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Targeted Isolation of Hemitheion from Mostuea brunonis, a Proposed Biosynthetic Intermediate of Theionbrunonines.

Elvis Otogo N'NangPierre Le PogamThiery Ndong MbaCédric Sima ObiangElisabeth MourayPhilippe GrellierBrice KumulunguiPierre ChampyMehdi A Beniddir
Published in: Journal of natural products (2021)
Hemitheion (1), a new sulfur-containing vobasane-type indole alkaloid, was isolated, together with three known compounds, vobasine (2), gelsedine (3), and gelsemicine (4), from the alkaloid extract of the stems of Mostuea brunonis Didr. (Gelsemiaceae). Compound 1 could be straightforwardly isolated. Its structure was elucidated by a combination of spectroscopic methods. Besides corresponding to a formerly postulated biosynthetic intermediate toward theionbrunonines, hemitheion (1) stands among the few monomeric vobasanes lacking an oxygen at C-3. Hemitheion (1) showed moderate antiplasmodial activity in the micromolar range against the strain FcB1 of Plasmodium falciparum and no cytotoxic activity against the MRC-5 cell line at 20 μM.
Keyphrases
  • plasmodium falciparum
  • molecular docking
  • high intensity
  • anti inflammatory
  • drug delivery
  • molecular dynamics simulations