JOURNAL 42


Records of Natural Products
VOLUME & ISSUE
Year: 2018 Issue: 2 March-April
PAGES
p.179 - 183
STATISTICS
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AUTHORS
    Seong Yeon Choi, Birang Jeong, Hyeon Seok Jang, Jiho Lee, Kiwon Ko, Hyunha Kim, Jua Hong, Young Soo Bae and Heejung Yang
PDF OF ARTICLE

GRAPHICAL ABSTRACT


ABSTRACT


A new dibenzofuran derivative, 1,2,4-trimethoxydibenzofuran-3,9-diol (7), was isolated from the ethyl acetate fraction of Sorbus commixta barks, along with six known compounds, lupeol (1), betulin (2), betulinic acid (3), ursolic acid (4)b -sitosterol (5) and b -pyrufuran (6). Their structures were determined by NMR spectroscopic analysis, including of 1H and 13C NMR, 1H- 1H COSY, HSQC and HMBC spectra data. Cytotoxic activities of seven compounds were evaluated in five cancer cell lines, HEp-2, A549, MCF-7, PC-3 and SKOV-3 at the concentrations ranging from 10 to 100 m M.

KEYWORDS
  • Sorbus commixta
  • triterpenes
  • dibenzofuran
  • 1
  • 2
  • 4-trimethoxydibenzofuran-3
  • 9-diol
  • cytotoxicity

SUPPORTING INFORMATION


Supporting Information
Download File 20-RNP-1706-112_ SI.pdf (1007.06 KB)