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苯妥英 /Phenytoin {[allProObj[0].p_purity_real_show]}

货号:A140185 同义名: 5,5-二苯基乙内酰脲 / 5,5-Diphenylhydantoin;NSC 8722

Phenytoin is an inactive voltage-gated sodium channel stabilizer.

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Phenytoin 化学结构 CAS号:57-41-0
Phenytoin 化学结构
CAS号:57-41-0
Phenytoin 3D分子结构
CAS号:57-41-0
Phenytoin 化学结构 CAS号:57-41-0
Phenytoin 3D分子结构 CAS号:57-41-0
规格 价格 会员价 库存 数量
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Phenytoin 纯度/质量文件 产品仅供科研

货号:A140185 标准纯度: {[allProObj[0].p_purity_real_show]}
批次查询: 批次纯度:

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产品名称 Sodium Channel 其他靶点 纯度
Tolperisone HCl 99%
Lamotrigine 98%
Vinpocetine 98%
Zonisamide 98%
Dronedarone Hydrochloride 95%
Procainamide hydrochloride 99%
Bupivacaine HCl 99+%
Benzocaine 98%
Carbamazepine ++

Sodium channel, IC50: 131 μM

98%
Quinidine sulfate dihydrate 98%
Ibutilide fumarate 99%+
Dibucaine HCl 99+%
Mexiletine HCl 99%
Phenytoin 99+%
Camostat Mesylate +++

epithelial sodium channel (ENaC), IC50: 50 nM

99%+
Levobupivacaine 97+%
Oxcarbazepine +

sodium channel, IC50: 160 μM

98%
Ambroxol 98+%
Primidone 99%
Propafenone 99%
A-803467 ++++

Na(V1.8) channel, IC50: 8 nM

99%+
Rufinamide 99%
Phenytoin sodium 98%
Proparacaine Hydrochloride +

Voltage-gated sodium channel, ED50: 3.4 mM

98+%
Riluzole 97%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Phenytoin 生物活性

靶点
  • Sodium Channel

描述 Phenytoin (5,5-Diphenylhydantoin) is a potent blocker of Voltage-gated Na+ channels (VGSCs). It is noted for its antiepileptic properties and its ability to reduce breast tumor growth and metastasis in mice[1].[2].
体内研究

In a specific study, Phenytoin (60 mg/kg; daily; for 28 days) was shown to decrease tumor growth in six-week-old female Rag2-/- Il2rg-/- mice implanted with MDA-MB-231 cells[1].

体外研究

As an antiepileptic medication, Phenytoin is effective in managing partial seizures and generalized tonic-clonic seizures, although it is not suitable for primary generalized seizures such as absence seizures or myoclonic seizures. Its mechanism involves a voltage-dependent blockade of voltage-gated sodium channels, which helps to prevent seizure activity[2].

Phenytoin exhibits low affinity for sodium channels that are in a resting state at hyperpolarized membrane potentials[3].

Phenytoin 动物研究

Animal study 牙龈增生模型
动物:BALB/cByJ小鼠,雄性,8周龄
给药:30 mg /kg,微渗透泵,0.5 μ L /h,2周。

Phenytoin 参考文献

[1]Michaela Nelson, et al. The sodium channel-blocking antiepileptic drug phenytoin inhibits breast tumour growth and metastasis. Mol Cancer. 2015 Jan 27;14(1):13.

[2]Rogawski, M.A. and W. Loscher, The neurobiology of antiepileptic drugs. Nat Rev Neurosci, 2004. 5(7): p. 553-64.

[3]Porter, R.J., et al., Mechanisms of action of antiseizure drugs. Handb Clin Neurol, 2012. 108: p. 663-81.

Phenytoin 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.96mL

0.79mL

0.40mL

19.82mL

3.96mL

1.98mL

39.64mL

7.93mL

3.96mL

Phenytoin 技术信息

CAS号57-41-0
分子式C15H12N2O2
分子量 252.268
别名 5,5-二苯基乙内酰脲 ;5,5-Diphenylhydantoin;NSC 8722;NCI-C55765;Lehydan;Hydantol;Diphenylhydantoin;Diphenylan;Diphenat;Diphedan;Dilabid;Dihycon;Di-Hydan
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Inert atmosphere,Store in freezer, under -20°C

溶解度

DMSO: 50 mg/mL(198.2 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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