Roidipedia.Compound reference & reporting
06 AUG 2026
CompoundsResearch chemical Troparil (beta-CPT / WIN 35065-2)
Research chemicalResearch chemicalDopamine reuptake inhibitorCocaine analoguePhenyltropane

Troparil (beta-CPT / WIN 35065-2)

Also known as Troparil · beta-CPT · WIN 35065-2

Troparil is a phenyltropane, a synthetic cocaine analogue developed as a research tool that acts as a potent, longer-lasting dopamine reuptake inhibitor. It has appeared on research-chemical markets as a cocaine-like stimulant, with extensive preclinical but essentially no human safety data.

01 Overview

Troparil (beta-CPT, WIN 35065-2) is one of the classic phenyltropanes synthesised to study the cocaine binding site at the dopamine transporter. Replacing cocaine's ester oxygen with a carbon makes it metabolically more stable and longer-acting.

There are no controlled human trials. Its pharmacology is well characterised in animals as a potent DAT inhibitor with cocaine-like reinforcing effects, predicting high abuse potential and cardiovascular risk in humans.

02 Mechanism

Potent dopamine (and norepinephrine) reuptake inhibitor; a phenyltropane cocaine analogue lacking the labile benzoyl ester.

03 Dosing

TierDoseRouteNotes
Common (approximate, anecdotal)5–20 mgOralPotent; no validated human dosing.

04 Effects

EffectMagnitudeEvidence
Potent stimulationCocaine-like euphoria and energy, longer-lasting; documented in animals, reported anecdotally in humans.StrongPreclinical
ReinforcementRobust self-administration in animal models predicts addictive potential.StrongPreclinical

05 Side effects

EffectSeverityFrequencyEvidenceCountermeasures
Cardiovascular toxicityTachycardia, hypertension and arrhythmia expected from potent stimulant action.SevereUnknown in humansUnconfirmed
Dependence and psychosis riskStrong reinforcement and dopaminergic drive risk dependence and paranoia.SevereUnknownUnconfirmed

07 References

Carroll FI et al. Phenyltropane dopamine transporter ligands (troparil/WIN 35065-2)Journal of Medicinal Chemistry

08 Discussion0 comments

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