Procaine is an inhibitor of sodium channel, NMDA receptor and nAChR with IC50 of 60 μM, 0.296 mM and 45.5 μM, which is also an inhibitor of 5-HT3 with KD of 1.7 μM.
Procaine is an inhibitor of sodium channel, NMDA receptor and nAChR with IC50 of 60 μM, 0.296 mM and 45.5 μM, which is also an inhibitor of 5-HT3 with KD of 1.7 μM.
动物 A (mg/kg) = 动物 B (mg/kg)×动物 B的Km系数/动物 A的Km系数 | |
例如,已知某工具药用于小鼠的剂量为88 mg/kg , 则用于大鼠的剂量换算方法:将88 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到该药物用于大鼠的等效剂量44 mg/kg。
[1] Carmen Herencia,et al. Procaine Inhibits Osteo/Odontogenesis through Wnt/β-Catenin Inactivation. PLoS One. 2016; 11(6): e0156788. Published online 2016 Jun 3. doi: 10.1371/journal.pone.0156788.
[2] Bryon Adinoff,et al. Psychiatry Res. Author manuscript; available in PMC 2010 Aug 30. Published in final edited form as: Psychiatry Res. 2009 Aug 30; 173(2): 135–142. Published online 2009 Jun 28. doi: 10.1016/j.pscychresns.2009.03.001.
分子式 C13H21ClN2O2 |
分子量 272.77 |
CAS号 51-05-8 |
储存方式 -20 ℃长期冷藏储存。冰袋运输 |
溶剂(常温) |
DMSO 55 mg/mL |
Water 55 mg/mL |
Ethanol <1 mg/mL |
体内溶解度
注:以上所有数据均来自公开文献,并不保证对所有实验均有效,数据仅供参考。
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