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Ethosuximide anticonvulsant

Ethosuximide Anticonvulsant used in absence seizures may block T-type Ca chaimels in... [Pg.555]

Succinimides. Ethosuximide [77-67-8] C2H22NO2 (41) and the related succinknide, methsuximide [77-41-8] C22H23NO2 (42) are used in absence seizure treatment. Like the other anticonvulsants discussed, the mechanism of action of the succinirnides is unclear. Effects on T-type calcium channels and -ATPase activity have been reported (20). Ethosuximide has significant CNS and gastrointestinal (GI) side effect HabiUties (13). [Pg.535]

The oxa2ohdinedione trimethadione [127-48-0] C H NO (50), at one time the dmg of choice for the treatment of absence sei2ures, has been replaced by ethosuximide (41) and valproate (49). (50) has a distinct profile from that of phenytoin but causes photophobia and night blindness in approximately 30% of the patients taking it and has the CNS and sedative properties seen for other anticonvulsants together with moderate neutropenia, hepatitis, and skin rashes (13). Trimethadione does not appear to produce its effects via modulation of GABA-mediated responses. [Pg.537]

Ethoheptazine as analgesic, 1, 167 Ethosuximide as anticonvulsant, 1, 166 Ethoxzolamide as diuretic, 1, 173 Ethylamine, o-bromophenyl-indole synthesis from, 4, 322 Ethylamine, 2-thienyl-biological activity, 4, 911 Ethylamine, 3-thienyl-biological activity, 4, 912 Ethylene... [Pg.623]

Anxiolytics clonazepam, diazepam, temazepam, triazolam, alprazolam, midazolam, buspirone Anticonvulsants ethosuximide, carbamazepine Calcium channel blockers diltiazem, felodipine, nifedipine, verapamil... [Pg.93]

Ethosuximide is an anticonvulsant drug that is used in minor forms of epilepsy. It is also prescribed under the name aximide, suxilene, rontone, and pyknolepsinum. [Pg.128]

RPC has found use in the analysis of barbiturates including the determination of drugs taken in an overdose (332). Thiopental was determined using a mobile phase comprised of methanol-0.1% sodium citrate buffer, pH 6.5 (45 55) (333). Hydantoins, along with other species which have anticonvulsant activity, have been determined with barbiturates. These include phenytoin in the presence of phenobarbital and primidone (334,335) and the related anticonvulsants ethosuximide and carbamazepine (336). [Pg.144]

Whether there is any other connection between anticonvulsant activity and camosine s antiaging actions is obviously highly speculative. It may be relevant to note that epileptic seizures and a shortened life span, together with altered protein accumulation, are consequences of PIMT-deficiency in mice, while treatment with valproic acid, an anticonvulsant, partially suppresses these symptoms including effects on life span (Yamamoto et ah, 1998). Conversely, PIMT overexpression can increase life span of Drosophila (Bennet et ah, 2003). Furthermore, the chemistry of some anticonvulsants (ethosuximide) resembles quite closely the structure of the succinimide intermediate formed during both asparagine deamidation and PIMT-mediated repair of isoaspartate residues. One conjectures whether there are any relationships between these... [Pg.102]

Anticonvulsant Carbamazepine, ethosuximide, lamotrigine, mesantoin, phenytoin, trimefhadione, valproic acid... [Pg.416]

Carbamazepine also can induce the enzymes that metabolize other anticonvulsant drugs, including phenytoin, primidone, phenobarbital, valproic acid, clonazepam, and ethosuximide, and metabolism of other drugs the patient may be taking. Similarly, other drugs may induce metabolism of carbamazepine the end result is the same as for autoinduction, and the dose of carbamazepine must be readjusted. A common drug-drug interaction is between carbamazepine and the macrolide antibiotics erythromycin and trolean-domycin. After a few days of antibiotic therapy, symptoms of carbamazepine toxicity develop this is readily reversible if either the antibiotic or carbamazepine is discontinued. [Pg.379]

Oxidation Aliphatic Carbon Atoms. Oxidation at the terminal carbon atom of an alkyl substituent is co-oxidation oxidation of the carbon atom located second from the end is co-1 oxidation. Unless specifically catalyzed by an enzyme, co-1 oxidation tends to occur more frequently. The anticonvulsant drug ethosuximide is metabolized at both the CO and co-1 position. [Pg.147]

The first report of the preparation of the dialkyl succinimide (29-3) dates back to early in the twentieth cenmry. It is consequently surprising to note that it was introduced as an anticonvulsant, under the name ethosuximide, well after its more recently synthesized congeners. The synthetic route starting from methyl ethyl ketone generally follows that above with the exception of the use of ammonia in the last step. The compound thus differs as well by possessing a somewhat acidic imide proton [30]. [Pg.257]

Of the succinimide anticonvulsants, ethosuximide is particularly effective in the control of absence seizures. The main side effects of this drug are singultus (hiccups) and sedation at high doses. Hallucinations have also been reputed to occur. Ethosuximide has no beneficial effect in generalized... [Pg.309]

M. Giaccone, Effect of enzyme inducing anticonvulsants on ethosuximide pharmacokinetics in epileptic patients. Br. J. Clin. Pharmacol. 41 575-579, 1996. [Pg.365]

High Pressure Liquid Chromatography. In plasma or serum ethosuximide and other anticonvulsants, sensitivity about 2 pg/ ml, UV detection—J. A. Christofides and D. E. Fry, Clin. Chem.,... [Pg.600]

Most anticonvulsants are excreted in the breast milk in limited amounts, and their use is not generally a contraindication to breastfeeding. Barbiturates, ethosuximide, lamotrigine, and to a lesser extent carbamazepine and benzodiazepines can reach appreciable serum concentrations in breast-fed infants, who should be carefully observed. [Pg.289]

Mesuximide (A,2-dimethyl-2-phenylsuccmimide) is a suc-cinimide anticonvulsant with actions similar to those of ethosuximide. Its activity is mostly due to its main metabolite, A-desmethylmesuximide, which has a half-hfe of about 48 hours (1). [Pg.2267]

The mechanisms of action, metabolism, and the adverse effect of the primary anticonvulsant drugs j (phenytoin, carbamazepine, ethosuximide, valproic acid, and the barbiturates and benzodiazepines) i are discussed. i... [Pg.173]

Anticonvulsants Phenobarbitone, phenytoin primidone, ethosuximide and carbamazepine in serum Partition ODS-SIL-X-I Water/acetonitrile (83 17)... [Pg.220]


See other pages where Ethosuximide anticonvulsant is mentioned: [Pg.121]    [Pg.121]    [Pg.327]    [Pg.471]    [Pg.228]    [Pg.127]    [Pg.610]    [Pg.159]    [Pg.425]    [Pg.674]    [Pg.516]    [Pg.166]    [Pg.159]    [Pg.557]    [Pg.307]    [Pg.318]    [Pg.127]    [Pg.600]    [Pg.166]    [Pg.296]    [Pg.115]    [Pg.297]    [Pg.367]    [Pg.188]    [Pg.193]    [Pg.323]    [Pg.251]   
See also in sourсe #XX -- [ Pg.6 , Pg.265 , Pg.267 , Pg.297 , Pg.298 ]




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