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4-PO-DMT

Psilocybin
Kekulé, skeletal formula of canonical psilocybin
Spacefill model of canonical psilocybin
Names
IUPAC name
[3-(2-Dimethylaminoethyl)-1H-indol-4-yl] dihydrogen phosphate
Identifiers
3D model (Jmol)
273158
ChEBI
ChemSpider
ECHA InfoCard 100.007.542
EC Number 208-294-4
KEGG
MeSH Psilocybine
PubChem CID
RTECS number NM3150000
Pharmacology
Low
Oral, intravenous
Pharmacokinetics:
Hepatic
oral: 163±64 min
intravenous: 74.1±19.6 min
Renal
Legal status
Properties
C12H17N2O4P
Molar mass 284.25 g·mol−1
Melting point 220–228 °C (428–442 °F)
soluble
Solubility soluble in methanol
slightly soluble in ethanol
negligible in chloroform, benzene
Hazards
Lethal dose or concentration (LD, LC):
LD50 (median dose)
285 mg/kg (mouse, i.v.)
280 mg/kg (rat, i.v.)
12.5 mg/kg (rabbit, i.v.)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY  (what is YesYN ?)
Infobox references

Psilocybin (/ˌsɪləˈsbɪn/ SIL-ə-SY-bin) is a naturally occurring psychedelic compound produced by more than 200 species of mushrooms, collectively known as psilocybin mushrooms. The most potent are members of the genus Psilocybe, such as P. azurescens, P. semilanceata, and P. cyanescens, but psilocybin has also been isolated from about a dozen other genera. As a prodrug, psilocybin is quickly converted by the body to psilocin, which has mind-altering effects similar, in some aspects, to those of LSD, mescaline, and DMT. In general, the effects include euphoria, visual and mental hallucinations, changes in perception, a distorted sense of time, and spiritual experiences, and can include possible adverse reactions such as nausea and panic attacks.


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Wikipedia

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