Journal
ORGANIC LETTERS
Volume 25, Issue 21, Pages 3961-3966Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.3c01391
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In this study, a poststage synthetic protocol for accessing novel ADP-2''-deoxyribosylderivatives through designing a light-induced biomimetic reaction was reported, and SPR assays revealed effective binding of ADP-2''-deoxyribosylpeptides to MacroH2A1.1 with a high affinity (K(D) = 3.75 x 10(-6) M).
Modifications on the hydroxyl groups of ADP-ribosyl unitscan providevaluable tools for investigating ADP-ribosylation-related molecularinteractions, but the chemical syntheses of these compounds are usuallydifficult due to their inherent complex structures. In this study,we report a poststage synthetic protocol for accessing novel ADP-2 ''-deoxyribosylderivatives through designing a light-induced biomimetic reaction,and SPR assays revealed effective binding of ADP-2 ''-deoxyribosylpeptides to MacroH2A1.1 with a high affinity (K (D) = 3.75 x 10(-6) M).
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