Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10591129 | Bioorganic & Medicinal Chemistry Letters | 2014 | 4 Pages |
Abstract
Here, we describe the synthesis of two new fluorescent derivatives of thiamethoxam and compared their toxicity on aphid Acyrthosiphon pisum and their mode of action on insect nicotinic acetylcholine receptors expressed on the sixth abdominal ganglion. The compound 3 with two 2-chlorothiazole moieties was found to be more toxic using toxicological bioassays 24Â h and 48Â h after exposure while compound 4 appeared more active using cockroach ganglionic depolarization. Interestingly, thiamethoxam appeared more effective than component 3 and 4, respectively. Our results demonstrated that component 3 and 4 act as agonists of insect nicotinic acetylcholine receptors.
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Authors
Emiliane Taillebois, Paul Langlois, Thomas Cunha, Denis Seraphin, Steeve H. Thany,