Back to Search
Start Over
Dimeric bisindole alkaloids from the stem bark of Strychnos nux-vomica L
- Source :
- Phytochemistry. 87:157-163
- Publication Year :
- 2013
- Publisher :
- Elsevier BV, 2013.
-
Abstract
- Strychnos nux-vomica L. (Loganiaceae) is famous for its monomeric alkaloid content, such as strychnine, a convulsant poison. The stem bark of the tree is traditionally used to treat intermittent fever in South East Asia. In various studies, it appeared that dimeric indolo-monoterpenic alkaloids possess a promising activity on Plasmodium falciparum. Three bisindolomonoterpenic alkaloids together with strychnochrysine, previously identified in the root bark of S. nux-vomica, were isolated from the stem bark. The structures of these compounds were established using NMR spectroscopy and mass spectrometry. Stereochemistry of the compounds was confirmed by molecular modelling. This then allowed the structural determination of strychnoflavine, a coloured bisindole alkaloid previously isolated from the root bark of the tree. Moreover, the conformational inversion in alkaloids possessing an ether bond in the strychnane moiety could be easily predicted by specific δ (13)C NMR values. These longicaudatine-type alkaloids were found to display in vitro antiplasmodial activity against a chloroquine resistant strain and a chloroquine sensitive strain. The most interesting was strychnochrysine showing an IC(50) value at around 10 μM.
- Subjects :
- Magnetic Resonance Spectroscopy
Stereochemistry
Plasmodium falciparum
Strychnos
Plant Science
Horticulture
complex mixtures
Biochemistry
Mass Spectrometry
Antimalarials
Alkaloids
Strychnos nux-vomica
Plant Bark
Animals
Humans
Organic chemistry
heterocyclic compounds
Molecular Biology
Plant Stems
biology
Chemistry
Alkaloid
General Medicine
Loganiaceae
Nuclear magnetic resonance spectroscopy
Carbon-13 NMR
biology.organism_classification
visual_art
visual_art.visual_art_medium
Bark
Subjects
Details
- ISSN :
- 00319422
- Volume :
- 87
- Database :
- OpenAIRE
- Journal :
- Phytochemistry
- Accession number :
- edsair.doi.dedup.....3c1e85e0ae77d7ecb11ac0c6ea2d113e
- Full Text :
- https://doi.org/10.1016/j.phytochem.2012.11.002