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Phenytoin Sodium

Cat. No. M5876
Phenytoin Sodium Structure
Synonym:

Diphenylhydantoin Sodium

Size Price Availability Quantity
Free Sample (0.5-1 mg)  USD 0 In stock
500mg USD 55  USD55 In stock
1g USD 65  USD65 In stock
5g USD 100  USD100 In stock
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Quality Control & Documentation
Biological Activity

Phenytoin Sodium is a potent Voltage-gated Na+ channels (VGSCs) blocker. 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 has antiepileptic activity and reduces breast tumour growth and metastasis in mice.

Chemical Information
Molecular Weight 274.25
Formula C15H11N2NaO2
CAS Number 630-93-3
Solubility (25°C) DMSO 42 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Erenberk U, et al. Drug Chem Toxicol. Melatonin attenuates phenytoin sodium-induced DNA damage.

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Keywords: Phenytoin Sodium, Diphenylhydantoin Sodium supplier, Sodium Channel, inhibitors, activators


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