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🔗 MergedComparePsychonautWikiTripSitPharmacology

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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PsychonautWikiTripSitPharmacology
Classification
Class / category
Also known as
mCPP
Safety
Dangerous interactions
Unsafe interactions
Dose · Oral
Threshold15 mg
Light20–50 mg
Common50–120 mg
Strong120–150 mg
Heavy150 mg+
Duration
Onset20–60 minutes
Pharmacology
Receptor activity
5-hydroxytryptamine receptor 1B5-hydroxytryptamine receptor 2C5-hydroxytryptamine receptor 2B5-hydroxytryptamine receptor 1ASerotonin 1 (5-HT1) receptor5-hydroxytryptamine receptor 2ASerotonin 2 (5-HT2) receptorSerotonin 3 (5-HT3) receptor5-hydroxytryptamine receptor 7Adrenergic receptor alpha-1Sodium-dependent serotonin transporterD(1A) dopamine receptorD(2) dopamine receptor5-hydroxytryptamine receptor 6Sigma non-opioid intracellular receptor 15-hydroxytryptamine receptor 5A
Half-lifeGroups of 5 male Wistar rats were dosed orally with 5 mg/kg of either (14)C-Mecoprop-P-EHE (radiochemical purity: 99.6%, spec. act.: 145.37 uCi/mg) (Groups A and C) or (14)C-Mecoprop-P-DMA (radiochemical purity (based on the acid): 99.8%, spec. act.: 114.79 uCi/mg) (Groups B and D). ... The half-life for elimination was 8.36 and 6.61 hours for Groups A and B, respectively. ... /In/ two cases of serious intoxication with phenoxy herbicides (MCPP) ... The plasma half-life was about 17 hr. MCPP plasma elimination probably follows first-order kinetics.

TripSit summary

A phenylpiperazine stimulant first developed in the 1970s before being sold in the RC market, often mislabelled as MDMA. Said to have very unpleasant effects such as anxiogenesis and headaches.

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