About: Ethosuximide     Goto   Sponge   Distinct   Permalink

An Entity of Type : http://linked.opendata.cz/ontology/drugbank/Drug, within Data Space : linked.opendata.cz associated with source document(s)

AttributesValues
rdf:type
http://linked.open...gbank/description
  • An anticonvulsant especially useful in the treatment of absence seizures unaccompanied by other types of seizures. [PubChem] (en)
http://linked.open...y/drugbank/dosage
http://linked.open...generalReferences
  • # Patsalos PN: Properties of antiepileptic drugs in the treatment of idiopathic generalized epilepsies. Epilepsia. 2005;46 Suppl 9:140-8. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/16302888 # Coulter DA, Huguenard JR, Prince DA: Specific petit mal anticonvulsants reduce calcium currents in thalamic neurons. Neurosci Lett. 1989 Mar 13;98(1):74-8. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/2710401 # Coulter DA, Huguenard JR, Prince DA: Characterization of ethosuximide reduction of low-threshold calcium current in thalamic neurons. Ann Neurol. 1989 Jun;25(6):582-93. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/2545161 # Coulter DA, Huguenard JR, Prince DA: Differential effects of petit mal anticonvulsants and convulsants on thalamic neurones: calcium current reduction. Br J Pharmacol. 1990 Aug;100(4):800-6. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/2169941 # Kostyuk PG, Molokanova EA, Pronchuk NF, Savchenko AN, Verkhratsky AN: Different action of ethosuximide on low- and high-threshold calcium currents in rat sensory neurons. Neuroscience. 1992 Dec;51(4):755-8. "Pubmed":http://www.ncbi.nlm.nih.gov/pubmed/1336826 (en)
http://linked.open...gy/drugbank/group
  • approved (en)
http://linked.open...drugbank/halfLife
  • 53 hours (en)
http://linked.open...ugbank/indication
  • For the treatment of petit mal epilepsy. (en)
http://linked.open...bank/manufacturer
sameAs
Title
  • Ethosuximide (en)
adms:identifier
http://linked.open...mechanismOfAction
  • Binds to T-type voltage sensitive calcium channels. Voltage-sensitive calcium channels (VSCC) mediate the entry of calcium ions into excitable cells and are also involved in a variety of calcium-dependent processes, including muscle contraction, hormone or neurotransmitter release, gene expression, cell motility, cell division and cell death. The isoform alpha-1G gives rise to T-type calcium currents. T-type calcium channels belong to the "low-voltage activated (LVA)" group and are strongly blocked by mibefradil. A particularity of this type of channels is an opening at quite negative potentials and a voltage-dependent inactivation. T-type channels serve pacemaking functions in both central neurons and cardiac nodal cells and support calcium signaling in secretory cells and vascular smooth muscle. They may also be involved in the modulation of firing patterns of neurons which is important for information processing as well as in cell growth processes. (en)
http://linked.open...drugbank/packager
http://linked.open.../drugbank/synonym
  • Ethosuximide (en)
  • Atysmal (en)
  • Thilopemal (en)
  • Aethosuximide (en)
  • Etosuximida (en)
  • (+-)-2-Ethyl-2-methylsuccinimide (en)
  • (±)-2-ethyl-2-methylsuccinimide (en)
  • 2-Methyl-2-ethylsuccinimide (en)
  • 2-ethyl-2-methylsuccinimide (en)
  • 3-Ethyl-3-methylsuccinimide (en)
  • 3-Methyl-3-ethylpyrrolidine-2,5-dione (en)
  • 3-Methyl-3-ethylsuccinimide (en)
  • 3-ethyl-3-methyl-2,5-pyrrolidinedione (en)
  • Ethosuximid (en)
  • Ethosuximidum (en)
  • alpha-Ethyl-alpha-methylsuccinimide (en)
  • alpha-Methyl-alpha-ethylsuccinimide (en)
  • gamma-Ethyl-gamma-methyl-succinimide (en)
  • gamma-Methyl-gamma-ethyl-succinimide (en)
  • γ-ethyl-γ-methyl-succinimide (en)
http://linked.open...drugbank/toxicity
  • Acute overdoses may produce nausea, vomiting, and CNS depression including coma with respiratory depression. (en)
http://linked.open.../drug/hasAHFSCode
http://linked.open...k/foodInteraction
  • Avoid alcohol. (en)
  • Take with food. (en)
http://linked.open...ynthesisReference
  • Miller, C.A. and Long, L.M.; U.S. Patent 2,993,835; July 25,1961; assigned to Parke, Davis and Company. (en)
foaf:page
http://linked.open...ugbank/IUPAC-Name
http://linked.open...gy/drugbank/InChI
http://linked.open...Molecular-Formula
http://linked.open.../Molecular-Weight
http://linked.open...noisotopic-Weight
http://linked.open...y/drugbank/SMILES
http://linked.open.../Water-Solubility
http://linked.open...ogy/drugbank/logP
http://linked.open...ogy/drugbank/logS
http://linked.open...l/drug/hasATCCode
http://linked.open...nd-Acceptor-Count
http://linked.open...-Bond-Donor-Count
http://linked.open...drugbank/InChIKey
http://linked.open...urface-Area--PSA-
http://linked.open...nk/Polarizability
http://linked.open...bank/Refractivity
http://linked.open...atable-Bond-Count
http://linked.open...ugbank/absorption
  • Bioavailability following oral administration is 93%. (en)
http://linked.open.../affectedOrganism
  • Humans and other mammals (en)
http://linked.open...casRegistryNumber
  • 77-67-8 (en)
http://linked.open...drugbank/category
  • (en)
http://linked.open...gbank/containedIn
http://linked.open...k/Bioavailability
http://linked.open...bank/Ghose-Filter
http://linked.open...nk/MDDR-Like-Rule
http://linked.open...ank/Melting-Point
http://linked.open...k/Number-of-Rings
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