| Weight | 284.252 g/mol |
|---|---|
| Formula | C12H17N2O4P |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 5 |
Psilocybine (520-52-5)
Psilocybin · Psilocibin
Score:
#568 in Neuroscience
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#2565 in Biology
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#3194 in Chemistry
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- Psilocybin induces schizophrenia-like psychosis in humans via a serotonin-2 agonist action (Neuroreport, 1998)
- Psilocybin can occasion mystical-type experiences having substantial and sustained personal meaning and spiritual significance (Psychopharmacology, 2006)
- Neural correlates of the psychedelic state as determined by fMRI studies with psilocybin (Proceedings of the National Academy of Sciences of the United States of America, 2012)
- Positron emission tomography and fluorodeoxyglucose studies of metabolic hyperfrontality and psychopathology in the psilocybin model of psychosis (Neuropsychopharmacology, 1997)
- Pilot Study of Psilocybin Treatment for Anxiety in Patients With Advanced-Stage Cancer (Archives of General Psychiatry, 2011)
- Mystical-type experiences occasioned by psilocybin mediate the attribution of personal meaning and spiritual significance 14 months later (Journal of Psychopharmacology, 2008)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Psilocybin
- Psilocibin
-
SMILESCN(C)CCC1=CNC2=C1C(=CC=C2)OP(=O)(O)O
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InChIKeyQVDSEJDULKLHCG-UHFFFAOYSA-N
- Pubchem - Psilocybine
- Wikipedia - psilocybine
Psilocybin ( sy-l-SY-bin) is a naturally occurring psychedelic prodrug compound produced by more than 200 species of mushrooms, collectively known as psilocybin mushrooms. Psilocybin evolved in mushrooms from its ancestor, muscarine, some 20 million years ago. 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.
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