Article ID Journal Published Year Pages File Type
1399046 European Journal of Medicinal Chemistry 2013 10 Pages PDF
Abstract

•3-Methyl-1-benzofurans derived from cercosporamide were synthesized.•Antiproliferative activity against human NSCLC cell lines was investigated.•Some 3-methyl-1-benzofuran-7-carboxamide derivatives exhibited cytotoxic activities.

A novel series of 3-methyl-1-benzofuran derivatives were synthesized and screened in vitro for their antiproliferative activity against two human NSCLC cell lines (NSCLC-N6 mutant p53 and A549 wild type p53). Most promising compounds presented a structural analogy with the west part of cercosporamide, a natural product of biological interest. In particular, compounds 10, 12 and 31 showed cytotoxic activities at micromolar concentrations (IC50 < 9.3 μM) and compounds 13, 18 and 32 displayed moderate IC50 values (25–40 μM).

Graphical abstractThe access to 3-methyl-1-benzofurans derived from cercosporamide and the corresponding antiproliferative activity against NSCLC cell lines are described.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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