Deschloroketamine: Difference between revisions
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==Chemistry== | ==Chemistry== | ||
Deschloroketamine, or 2-Phenyl-2-(methylamino)cyclohexanone, is classed as an [[arylcyclohexylamine]] drug. | Deschloroketamine, or 2-Phenyl-2-(methylamino)cyclohexanone, is classed as an [[arylcyclohexylamine]] drug. Arylcyclohexylamine drugs are named for their structures which include a cyclohexane ring bound to an aromatic ring along with an amine group. Descholoroketamine contains a phenyl ring bonded to a cyclohexane ring substituted with an oxo group (cyclohexanone). An amino methyl chain (-N-CH<sub>3</sub>) is bound to the adjacent alpha carbon (R<sub>2</sub>) of the cyclohexanone ring. | ||
Descholoroketamine is a chiral molecule and is often produced as a racemate. Des- is a prefix used in chemistry to denote the absence of a functional group (in this case "chloro") hence deschloroketamine is named for lacking a chlorine substitution on its phenyl ring, which is found in ketamine. | Descholoroketamine is a chiral molecule and is often produced as a racemate. Des- is a prefix used in chemistry to denote the absence of a functional group (in this case "chloro") hence deschloroketamine is named for lacking a chlorine substitution on its phenyl ring, which is found in ketamine. |