Difference between revisions of "Methoxetamine"

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| C = 13 | H = 16 | Cl = 1 | N = 1 | O = 1
 
| C = 13 | H = 16 | Cl = 1 | N = 1 | O = 1
 
| molecular_weight        = 237.73 g/mol
 
| molecular_weight        = 237.73 g/mol
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| smiles                  = O=C1CCCCC1(NCC)c2cccc(c2)OC
 
| bioavailability          =
 
| bioavailability          =
 
| metabolism              =
 
| metabolism              =
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}}
 
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'''Methoxetamine''' is a novel [[designer drug]] of the [[arylcyclohexylamine]] class. It is an [[structural analog|analogue]] of [[ketamine]] where the 2-[[chloro]] [[functional group|group]] on the [[phenyl]] [[functional group|ring]] and the ''N''-[[methyl]] group on the [[amine]] have been replaced by 3-[[methoxy]] and ''N''-[[ethyl]] groups, respectively. Accordingly to anecdotal reports, in comparison to ketamine, methoxetamine is similarly [[dissociative]] but is much more [[euphoric]], while also having diminished [[side effect]]s such as [[confusion]], [[anxiety]], and [[motor dysfunction]].{{Citation needed|date=September 2010}}
+
'''Methoxetamine''' is a novel [[designer drug]] of the [[arylcyclohexylamine]] class. It is an [[structural analog|analogue]] of [[ketamine]] where the 2-[[chloro]] [[functional group|group]] on the [[phenyl]] [[functional group|ring]] and the ''N''-[[methyl]] group on the [[amine]] have been replaced by 3-[[methoxy]] and ''N''-[[ethyl]] groups, respectively. Accordingly to anecdotal reports, in comparison to ketamine, methoxetamine is similarly [[dissociative]] but more [[euphoric]], while also having diminished [[side effect]]s such as [[confusion]], [[anxiety]], and [[motor dysfunction]].{{Citation needed|date=September 2010}}  
  
 
==See also==
 
==See also==

Revision as of 09:07, 20 September 2010

Methoxetamine
File:Methoxetamine.png
Systematic (IUPAC) name
2-(3-methoxyphenyl)-2-(ethylamino)cyclohexanone
Identifiers
ATC code None
Chemical data
Formula C13H16ClNO
Molar mass 237.73 g/mol[[Script error: No such module "String".]]
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Methoxetamine is a novel designer drug of the arylcyclohexylamine class. It is an analogue of ketamine where the 2-chloro group on the phenyl ring and the N-methyl group on the amine have been replaced by 3-methoxy and N-ethyl groups, respectively. Accordingly to anecdotal reports, in comparison to ketamine, methoxetamine is similarly dissociative but more euphoric, while also having diminished side effects such as confusion, anxiety, and motor dysfunction.[citation needed]

See also

References

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External links