Bioassay-guided fractionation of an ethyl acetate extract of Fissistig
ma lanuginosum led to the isolation of the known chalcone pedicin [1],
which inhibited tubulin assembly into microtubules (IC50 value of 300
mu M). From the same EtOAc fraction, two new condensed chalcones, fis
sistin [2] and isofissistin [3], which showed cycotoxicity against KB
cells, were also obtained, together with the inactive dihydropedicin [
4] and 6,7-dimethoxy-5,8-dihydroxyflavone [5] In addition, the aminoqu
inones 6, 8, and 9 were isolated from the alkaloid extract. These comp
ounds were artifacts, prepared by treatment of 1, 4, and 2, respective
ly, with NH4OH. The structures of the new compounds were elucidated by
spectral methods, especially 2D nmr.