Substituted phenidates
Substituted phenidates (also known as phenidates) are a class of chemicals that include compounds that predominantly produce traditional stimulant effects when administered. They may be defined as esters of ritalinic acid and its analogs.

Chemistry
Substituted phenidates are a chemical class based upon the molecule methylphenidate. The molecular structure of methylphenidate is comprised of a phenethylamine core with a carbon chain substitution at the Rα position that links to the RN position, forming a piperidine ring. It also includes a substitution at the Rβ position of methyl acetate.
Pharmacology
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Substituted phenidates primarily act as reuptake inhibitors of the monoamine neurotransmitters dopamine, norepinephrine, and to a minor degree, serotonin.[citation needed]
List of substituted phenidates
Compound | R3 | R4 | RO | Structure |
---|---|---|---|---|
Methylphenidate | H | H | CH3 | |
Ethylphenidate | H | H | CH2CH3 | |
Isopropylphenidate | H | H | CH(CH3)2 | |
Propylphenidate | H | H | CH2CH2CH3 | |
4-Methylmethylphenidate | H | CH3 | CH3 | |
3,4-CTMP | Cl | Cl | CH3 | |
4F-MPH | H | F | CH3 | |
4F-EPH | H | F | CH2CH3 | |
Methylnaphthidate (HDMP-28) | CH=CH- | CH=CH- | CH3 | |
Ethylnaphthidate (HDEP-28) | CH=CH- | CH=CH- | CH2CH3 |