Elemicin
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General | |||||||||||||||||||
Surname | Elemicin | ||||||||||||||||||
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Molecular formula | C 12 H 16 O 3 | ||||||||||||||||||
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properties | |||||||||||||||||||
Molar mass | 208.25 g mol −1 | ||||||||||||||||||
Physical state |
liquid |
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Elemicin is a natural substance found in nutmeg ( Myristica fragrans ).
Like the related compounds safrole and myristicin also contained in nutmeg, elemicin also has a delirious hallucinogenic effect. In addition to nutmeg, about 2% of Elemicin is found in the Elemi tree resin from Canarium luzonicum .
The exact metabolism of elemicin in the body is not yet understood. The substance is thought to be metabolized to 3,4,5-trimethoxyamphetamine (TMA). TMA is very similar in structure to the alkaloid mescaline .
further reading
- E. Solheim and RR Scheline: Metabolism of alkenebenzene derivatives in the rat. III. Elemicin and isoelemicin. In: Xenobiotica 10, 1980, pp. 371-380. PMID 7415220 .
- M. De Vincenzi et al: Constituents of aromatic plants: elemicin. In: Fitoterapia 75, 2004, pp. 615-618. doi : 10.1016 / j.fitote.2004.05.003 , PMID 15351123 .
Individual evidence
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ^ MA Villanueva et al .: The Composition of Manila Elemi Oil. In: Flavor And Fragrance Journal 8, 1993, pp. 35-37. doi : 10.1002 / ffj.2730080107 .
- ↑ O. Sauer and S. Weilemann: Drugs: Properties, Effects, Intoxications. Schlütersche Verlagsanstalt, 2001, ISBN 3-87706-601-1 , p. 65.