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Substituted phenidates: Difference between revisions

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>BronzeManul
Created page, addition of pharmacology would be appreciated
 
>Dextromethorphan
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! scope="col" | '''Structure'''
! scope="col" | '''Structure'''
|-
|-
| [[Methylphenidate]] || H || H || H || H || H || Methyl || [[File:Methyllphenidate.png|170px]]
| [[Methylphenidate]] || H || H || H || H || H || CH<sub>3</sub> || [[File:Methyllphenidate.png|170px]]
|-
|-
| [[Ethylphenidate]] || H || H || H || H || H || Ethyl || [[File:Ethyllphenidate.png|170px]]
| [[Ethylphenidate]] || H || H || H || H || H || CH<sub>2</sub>CH<sub>3</sub> || [[File:Ethyllphenidate.png|170px]]
|-
|-
| [[Isopropylphenidate]] || H || H || H || H || H || Isopropyl || [[File:Isopropylphenidate.png|170px]]
| [[Isopropylphenidate]] || H || H || H || H || H || CH(CH<sub>3</sub>)<sub>2</sub> || [[File:Isopropylphenidate.png|170px]]
|-
|-
| [[Propylphenidate]] || H || H || H || H || H || Propyl || [[File:Propylphenidate.png|170px]]
| [[Propylphenidate]] || H || H || H || H || H || CH<sub>2</sub>CH<sub>2</sub>CH<sub>3</sub> || [[File:Propylphenidate.png|170px]]
|-
|-
| [[3,4-CTMP]] || H || Cl || Cl || H || H || Methyl || [[File:34-ctmp.png|170px]]
| [[3,4-CTMP]] || H || Cl || Cl || H || H || CH<sub>3</sub> || [[File:34-ctmp.png|170px]]
|-
|-
| [[4F-MPH]] || H || H || F || H || H || Methyl || [[File:4-Fluoromethylphenidate.png|170px]]
| [[4F-MPH]] || H || H || F || H || H || CH<sub>3</sub> || [[File:4-Fluoromethylphenidate.png|170px]]
|-
|-
| [[4F-EPH]] || H || H || F || H || H || Ethyl || [[File:4F-EPH.png|170px]]
| [[4F-EPH]] || H || H || F || H || H || CH<sub>2</sub>CH<sub>3</sub> || [[File:4F-EPH.png|170px]]
|-
|-
| [[Methylnaphthidate]] || H || Benzene || Benzene || H || H || Methyl || [[File:Methylnaphthidate.png|170px]]
| [[Methylnaphthidate]] || H || CH=CH- || CH=CH- || H || H || CH<sub>3</sub> || [[File:Methylnaphthidate.png|170px]]
|-
|-
| [[Ethylnaphthidate]] || H || Benzene || Benzene || H || H || Ethyl || [[File:Ethylnaphthidate.png|170px]]
| [[Ethylnaphthidate]] || H || CH=CH- || CH=CH- || H || H || CH<sub>2</sub>CH<sub>3</sub> || [[File:Ethylnaphthidate.png|170px]]
|-
|-
|}
|}

Revision as of 06:17, 25 October 2016

General formula of a phenidate molecule.

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

Chemistry

Substituted phenidates are a chemical class based upon the molecule Methylphenidate. Methylphenidate is made up of a phenethylamine molecule with a carbon chain substitution at the Rα position that links to the RN position forming a piperidine ring, and a substitution at the Rβ position of methyl acetate.

List of substituted phenidates

Compound R2 R3 R4 R5 R6 RO Structure
Methylphenidate H H H H H CH3
Ethylphenidate H H H H H CH2CH3
Isopropylphenidate H H H H H CH(CH3)2
Propylphenidate H H H H H CH2CH2CH3
3,4-CTMP H Cl Cl H H CH3
4F-MPH H H F H H CH3
4F-EPH H H F H H CH2CH3
Methylnaphthidate H CH=CH- CH=CH- H H CH3
Ethylnaphthidate H CH=CH- CH=CH- H H CH2CH3

See also

Retrieved from "http://psy.st/w/index.php?title=Substituted_phenidates&oldid=71252"