A new acyclic diterpene (1) and a known acyclic diterpene, 12(S)-hydroxyger
anylgeraniol (2) were isolated from the aerial parts of Carpesium divaricat
um. The structure of 1 was determined to be (2E,10E)-1, 12-dihydroxy-18-ace
toxy-3,7,15-trimethylhexadeca-2,10,14-triene (1) on the basis of spectrosco
pic studies. Compounds 1 and 2 exhibited cytotoxicity against cultured huma
n tumor cell lines, A549, SK-OV-3, SK-MEL-2, XF498, and HCT15, with ED50 va
lues ranging from 4.3-10.2 mu g/ml and 4.1-8.3 mu g/ml, respectively.