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Mepivacaine 是一种酰胺型药剂,可暂时使局部失去知觉。Mepivacaine 与神经元细胞膜上特定的电压门控钠离子通道结合,抑制钠离子内流和膜去极化。
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更新时间:2026/10/7 8:41:36关注度:2455
关键词标签:Carbocaine
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CAS No. : 96-88-8
MCE 国际站:Mepivacaine
产品活性:Mepivacaine 是一种酰胺型药剂,可暂时使局部失去知觉。Mepivacaine 与神经元细胞膜上特定的电压门控钠离子通道结合,抑制钠离子内流和膜去极化。
研究领域:Membrane Transporter/Ion Channel
作用靶点:Sodium Channel
In Vitro: Mepivacaine binds to specific voltage-gated sodium ion channels in neuronal cell membranes, which inhibits both sodium influx and membrane depolarization. This leads to a blockage of nerve impulse initiation and conduction and results in a reversible loss of sensation. Compared to other local anesthetics, this agent has a more rapid onset and moderate duration of action.
Mepivacaine has a reasonably rapid onset (more rapid than that of procaine) and medium duration of action (shorter than that of procaine).
Mepivacaine displays a preferential use-dependent block of Na(v)1.8, S(-)-bupivacaine displays a preference for TTXs Na(+) channels.
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