Ethylone
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Routes of administration |
Oral, nasal, IV |
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Identifiers | |
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CAS Number | 1112937-64-0 N |
PubChem (CID) | 57252245 |
ChemSpider | 21106271 N |
UNII | L91C78FW96 N |
Chemical and physical data | |
Formula | C12H15NO3 |
Molar mass | 221.2524 g/mol |
3D model (Jmol) | Interactive image |
Chirality | Racemic mixture |
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NY (what is this?) (verify) |
Ethylone, also known as 3,4-methylenedioxy-N-ethylcathinone (MDEC, βk-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[edit]
Analysis of human and rat urine for the metabolites of bk-amphetamines suggested that ethylone was degraded in the following metabolic steps:[2]
- N-deethylation to the primary amine.
- Reduction of the keto moiety to the respective alcohol.
Legal Status[edit]
As of October 2015 Ethylone is a controlled substance in China.[3]
See also[edit]
References[edit]
- ^ a b Dayong Lee; Chris W. Chronister; Jennifer Hoyer; Bruce A. Goldberger (September 2015). "Ethylone-Related Deaths: Toxicological Findings". Journal of Analytical Toxicology. 39 (7): 567–571. doi:10.1093/jat/bkv053. PMID 26025164.
- ^ Meyer, Markus R; Jens Wilhelm; Frank T. Peters; Hans H. Maurer (June 2010). "Beta-keto amphetamines: studies on the metabolism of the designer drug mephedrone and toxicological detection of mephedrone, butylone, and methylone in urine using gas chromatography–mass spectrometry". Analytical and Bioanalytical Chemistry. 397 (3): 1225–1233. doi:10.1007/s00216-010-3636-5. PMID 20333362.
- ^ "关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and Drug Administration. 27 September 2015. Retrieved 1 October 2015.
External links[edit]
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