Difference between revisions of "Pesticide Science (1999) 55, 909-918"
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{{Publication | {{Publication | ||
− | |Publication authors=[[Yoshiaki Nakagawa|Y. Nakagawa]], [[Guy Smagghe|G. Smagghe]], S. Kugimiya, K. Hattori, T. Ueno, L. Tirry and T. Fujita | + | |Publication authors=[[Yoshiaki Nakagawa|Y. Nakagawa]], [[Guy Smagghe|G. Smagghe]], S. Kugimiya, K. Hattori, T. Ueno, [[Luc Tirry|L. Tirry]] and T. Fujita |
− | |Author Page=Yoshiaki Nakagawa, Guy Smagghe | + | |Author Page=Yoshiaki Nakagawa, Guy Smagghe, Luc Tirry |
|Publication date=1999 | |Publication date=1999 | ||
|dc:title=Quantitative structure-activity studies of insect growth regulators: XVI. Substituent effects of dibenzoylhydrazines on the insecticidal activity to Colorado potato beetle ''[[Leptinotarsa decemlineata]] '' | |dc:title=Quantitative structure-activity studies of insect growth regulators: XVI. Substituent effects of dibenzoylhydrazines on the insecticidal activity to Colorado potato beetle ''[[Leptinotarsa decemlineata]] '' |
Latest revision as of 18:50, 18 November 2018
Y. Nakagawa, G. Smagghe, S. Kugimiya, K. Hattori, T. Ueno, L. Tirry and T. Fujita (1999)
Quantitative structure-activity studies of insect growth regulators: XVI. Substituent effects of dibenzoylhydrazines on the insecticidal activity to Colorado potato beetle Leptinotarsa decemlineata
Pesticide Science 55 (9), 909-918
Abstract: Insecticidal activity against the Colorado potato beetle, Leptinotarsa decemlineata, was measured for a series of substituted N-tert-butyl-dibenzoylhydrazines, in which one of the benzoyl moieties closer to the tert-butyl group was fixed as being 2-chloro-substitued and the other variously substituted singly or doubly. The effects of substituents on the activity were quantitatively analysed using the classical quantitative structure-activity relationship (QSAR) procedure. The activity against the Colorado potato beetle increases with the molecular hydrophobicity. In addition, various types of steric effect are at work, depending upon the positions. Hydrogen-bonding acceptor substituents at the para position enhance the activity. There seem to be threshold (or optimum) values, albeit position-dependent, in the molecular hydrophobicity, above which the activity starts to decrease. This biphasic contribution of the molecular hydrophobicity to activity against coleopterous larvae is the most conspicuous difference in substituent effects from those found for similar compounds against lepidopterous pest insects, and may be the basis of the variations in the activity spectrum for certain compounds in this series. The introduction of bulkier substituents into the meta- and para-positions of the benzene ring, apart from the tert-butyl group, is unfavorable to activity. LD50 values against Colorado potato beetle larvae of methoxyfenozide (RH-2485) and tebufenozide (RH-5992) were in the order of 10-7 mol per insect, whereas those of RH-5849, and halofenozide (RH-0345) were very low, 10-9-10-10 mol per insect being selective to the coleopterous larvae.
(The abstract is excluded from the Creative Commons licence and has been copied with permission by the publisher.)
Database assignments for author(s): Yoshiaki Nakagawa, Guy Smagghe, Luc Tirry
Research topic(s) for pests/diseases/weeds:
control - general
Pest and/or beneficial records:
Beneficial | Pest/Disease/Weed | Crop/Product | Country | Quarant.
|
---|---|---|---|---|
Leptinotarsa decemlineata |