Unravelling nicotinic receptor and ligand features underlying neonicotinoid knockdown actions on the malaria vector mosquito .

With the spread of resistance to long-established insecticides targeting malaria vectors, understanding the actions of compounds newly identified for vector control is essential. With new commercial vector-control products containing neonicotinoids under development, we investigate the actions of 6 neonicotinoids (imidacloprid, thiacloprid, clothianidin, dinotefuran, nitenpyram and acetamiprid) on 13 nicotinic acetylcholine receptor (nAChR) subtypes produced by expression of combinations of the Ag1, Ag2, Ag3, Ag8 and Ag1 subunits in oocytes, the orthologues of which we have previously shown to be important in neonicotinoid actions. The presence of the Ag2 subunit reduces neonicotinoid affinity for the mosquito nAChRs, whereas the Ag3 subunit increases it.

Divergent Nine-Step Syntheses of Perhydrohistrionicotoxin Analogs and Their Inhibition Activity Toward Chicken α4β2-Neuronal Nicotinic Acetylcholine Receptors.

Histrionicotoxin (HTX) alkaloids, which are isolated from Colombian poison dart frogs, are analgesic neurotoxins that modulate nicotinic acetylcholine receptors (nAChRs) as antagonists. Perhydrohistrionicotoxin (pHTX) is the potent synthetic analogue of HTX and possesses a 1-azaspiro[5.5]undecane skeleton common to the HTX family.