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Ephenidine Facts

Dissociative; Diarylethylamine; NMDA receptor antagonist

Description

Ephenidine (N-ethyl-1,2-diphenylethylamine) — NEDPA, EPE — is a synthetic dissociative of the diarylethylamine class. It blocks glutamate signaling in the brain,[1] cutting off communication between brain regions and producing the dissociative state.

Subjective effects include dissociation, mood lift, physical energy, visual distortions, and cognitive disconnection. The experience is longer and more activating than ketamine — closer in character to PCP, with a warmth and stimulant drive that pure dissociatives lack.[2]

Addictive potential is assessed as highly probable; the class has been linked to 48 deaths globally, one-third involving no other substance.[3]safety citation needed The stimulant-dissociative dual action stacks cardiovascular strain, and opioid co-use adds fatal respiratory risk.[3]

Dose and durationby route · individual sensitivity varies

Oral(mg)
Threshold< 30 mgLight30 – 70 mgCommon70 – 100 mgStrong100 – 150 mgHeavy150+ mg

Starts in 10 – 30 minLasts 5 – 7 hoursAfter-effects 6 – 12 hours

Body and dependence

Acute toxicity
Moderate
Chronic toxicity
Moderate
Physical dependence
Low
Psychological dependence
Moderate
Withdrawal
None recorded
Compulsive redosing
High

Tolerance

Builds
Moderate
Fully resets after
10 days
Carries over to
ketamine; phencyclidine; methoxetamine; dextromethorphan; diphenidine; methoxphenidine

Effectslikely at a common dose

Perception
none likely · 20 possible, including Spatial disorientation, Vestibular distortion, Visual acuity suppression
Body
Motor control impairment; +28 possible, including Dizziness, Nystagmus (eye wobbles), Nausea
Thinking
none likely · 26 possible, including Cognitive impairment, Confusion, Memory suppression
Feeling
none likely · 7 possible, including Anxiety, Emotional lability, Dysphoria
Self
none likely · 9 possible, including Depersonalization, Derealization, Social disconnection
Time
none likely · 5 possible, including Temporal disorientation

Who shouldn't take it

Absolute
Cardiovascular disease; Psychotic disorders; Pregnancy; MAO inhibitor therapy
Relative
Bipolar disorder; Renal impairment

Combinations61 recorded

Lethal (1)
GHB, GBL
Dangerous (35)
Amphetamines; Benzodiazepines; Benzodiazepines, Barbiturates; Buprenorphine, Kratom; Ephedrine, Pseudoephedrine; MAOIs; Naltrexone; NSAIDs; Stimulants; Alpha-2 adrenergic receptor antagonist; Anticholinergics; Antihistamines; Antipsychotics; Caffeine; Clonidine, Guanfacine; Dopamine agonists; Gabapentin, Pregabalin; GHB, Baclofen; Ibogaine; Ketamine, DXM, PCP; Lithium; Local anesthetics; MDMA, Amphetamines; MDMA, MDA; and 11 more, see full page
Caution (23)
See full page: psychedex.org/substances/ephenidine
Not graded (2)
Not listed never means safe.

Seek help immediately if

  • Severe disorientation; unable to move or speak (deep dissociation / "k-hole")
  • Complete loss of coordination — cannot stand or walk safely
  • Vomiting while incapacitated (choking / aspiration risk)
  • Very high blood pressure; fast heart rate
  • Slow or shallow breathing at high doses (especially mixed with depressants)
  • Unconsciousness; rarely, seizures

What to do

  1. Move them somewhere safe, away from stairs, water, roads, and sharp edges — they cannot protect themselves
  2. Place in the recovery position if vomiting or unconscious (aspiration is a key risk)
  3. Stay with them and reassure calmly; keep the environment quiet
  4. If breathing is slow/shallow or they are unresponsive, call emergency services
  5. Do not let them wander; do not leave them alone
  6. Be ready to give rescue breaths / CPR

Effects wear off with time in a safe, monitored setting. The main dangers are physical injury and aspiration while incapacitated, and respiratory depression when combined with other depressants — not the dissociation itself.

988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE

Version r1 · Not medical advice

References

  1. [1]
    ^Kang H, Park P, Bortolotto ZA, Brandt SD, Colestock T, Wallach J, Collingridge GL, Lodge D (2017) Ephenidine: A new psychoactive agent with ketamine-like NMDA receptor antagonist properties — Neuropharmacology doi:10.1016/j.neuropharm.2016.08.004
  2. [2]
    ^Eiden C, Leone-Burgos S, Serre A, Carton L, Gerardin M, Le Boisselier R, Gibaja V, Monzon E, Fouilhe N, Boucher A, Peyriere H (2018) Ephenidine, diphenidine, and methoxphenidine complications reported to the French Addictovigilance Network — Fundamental & Clinical Pharmacology doi:10.1111/fcp.12395
  3. [3]
    ^abCorkery JM, Copeland C, Schifano F (2025) Deaths related to the use of diarylethylamines, with a focus on the United Kingdom: A systematic review and case series report — Journal of Psychopharmacology doi:10.1177/02698811251349203
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