptor insects intestine membrane; fatty acid synthesis inhibitor, preferably tetronicacid and tetramic acid; carboxamide; octopamine agonist; magnesium-stimulater ATPase-inhibitor; phthalamide; nereistoxin analog; biological hormone or pheromone; and aeration agent, worm inhibitor and mite growth inhibitor. R 1,>; R 3>;, R 7>;, R 10>; : H, halo, 1-3C-alkyl or 1-3C-haloalkyl with 1-7 F, Cl or Br; R 2>; : 1-3C alkyl; R 4>; : H, halo, or 1-3C-alkyl; A : 8 heterocyclic compounds e.g. of formulae (II)-(IX)
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