Substance

ID:703

Names and Identifiers
Synonyms
DisulfiramTetraethylthiuram DisulfideTETDTATDTetraethylthiuram SulfideTetraethylthiram DisulfideTetraethylthiram DisulphideTetraethylthiuramTTDUsaf B-33Tetraethylthioperoxydicarbonic DiamideDupon 4472Dupont Fungicide 4472Tetraethylthiuram DisulphideTetraethylthiuran DisulfideDisulfuramDisulphuram
IUPAC Traditional name
disulfiram
IUPAC name
N,N-diethyl[(diethylcarbamothioyl)disulfanyl]carbothioamide
Brand Name
AntabuseAntaethanAntetilAntivitiumCronetalDicupralEkagom TedsTeturamGababentinNoxalSuper RodiatoxTTSTenutexTetidisAnthethylAnti-EthylAntietanolBonibalContralinEkagom TetdsAbstinilAccel TetAntaenylAntetanAnteylTetraetilThioscabinThireranideTTS XEthyl TuexNocbinRefusalRo-SulfiramSanceler TetSanceler Tet-GDisulframEkagom DtetEkaland TetdEthyl ThiuradEthyl TuadsEthyl Tuads RodformAntaetilAntiaethanAnticolAverzanContrapotDisulfanAbstensilAccel Tet-RAkrochem TetdAncazide EtAntabusAntadixTiuramStopethylStopetyStopetylTetradinTetradineThiocidDisetilEphorranEtabusEthyl ThiudadEthyldithiurameEtyl TuexAntaethylAntalcolAntethylAntietilAntikolAversanAbstinylAlcophobinAlk-AubsSoxinol TetStopaethylTenuridTeturaminThiophosTillramHocaKrotenalNocceler TetNocceler Tet-GPerkacit TetdPerkait TetdEspenalEsperalEthyl ThiramEthyldithiourameExhoranExhorran
Registration numbers
CAS Number
PubChem CID
PubChem SID
Properties
Physical Property
Solubility
4.09 mg/L
Hydrophobicity(logP)
1.9
Molecule Details
Drug Groups
approved
Description
A carbamate derivative used as an alcohol deterrent. It is a relatively nontoxic substance when administered alone, but markedly alters the intermediary metabolism of alcohol. When alcohol is ingested after administration of disulfiram, blood acetaldehyde concentrations are increased, followed by flushing, systemic vasodilation, respiratory difficulties, nausea, hypotension, and other symptoms (acetaldehyde syndrome). It acts by inhibiting aldehyde dehydrogenase. [PubChem]
Indication
For the treatment and management of chronic alcoholism
Pharmacology
Disulfiram produces a sensitivity to alcohol which results in a highly unpleasant reaction when the patient under treatment ingests even small amounts of alcohol. Disulfiram blocks the oxidation of alcohol at the acetaldehyde stage during alcohol metabolism following disulfiram intake, the concentration of acetaldehyde occurring in the blood may be 5 to 10 times higher than that found during metabolism of the same amount of alcohol alone. Accumulation of acetaldehyde in the blood produces a complex of highly unpleasant symptoms referred to hereinafter as the disulfiram-alcohol reaction. This reaction, which is proportional to the dosage of both disulfiram and alcohol, will persist as long as alcohol is being metabolized. Disulfiram does not appear to influence the rate of alcohol elimination from the body. Prolonged administration of disulfiram does not produce tolerance; the longer a patient remains on therapy, the more exquisitely sensitive he becomes to alcohol.
Toxicity
LD50=8.6g/kg (orally in rats). Symptoms of overdose include irritation, slight drowsiness, unpleasant taste, mild GI disturbances, and orthostatic hypotension.
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic.
Absorption
Disulfiram is absorbed slowly from the gastrointestinal tract (80 to 90% of oral dose).
References
• Nash T, Rice WG: Efficacies of zinc-finger-active drugs against Giardia lamblia. Antimicrob Agents Chemother. 1998 Jun;42(6):1488-92. [Pubmed]
• Bouma MJ, Snowdon D, Fairlamb AH, Ackers JP: Activity of disulfiram (bis(diethylthiocarbamoyl)disulphide) and ditiocarb (diethyldithiocarbamate) against metronidazole-sensitive and -resistant Trichomonas vaginalis and Tritrichomonas foetus. J Antimicrob Chemother. 1998 Dec;42(6):817-20. [Pubmed]
• Gaval-Cruz M, Weinshenker D: mechanisms of disulfiram-induced cocaine abstinence: antabuse and cocaine relapse. Mol Interv. 2009 Aug;9(4):175-87. [Pubmed]
External Links
Molecular Spectra
No Data Available
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References
• Bouma MJ, Snowdon D, Fairlamb AH, Ackers JP: Activity of disulfiram (bis(diethylthiocarbamoyl)disulphide) and ditiocarb (diethyldithiocarbamate) against metronidazole-sensitive and -resistant Trichomonas vaginalis and Tritrichomonas foetus. J Antimicrob Chemother. 1998 Dec;42(6):817-20. Pubmed
• Gaval-Cruz M, Weinshenker D: mechanisms of disulfiram-induced cocaine abstinence: antabuse and cocaine relapse. Mol Interv. 2009 Aug;9(4):175-87. Pubmed
• Nash T, Rice WG: Efficacies of zinc-finger-active drugs against Giardia lamblia. Antimicrob Agents Chemother. 1998 Jun;42(6):1488-92. Pubmed