Names | |
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IUPAC name
2-(2-Methoxyphenyl)-2-(methylamino)cyclohexanone
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Identifiers | |
3D model (
JSmol)
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ChemSpider | |
PubChem
CID
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UNII |
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CompTox Dashboard (
EPA)
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Properties | |
C14H19NO2 | |
Molar mass | 233.311 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
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Methoxyketamine or 2-MeO-2-deschloroketamine is a designer drug of the arylcyclohexylamine class first reported in 1963. [1] It is an analog of ketamine in which the chlorine atom has been replaced with a methoxy group. Its synthesis by rearrangement of an amino ketone has been reported. [2] As an arylcyclohexylamine, methoxyketamine most likely functions as an NMDA receptor antagonist. It produces sedative, hallucinogenic, and (at high doses) anesthetic effects, but with a lower potency than ketamine itself.
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This article about an organic compound is a stub. You can help Wikipedia by expanding it. |
Names | |
---|---|
IUPAC name
2-(2-Methoxyphenyl)-2-(methylamino)cyclohexanone
| |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
PubChem
CID
|
|
UNII |
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C14H19NO2 | |
Molar mass | 233.311 g·mol−1 |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Methoxyketamine or 2-MeO-2-deschloroketamine is a designer drug of the arylcyclohexylamine class first reported in 1963. [1] It is an analog of ketamine in which the chlorine atom has been replaced with a methoxy group. Its synthesis by rearrangement of an amino ketone has been reported. [2] As an arylcyclohexylamine, methoxyketamine most likely functions as an NMDA receptor antagonist. It produces sedative, hallucinogenic, and (at high doses) anesthetic effects, but with a lower potency than ketamine itself.
Psychedelics ( 5-HT2A agonists) |
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Dissociatives ( NMDAR antagonists) |
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Deliriants ( mAChR antagonists) |
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Others |
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This article about an organic compound is a stub. You can help Wikipedia by expanding it. |