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Fluorescent probes for insect ryanodine receptors: candidate anthranilic diamides.


ABSTRACT: 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.

SUBMITTER: Wang Y 

PROVIDER: S-EPMC6270845 | biostudies-literature | 2014 Apr

REPOSITORIES: biostudies-literature

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Fluorescent probes for insect ryanodine receptors: candidate anthranilic diamides.

Wang Yi Y   Guo Lei L   Qi Suzhen S   Zhang Hao H   Liu Kechang K   Liu Ruiquan R   Liang Pei P   Casida John E JE   Liu Shangzhong S  

Molecules (Basel, Switzerland) 20140402 4


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  ...[more]

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