Triterpenoids from Camellia japonica and Their Cytotoxic Activity

From the ethyl acetate fraction of the stem bark of Camellia japonica, three new triterpenoids, 3 beta-O-acetyl-16 beta-hydroxy-12-oxoolean (6), 3 beta-O-acetyl-16 beta-hydroxy-11-oxoolean-12-ene (7), and 3 beta-O-acetyl-16 beta-hydroxy-olean-12-ene (8), along with seven known compounds, 3 alpha-hydroxy-1-oxofriedelan (1), friedelin (2), 3 beta-friedelanol (3), canophyllol (4), 3-oxofriedelan-1(2)-ene (5), beta-amyrin (9), camellenodiol (10), and camelledionol (11) were isolated. Their structures were established on the basis of spectroscopic analysis and chemical evidence. The isolated compounds were tested in vitro for their cytotoxic activities against the A549, LLC, HL-60 and MCF-7 cancer cell lines. Among them, compound 8 showed cytotoxicity against LLC and HL-60 cancer cell lines with IC50 values of 25.2 and 21.7 mu M, respectively.