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Ibogaine

anti-addictive

Ibogaine ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Ibogaine ballicule

What it isIboga alkaloid with NMDA antagonism, kappa agonism and SERT inhibition; unapproved treatment for opioid dependence.

Why this oneA single dose is reported to interrupt withdrawal and craving, which no approved agent does.

What limits it⚑ Fatal arrhythmias from QT prolongation have occurred in unmonitored clinic settings. Not approved anywhere in the US.

Ibogaine molecular structure (skeletal formula)
Molecular structure: Ibogaine

FDA-approved for

Off-label

NO BOXED WARNINGS

Principal risk⚑ Fatal arrhythmias from QT prolongation have occurred in unmonitored clinic settings

Classes and tags

Clinical profile

Therapeutic safety burden4 / 4
Overdose danger3 / 4
QT / Torsades4 / 4
Direct muscarinic antagonism0 / 4

Defining liabilityMarked QT prolongation, proarrhythmia and severe ataxia

Serotonin and MAOI

Provisional washout figures

SRI significance1 / 4
Serotonin release0 / 4

Elevating mechanismSRI (noncompetitive)

Evidence confidenceModerate

InterpretationA confirmed but atypical SERT inhibitor: cryo-EM shows binding at the central site with the extracellular gate closed, competitive with SSRIs for binding yet NONcompetitive for transport, trapping the transporter inward-open. Weak -- less potent than S-citalopram or cocaine -- but real, with in vivo 5-HT increases and a stated serotonin-toxicity concern alongside other serotonergic agents.

Active metabolites

Open Ibogaine in the interactive console ↗