Green Drug Discovery: Novel Fragment Space from the Biomass-Derived Molecule Dihydrolevoglucosenone (CyreneTM)

Tom Dekker, Jaap W. Harteveld, Gábor Wágner, Max C.M. de Vries, Hans Custers, Andrea C. van de Stolpe, Iwan J.P. de Esch, Maikel Wijtmans

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Biomass-derived molecules can provide a basis for sustainable drug discovery. However, their full exploration is hampered by the dominance of millions of old-fashioned screening compounds in classical high-throughput screening (HTS) libraries frequently utilized. We propose a fragment-based drug discovery (FBDD) approach as an efficient method to navigate biomass-derived drug space. Here, we perform a proof-of-concept study with dihydrolevoglucosenone (CyreneTM), a pyrolysis product of cellulose. Diverse synthetic routes afforded a 100-membered fragment library with a diversity in functional groups appended. The library overall performs well in terms of novelty, physicochemical properties, aqueous solubility, stability, and three-dimensionality. Our study suggests that Cyrene-based fragments are a valuable green addition to the drug discovery toolbox. Our findings can help in paving the way for new hit drug candidates that are based on renewable resources.

Original languageEnglish
Article number1777
Pages (from-to)1-19
Number of pages19
JournalMolecules (Basel, Switzerland)
Volume28
Issue number4
DOIs
Publication statusPublished - 2 Feb 2023

Bibliographical note

This article belongs to the Special Issue: Fragment-to-Lead Optimization in Drug Discovery

Funding

This work was partially funded by the Dutch Research Council under Applied and Engineering Sciences grant number 18019 (“Ready for growth: a new generation of highly versatile fragment libraries”).

FundersFunder number
Nederlandse Organisatie voor Wetenschappelijk Onderzoek18019

    Keywords

    • biomass
    • CyreneTM
    • drug discovery
    • fragment-based drug discovery
    • organic synthesis
    • sustainability

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