- Ethylphenidate
drugbox
IUPAC_name = ethyl 2-phenyl-2-piperidin-2-ylacetate
CAS_number = 57413-43-1
ATC_prefix =
ATC_suffix =
PubChem = 3080846
DrugBank =
C=15|H=21|N=1|O=2
molecular_weight = 247.33274 g/mol
smiles = CCOC(=O)C(C1CCCCN1)C2=CC=CC=C2
bioavailability = Variable
protein_bound = Unknown
metabolism = Hepatic transesterification of prodrugs methylphenidate and ethanol
elimination_half-life = Dependent onmethylphenidate administrationMarkowitz JS, DeVane CL, Boulton DW, Nahas Z, Risch SC, Diamond F, Patrick KS. Ethylphenidate formation in human subjects after the administration of a single dose of methylphenidate and ethanol. "Drug Metabolism and Disposition". 2000 Jun;28(6):620-4.]
excretion =Urine
pregnancy_AU =
pregnancy_US =
pregnancy_category=
legal_AU =
legal_CA =
legal_UK =
legal_US =
legal_status = Presumably Controlled in the US
routes_of_administration = N/AEnantiomer ic (dl)-"threo"-Ethylphenidate is a potent psychostimulant that acts as both adopamine reuptake inhibitor andnorepinephrine reuptake inhibitor , meaning it effectively boosts the levels of thenorepinephrine anddopamine neaurotransmitters in the brain, by binding to, and partially blocking the transporterprotein s that normally remove thosemonoamine s from thesynaptic cleft . It is formed when ethanol andmethylphenidate are coingested, via hepatictransesterification . Ethylphenidate formation appears to be more common when large quantities of methylphenidate and alcohol are consumed at the same time, such as in abuse oroverdose scenarios. [Markowitz JS, Logan BK, Diamond F, Patrick KS. Detection of the novel metabolite ethylphenidate after methylphenidate overdose with alcohol coingestion. "Journal of Clinical Psychopharmacology". 1999 Aug;19(4):362-6.] Thiscarboxylesterase -dependent transesterification process is also known to occur whencocaine and alcohol are consumed together, formingcocaethylene . [Bourland JA, Martin DK and Mayersohn M (1997) Carboxylesterase transesterification of meperidine (Demerol) and methylphenidate (Ritalin) in the presence of [2H6] ethanol: Preliminary in vitro findings using a rat liver preparation. J Pharm Sci 86: 1494-1496]Ethylphenidate is more selective to the
dopamine transporter (DAT) than methylphenidate, having approximately the same efficacy as the parent compound, [Patrick KS, Williard RL, VanWert AL, Dowd JJ, Oatis JE Jr, Middaugh LD. Synthesis and pharmacology of ethylphenidate enantiomers: the human transesterification metabolite of methylphenidate and ethanol. "Journal of Medicinal Chemistry". 2005 Apr 21;48(8):2876-81.] but has significantly less activity on thenorepinephrine transporter (NET). [Williard RL, Middaugh LD, Zhu HJ, Patrick KS. Methylphenidate and its ethanol transesterification metabolite ethylphenidate: brain disposition, monoamine transporters and motor activity. "Behavioural Pharmacology". 2007 Feb;18(1):39-51.] It has nearly a identical dopaminergic pharmacodynamic profile as methylphenidate, possessing appreciable affinity for the inhibitory G protein-coupled dopamine subtype-2 receptors in thestriatum and mesolimbic regions of the brain, [Schweri MM, Skolnick P, Rafferty MF, Rice KC, Janowsky AJ and Paul SM (1985) [3H] Threo-(±)-methylphenidate binding to 3,4-dihydroxyphenylethylamine uptake sites in corpus striatum: Correlation with the stimulant properties of ritalinic acid esters. J Neurochem 45: 1062-1070] including thenucleus accumbens , [Volkow ND, Ding Y-S, Wang G-L, Logan J, Gatley JS, Dewey S, Ashby C, Lieberman J, Hitzemann R and Wolf AP (1995) Is methylphenidate like cocaine? Studies on their pharmacokinetics and distribution in the human brain. Arch Gen Psychiatry 52: 456-463] which is primarily responsible for its pro-euphorant and reinforcing effects. [Jatlow P, Elsworth JD, Bradberry CW, Winger G, Taylor JR, Russell R and Roth RH (1991) Cocaethylene: A neuropharmacologically active metabolite associated with concurrent cocaine-ethanol ingestion. Life Sci 48: 1787-1794]References
ee also
*
Cocaethylene (compound formed whencocaine andethanol are taken together)
*Methylphenidate
*Ethanol (drinking alcohol)
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