• The Korean Journal of Pesticide Science
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• v.6 no.3
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• pp.224-229
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• 2002

In vivo metabolism study was carried out to find out the biochemical or metabolic tolerance mechanism between Diamond backmoth (DBM), Plutella xylostella and Beet armywarm (BAW), Spodoptera exigua to flupyrazofos. They showed some differences between the DBM and BAW. About 20% of flupyrazofos applied to the 3rd instar larvae of DBM was metabolized within 1 h and about 50% of that was metabolized within 4 h. The metabolites of flupyrazofos-oxon in 3rd instar larvae of DBM were increased 10 times more at 4 h than 1 h after application. The amounts of flupyrazol were nearly same between at 1 h and 4 h. The amount of unknown and origin increased 2 and 3 times more at 1 h than 4 h after application, respectively. In the 4th instar BAW larva, about 50% of flupyrazofos was metabolized within 1 h and about 70% of that was metabolized within 4 h. As metabolites, the amounts of flupyrazofos-oxon increased 2 times more at 4 h than 1 h after application. The amounts of flupyrazol increased 4 times more at 4 h than 1 h after application. The amount of unknown and origin increased 2.5 and 2 times more at 4 h than 1 h after application, respectively. From the study, it is supposed that hydrolytic enzyme, esterase, cleave the alkyl bond of flupyrazofos and conjugates with flupyrazofos. This seems to be the main tolerance mechanism of BAW to flupyrazofos.

• The Korean Journal of Pesticide Science
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• v.9 no.1
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• pp.97-101
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• 2005

Flupyrazofos (O,O-diethyl O-1-phenyl-3-trifluoromethylpyrazo-5-yl phosphorothioate) is an organophosphorus insecticide with a pyrazole moiety which is newly developed and commercialized by SUNGBO chemical company and Korean Research Institute of Chemical Technology for effectively control against diamond back moth. This study was conducted to determine the composition and quantity of impurities in technical 1 (94.5%), technical 2 (97.6%) and purified (99.2%) flupyrazofos using GLC/MSD. Bimolecular inhibition rate constant($k_i$) with acethylcholinesterase (in vitro) and $I_{50}$ with mouse brain acetylcholinesterase (in vivo) were measured for comparing inhibitory patterns of two technicals and purified flupyrazofos. Impurities of flupyrazofos were identified as O,O,O-triethylthio-phosphoric acid (TEA), 1-phenyl-3-trifluoromethyl-5-ethoxy pyrazole(PTMEP), O,O-diethyl O-1-phenyl-3-trifluoromethylpyrazo-5-yl phosphoric acid ester(flupyrazofos oxen), O,S-diethyl O-1-phenyl-3-trifluoromethylpyrazo-5-yl phosphorothionate (S-ethyl flupyrazofos). In in vitro, technical 1 showed the fastest inhibition on AChE activity among them. And technical 1 and 2 showed 40% higher in vivo inhibition against mouse brian AChE than purified flupyrazofos did. These results could be caused by the impurities such as flupyrazofos oxen and S-methyl flupyrazofos contained in technical grades of flupyrazofos.