JOURNAL 377


Records of Natural Products
VOLUME & ISSUE
Year: 2016 Issue: 3 May-June
PAGES
p.332 - 340
STATISTICS
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AUTHORS
    Bui Linh Chi Huynh, Thuc Huy Duong, Thi My Lien Do, Travis George Pinnock, Lawrence Michael Pratt, Shigeki Yamamoto, Hitoshi Watarai, Takao Tanahashi and Kim Phi Phung Nguyen
PDF OF ARTICLE

GRAPHICAL ABSTRACT


ABSTRACT


From the lichen Parmotrema praesorediosum (Nyl.) Hale, Parmeliaceae, collected in Vietnam, five new (1, 2, 3, 5, 6) and one known (4) g -lactonic acids were isolated. The structures of the new compounds were established by 1D and 2D NMR spectroscopy, as well as high resolution-electrospray ionization (HR-ESI)-MS analysis. The absolute configuration of new compounds was determined by ultraviolet circular dichroism spectroscopy. Compounds were evaluated for their cytotoxic activity against HeLa (human epithelial carcinoma), NCI-H460 (human lung cancer) and MCF-7 (human breast cancer) cell lines at the concentration of 100 µg/mL. Among six compounds, 1 possessed medium activity against MCF-7 cell line with the inhibition of 52.5%. Meanwhile, the rest showed no cytotoxic activity against three surveyed cancer cell lines.

KEYWORDS
  • Parmotrema praesorediosum
  • Parmeliaceae
  • lichen
  • aliphatic acids

SUPPORTING INFORMATION


Supporting Information
Download File 41-RNP-1503-054-SI.pdf (7.35 MB)