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受體一樣）。[8]菸鹼型乙酰膽鹼受體是離子型受體中被研究得最透徹的 Nicotinic acetylcholine receptors are the best-studied of the ionotropic receptors.。 由於菸鹼受體有助於傳遞交感神經系統和副交感神經系統的輸出信號，
3-Pyridyl ethers with subnanomolar affinity for central neuronal nicotinic acetylcholine receptors. Journal of Medicinal Chemistry. February 1996, 39 (4): 817–25
美國雅培公司开发，可作为菸鹼型乙醯膽鹼受體的激动剂，未经过臨床試驗。 Jain KK. Modulators of nicotinic acetylcholine receptors as analgesics. Current Opinion in Investigational Drugs. January
properties of oxime reactivators: the interaction with muscarinic and nicotinic receptors. Archives of Toxicology. 21 November 2012, 87 (4): 711–719. PMID 23179755
Bouzat, C. The local anaesthetics proadifen and adiphenine inhibit nicotinic receptors by different molecular mechanisms. British Journal of Pharmacology