Pseudo‐Natural Products Inspired by Aspidospermidine‐, Strychnos‐, and Koumine Monoterpene Indole Alkaloids Reveal Pyrimidine Biosynthesis Inhibitors

ABSTRACT In pseudo‐natural product (PNP) design, natural product fragments are combined in arrangements not found in nature to afford novel biologically relevant NP‐related compound classes. A pseudo‐natural product compound collection inspired by aspidospermidine‐, strychnos‐, and koumine monoterpene alkaloids was designed and rapidly synthesized to afford a collection of 78 compounds representing eight structurally different PNP classes. Evaluation of the collection for biological relevance by means of the cell painting assay, including a recently reported subprofile analysis, revealed that one of the structural classes is enriched in and defines a new chemotype of de novo pyrimidine biosynthesis inhibitors. Our results exemplify the combination of pseudo‐natural product design and unbiased morphological screening technologies as an efficient means to rapidly access and identify novel biologically relevant chemotypes.

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Publication Details

Journal
Helvetica Chimica Acta
Published
2025-11-08
DOI
https://doi.org/10.1002/hlca.202500155
Citations
1
Primary Topic
Advanced Synthetic Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.94

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article

Pseudo‐Natural Products Inspired by Aspidospermidine‐, Strychnos‐, and Koumine Monoterpene Indole Alkaloids Reveal Pyrimidine Biosynthesis Inhibitors

Axel Pahl, Sonja Sievers, Michael Grigalunas, Annika Schmidt et al.
1 citations
Helvetica Chimica Acta
Advanced Synthetic Organic Chemistry
0.94
article

Pseudo‐Natural Products Inspired by Aspidospermidine‐, Strychnos‐, and Koumine Monoterpene Indole Alkaloids Reveal Pyrimidine Biosynthesis Inhibitors

Axel Pahl, Sonja Sievers, Michael Grigalunas, Annika Schmidt, Carsten Strohmann, Jana Bonowski, Herbert Waldmann, Slava Ziegler, Luca C. Greiner, Animesh Biswas
article en
1 citations

Abstract

ABSTRACT In pseudo‐natural product (PNP) design, natural product fragments are combined in arrangements not found in nature to afford novel biologically relevant NP‐related compound classes. A pseudo‐natural product compound collection inspired by aspidospermidine‐, strychnos‐, and koumine monoterpene alkaloids was designed and rapidly synthesized to afford a collection of 78 compounds representing eight structurally different PNP classes. Evaluation of the collection for biological relevance by means of the cell painting assay, including a recently reported subprofile analysis, revealed that one of the structural classes is enriched in and defines a new chemotype of de novo pyrimidine biosynthesis inhibitors. Our results exemplify the combination of pseudo‐natural product design and unbiased morphological screening technologies as an efficient means to rapidly access and identify novel biologically relevant chemotypes.

Helvetica Chimica ActaVol. 108(12)
TU Dortmund University (DE), Fraunhofer Institute for Translational Medicine and Pharmacology (DE), Max Planck Institute of Molecular Physiology (DE)
European Federation of Pharmaceutical Industries and Associations, European Commission, Max-Planck-Gesellschaft, European Regional Development Fund
Openalex Percentile: Top 20%
Advanced Synthetic Organic Chemistry
0.94
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