Substituted amphetamines

Revision as of 14:16, 28 January 2017 by >Kenan (Reverted edits by Kaylee (talk) to last revision by Clarity)

Substituted amphetamines are a family of modified amphetamine molecules that include compounds with psychoactive effects, which typically have classical stimulant but may also include entactogenic (e.g. MDA and MDMA) and psychedelic effects (e.g. DOx or TMA-6).

Generic structure of an amphetamine molecule

Chemistry

Substituted amphetamines are a chemical class based upon the molecule amphetamine. Amphetamine is made up of a phenethylamine molecule. The chemical structure of a substituted amphetamine is the same as the organic molecule amphetamine, except some substitutions are made at the phenyl and amine sites, typically of methyl and ethyl chains.

Pharmacology

The substituted amphetamine class of psychedelic, entactogenic and stimulant drugs works via their action upon numerous receptors. Psychedelic effects can be attributed to action on the 5-HT2A receptor. Entactogenic and stimulant effects are due to their action as releasing agents of serotonin, adrenaline and noradrenaline or as agonists on the receptors of the previous neurotransmitters. The agonism of this set of receptors leads to an increased rate firing of the post-synaptic neuron, triggering both cognitive and physical stimulation within the user.

List of substituted amphetamines

Note: This list does not include phenethylamines, phenidates, cathinones, MDxxs, DOxs, Benzofurans or aminoindanes.

Compound R2 R3 R4 R5 R6 Rα Rβ RN1 RN2 Structure
Amphetamine H H H H H H H H H  
Methamphetamine H H H H H H H H CH3  
Ethylamphetamine (Etilamfetamine) H H H H H H H H CH3  
Propylamphetamine H H H H H H H H CH2CH2CH3  
Isopropylamphetamine H H H H H H H H CH(CH3)2  
Bromo-DragonFLY OCH=CH- - Br OCH=CH- - H H H H  
Lisdexamfetamine H H H H H H H H COCH(NH2)(CH2)4NH2  
Clobenzorex H H H H H H H H CH2C6H4Cl  
Dimethylamphetamine H H H H H H H CH3 CH3  
Selegiline H H H H H H H CH3 CH2CCH  
Benzphetamine H H H H H H H CH3 CH2C6H5  
Ortetamine CH3 H H H H H H H H  
3-Methylamphetamine H CH3 H H H H H H H  
4-Methylamphetamine H H CH3 H H H H H H  
4-MMA H H CH3 H H H H H CH3  
Xylopropamine H CH3 CH3 H H H H H H  
β-methylamphetamine H H H H H H CH3 H H  
2-FA F H H H H H H H H  
2-FMA F H H H H H H H CH3  
3-FA H F H H H H H H H  
3-FMA H F H H H H H H CH3  
3-FEA H F H H H H H H CH2CH3  
4-FA H H F H H H H H H  
4-FMA H H F H H H H H CH3  
4-CA H H Cl H H H H H H  
4-BA H H Br H H H H H H  
4-IA H H I H H H H H H  
DCA H Cl Cl H H H H H H  
4-HA H H OH H H H H H H  
4-HMA H H OH H H H H H CH3  
3,4-DHA H OH OH H H H H H H  
OMA OCH3 H H H H H H H H  
3-MA H OCH3 H H H H H H H  
MMMA H OCH3 H H H H H H CH3  
MMA H OCH3 CH3 H H H H H H  
PMA H H OCH3 H H H H H H  
PMMA H H OCH3 H H H H H CH3  
PMEA H H OCH3 H H H H H CH2CH3  
4-ETA H H OCH2CH3 H H H H H H  
4-MTA H H SCH3 H H H H H H  
Cathine H H H H H H OH H H  

See also

References

 

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