| Reference : Strychnogucines a and B, Two New Antiplasmodial Bisindole Alkaloids from Strychnos Icaja |
| Scientific journals : Article | |||
| Human health sciences : Immunology & infectious disease Life sciences : Phytobiology (plant sciences, forestry, mycology...) Human health sciences : Pharmacy, pharmacology & toxicology | |||
| http://hdl.handle.net/2268/13887 | |||
| Strychnogucines a and B, Two New Antiplasmodial Bisindole Alkaloids from Strychnos Icaja | |
| English | |
Frederich, Michel [Université de Liège - ULg > Département de pharmacie > Pharmacognosie >] | |
Gillet, Marie-Claire [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Histologie - Cytologie - Département des sciences biomédicales et précliniques >] | |
Prosperi, Christelle [Université de Liège - ULg > Département de physique > Département de physique >] | |
Tits, Monique [Université de Liège - ULg > Département de pharmacie > Phytochimie et phytothérapie >] | |
| Brandt, V. [> > > >] | |
| Penelle, J. [> > > >] | |
Hayette, Marie-Pierre [Centre Hospitalier Universitaire de Liège - CHU > > Microbiologie médicale >] | |
De Mol, Patrick [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Microbiologie médicale et virologie médicale] | |
Angenot, Luc [Université de Liège - ULg > Département de pharmacie > Pharmacognosie >] | |
| Jan-2001 | |
| Journal of Natural Products | |
| 64 | |
| 1 | |
| 12-16 | |
| Yes (verified by ORBi) | |
| International | |
| 0163-3864 | |
| 1520-6025 | |
| [en] A reinvestigation of Strychnos icaja roots has resulted in the isolation of two tertiary quasi-symmetric bisindole alkaloids named strychnogucines A (1) and B (2). Their structures were identified by means of spectroscopic data interpretation. Compound 2 was highly active in vitro and compound 1 moderately active against four strains of Plasmodium falciparum. Strychnogucine B (2) was more active against a chloroquine-resistant strain than against a chloroquine-sensitive one (best CI(50), 80 nM against the W2 strain). In addition, this compound showed a selective antiplasmodial activity with 25-180 times greater toxicity toward P. falciparum, relative to cultured human cancer cells (KB) or human fibroblasts (WI38). | |
| http://hdl.handle.net/2268/13887 |
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