| Weight | 406.242 g/mol |
|---|---|
| Formula | C16H13N2Na2O6P |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
Fosphenytoin sodium (92134-98-0)
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- Safety of fosphenytoin sodium (American Journal of Health-system Pharmacy, 1996)
- Stability of Fosphenytoin Sodium with Intravenous Solutions in Glass Bottles, Polyvinyl Chloride Bags, and Polypropylene Syringes (Annals of Pharmacotherapy, 1997)
- Population pharmacokinetics of phenytoin after intravenous administration of fosphenytoin sodium in pediatric patients, adult patients, and healthy volunteers. (European Journal of Clinical Pharmacology, 2012)
- Pharmacokinetics of phenytoin following intravenous and intramuscular administration of fosphenytoin and phenytoin sodium in the rabbit. (European Journal of Drug Metabolism and Pharmacokinetics, 2002)
- Bioavailability of intravenous fosphenytoin sodium in healthy Japanese volunteers (European Journal of Drug Metabolism and Pharmacokinetics, 2013)
- Process for the preparation of sodium fosphenytoin (2005)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C2(C(=O)N(C(=O)N2)COP(=O)([O-])[O-])C3=CC=CC=C3.[Na+].[Na+]
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InChIKeyGQPXYJNXTAFDLT-UHFFFAOYSA-L
- Pubchem - Fosphenytoin sodium
- Wikipedia - fosphenytoin sodium
Fosphenytoin (fosphenytoin sodium, trade names Cerebyx, Parke-Davis; Prodilantin, Pfizer Holding France) is a water-soluble phenytoin prodrug that is administered intravenously to deliver phenytoin, potentially more safely than intravenous phenytoin. It is most commonly used in the acute treatment of convulsive status epilepticus. Fosphenytoin was developed in 1996.
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