3-HO-PCE
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3 sources
How the databases line up — = agree, ≈ partial, ≠ differ. In lists, shared items appear in every source and unique ones in only one (matched case-insensitively).
| PsychonautWiki | TripSit | Pharmacology | ||
|---|---|---|---|---|
| Classification | ||||
| Class / category | — | ≈ | ||
| Also known as | 3-HO-PCEHydroxyeticyclidine | 3hopce | — | ≈ |
| Safety | ||||
| Addiction potential | moderately addictive with a moderate potential for adverse side effects such as psychosis | — | — | |
| Toxicity | toxic dosage is unknown | — | — | |
| Dangerous interactions | — | — | ||
| Dose · Oral | ||||
| Threshold | 5 mg | — | — | |
| Light | 5–10 mg | 2–5 mg | — | ≠ |
| Common | 10–15 mg | 5–10 mg | — | ≠ |
| Strong | 15–25 mg | 10–15 mg | — | ≠ |
| Heavy | 25 mg+ | — | — | |
| Duration | ||||
| Onset | — | 20–40 minutes | — | |
| Total | 4–6 hours | 3–4 hours | — | ≠ |
| After-effects | — | 2 hours | — | |
| Pharmacology | ||||
| Receptor activity | — | — | Vasopressin V1a receptor | |
Dose at a glance
Each database's primary-route ladder on one shared scale — see where ranges line up or shift.
Duration at a glance
Total duration on one shared scale.
PsychonautWiki summary
Not to be confused with 3-HO-PCP. Summary sheet: 3-HO-PCE
TripSit summary
A rare and very potent PCP analogue, eight times more potent than PCP as NMDA receptor antagonist and also a μ-opioid receptor agonist. Similar in structure to methoxetamine.
Fact-sheets from PsychonautWiki. Harm-reduction reference only — not medical advice.