Substituted amphetamines

Revision as of 22:44, 26 October 2016 by >BronzeManul

Substituted amphetamines, also known as amphetamines, are a class of chemicals that include compounds with psychoactive effects.

General formula 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 phenidates, cathinones, MDxxs, DOxs, Benzofurans or aminoindanes, nor does it contain any of the DMA or TMA isomers.

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 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 CH2(CH3)2  
Lisdexamfetamine H H H H H H H H COCH(NH2)(CH2)4NH2  
Clobenzorex H H H H H H H H CH2C6H42Cl  
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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