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Contents

   



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1 See also  




2 References  













Norbaeocystin






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From Wikipedia, the free encyclopedia
  

Norbaeocystin
Skeletal formula of norbaeocystin
Space-filling model of the norbaeocystin molecule as a zwitterion
Clinical data
Routes of
administration		Oral
ATC code
  • none
Legal status
Legal status
Identifiers

  • 3-(2-ammonioethyl)-1H-indol-4-yl hydrogen phosphate

CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEBI
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC10H13N2O4P
Molar mass256.198 g·mol−1
3D model (JSmol)

  • NCCc1c[nH]c2cccc(OP(=O)(O)O)c12

  • InChI=1S/C10H13N2O4P/c11-5-4-7-6-12-8-2-1-3-9(10(7)8)16-17(13,14)15/h1-3,6,12H,4-5,11H2,(H2,13,14,15)

  • Key:IKQGYCWFBVEAKF-UHFFFAOYSA-N

  (verify)

Norbaeocystin is a psilocybin mushroom alkaloid and analogofpsilocybin. It is found as a minor compound in most psilocybin mushrooms together with psilocin, psilocybin, aeruginascin, and baeocystin, from which it is a derivative.[1][2]

Norbaeocystin is an N-demethylated derivative of baeocystin (itself an N-demethylated derivative of psilocybin), and a phosphorylated derivative of 4-hydroxytryptamine. The latter is notable as a positional isomer of serotonin, which is 5-hydroxytryptamine.

See also[edit]

References[edit]

  1. ^ Leung AY, Paul AG (October 1968). "Baeocystin and norbaeocystin: new analogs of psilocybin from Psilocybe baeocystis". Journal of Pharmaceutical Sciences. 57 (10): 1667–1671. doi:10.1002/jps.2600571007. PMID 5684732.
  • ^ Gotvaldová K, Borovička J, Hájková K, Cihlářová P, Rockefeller A, Kuchař M (November 2022). "Extensive Collection of Psychotropic Mushrooms with Determination of Their Tryptamine Alkaloids". International Journal of Molecular Sciences. 23 (22): 14068. doi:10.3390/ijms232214068. PMC 9693126. PMID 36430546.


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