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🔗 MergedComparePsychonautWikiTripSitPharmacologyTiHKAL

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).

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PsychonautWikiTripSitPharmacologyTiHKAL
Classification
Class / category
Also known as
4-HO-MiPTMiprocin
4homipthomipt4-homiprocin
4-INDOLOL, 3-[2-(ISOPROPYLMETHYLAMINO)ETHYL]4-HYDROXY-N-ISOPROPYL-N-METHYLTRYPTAMINE3-[2-(ISOPROPYLMETHYLAMINO)ETHYL]-4-INDOLOL
Safety
Addiction potentialnot habit-forming
Toxicity
toxic dose is unknown
Dangerous interactions
Unsafe interactions
Dose · Oral
Threshold5 mg5 mg=
Light10–15 mg10–15 mg=
Common15–25 mg15–20 mg12–25 mg
Strong25–35 mg20–30 mg
Heavy35 mg+40 mg+
Duration
Onset15–45 minutes20–90 minutes
Total4–6 hours3–6 hours4–6 hours
After-effects2–12 hours1–8 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.

PsychonautWiki oral
TripSit Oral
TiHKAL oral
050 mg
LightCommonStrongHeavy

Duration at a glance

Total duration on one shared scale.

PsychonautWiki
4–6 hours
TripSit
3–6 hours
TiHKAL
4–6 hours

TripSit summary

A reasonably popular tryptamine deriviative and Psilocin analogue, first synthesised by Alexander Shulgin. It has been reported as having comparable effects to psychedelic mushrooms, though with a shorter duration.

TiHKAL summary

An orally active two-carbon relative of psilocin, with one comparison putting 20 milligrams on par with 50 milligrams of psilocin, though another trial with the acetate ester was much milder. Onset at higher doses came within the first half hour.

Fact-sheets from PsychonautWiki. Harm-reduction reference only — not medical advice.