硝基还原酶
生物催化
药物发现
组合化学
化学
芳基
苯胺
酶
生物化学
催化作用
有机化学
反应机理
烷基
作者
Lauren Holder,Eda Yuce,Gabriel Oriomah,Alec Jenkins,Jóhannes Reynisson,Anja Winter,Sebastian C. Cosgrove
标识
DOI:10.1002/cbic.202400428
摘要
Biocatalysis has played a limited role in the early stages of drug discovery. This is often attributed to the limited substrate scope of enzymes not affording access to vast areas of novel chemical space. Here, we have shown a promiscuous nitroreductase enzyme (NR‐55) can be used to produce a panel of functionalised anilines from a diverse panel of aryl nitro starting materials. After screening on analytical scale, we show that sixteen substrates could be scaled to 1 mmol scale, with several poly‐functional anilines afforded with ease under the standard conditions. The aniline products were also screened for activity against several cell lines of interest, with modest activity observed for one compound. This study demonstrates the potential for nitroreductase biocatalysis to provide access to functional fragments under benign conditions.
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