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.
Fluorescent probes for insect ryanodine receptors: candidate anthranilic diamides.
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作者:Wang Yi, Guo Lei, Qi Suzhen, Zhang Hao, Liu Kechang, Liu Ruiquan, Liang Pei, Casida John E, Liu Shangzhong
| 期刊: | Molecules | 影响因子: | 4.600 |
| 时间: | 2014 | 起止号: | 2014 Apr 2; 19(4):4105-14 |
| doi: | 10.3390/molecules19044105 | ||
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