4-HO-DET
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4 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 | TiHKAL | ||
|---|---|---|---|---|---|
| Classification | |||||
| Class / category | — | — | ≈ | ||
| Also known as | 4-HO-DETEthocinCZ-74 | 4hodet4-hydroxy-det | — | 4-INDOLOL, 3-[2-(DIETHYLAMINO)ETHYL]N,N-DIETHYL-4-HYDROXYTRYPTAMINE3-[2-(DIETHYLAMINO)ETHYL]-4-INDOLOLCZ-744-HO-DET PHOSPHATE ESTER | ≠ |
| Safety | |||||
| Addiction potential | not habit-forming | — | — | — | |
| Toxicity | toxic dose is unknown | — | — | — | |
| Dangerous interactions | — | — | — | ||
| Unsafe interactions | — | — | — | ||
| Dose · Oral | |||||
| Threshold | 5 mg | — | — | — | |
| Light | 10–15 mg | 10–15 mg | — | — | = |
| Common | 20–30 mg | 15–20 mg | — | 10–25 mg | ≠ |
| Strong | 30–45 mg | 20–30 mg | — | — | ≠ |
| Heavy | 45 mg+ | — | — | — | |
| Duration | |||||
| Onset | 20–45 minutes | 30–60 minutes | — | — | ≠ |
| Total | 5–7 hours | 3–7 hours | — | 4–6 hours | ≠ |
| After-effects | 1–4 hours | 1–12 hours | — | — | ≠ |
| Pharmacology | |||||
| Receptor activity | — | — | Sodium/potassium-transporting ATPase subunit alpha-2/beta-3Sodium/potassium-transporting ATPase subunit alpha-2/beta-2Sodium/potassium-transporting ATPase subunit alpha-2/beta-1Sodium/potassium-transporting ATPase subunit alpha-1/beta-1 | — | |
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.
TripSit summary
A rare compound first produced by Albert Hoffman, also known as ethocin. Structurally related to 4-HO-MET (metocin) and psilocin (4-HO-DMT), this drug has similar psychedelic effects but little recorded human usage. Probably similar to mushrooms. Potentially stimulating.
TiHKAL summary
This diethyl relative of psilocin is described as a potent drug, and the author argues that, like psilocin and psilocybin, the phenol and its esters likely act on the brain as the same end product. Notably, certain mushroom species will enzymatically convert fed precursors into this non-natural compound.
Fact-sheets from PsychonautWiki. Harm-reduction reference only — not medical advice.