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ETHOSUXIMIDE

ETHOSUXIMIDE Structure
CAS No.
77-67-8
Chemical Name:
ETHOSUXIMIDE
Synonyms
Zarontin;h940;Suxin;ci366;H 940;H-490;Pemal;pm671;Asamid;CI-366
CBNumber:
CB1420630
Molecular Formula:
C7H11NO2
Molecular Weight:
141.17
MOL File:
77-67-8.mol
Modify Date:
2024/7/2 8:55:00

ETHOSUXIMIDE Properties

Melting point 51 °C
Boiling point 150 °C / 12mmHg
Density 1.1522 (rough estimate)
refractive index 1.5026 (estimate)
storage temp. 2-8°C
solubility ethanol: 100 mg/mL
pka pKa 9.5 (Uncertain)
form Solid
color White to Off-White
Water Solubility 190g/L(25 ºC)
Merck 14,3748
BCS Class 1,3
CAS DataBase Reference 77-67-8

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P501
Hazard Codes  Xn,T,F
Risk Statements  22-39/23/24/25-23/24/25-11
Safety Statements  36-45-36/37-16-7
WGK Germany  3
RTECS  WN2800000
HS Code  2925190100
Toxicity LD50 in mice (g/kg): 1.65 i.p.; 1.75 orally (Najer)
NFPA 704
0
1 0

ETHOSUXIMIDE price More Price(7)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) E7138 Ethosuximide 77-67-8 5G ₹8237.83 2022-06-14 Buy
Sigma-Aldrich(India) PHR1413 Ethosuximide Pharmaceutical Secondary Standard; Certified Reference Material 77-67-8 1G ₹30082.68 2022-06-14 Buy
Sigma-Aldrich(India) E7138 Ethosuximide 77-67-8 100G ₹38731.85 2022-06-14 Buy
Sigma-Aldrich 68459 Ethosuximide analytical standard 77-67-8 100MG ₹6365.1 2022-06-14 Buy
Sigma-Aldrich(India) 68459 Ethosuximide analytical standard 77-67-8 100MG ₹6365.1 2022-06-14 Buy
Product number Packaging Price Buy
E7138 5G ₹8237.83 Buy
PHR1413 1G ₹30082.68 Buy
E7138 100G ₹38731.85 Buy
68459 100MG ₹6365.1 Buy
68459 100MG ₹6365.1 Buy

ETHOSUXIMIDE Chemical Properties,Uses,Production

Chemical Properties

White to Off-White Solid

Uses

Ethosuximide is an anticonvulsant drug that is used in minor forms of epilepsy.

Definition

ChEBI: A dicarboximide that is pyrrolidine-2,5-dione in which the hydrogens at position 3 are substituted by one methyl and one ethyl group. An antiepileptic, it is used in the treatment of absence seizures and may be used for myoclonic seizures, but is ineffect ve against tonic-clonic seizures.

brand name

Epileo Petitmal (Eisai), Pemal (Benzon), Petnidan (Desitin Arzneimittel), Suxilep (Parke – Davis, Jenapharm), Suxinutin/Zarontin (Parke – Davis).

Biological Functions

It is now generally accepted that the specific antiepileptic action of ethosuximide (and the older agent trimethadione, no longer employed) against absence epilepsy is its ability to reduce the low-threshold calcium current (LTCC) or T (transient) current. These currents underlie the 3-Hz spike wave discharges that are characteristic of absence epilepsy. A blockade of T-calcium current is likely also to be a mechanism used by valproic acid.
The only clinical use for ethosuximide (Zarontin) is in the treatment of absence epilepsy. If absence attacks are the only seizure disorder present, ethosuximide alone is effective. If other types of epilepsy are present, ethosuximide can be readily combined with other agents.
For the most part, ethosuximide is a safe drug. Most of the side effects are dose related and consist of nausea, gastrointestinal irritation, drowsiness, and anorexia. A variety of blood dyscrasias have been reported, but serious blood disorders are quite rare.

General Description

Ethosuximide is considered the prototypical anticonvulsantneeded for treating patients with absence seizures.Ethosuximide and the N-dealkylated active metabolite ofmethsuximide work by blocking the lowthresholdT-type calcium channels, thereby reducing thehyperexcitability of thalamic neurons that is specifically associatedwith absence seizure.

Clinical Use

Although ethosuximide is the drug of choice for treatment of simple absence seizures, it is not effective against partial complex or tonic-clonic seizures and may increase the frequency of grand mal attacks. Thus, it must be administered in combination with other AEDs when treating persons with mixed seizure types. Ethosuximide is a substrate for both CYP3A4 and CYP2E1. The major metabolite for ethosuximide is 3-(1-hydroxyethyl) succinimide, which is inactive and excreted unconjugated into the urine Several additional metabolites have been characterized recently. Approximately 20% of an oral dose is excreted unchanged.
Although ethosuximide is thought to be the least toxic of the succinimides, it can cause gastrointestinal disturbances and dose-related CNS effects, such as drowsiness, dizziness, ataxia, sleep disturbances and depression. Idiosyncratic hypersensitivity reactions include severe rashes, leukopenia, agranulocytosis (some fatal), systemic lupus erythematosus, and parkinsonian-like symptoms. In addition to being less toxic than trimethadione, ethosuximide offers a wider range of protection against different kinds of absence seizures.

Global( 166)Suppliers
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career henan chemical co +86-0371-86658258 +8613203830695 China 29826 58 Inquiry

ETHOSUXIMIDE Spectrum

Suxilep Suximal Suxin Suxinutin Thetamid 2-Methyl-2-ethylsuccinimide 3-Methyl-3-ethylsuccinimide 3-ethyl-3-methyl-5-pyrrolidinedione 3-Ethyl-3-methylpyrrolidine-2,5-dione 3-Ethyl-3-methylpyrroline-2,5-dione 3-ethyl-3-methylsuccinimide 3-Methyl-3-ethylpyrrolidine-2,5-dione Aethosuximide alpha-Ethyl-alpha-methylsuccinimide alpha-methyl-alpha-ethylsuccinimide Asamid Atysmal C.I. 366 Capitus ci366 CI-366 Cl 366 CN-10,395 Emeside Epileo petit mal epileopetitmal Thilopemal Uritone Urodeine Zaraondan Zarodan Zarondan Zarondan-Saft Zartalin Succinimide, 2-ethyl-2-methyl- (6CI, 7CI, 8CI) α-Ethyl-α-methylsuccinimide α-Methyl-α-ethylsuccinimide 3-ethyl-3-methyl-pyrrolidine-2,5-quinone EthosuxiMide, USP Ethosuximide (500 mg) 3-Ethyl-3-Methyl- Ethosuximide solution ETHOSUXIMIDE 3-Ethyl-3-methyl-2,5-pyrrolidinedione 3-ethyl-3-methyl-2,5-pyrrolidine-dione 2-ETHYL-2-METHYLSUCCINIMIDE 2,5-Pyrrolidinedione, 3-ethyl-3-methyl- 2-ethyl-2-methyl-succinimid Ethosuccimide Ethosuccinimide Ethosuxide Ethymal Etomal Etosuximid Etosuximida gamma-Methyl-gamma-ethylsuccinimide gamma-methyl-gamma-ethyl-succinimide H 940