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Merck

BODIPY-modified 2'-deoxyguanosine as a novel tool to detect DNA damages.

Bioorganic & medicinal chemistry letters (2011-06-21)
Takeji Takamura-Enya, Ryoko Ishii
RESUMEN

BODIPY-modified 2'-deoxyguanosine was synthesized for use as a detection reagent for genotoxic compounds. BODIPY-FL is a well known fluorescence reagent whose fluorescent light emission diminishes near a guanine base by a photo-induced electron transfer process. We attached BODIPY-Fl to the 5' position of the deoxyribose moiety of 2'-deoxyguanosine. Although this compound has low fluorescence activity, when depurination by the action of alkylating reagents and dG oxidation by singlet oxygen occurred, the emission of strong fluorescence was observed. BODIPY-dG was found, therefore, to be a very useful tool for selectively detecting DNA damaging activity particularly in natural environmental extracts.

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Sigma-Aldrich
2′-Deoxyguanosine monohydrate, 99-100%