Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1397155 | European Journal of Medicinal Chemistry | 2006 | 7 Pages |
Abstract
In this work we report our results concerning the study on the in vitro antiproliferative activity of 18 Baylis–Hillman adducts and some derivatives against a panel of humor tumor cell lines. A brief qualitative structure–activity relationship study indicated that carbon-carbon double bond and the presence of an electron-withdrawing substituent at the aromatic ring are essential for the activity. A quinoline–phthalide derivative has exhibited a potent effect on the proliferation of all cell lines. It is interesting to note their special cytotoxic activity against NCIADR cell line.
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Organic Chemistry
Authors
Luciana K. Kohn, C.H. Pavam, D. Veronese, F. Coelho, J.E. De Carvalho, Wanda P. Almeida,