Phenytoin
For Laboratory Research Only. Not for Clinical or Personal Use.
- Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
- Dry Ice Shipment: No


Phenytoin
Description :
Phenytoin (5,5-Diphenylhydantoin) is a potent Voltage-gated Na+ channels (VGSCs) blocker. Phenytoin has antiepileptic activity and reduces breast tumour growth and metastasis in mice[1][2].Product Name Alternative :
5,5-DiphenylhydantoinUNSPSC :
12352005Hazard Statement :
H302, H351, H360Target :
Sodium Channel; Virus ProteaseType :
Reference compoundRelated Pathways :
Anti-infection; Membrane Transporter/Ion ChannelApplications :
Neuroscience-NeuromodulationField of Research :
Neurological Disease; CancerAssay Protocol :
https://www.medchemexpress.com/phenytoin.htmlPurity :
99.95Solubility :
DMSO : 50 mg/mL (ultrasonic)Smiles :
O=C1NC(C(C2=CC=CC=C2)(C3=CC=CC=C3)N1)=OMolecular Formula :
C15H12N2O2Molecular Weight :
252.27Precautions :
H302, H351, H360References & Citations :
[1]Rogawski, M.A. and W. Loscher, The neurobiology of antiepileptic drugs. Nat Rev Neurosci, 2004. 5 (7) : p. 553-64.|[2]Porter, R.J., et al., Mechanisms of action of antiseizure drugs. Handb Clin Neurol, 2012. 108: p. 663-81.|[3]Balaji, S., Medical therapy for sudden death. Pediatr Clin North Am, 2004. 51 (5) : p. 1379-87.|[4]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.|[5]Assaggaf MA, et al. Prevention of phenytoin-induced gingival overgrowth by lovastatin in mice. Am J Pathol. 2015 Jun;185 (6) :1588-99.Shipping Conditions :
Room TemperatureStorage Conditions :
-20°C, 3 years; 4°C, 2 years (Powder)Scientific Category :
Reference compound1Clinical Information :
LaunchedCitation 01 :
Cell Rep Methods. 2023 Oct 23;3 (10) :100599.|Oxid Med Cell Longev. 2022 Mar 28;2022:8538296.|Regen Ther. 2023 Jul 6:24:201-210.|Int Immunopharmacol. 2023 Feb:115:109706.|University of Glasgow. School of Cancer Sciences.CAS Number :
[57-41-0]

