Abstract
New series of analogues of N-(pyridin-4-yl)-2-[1-(4-chlorobenzyl)-indol- 3-yl]glyoxamide D-24851 were synthesized, characterized and tested for their in vitro anticancer properties. In the first series, an amino acid spacer was introduced in the glyoxamide chain of D-24851. In the second series, the glyoxamide chain was moved to positions 4 and 5 of indole skeleton. These new compounds were tested on four cancer cell lines (KB, SK-OV-3, NCI-H460 and SF-268), with promising activity for the glycine derivative.
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Antoine, M., Marchand, P., Le Baut, G., Czech, M., Baasner, S., & Gunther, E. (2008). Side chain modifications of (indol-3-yl)glyoxamides as antitumor agents. Journal of Enzyme Inhibition and Medicinal Chemistry, 23(5), 686–695. https://doi.org/10.1080/14756360802207998
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