Eleven phenolic compounds have been isolated from the ethanolic extrac
t of Selaginella doederleinii by a combination of chromatographic tech
niques. These are five lignans: (-)-lirioresinol A, (-)-lirioresinol B
, (+)-wikstromol, (-)-nortracheloside, (+)-matairesinol (1), two pheny
lpropanones: 3-hydroxy-1(3 -methoxy-4-hydroxyphenyl)-propan-1-one (2),
oxy-1-(3,5-dimethoxy-4-hydroxyphenyl)-propan-1-one (3), and four bifl
avonoids: amentoflavone, 7,7''-di-O-methylamentoflavone, 7,4',7'',4'''
-tetra-O-methylamentoflavone, and heveaflavone (4). Compounds 1, 2, an
d 3 are novel natural secondary metabolites. Their structures were ded
uced from their spectral data (mainly H-1-NMR, mass, and CD). Lignans
are described here for the first time in the family Selaginellaceae. T
heir cytotoxic activity against L 929 murine cells accounts for the us
e of the plant in traditional Chinese medicine as an anticancer agent.