部分
化学
立体化学
粘细菌
聚酮
代谢物
生物活性
三肽
组合化学
生物化学
氨基酸
生物
体外
生物合成
酶
细菌
遗传学
作者
Holger Hoffmann,Herbert Kogler,Winfried Heyse,Hans Matter,Michael Caspers,Dietmar Schummer,Christine Klemke‐Jahn,Armin Bauer,Géraldine Pénarier,Laurent Debüssche,Mark Brönstrup
标识
DOI:10.1002/ange.201411377
摘要
Abstract Microbial natural products are a rich source of bioactive molecules to serve as drug leads and/or biological tools. We investigated a little‐explored myxobacterial genus, Nannocystis sp., and discovered a novel 21‐membered macrocyclic scaffold that is composed of a tripeptide and a polyketide part with an epoxyamide moiety. The relative and absolute configurations of the nine stereocenters was determined by NMR spectroscopy, molecular dynamics calculations, chemical degradation, and X‐ray crystallography. The compound, named nannocystin A ( 1 ), was found to inhibit cell proliferation at low nanomolar concentrations through the early induction of apoptosis. The mode of action of 1 could not be matched to that of standard drugs by transcriptional profiling and biochemical experiments. An initial investigation of the structure–activity relationship based on seven analogues demonstrated the importance of the epoxide moiety for high activity.
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