Häggblad J, Eriksson H, Heilbronn E
Acta Pharmacol Toxicol (Copenh). 1985 Nov;57(5):317-21. doi: 10.1111/j.1600-0773.1985.tb00051.x.
Oxotremorine, a compound widely used as a muscarinic agonist, was found to inhibit binding of 125I-alpha-bungarotoxin to chick myotube nicotinic acetylcholine receptors, IC50 = 79 +/- 5 microM. Oxotremorine also induced a d-tubocurarine sensitive influx of 86Rb in the myotubes (EC50 = 50 +/- 15 microM). Comparative ion-flux studies with carbachol suggested a partial agonist mode of action of oxotremorine.
氧化震颤素是一种广泛用作毒蕈碱激动剂的化合物,它能抑制125I-α-银环蛇毒素与鸡肌管烟碱型乙酰胆碱受体的结合,半数抑制浓度(IC50)为79±5微摩尔。氧化震颤素还能诱导肌管中86Rb的d-筒箭毒碱敏感内流(半数有效浓度(EC50)为50±15微摩尔)。与卡巴胆碱进行的比较离子通量研究表明氧化震颤素具有部分激动剂的作用模式。