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Isolation and Biological Characterization of Homoisoflavanoids and the Alkylamide N-p-Coumaroyltyramine from Crinum biflorum Rottb., an Amaryllidaceae Species Collected in Senegal.

Abstract
Crinum biflorum Rottb. (syn. Crinum distichum) is an Amaryllidaceae plant used in African traditional medicine but very few studies have been performed on this species from a chemical and applicative point of view. Bulbs of C. biflorum, collected in Senegal, were extracted with ethanol by Soxhlet and the corresponding organic extract was purified using chromatographic methods. The pure compounds were chemically characterized by spectroscopic techniques (1D and 2D 1H and 13C NMR, HR MS and ECD) and X-ray analysis. Four homoisoflavonoids (1-4) and one alkylamide (5) were isolated and characterized as 5,6,7-trimethoxy-3-(4-hydroxybenzyl)chroman-4-one (1), as 3-hydroxy-5,6,7-trimethoxy-3-(4-hydroxybenzyl)chroman-4-one (2), as 3-hydroxy-5,6,7-trimethoxy-3-(4-methoxybenzyl)chroman-4-one (3) and as 5,6,7-trimethoxy-3-(4-methoxybenzyl)chroman-4-one (4), and the alkylamide as (E)-N-(4-hydroxyphenethyl)-3-(4-hydroxyphenyl)acrylamide (5), commonly named N-p-coumaroyltyramine. The relative configuration of compound 1 was verified thanks to the X-ray analysis which also allowed us to confirm its racemic nature. The absolute configurations of compounds 2 and 3 were assigned by comparing their ECD spectra with those previously reported for urgineanins A and B. Flavanoids 1, 3 and 4 showed promising anticancer properties being cytotoxic at low micromolar concentrations towards HeLa and A431 human cancer cell lines. The N-p-coumaroyltyramine (5) was selectively toxic to A431 and HeLa cancer cells while it protected immortalized HaCaT cells against oxidative stress induced by hydrogen peroxide. Compounds 1-4 also inhibited acetylcholinesterase activity with compound 3 being the most potent. The anti-amylase and the strong anti-glucosidase activity of compound 5 were confirmed. Our results show that C. biflorum produces compounds of therapeutic interest with anti-diabetic, anti-tumoral and anti-acetylcholinesterase properties.
AuthorsMarco Masi, Manoj Koirala, Antonella Delicato, Roberta Di Lecce, Natacha Merindol, Seydou Ka, Matar Seck, Angela Tuzi, Isabel Desgagne-Penix, Viola Calabrò, Antonio Evidente
JournalBiomolecules (Biomolecules) Vol. 11 Issue 9 (08 31 2021) ISSN: 2218-273X [Electronic] Switzerland
PMID34572511 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antiviral Agents
  • Cholinesterase Inhibitors
  • Coumaric Acids
  • Flavonoids
  • Fluoresceins
  • Hypoglycemic Agents
  • N-(4-hydroxy-beta-phenethyl)-4-hydroxycinnamide
  • diacetyldichlorofluorescein
  • Acetylcholinesterase
  • alpha-Amylases
Topics
  • Acetylcholinesterase (metabolism)
  • Amaryllidaceae (chemistry)
  • Antiviral Agents (pharmacology)
  • Cell Death (drug effects)
  • Cell Survival (drug effects)
  • Cholinesterase Inhibitors (pharmacology)
  • Coumaric Acids (chemistry, isolation & purification)
  • Crinum (chemistry)
  • Flavonoids (chemistry, isolation & purification)
  • Fluoresceins (metabolism)
  • HIV-1 (drug effects)
  • HaCaT Cells
  • HeLa Cells
  • Humans
  • Hypoglycemic Agents (pharmacology)
  • Metabolome
  • Molecular Conformation
  • Senegal
  • alpha-Amylases (metabolism)

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