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A series of novel curcumin analogues were synthesized by optimization of its aromatic ring. The antiproliferative activities of these analogues were screened against four human cancer cell lines by MTT assay and some displayed significant improvement in antiproliferative activity compared with curcumin. The most potent compound 10 exhibited antiproliferative activity against Caco-2, Bel-7402, MDA-MB-231,...
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