4.7 Article

Cytotoxic Guaianolide Sesquiterpenoids from Ainsliaea fragrans

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 84, Issue 9, Pages 2568-2574

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.1c00587

Keywords

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Funding

  1. National Key RD Program [2019YFC1711500]
  2. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX20_1500]
  3. Nature Science Foundation of Jiangsu Higher Education Institutions of China [19KJA180008]
  4. Jiangsu Provincial Innovation and Entrepreneurship Talent Plan [202010528]

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Twelve guaianolide-type sesquiterpene oligomers, including a novel trimer and two new dimers, were isolated from the whole plants of Ainsliaea fragrans. The chemical structures of the new compounds were elucidated through spectroscopic data interpretation and computational calculations. Ainsfragolide exhibited potent cytotoxicity against five cancer cell lines.
Twelve guaianolide-type sesquiterpene oligomers with diverse structures were isolated from the whole plants of Ainsliaea fragrans, including a novel trimer (1) and two new dimers (2, 3). The chemical structures of the new compounds were elucidated through spectroscopic data interpretation and computational calculations. Ainsfragolide (1) is an unusual guaianolide sesquiterpene trimer generated with a novel C-C linkage at C-2' -C-15 '', which may be biosynthesized prospectively through a further Michael addition. Cytotoxicity results showed that ainsfragolide (1) was the most potent compound against five cancer cell lines with IC50 values in the range of 0.4-8.3 mu M.

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