Department of Chemical Biology, Max Planck Institute of Molecular Physiology, Dortmund, Germany.
Technical University Dortmund, Faculty of Chemistry and Chemical Biology, Dortmund, Germany.
Nat Commun. 2021 Mar 25;12(1):1883. doi: 10.1038/s41467-021-22174-4.
Natural product structure and fragment-based compound development inspire pseudo-natural product design through different combinations of a given natural product fragment set to compound classes expected to be chemically and biologically diverse. We describe the synthetic combination of the fragment-sized natural products quinine, quinidine, sinomenine, and griseofulvin with chromanone or indole-containing fragments to provide a 244-member pseudo-natural product collection. Cheminformatic analyses reveal that the resulting eight pseudo-natural product classes are chemically diverse and share both drug- and natural product-like properties. Unbiased biological evaluation by cell painting demonstrates that bioactivity of pseudo-natural products, guiding natural products, and fragments differ and that combination of different fragments dominates establishment of unique bioactivity. Identification of phenotypic fragment dominance enables design of compound classes with correctly predicted bioactivity. The results demonstrate that fusion of natural product fragments in different combinations and arrangements can provide chemically and biologically diverse pseudo-natural product classes for wider exploration of biologically relevant chemical space.
天然产物结构和基于片段的化合物开发通过给定的天然产物片段集的不同组合来启发伪天然产物设计,以产生预期在化学和生物学上具有多样性的化合物类别。我们描述了将片段大小的天然产物奎宁、奎尼丁、青藤碱和灰黄霉素与色酮或吲哚片段进行合成组合,以提供一个包含 244 个成员的伪天然产物集合。化学信息学分析表明,由此产生的八个伪天然产物类别在化学上具有多样性,并具有药物和天然产物的共同特性。通过细胞染色进行无偏生物评估表明,伪天然产物、导向天然产物和片段的生物活性不同,并且不同片段的组合主导着独特生物活性的确立。表型片段优势的鉴定能够设计出具有正确预测生物活性的化合物类别。结果表明,不同组合和排列的天然产物片段融合可以提供化学和生物学上具有多样性的伪天然产物类别,从而更广泛地探索具有生物学相关性的化学空间。