Quantitative structure-activity studies of pyrethroids

Nishimura, Keiichiro; Kitahaba, Tetsuo; Ikemoto, Yuji; Fujita, Toshio

doi:10.1016/0048-3575(88)90017-x

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Cited by 12 publications

References 117 publications

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Miticidal pyrethroids having an isobutyranilidoxime ether skeleton

et al. 1998

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: Isobutyranilidoxime meta-phenoxybenzyl ethers and related compounds were synthesized. Their insecticidal activities measured against Periplaneta americana by injection were lower than that of phenothrin by factors of at least 1/60. However, some compounds were comparable to or only slightly less potent than phenothrin and tetramethrin in miticidal activity tested by a contact method against Dermatophagoides farinae, D. pteronyssinus and T yrophagus putrescentiae.

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Miticidal pyrethroids having an isobutyranilidoxime ether skeleton

et al. 1998

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Comparison of symptomatic and neurophysiological activities of enantiomers of the insecticide 3‐phenoxybenzyl 1‐(4‐ethoxyphenyl)‐2,2‐dichlorocyclopropane‐1‐carboxylate

et al. 1992

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The insecticidal activities of optical isomers of 3‐phenoxybenzyl 1‐(4‐ethoxyphenyl)‐2,2‐dichlorocyclopropanecarboxylate and related compounds were measured with American cockroaches and their knockdown activities were evaluated with house flies. The activities of the S(−)‐isomer of the dichlorocyclopropanecarboxylate were higher than those of the R(+)‐isomer. The effects of the compounds on the inward membrane currents induced by a stepdepolarizing pulse in crayfish axonal membranes were examined under voltage clamp conditions by the sucrose gap method. The compounds induced a tail current upon step repolarization of the membrane. The tail current decayed to zero in each record, but developed with time after the start of application of the compound until a steady level was reached. The rate of decay of the tail current observed in axonal membranes treated with the S(−)‐isomer was slower than with the R(+)‐isomer. The rates of development of the tail current induced by the two isomers were not very different.

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Structure-Activity Relationship and Molecular Design of Peroxidizing Herbicides with Cyclic Imide Structures and Their Relatives

Fujita¹,

Nakayama

1999

Peroxidizing Herbicides

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Quantitative structure-activity studies of pyrethroids

Cited by 12 publications

References 117 publications

Miticidal pyrethroids having an isobutyranilidoxime ether skeleton

Miticidal pyrethroids having an isobutyranilidoxime ether skeleton

Comparison of symptomatic and neurophysiological activities of enantiomers of the insecticide 3‐phenoxybenzyl 1‐(4‐ethoxyphenyl)‐2,2‐dichlorocyclopropane‐1‐carboxylate

Structure-Activity Relationship and Molecular Design of Peroxidizing Herbicides with Cyclic Imide Structures and Their Relatives

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