Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1371073 | Bioorganic & Medicinal Chemistry Letters | 2011 | 4 Pages |
Abstract
Novel nucleoside–Cinchona alkaloid conjugates were synthesized using ‘click’ chemistry approach based on the copper(I) catalyzed Huisgen azide–alkyne cycloaddition. Two series of conjugates were prepared employing 3′-azido-3′-deoxythymidine (AZT) as the azide component and the four 10,11-didehydro Cinchona alkaloids as well as their 9-O-propargyl ethers as the alkyne components. All obtained conjugates showed strong fluorescence emission and some of them exhibited marked cytotoxic activity in vitro.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Dagmara Baraniak, Karol Kacprzak, Lech Celewicz,