Diamide insecticides with high efficacy against pests and good environmental safety are broadly applied in crop protection. They act at a poorly-defined site in the very complex ryanodine (Ry) receptor (RyR) potentially accessible to a fluorescent probe. Two N-propynyl analogs of the major anthranilic diamide insecticides chlorantraniliprole (Chlo) and cyantraniliprole (Cyan) were accordingly synthesized and converted into two fluorescent ligands by click reaction coupling with 3-azido-7-hydroxy-2H- chromen-2-one. The new diamide analogs and fluorescent ligands were shown to be nearly as potent as Chlo and Cyan in inhibition of [3H]Chlo binding and stimulation of [3H]Ry binding in house fly thoracic muscle RyR. Although the newly synthesized compounds had only moderate activity in insect larvicidal activity assays, their high in vitro potency in a validated insect RyR binding assay encourages further development of fluorescent probes for insect RyRs.©2014 by the authors; licensee MDPI, Basel, Switzerland.
CITATION STYLE
Wang, Y., Guo, L., Qi, S., Zhang, H., Liu, K., Liu, R., … Liu, S. (2014). Fluorescent probes for insect ryanodine receptors: Candidate anthranilic diamides. Molecules, 19(4), 4105–4114. https://doi.org/10.3390/molecules19044105
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