化学
化学
天然产物
药物发现
化学空间
化学生物学
组合化学
计算生物学
生物化学
生物
作者
Luca C. Greiner,Axel Pahl,Anna Lina Heinzke,Barbara Zdrazil,Andrew R. Leach,Robert J. Young,Paul D. Leeson,Herbert Waldmann
标识
DOI:10.1021/acs.jmedchem.5c00643
摘要
Natural product (NP) structures have provided invaluable inspiration for the discovery of bioactive compound discovery. In the pseudonatural product (PNP) concept unprecedented combinations of NP fragments combine the biological relevance of NPs with exploration of wider chemical space by fragment-based design. We describe the principles underlying the PNP design and discovery of selected PNPs with unexpected or novel bioactivity. Cheminformatic analyses of ChEMBL 32, the Enamine screening library, phase 1-3 clinical compounds, and approved drugs reveal that ca. 1/3 of historically developed biologically active compounds and of currently commercially available screening compounds are PNPs, and that PNPs are increasing over time. PNPs are 54% more likely to be found in clinical compounds versus nonclinical compounds, and 67% of recent clinical compounds are PNPs. 63% of the core scaffolds in recent clinical compounds are made up of just 176 NP fragments, which suggests that PNPs open up a multitude of unexploited opportunities for drug discovery.
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