Novel guanidine compounds having the formula
in which R1, R2 and R4 are as defined, are effective as sodium channel dockers in neuronal mammalian cells and as anesthetics and/or analgesics, particularly local spinal and/or epidural anesthetics, for alleviation of neuropathic pain, for providing a neuroprotective effect, and for producing anti-convulsant effects.
具有以下结构式的新型
胍类化合物,在神经元哺乳动物细胞中作为
钠通道的停靠剂,并作为
麻醉剂和/或镇痛剂,特别是局部脊髓和/或硬膜外
麻醉剂,用于缓解神经病性疼痛,提供神经保护作用和产生抗惊厥作用,其中R1、R2和R4如定义。