S. Ducki et al., POTENT ANTIMITOTIC AND CELL-GROWTH INHIBITORY PROPERTIES OF SUBSTITUTED CHALCONES, Bioorganic & medicinal chemistry letters, 8(9), 1998, pp. 1051-1056
A series of substituted chalcones was synthesised and screened for cyt
otoxic activity against the K562 human leukaemia cell line. thyl-1-(3'
,4',5'-trimethoxyphenyl)-prop-2-en-1-one [IC50 (K562) 0.21 nM] was fou
nd to be the most active. A relationship between the conformation and
cytotoxicity of the chalcones is discussed. (C) 1998 Elsevier Science
Ltd. All rights reserved.