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Glutethimide

From Wikipedia, the free encyclopedia

Chemical structure of Glutethimide
Glutethimide
Systematic (IUPAC) name
3-ethyl-3-phenyl-piperidine-2,6-dione
Identifiers
CAS number 77-21-4
ATC code N05CE01
PubChem 3487
DrugBank N/A
Chemical data
Formula C13H15NO2 
Mol. mass 217.264 g/mol
Pharmacokinetic data
Bioavailability Variable
Metabolism Hepatic
Half life 10-12 hours
Excretion Renal:2%
Fecal:2%
Lactic (in lactiferous females)
Therapeutic considerations
Pregnancy cat.

C: (USA)

Legal status

Schedule II

Routes Oral

Glutethimide is a hypnotic sedative that was introduced in 1954 as a safe alternative to barbiturates to treat insomnia. Before long, however, it had become clear that glutethimide was just as likely to cause addiction and caused similarly severe withdrawal symptoms. It was originally a Schedule III drug in the United States under the Controlled Substances Act, but in 1991 it was upgraded to Schedule II more than a decade after recreational abusers discovered that combining the drug with codeine produced a euphoria which closely resembles that obtained from heroin. The street name for a combination of two doriden and four Codeine #4s a "load" or "doors and fours" . Glutethimide is a Schedule II drug under the Convention on Psychotropic Substances[1]. Doriden is the brand-name version of the drug, which is rarely prescribed today.

[edit] See also


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