Ethylone

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Ethylone
Bk-MDEA.svg
Systematic (IUPAC) name
(RS)-1-(1,3-benzodioxol-5-yl)-2-(ethylamino)propan-1-one
Clinical data
Pregnancy
category
  • N (US)
Legal status
Routes of
administration
Oral, nasal, IV
Identifiers
CAS Number 1112937-64-0 YesY
ChemSpider 21106271 N
Chemical data
Formula C12H15NO3
Molecular mass 221.2524 g/mol
  • CC(NCC)C(=O)c1ccc2OCOc2c1
  • InChI=1S/C12H15NO3/c1-3-13-8(2)12(14)9-4-5-10-11(6-9)16-7-15-10/h4-6,8,13H,3,7H2,1-2H3 N
  • Key:MJEMIOXXNCZZFK-UHFFFAOYSA-N N
 NYesY (what is this?)  (verify)

Ethylone, also known as 3,4-methylenedioxy-N-ethylcathinone (MDEC, bk-MDEA), is recreational designer drug classified as an entactogen, stimulant, and psychedelic of the phenethylamine, amphetamine, and cathinone chemical classes. It is the β-keto analogue of MDEA ("Eve"). Ethylone has only a short history of human use and is reported to be less potent than its relative methylone.[citation needed] In the United States, it began to be found in cathinone products in late 2011.[1]

Very little data exists about the pharmacological properties, metabolism, and toxicity of ethylone, but several ethylone-related deaths have been reported.[1]

Pharmacokinetics

Analysis of human and rat urine for the metabolites of bk-amphetamines suggested that ethylone was degraded in the following metabolic steps:[2]

  1. N-deethylation to the primary amine.
  2. Reduction of the keto moiety to the respective alcohol.

Legal Status

As of October 2015 Ethylone is a controlled substance in China.[3]

See also

References

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External links


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