Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1374908 | Bioorganic & Medicinal Chemistry Letters | 2009 | 4 Pages |
Abstract
A total of seven new oxyranylmethyloxy or thiiranylmethyloxy group substituted 5-azaxanthones and -acridones analogues were synthesized and tested for their biological activities for cancer cell lines and topoisomerases. Among the compounds, compound 5, 3-thiiranylmethyloxy-1-hydroxy-5-azaxanthone, showed effective topoisomerase I inhibitory activity, 50% and 27% inhibition ratio at 100 and 20 μM, respectively. This result is the first finding of the function of 5-azaxanthone compounds for topoisomerase I inhibition and can provide a novel skeleton for the anticancer drug development process.
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Related Topics
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Chemistry
Organic Chemistry
Authors
Hee-Ju Cho, Mi-Ja Jung, Youngjoo Kwon, Younghwa Na,