Systematic (IUPAC) name | |
---|---|
5-phenyl-5-ethyl- 3-methylbarbituric acid |
|
Clinical data | |
AHFS/Drugs.com | International Drug Names |
MedlinePlus | a605022 |
Pregnancy cat. | ? |
Legal status | Schedule IV (US) |
Routes | ? |
Pharmacokinetic data | |
Bioavailability | ? |
Protein binding | 70-76% |
Metabolism | Hepatic |
Half-life | 34 hours |
Excretion | ? |
Identifiers | |
CAS number | 115-38-8 |
ATC code | N03AA01 |
PubChem | CID 8271 |
DrugBank | APRD00047 |
ChemSpider | 7972 |
UNII | 5NC67NU76B |
KEGG | D00700 |
ChEBI | CHEBI:6758 |
ChEMBL | CHEMBL45029 |
Chemical data | |
Formula | C13H14N2O3 |
Mol. mass | 246.3 g/mol |
SMILES | eMolecules & PubChem |
|
|
(verify) |
(what is this?)
Methylphenobarbital (INN), also known as mephobarbital (USAN, JAN) and mephobarbitone (BAN), marketed under brand names such as Mebaral, Mephyltaletten, Phemiton, and Prominal, is a drug which is a barbiturate derivative and is used primarily as an anticonvulsant, but also as a sedative and anxiolytic. It is the N-methylated analogue of phenobarbital and has similar indications, therapeutic value, and tolerability.
Contents |
Symptoms of overdose of mephobarbital include confusion, decrease in or loss of reflexes, somnolence, fever, irritability, hypothermia, poor judgment, shortness of breath or slow/troubled breathing, slow heartbeat, slurred speech, staggering, trouble in sleeping, unusual movements of the eyes, weakness.
Mephobarbital (5-ethyl-1-methyl-5-phenylbarbituric acid) is synthesized according to one of the diagrams used for the phenobarbital synthesis, except one uses methylurea instead.
|