Quaternary ammonium 3-(aminoethoxy)pyridines as antinociceptive agents
摘要:
Quaternization via N-methylation of the terminal amines of a series of 3-(dialkylaminoethoxy)pyridines resulted in analogues that displayed up to 50-60-fold enhanced affinity for nicotinic acetylcholinergic (nACh) receptors. Several of these compounds displayed antinociceptive properties in mice using the tail-flick assay and serve as possible leads for the development of novel analgesic agents. (C) 2003 Elsevier Ltd. All rights reserved.
Quaternary ammonium 3-(aminoethoxy)pyridines as antinociceptive agents
作者:Rahime Simsek、Jean Chang-Fong、Mase Lee、Malgorzata Dukat、M. Imad Damaj、Billy R. Martin、Richard A. Glennon
DOI:10.1016/s0960-894x(03)00585-7
日期:2003.9
Quaternization via N-methylation of the terminal amines of a series of 3-(dialkylaminoethoxy)pyridines resulted in analogues that displayed up to 50-60-fold enhanced affinity for nicotinic acetylcholinergic (nACh) receptors. Several of these compounds displayed antinociceptive properties in mice using the tail-flick assay and serve as possible leads for the development of novel analgesic agents. (C) 2003 Elsevier Ltd. All rights reserved.