CAS 83-94-3
:Tabernanthine
Description:
Tabernanthine is an indole alkaloid primarily derived from the plant Tabernaemontana species, particularly Tabernaemontana divaricata. It is known for its complex structure, which includes a bicyclic framework characteristic of many alkaloids. Tabernanthine exhibits a range of biological activities, including potential analgesic and anti-inflammatory effects, making it of interest in pharmacological research. The compound is typically found in a crystalline form and is soluble in organic solvents, but its solubility in water is limited. Its molecular formula reflects a specific arrangement of carbon, hydrogen, nitrogen, and oxygen atoms, contributing to its unique properties. Tabernanthine's mechanism of action and therapeutic potential are subjects of ongoing studies, particularly in the context of traditional medicine and modern pharmacology. As with many alkaloids, caution is advised regarding its use, as it may exhibit toxicity at certain doses. Overall, Tabernanthine represents a fascinating area of study within natural product chemistry and medicinal research.
Formula:C20H26N2O
InChI:InChI=1/C20H26N2O/c1-3-13-8-12-9-17-19-16(6-7-22(11-12)20(13)17)15-5-4-14(23-2)10-18(15)21-19/h4-5,10,12-13,17,20-21H,3,6-9,11H2,1-2H3/t12-,13+,17+,20+/m1/s1
InChI key:InChIKey=UCIDWKVIQZIKEK-CFDPKNGZSA-N
SMILES:C(C)[C@@H]1[C@]2([C@@]3(C4=C(C=5C(N4)=CC(OC)=CC5)CC[N@]2C[C@@](C3)(C1)[H])[H])[H]
Synonyms:- 6,9-Methano-5H-pyrido[1′,2′:1,2]azepino[4,5-b]indole, ibogamine deriv.
- Ibogamine, 13-methoxy-
- Tabernanthin
- 13-Methoxyibogamine
- Tabernanthine
- (2alpha)-13-methoxyibogamine
- 13-Methoxyibogamine
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Found 2 products.
Tabernanthine
CAS:Tabernanthine is an indole alkaloid, which is a potent psychotropic compound sourced from the root bark of the plant Tabernanthe iboga, native to Central Africa. As a naturally occurring compound, Tabernanthine shares structural similarities with other indole alkaloids, such as ibogaine, found in the same plant. Its mode of action primarily involves interaction with neurotransmitter systems, including antagonism at the NMDA receptor and modulation of serotonin and dopamine pathways. This interaction can disrupt or alter neural signaling, consequently producing significant effects on perception and cognition.Formula:C20H26N2OPurity:Min. 95%Molecular weight:310.40 g/mol

