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Phenacemide | CAS No: 63-98-9 | GMP-certified suppliers

A medication that controls refractory epilepsy by managing complex partial seizures through anticonvulsant effects within the central nervous system.

Therapeutic categories

AcetamidesAmidesAnticonvulsantsBenzene DerivativesCentral Nervous System DepressantsNervous System
Generic name
Phenacemide
Molecule type
small molecule
CAS number
63-98-9
DrugBank ID
DB01121
Approval status
Approved drug
ATC code
N03AX07

Primary indications

  • Used to control certain seizures in the treatment of epilepsy

Product Snapshot

  • Phenacemide is a small molecule formulated for oral administration
  • It is primarily indicated for the control of seizure activity in epilepsy management
  • Phenacemide holds approved status in key regulatory markets

Clinical Overview

Phenacemide (CAS Number 63-98-9) is an anticonvulsant agent utilized in the management of epilepsy, specifically for controlling certain seizure types. It is classified chemically as a phenylacetamide, which is a subclass of amide derivatives of phenylacetic acids. Clinically, phenacemide is indicated for patients with severe epilepsy, particularly those exhibiting mixed forms of complex partial seizures, including psychomotor or temporal lobe seizures, which are refractory to other anticonvulsant therapies.

Pharmacodynamically, phenacemide functions as a ureal anticonvulsant by increasing the seizure threshold. It elevates the threshold for minimal electroshock-induced convulsions and abolishes the tonic phase of maximal electroshock seizures. Additionally, phenacemide is effective in preventing or modifying seizures induced by chemical convulsants such as pentylenetetrazol.

The primary mechanism of action of phenacemide involves its interaction with neuronal ion channels. It binds to and blocks voltage-sensitive sodium channels and calcium channels in neurons. This inhibition decreases neuronal depolarization and reduces hypersynchronization of neuronal activity—a pathological process commonly underlying seizure generation.

Regarding absorption, distribution, metabolism, and excretion (ADME) properties, specific data are limited; however, as a central nervous system depressant, phenacemide crosses the blood-brain barrier to exert its therapeutic effect. Safety considerations include potential toxicity related to central nervous system depression, with particular attention required to avoid adverse effects in vulnerable populations. Due to its mechanism and side effect profile, phenacemide has been largely superseded by newer anticonvulsants but remains a reference compound in pharmacological contexts.

Phenacemide has historical usage in epilepsy treatment with limited current commercial presence. Notable brand names have largely been phased out in favor of agents with improved safety margins.

For sourcing and quality assurance of phenacemide as an active pharmaceutical ingredient, suppliers should provide comprehensive analytical data confirming identity, purity, and compliance with pharmacopeial standards. Given its central nervous system pharmacology and narrow therapeutic index, stringent quality control is essential to ensure consistent clinical performance and patient safety.

Identification & chemistry

Generic name Phenacemide
Molecule type Small molecule
CAS 63-98-9
UNII PAI7J52V09
DrugBank ID DB01121

Pharmacology

SummaryPhenacemide is an anticonvulsant agent that targets neuronal sodium channels and voltage-sensitive calcium channels to inhibit neuronal depolarization and hypersynchronization associated with seizure activity. It is used to manage severe epilepsy, particularly complex partial seizures refractory to other treatments. Phenacemide elevates seizure thresholds and suppresses both tonic and induced seizure phases through modulation of neuronal excitability.
Mechanism of actionPhenacemide binds to and blocks neuronal sodium channels or voltage sensitive calcium channels. This blocks or suppresses neuronal depolarization and hypersynchronization. Hypersynchronization is what often causes seizures.
PharmacodynamicsPhenacemide is a ureal anticonvulsant indicated for control of severe epilepsy, particularly mixed forms of complex partial (psychomotor or temporal lobe) seizures, refractory to other anticonvulsants. Phenacemide elevates the threshold for minimal electroshock convulsions and abolishes the tonic phase of maximal electroshock seizures. It also prevents or modifies seizures induced by pentylenetetrazol or other convulsants.
Targets
TargetOrganismActions
Sodium channel protein type 1 subunit alphaHumansinhibitor

ADME / PK

AbsorptionAlmost completely absorbed.
Half-life22-25 hours.
MetabolismMetabolized in the liver by hepatic microsomal enzymes, where it is inactivated by p-hydroxylation.

Formulation & handling

  • Phenacemide is a small molecule compound suitable for oral administration.
  • It exhibits moderate water solubility and low lipophilicity, facilitating formulation in aqueous media.
  • Co-administration with food may reduce gastrointestinal upset, although it can be taken without regard to meals.

Regulatory status

Safety

ToxicityOral, mouse: LD<sub>50</sub> = 987 mg/kg; Oral, rabbit: LD<sub>50</sub> = 2500 mg/kg; Oral, rat: LD<sub>50</sub> = 1600 mg/kg
High Level Warnings:
  • Handle with appropriate personal protective equipment to minimize inhalation and skin contact due to moderate oral toxicity
  • Avoid environmental release as compound may pose toxicity risks to wildlife based on animal LD₅₀ data
  • Store according to recommended conditions to maintain chemical stability and reduce degradation-related hazards