Tabernanthin
Structural formula | |||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
![]() |
|||||||||||||
General | |||||||||||||
Surname | Tabernanthin | ||||||||||||
Molecular formula | C 20 H 26 N 2 O | ||||||||||||
External identifiers / databases | |||||||||||||
|
|||||||||||||
properties | |||||||||||||
Molar mass | 310.43 g mol −1 | ||||||||||||
Physical state |
firmly |
||||||||||||
Melting point |
211-212 ° C |
||||||||||||
safety instructions | |||||||||||||
|
|||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Tabernanthin is a chemical compound from the group of the apocynaceae alkaloids and iboga alkaloids and is structurally related to ibogaine .
Occurrence
Tabernanthin occurs naturally in plants such as Tabernanthe iboga and Tabernaemontana laurifolia , both representatives of the dog-poison family .
safety instructions
Tabernanthin has neurotoxic effects.
Individual evidence
- ↑ Burkhard Fugmann, Susanne Lang-Fugmann, Wolfgang Steglich: RÖMPP Encyclopedia Natural Products, 1st Edition, 2000 . Georg Thieme Verlag, 2014, ISBN 3-13-179311-2 , p. 309 ( limited preview in Google Book search).
- ↑ This substance has either not yet been classified with regard to its hazardousness or a reliable and citable source has not yet been found.
- ^ WI Taylor: Iboga Alkaloids. II. The Structures of Ibogaine, Ibogamine and Tabernanthine. In: Journal of the American Chemical Society. 79, 1957, p. 3298, doi : 10.1021 / ja01569a093 .
- ↑ E. Breitmaier: Alkaloids . Springer Fachmedien, Wiesbaden 1997, ISBN 978-3-519-03542-8 , pp. 56 .
- ↑ M. Hesse: Indole alkaloids . Springer-Verlag, Berlin Heidelberg 1968, ISBN 978-3-540-04194-8 , p. 30 .
- ↑ M. Prioux-Guyonneau, E. Mocaër-Cretet, Y. Cohen, C. Jacquot: Evidence for an activating effect of tabernathine on rat brain catechlomine synthesis and elimination. In: Experientia. 40, 1984, p. 1388, doi : 10.1007 / BF01951904 .