Mephenytoin
目录号: PL14554 纯度: ≥99%
Mephenytoin 是一种抗惊厥剂,是 CYP2C19 和 CYP2B6 的底物。
CAS No. :50-12-4
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中文名称
Mephenytoin
中文别名
美芬妥英;美芬妥因;美芬妥因 USP标准品;美芬妥因标准品;5-乙基于-3-甲基-5-苯基乙内酰脲
英文名称
Mephenytoin
英文别名
Mephenytoin;Methoin;2,4-Imidazolidinedione,5-ethyl-3-methyl-5-phenyl-;rac-Mephenytoin;(±)-Mephenytoin;(S)-MEPHENYTOIN;5-ethyl-3-methyl-5-phenylhydantoin;Epiazin;Insulton;mephenytoine;Mesantoin;methyl Hydantoin;Methylphenetoin;Phenantoin;Sedantoin;Sedantoinal;Triantoin;(±)-5-Ethyl-3-methyl-5-phenyl-2,4-imidazolidinedione;(±)-5-Ethyl-3-methyl-5-phenylhydantoin;5-ethyl-3-methyl-5-phenyl-4-imidazolidinedione;3-ethylnirvanol;3-methyl-5,5-ethylphenylhydantoin;3-methyl-5,5-phenylethylhydantoin;3-methyl-5-ethyl-5-phenylhydantoin;5-ethyl-3-methyl-5-phenyl-2,4(3h,5h)-imidazoledione;5-ethyl-3-methyl-5-phenyl-2,4-imidazolidinedione;5-ethyl-3-methyl-5-phenylimidazolidin-2,4-dione;(+/-)-Mephenytoin;3-Methyl-5-ethyl-5-phenylhydantoin
Cas No.
50-12-4
分子式
C12H14N2O2
分子量
218.25
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
Mephenytoin 是一种抗惊厥剂,是 CYP2C19 和 CYP2B6 的底物。
生物活性
Mephenytoin, an anticonvulsant, is the CYP2C19 and CYP2B6 substrate.
性状
Solid
IC50 & Target[1][2]
CYP2
体内研究(In Vivo)
Mephenytoin (orally administration, 100 mg/kg, 200 mg/kg) can reduce maternal weight gain and increase offspring mortality at 200 mg/kg but not produce excessive offspring mortality at 100 mg/kg in Pregnant Sprague-Dawley CD rats.
Mephenytoin (i.p., 20 mg/kg per day for 16 days) significantly reduces serum cholesterol and triglyceride levels in mice, which may have a hypolipidemic effect.
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
Powder -20°C 3 years;4°C 2 years
ClinicalTrial
参考文献
[1]. Klaassen T, et al. Assessment of urinary mephenytoin metrics to phenotype for CYP2C19 and CYP2B6 activity. Eur J Clin Pharmacol. 2008;64(4):387-398.
[2]. D R Minck, et al. Comparison of the behavioral teratogenic potential of phenytoin, mephenytoin, ethotoin, and hydantoin in rats. Teratology. 1991 Apr;43(4):279-93. 
溶解度数据
In Vitro: DMSO : 50 mg/mL (229.10 mM; Need ultrasonic and warming)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。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2