<p><i>Excoecaria cochinchinensis</i> Lour. is a well-known medicinal plant in Vietnam, whose parts, particularly leaves, are applied as essential medicine in folk remedies. In this study, the chemical constituents of the plant’s aerial parts, together with their feasibility in enzyme inhibition and antioxidants, were investigated. Seven compounds, including a new coumarino lignan – excochinlignan (<b>1</b>), five known flavonol derivatives (<b>2</b>-<b>6</b>) and one monophenolic (<b>7</b>), were isolated and identified <i>via</i> chromatographic and spectroscopic approaches. In vitro biological evaluation of these compounds revealed the potential of kaempferol (<b>2</b>) and its glycosides (<b>3</b>-<b>6</b>) in all assays. Among them, kaempferol (<b>2</b>) was determined as the most active antioxidant (IC<sub>50</sub> 2.86 μM) while its 3-<i>O</i>-xylose derivatives (<b>3</b>) displayed the most significant <i>α</i>-glucosidase (IC<sub>50</sub> 65.88 μM) and tyrosinase (IC<sub>50</sub> 58.97 μM) inhibition. In silico evaluation <i>via</i> molecular docking simulation suggested the supportive effect of 3-<i>O</i>-xylose, C-4′ hydroxyl and C-4 ketone moieties in the structure of the isolated flavanols (<b>2</b>-<b>6</b>) on their enzyme inhibition and antioxidant properties.</p><p></p>

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Excochinlignan: A new coumarino lignan from Excoecaria cochinchinensis Lour

  • Huong Thi Thu Le,
  • Phan-Si-Nguyen Dong,
  • Le-Thuy-Thuy-Trang Hoang,
  • Hoai-Vu Nguyen-Si,
  • Hoang-Vinh-Truong Phan,
  • Thi-Minh-Thao Vo,
  • Thi-Tu-Linh Tran,
  • Tin-Thanh Le,
  • Van-Kieu Nguyen

摘要

Excoecaria cochinchinensis Lour. is a well-known medicinal plant in Vietnam, whose parts, particularly leaves, are applied as essential medicine in folk remedies. In this study, the chemical constituents of the plant’s aerial parts, together with their feasibility in enzyme inhibition and antioxidants, were investigated. Seven compounds, including a new coumarino lignan – excochinlignan (1), five known flavonol derivatives (2-6) and one monophenolic (7), were isolated and identified via chromatographic and spectroscopic approaches. In vitro biological evaluation of these compounds revealed the potential of kaempferol (2) and its glycosides (3-6) in all assays. Among them, kaempferol (2) was determined as the most active antioxidant (IC50 2.86 μM) while its 3-O-xylose derivatives (3) displayed the most significant α-glucosidase (IC50 65.88 μM) and tyrosinase (IC50 58.97 μM) inhibition. In silico evaluation via molecular docking simulation suggested the supportive effect of 3-O-xylose, C-4′ hydroxyl and C-4 ketone moieties in the structure of the isolated flavanols (2-6) on their enzyme inhibition and antioxidant properties.