Molecular Features of Neonicotinoid Pharmacophore Variants Interacting with the Insect Nicotinic Receptor

Molecular interactions of neonicotinoid insecticides with the nicotinic acetylcholine receptor have been mapped by chemical and structural neurobiology approaches, thereby encouraging the biorational design of novel nicotinic ligands. This investigation designs, prepares, and evaluates the target site potency of neonicotinoid analogues with various types of electronegative pharmacophores and subsequently predicts their molecular recognition in the ligand-binding pocket. The N-nitroimino (═NNO2) neonicotinoid pharmacophore is systematically replaced by N-nitrosoimino (═NNO), N-formylimino [═NC(O)H], N-alkyl- and N-arylcarbonylimino [═NC(O)R], and N-alkoxy- and N-aryloxycarbonylimino [═NC(O)OR] variants. The ═NNO analogues essentially retain the binding affinity of the ═NNO2 compounds, while the isosteric ═NC(O)H congeners have diminished potency. The ═NC(O)R and ═NC(O)OR analogues, where R is methyl, trifluoromethyl, phenyl, or pyridin-3-yl, have moderate to high affinities. Orientation of the tip oxygen p...