4.7 Article

Alkaloids of Zephyranthes citrina (Amaryllidaceae) and their implication to Alzheimer's disease: Isolation, structural elucidation and biological activity

Journal

BIOORGANIC CHEMISTRY
Volume 107, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2020.104567

Keywords

Zephyranthes citrina; Amaryllidaceae; Alkaloids; Narcieliine; Alzheimer's disease; Docking studies

Funding

  1. Charles University [178518, SVV UK 260 548, SVV 260 547, Progres/UK Q42]
  2. Long-term development plan (Faculty of Military Health Sciences)
  3. Pre-application research into innovative medicines and medical technologies project - European Union
  4. CESNET [LM2015042]
  5. CERIT Scientific Cloud [LM2015085]

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The alkaloids extracted from fresh bulbs of Zephyranthes citrina, including a newly described compound narcieliine, were identified using various spectroscopic techniques and compared with literature data. Narcieliine showed significant inhibitory activity against human AChE/BuChE, with the ability to cross the blood-brain barrier through passive diffusion, as predicted and supported by in vitro and in silico studies.
Twenty known Amaryllidaceae alkaloids of various structural types, and one undescribed alkaloid of narcikachnine-type, named narcieliine (3), have been isolated from fresh bulbs of Zephyranthes citrina. The chemical structures of the isolated alkaloids were elucidated by a combination of MS, HRMS, 1D and 2D NMR, and CD spectroscopic techniques, and by comparison with literature data. The absolute configuration of narcieliine (3) has also been determined. Compounds isolated in a sufficient quantity were evaluated for their in vitro acetylcholinesterase (AChE; E.C. 3.1.1.7), butyrylcholinesterase (BuChE; E.C. 3.1.1.8), and prolyl oligopeptidase (POP; E.C. 3.4.21.26) inhibition activities. Significant human AChE/BuChE (hAChE/hBuChE) inhibitory activity was demonstrated by the newly described alkaloid narcieliine (3), with IC50 values of 18.7 +/- 2.3 mu M and 1.34 +/- 0.31 mu M, respectively. This compound is also predicted to cross the blood-brain barrier (BBB) through passive diffusion. The in vitro data were further supported by in silico studies of 3 in the active site of hAChE/hBuChE.

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