4.6 Article

Cytotoxic guaianolides and seco-guaianolides from Artemisia atrovirens

Journal

FITOTERAPIA
Volume 151, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.fitote.2021.104900

Keywords

Artemisia atrovirens; Guaianolide; TDDFT ECD calculation; Cytotoxicity

Funding

  1. National Natural Science Foundation of China [81903485, 21920102003]
  2. Key-Area Research and Development Program of Guangdong Province [2020B0303070002]
  3. Ningxia Key Research and Development Program

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A phytochemical investigation of Artemisia atrovirens led to the discovery of several new compounds, with their structures and absolute configurations confirmed through various analytical methods. Testing in vitro showed moderate cytotoxicity of some compounds against HL-60 cell lines.
A phytochemical investigation of a medicinal plant Artemisia atrovirens was carried out, resulting in the characterization of a novel bis-nor seco-guaianolide, seco-atrovirenolide A (1), a new 1,10-seco-guaianolide derivative, seco-atrovirenoic acid A (2), and a new artifact 10-methanoyloxy-seco-atrovirenoic acid A (3), together with eight known guaianolide and seco-guaianolide derivatives (4-11). The structures of new compounds were fully established by extensive analysis of MS, 1D and 2D NMR spectroscopic data. The absolute configurations of the isolated compounds were confirmed by TDDFT ECD calculation, Mosher's method, and X-ray crystal diffraction experiment. All the compounds were tested in vitro for their cytotoxicity against HL-60 and A549 cell lines. Some of them showed moderate inhibitory activity against HL-60 cell lines with IC50 values ranging from 5.99 to 11.74 mu M.

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