摘要

Benzimidazole-based nucleotides and dinucleotides have been synthesised to increase the range of chemical tools available to probe the NAD(+) biology space. They were examined for their reactivity in alkylation-type reactions, where they yielded unstable alkylated heteoaromatic adducts, both chemically and enzymatically. While unsuited for NAD(+) cyclases, these NAD(+) analogues could be viable substrates for non-adenine modifying NAD(+)-dependent enzyme classes.

  • 出版日期2014-10

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