4.5 Article

17-O-Acetyl, 10-hydroxycorynantheol, a Selective Antiplasmodial Alkaloid Isolated from Strychnos usambarensis Leaves

期刊

PLANTA MEDICA
卷 77, 期 18, 页码 2050-U102

出版社

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0031-1280124

关键词

Strychnos usambarensis Gilg.; Loganiaceae; monomeric indole alkaloid; antiplasmodial; selectivity

资金

  1. Belgian National Fund for Scientific Research (FNRS) [3.4533.10]
  2. CUD (Cooperation Universitaire au Developpement)

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In the course of our investigations on Strychnos usambarensis leaves in order to isolate isostrychnopentamine, the main alkaloid responsible for the antiplasmodial activity of the plant, a new tertiary indolic alkaloid has been isolated: 17-O-acetyl, 10-hydroxycorynantheol 1. Its structure was determined by means of spectroscopic and spectrometric methods such as UV, IR, CD, NMR, and ESI-MS. 17-O-acetyl, 10-hydroxycorynantheol 1 is one of the most active monomeric indole alkaloids known to date showing an in vitro activity against Plasmodium falciparum close to 5 mu M and a high selectivity.

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