Structure-activity studies on a novel series of cholinergic channel activators based on a heteroaryl ether framework
作者:Nan-Horng Lin、Melwyn A. Abreo、David E. Gunn、Suzanne A. Lebold、Edmund L. Lee、James T. Wasicak、Ann-Marie Hettinger、Jerome F. Daanen、David S. Garvey、Jeffrey E. Campbell、James P. Sullivan、Michael Williams、Stephen P. Arneric
DOI:10.1016/s0960-894x(99)00462-x
日期:1999.9
Analogs of compound 1 with a variety of azacycles and heteroaryl groups were synthesized. These analogs exhibited K-i values ranging from 0.15 to 1 10,000 nM when tested in vitro for cholinergic channel receptor binding activity (displacement of [H-3](-) cytisine from whole rat brain synaptic membranes). (C) 1999 Elsevier Science Ltd. All rights reserved.
Asymmetric Induction in the Electrochemical Cross-Coupling of Aryl Halides with α-Chloropropionic Acid Derivatives Catalyzed by Nickel Complexes