Phenytoin sodium

本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断

苯妥英钠是一种无活性的电压门控钠通道稳定剂。

Phenytoin sodium is an inactive voltage-gated sodium channel stabilizer. (In Vitro):Phenytoin sodium is an antiepileptic drug. It is useful to treat partial seizures and generalized tonic-clonic seizures but not primary generalized seizures such as absence seizures or myoclonic seizures. Phenytoin is believed to protect against seizures by causing voltage-dependent block of voltage-gated sodium channels.Phenytoin has low affinity for resting sodium channels at hyperpolarized membrane potentials.When neurons are depolarized and the channels transition into the open and inactivated states, greater binding and block occur. The inhibitory potency is strongly use dependent, so that block accumulates with prolonged or repetitive activation, such as occurs during a seizure discharge. The blocking of sodium channels by phenytoin is of slow onset. The time course of fast sodium currents is therefore not altered in the presence of the drug and action potentials evoked by synaptic depolarizations of ordinary duration are not blocked. Thus phenytoin is able to selectively inhibit pathological hyperexcitability in epilepsy without unduly impairing ongoing activity. Phenytoin also blocks persistent sodium current and this may be of particular importance in seizure control. Phenytoin is a class 1b antiarrhythmic.

Phenytoin sodium is an antiepileptic drug. It is useful to treat partial seizures and generalized tonic-clonic seizures but not primary generalized seizures such as absence seizures or myoclonic seizures. Phenytoin is believed to protect against seizures by causing voltage-dependent block of voltage-gated sodium channels. Phenytoin has low affinity for resting sodium channels at hyperpolarized membrane potentials. When neurons are depolarized and the channels transition into the open and inactivated states, greater binding and block occur. The inhibitory potency is strongly use dependent, so that block accumulates with prolonged or repetitive activation, such as occurs during a seizure discharge. The blocking of sodium channels by phenytoin is of slow onset. The time course of fast sodium currents is therefore not altered in the presence of the drug and action potentials evoked by synaptic depolarizations of ordinary duration are not blocked. Thus phenytoin is able to selectively inhibit pathological hyperexcitability in epilepsy without unduly impairing ongoing activity. Phenytoin also blocks persistent sodium current and this may be of particular importance in seizure control. Phenytoin is a class 1b antiarrhythmic.

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Phenytoin Sodium | Dilantin sodium | Diphenylhydantoin Sodium | 5,5-Diphenylhydantoin sodium salt | Diphantoine

Membrane Transporter/Ion Channel

Sodium Channel

Sodium Channel

Neurological Disease

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630-93-3

274.25

C15H11N2NaO2

>98% (HPLC)

Ethanol: 11 mg/mL (40.1 mM); Water: 3 mg/mL (10.93 mM); DMSO: 32 mg/mL (116.68 mM)

O=C1NC(=O)C(N1)(C1=CC=CC=C1)C1=CC=CC=C1

sodium;5,5-diphenylimidazolidin-3-ide-2,4-dione

(-20℃)

With Ice Pack

≥ 2 years