4.7 Article

Bibenzyl-Based Meroterpenoid Enantiomers from the Chinese Liverwort Radula sumatrana

Journal

JOURNAL OF NATURAL PRODUCTS
Volume 80, Issue 12, Pages 3144-3151

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jnatprod.7b00394

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Funding

  1. National Natural Science Foundation of China [81630093, 81473107]

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Six new pairs of bibenzyl-based meroterpenoid enantiomers, (+/-)-rasumatranin A-D (1-4) and (+/-)-radulanin M and N (5 and 6), and six known compounds were isolated from the adnascent Chinese liverwort, Radula sumatrana. Their structures were elucidated based on spectroscopic data and chiral phase HPLC-ECD analyses. The structures of 1 and 7 were also confirmed by single-crystal X-ray diffraction analysis. Cytotoxicity tests of the isolated compounds showed that 6-hydroxy-3-methyl-8-phenylethylbenzo[b]oxepin-5-one (8) showed activity against the human cancer cell lines MCF-7, PC-3, and SMMC-7721, with IC50 values of 3.86, 6.60, and 3.58 mu M, respectively, and induced MCF-7 cell death through a mitochondria-mediated apoptosis pathway.

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