Synthesis and bio-evaluation of aryl hydrazono esters for oviposition responses in Aedes albopictus

A novel series of aryl hydrazono esters (AHE) (1–13) were synthesized (yield 76–98%) to study the oviposition responses in Aedes albopictus (Skuse) mosquitoes for the first time. At a concentration of 10 μg ml −1 in dual choice experiment, among the screened compounds, AHE-12 showed remarkable ovipo...

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Veröffentlicht in:Bioorganic & medicinal chemistry letters 2011-01, Vol.21 (2), p.794-797
Hauptverfasser: Bandyopadhyay, Prabal, Guha, Lopamudra, Seenivasagan, T., Sathe, Manisha, Sharma, Pratibha, Parashar, B.D., Kaushik, M.P.
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Sprache:eng
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Zusammenfassung:A novel series of aryl hydrazono esters (AHE) (1–13) were synthesized (yield 76–98%) to study the oviposition responses in Aedes albopictus (Skuse) mosquitoes for the first time. At a concentration of 10 μg ml −1 in dual choice experiment, among the screened compounds, AHE-12 showed remarkable oviposition attractant activity with an oviposition activity index (OAI) of +0.299 (greater than 95% confidence limit) comparable to p-cresol (OAI +0.320) which is well-reported oviposition attractant for Aedes aegypti. Conversely, AHE-10 exhibited highest oviposition deterrent activity with OAI −0.247. The possible utilization of these compounds will be in integrated vector management strategies. A novel series of aryl hydrazono esters (AHE) (1–13) were synthesized (yield 76–98%) to study the oviposition responses in Aedes albopictus (Skuse) mosquitoes for the first time. At a concentration of 10 μg ml −1 in dual choice experiment, among the screened compounds, AHE-12 showed remarkable oviposition attractant activity with an oviposition activity index (OAI) of +0.299 (greater than 95% confidence limit) comparable to p-cresol (OAI +0.320) which is well-reported oviposition attractant for Aedes aegypti. Conversely, AHE-10 exhibited highest oviposition deterrent activity with OAI −0.247. The possible utilization of these compounds will be in integrated vector management strategies.
ISSN:0960-894X
1464-3405
DOI:10.1016/j.bmcl.2010.11.101