Difference between revisions of "Methoxetamine"
From Self-sufficiency
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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 | ||
+ | | smiles = O=C1CCCCC1(NCC)c2cccc(c2)OC | ||
| bioavailability = | | bioavailability = | ||
| metabolism = | | metabolism = | ||
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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group|group]] on the [[phenyl]] [[functional group|ring]] and the ''N''-[[methyl]] group on the [[amine]] have been replaced by 3-[[methoxy]] and ''N''-[[ethyl]] groups, respectively.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 | + | '''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group|group]] on the [[phenyl]] [[functional group|ring]] and the ''N''-[[methyl]] group on the [[amine]] have been replaced by 3-[[methoxy]] and ''N''-[[ethyl]] groups, respectively.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 08:07, 20 September 2010
Not to be confused with methoxamine.
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".]] |
Script error: No such module "collapsible list". |
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 It is an analogue of ketamine where the 2-chloro group on the phenyl ring and the N-methyl group on the amine have been replaced by 3-methoxy and N-ethyl groups, respectively.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
This article does not cite any references or sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (September 2010) |
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