Comprehensive Molecular Insect Science 2005
DOI: 10.1016/b0-44-451924-6/00065-x
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The Insecticidal Macrocyclic Lactones

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Cited by 35 publications
(33 citation statements)
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“…The absence of cross‐resistance in pyrethroids resistance population to newer insecticides is consistence with the result reported for different insect populations across the globe (Liang et al. 2003; Rugg et al. 2005).…”
Section: Discussionsupporting
confidence: 86%
“…The absence of cross‐resistance in pyrethroids resistance population to newer insecticides is consistence with the result reported for different insect populations across the globe (Liang et al. 2003; Rugg et al. 2005).…”
Section: Discussionsupporting
confidence: 86%
“…Alternatively, insight could be obtained by exploring the resistance mechanisms to the insecticides. For example, Abamectin acts on the GABA receptor/ chloride ionophore complex and glutamate-gated chloride channel (Clark et al 1995;Rugg et al 2005). Any variation Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Tebufenozide was first developed by Rohm and Haas Co. as an agonist of 20-hydroxyecdysone, and kills insects by initiating premature molting (Wing 1988;Wing et al 1988). Abamectin is a bacterial (Streptomyces avermitilis) based toxin that acts on the GABA receptor/ chloride ionophore complex and glutamate-gated chloride channel (Clark et al 1995;Rugg et al 2005). Resistance of DBM to Tebufenozide has been reported in laboratory selected strains, and to Abamectin in field populations (Cao and Han 2006;Qian et al 2008).…”
Section: Introductionmentioning
confidence: 98%
“…Some of the NPs listed above, including abamectin and spinosad, have been synthetically modified, leading to insecticides that have an altered spectrum, improved efficacy and/or improved residual. For example, synthetic modification to the 4″‐hydroxy of abamectin to form the 4″‐ N ‐methylamine yields emamectin benzoate, which possesses greatly improved efficacy for lepidopteran species . Likewise, synthetic modifications (ethoxylation of the 3′‐hydroxy on the rhamnose; reduction of the 5,6‐double bond of spinosyn J) to a mixture of spinosyns J and L results in spinetoram, a semi‐synthetic spinosyn insecticide .…”
Section: Insecticidesmentioning
confidence: 99%