Tocainide hydrochloride
目录号: PL11348 纯度: ≥98%
CAS No. :71395-14-7
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中文名称
Tocainide hydrochloride
中文别名
N-(2-氨基丙酰基)-2,6-二甲基苯胺;妥卡尼;2-Amino-N-(2,6-dimethylphenyl)propanamide 盐酸盐
英文名称
Tocainide hydrochloride
英文别名
Propanamide,2-amino-N-(2,6-dimethylphenyl)-, hydrochloride (1:1);Tocainide Hydrochloride;(+-)-2-amino-N-(2,6-dimethylphenyl)propionamide hydrochloride;4-Amino-2-[4,6-diamino-3-[3-amino-6-(aminomethyl)-5-hydroxyoxan-2-yl]oxy-2-hydroxycyclohexyl]oxy-6-(hydroxymethyl)oxane-3,5-diol sulfate;6'-propionoxylidide hydrochloride;Dartobcin;Dicon;Nebcine;Tobra gobens;Tobramycin sulfate [usan];TOBRAMYCIN SULFATE SALT;TOBRAMYCIN SULPHATE;Tobraneg;Tocainidhydrochlorid
Cas No.
71395-14-7
分子式
C11H16N2O.HCl
分子量
228.72
包装储存
4°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
产品详情
Tocainide hydrochloride 是一种 sodium channel 阻滞剂,在产生疼痛的病灶中(神经膜上) 阻断钠通道。Tocainide hydrochloride 是利多卡因 (lignocaine) 的一种伯胺类似物,用于心律不齐的研究。
生物活性
Tocainide hydrochloride is a sodium channel blocker, it blocks the sodium channels in the pain-producing foci in the nerve membranes. Tocainide hydrochloride is a primary amine analog of lidocaine, can be used for the treatment of tinnitus.
性状
Solid
IC50 & Target[1][2]
IC50: sodium channel
体内研究(In Vivo)
Tocainide (100 mg/kg) effectively suppresses ventricular ectopic activity in unanesthetized dogs with coronary occlusion. Termination of tocainide infusion in both digitalis toxicity and coronary occlusion models results in prompt return of ventricular ectopic activity. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, stored under nitrogen In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)
参考文献
[1]. Alpert JS, et al. Chemistry, pharmacology, antiarrhythmic efficacy and adverse effects of tocainide hydrochloride, an orally active structural analog of lidocaine. Pharmacotherapy. 1983 Nov-Dec;3(6):316-23.
[2]. De Luca A,et al.Optimal requirements for high affinity and use-dependent block of skeletal muscle sodium channel by N-benzyl analogs of tocainide-like compounds.Mol Pharmacol. 2003 Oct;64(4):932-45.
溶解度数据
In Vitro: DMSO : 125 mg/mL (546.52 mM; Need ultrasonic)H2O : 50 mg/mL (218.61 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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