Synthesis and Antiviral Evaluation of Sugar‐Modified Pseudouridine Analogs
The pyrimidine C ‐nucleoside pseudouridine (Ψ) is a ubiquitous RNA modification that enhances the stability, modulates immunogenicity, and influences the biological function of natural and synthetic RNA. Despite its biological importance, the antiviral potential of pseudouridine analogs remains largely unexplored. Furthermore, although several sugar‐modified pseudouridine analogs have been synthesized, a systematic approach to access these derivatives is still lacking. In this study, we present the synthesis of novel pseudouridine analogs with structural modifications at different positions of the carbohydrate moiety.
Authors
- Steven De Jonghe (ORCID: https://orcid.org/0000-0002-3872-6558)
- Eveline Lescrinier (ORCID: https://orcid.org/0000-0001-7066-4329)
- Jef Rozenski (ORCID: https://orcid.org/0000-0001-9624-5536)
- Elisabetta Groaz (ORCID: https://orcid.org/0000-0002-8866-2265)
- Zhiyuan Chen (ORCID: https://orcid.org/0009-0003-2229-2091)
Institutions
- Rega Institute for Medical Research (BE)
Publication Details
- Journal
- European Journal of Organic Chemistry
- Published
- 2026-08-25
- DOI
- https://doi.org/10.1002/ejoc.70799
- Primary Topic
- RNA modifications and cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- China Scholarship Council
- Rega Foundation