药物发现
天然产物
加合物
化学空间
化学
计算生物学
组合化学
生物
生物化学
有机化学
作者
Nicholas A. Zill,Yongle Du,Samantha Marinkovich,Di Gu,Jeremy Seidel,Wenjun Zhang
标识
DOI:10.1021/acschembio.3c00083
摘要
The discovery of bioactive natural products lies at the forefront of human medicine. The continued discovery of these molecules is imperative in the fight against infection and disease. While natural products have historically dominated the drug market, discovery in recent years has slowed significantly, partly due to limitations in current discovery methodologies. This work demonstrates a new workflow, deuterium adduct bioactivity screening (DABS), which pairs untargeted isotope labeling with whole cell binding assays for bioactive natural product discovery. DABS was validated and led to the discovery of a new isoprenyl guanidine alkaloid, zillamycin, which showed anti-cancer and anti-microbial activities. DABS thus represents a new workflow to accelerate discovery of natural products with a wide range of bioactive potentials.
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