Synthesis and evaluation of new β-carboline-3-(4-benzylidene)- 4H-oxazol-5-one derivatives as antitumor agents

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Abstract

In the present work, we report the synthesis and in vitro anticancer and antimicrobial activity evaluation of a new series of 1-substituted-β- carboline derivatives bearing a 4-benzylidene-4H-oxazol-5-one unity at C-3. The compound 2-[1-(4- methoxyphenyl)-9H-β-carbolin-3-yl]-4-(benzylidene)-4H- oxazol-5-one (11) was the most active derivative, exhibiting a potent cytotoxic activity against glioma (U251), prostate (PC-3) and ovarian (OVCAR-03) cancer cell lines with IC 50 values of 0.48, 1.50 and 1.07 μM, respectively. An in silico study of the ADME properties of the novel synthesized β-carboline derivatives was also performed. © 2012 by the Authors.

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Savariz, F. C., Foglio, M. A., De Carvalho, J. E., Ruiz, A. L. T. G., Duarte, M. C. T., Da Rosa, M. F., … Sarragiotto, M. H. (2012). Synthesis and evaluation of new β-carboline-3-(4-benzylidene)- 4H-oxazol-5-one derivatives as antitumor agents. Molecules, 17(5), 6100–6113. https://doi.org/10.3390/molecules17056100

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