4.7 Article

Brujavanoids A-U, structurally diverse apotirucallane-type triterpenoids from Brucea javanica and their anti-inflammatory effects

Journal

BIOORGANIC CHEMISTRY
Volume 127, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2022.106012

Keywords

Simaroubaceae; Brucea javanica; Triterpenoid; Apotirucallane; Anti-inflammatory

Funding

  1. National Natural Science Foundation of China [31870330, 82003605, 81773869]
  2. Open Foundation of Hebei Technological Innovation Center of Chiral Medicine [ZXJJ20210201]
  3. Analytical and Testing Center of Huazhong University of Science and Technology (HUST)

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A total of 27 triterpenoids, including 21 previously undescribed compounds, were isolated and identified from the methanol extract of the inflorescences, twigs, and leaves of Brucea javanica. Among them, brujavanoid A is the first apotirucallane-type triterpenoid with a novel 19(10 & RARR; 9)abeo motif, and brujavanoids B and C are the first apotirucallane-type triterpenoids with a rarely occurring 14-hydroxy-15,16-epoxy fragment. The most active compound, brujavanoid E, exhibits significant anti-inflammatory effects.
Extensive phytochemical investigation on the methanol extract of the inflorescences, twigs, and leaves of Brucea javanica led to the isolation and identification of 27 triterpenoids, including 21 previously undescribed ones, named brujavanoids A-U (1-21). Their structures were determined based on comprehensive spectroscopic analysis and single-crystal X-ray diffraction. Of these compounds, brujavanoid A (1) represents the first apotirucallane-type triterpenoid with a novel 19(10 & RARR; 9)abeo motif, and brujavanoids B and C (2-3) are the first apotirucallane-type triterpenoids with a rarely occurring 14-hydorxy-15,16-epoxy fragment. All the isolates were evaluated for their anti-inflammatory effect in an LPS-activated RAW264.7 cells model. Furthermore, the most active one, brujavanoid E (5), can suppress the transcriptional expression of typical pro-inflammatory mediators and inhibit the nuclear translocation of NF -KB p65 in the LPS-activated RAW264.7 cells.

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