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 language | English |
|---|---|
| Article number | 1777 |
| Pages (from-to) | 1-19 |
| Number of pages | 19 |
| Journal | Molecules (Basel, Switzerland) |
| Volume | 28 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 2 Feb 2023 |
Bibliographical note
This article belongs to the Special Issue: Fragment-to-Lead Optimization in Drug DiscoveryFunding
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”).
| Funders | Funder number |
|---|---|
| Nederlandse Organisatie voor Wetenschappelijk Onderzoek | 18019 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- biomass
- CyreneTM
- drug discovery
- fragment-based drug discovery
- organic synthesis
- sustainability
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