JOURNAL 3015


Records of Natural Products
VOLUME & ISSUE
Year: 2024 Issue: 2 March-April
PAGES
p.296 - 301
STATISTICS
Viewed 299 times.
AUTHORS
  • Aifen Zeng
  • Zhengkuan Zhang
  • Guobo Xu
  • Shanggao Liao
  • Qin-Feng Zhu
  • Xun He
PDF OF ARTICLE

GRAPHICAL ABSTRACT


ABSTRACT


A new prenylated coumarin, 5, 7-dimethoxy-6-[(Z)-3'-methylbutan-1',3'-d-ienyl] coumarin (1), along with ten known compounds (2-11), was obtained from the roots of Toddalia asiatica (Linn.) Lam. Their structures were determined based on 1 D and 2 D NMR spectroscopy as well as high-resolution mass spectrometry. Notably, the structure of (3S, 4R)-3,4-epoxypimpinellin was revised as its cis-epimer, compounds (2-7) were isolated from this genus for the first time. The cytotoxic activities of the isolated compounds 1-11 were evaluated against SW480, A549, MDA-MB-231, HepG 2, HEp-2, SGC7901 cancer cell lines. Compound 10 exhibited weak cytotoxicity against HEP 2 with IC50 value of 75.19 ± 1.17 µM. KEYWORDS
  • Toddalia asiatica
  • coumarins
  • chemical constituents
  • cytotoxic activity

SUPPORTING INFORMATION


Supporting Information
Download File A12-449-RNP-2401-3015-SI.pdf (1.94 MB)