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Facile access to 4′-(<i>N</i>-acylsulfonamide) modified nucleosides and evaluation of their inhibitory activity against SARS-CoV-2 RNA cap <i>N</i>7-guanine-methyltransferase nsp14

Romain Amador, Adrien Delpal, Bruno Canard, Jean‐Jacques Vasseur, Étienne Decroly, Françoise Debart, Guillaume Clavé, Michaël Smietana

2022Organic & Biomolecular Chemistry15 citationsDOI

Abstract

4′-( N -Acylsulfonamide) adenosine derivatives have been efficiently synthetized via the sulfo-click reaction and their biological activity has been evaluated as potential inhibitors of the SARS-CoV-2 RNA cap N 7-guanine- methyltransferase nsp14.

Topics & Concepts

ChemistrySulfonamideSynthonMoietyGuanineNucleosideAcylationRNAStereochemistryMethyltransferaseCombinatorial chemistryBiochemistryNucleotideDNACatalysisMethylationGeneHIV/AIDS drug development and treatmentCRISPR and Genetic EngineeringSulfur-Based Synthesis Techniques
Facile access to 4′-(<i>N</i>-acylsulfonamide) modified nucleosides and evaluation of their inhibitory activity against SARS-CoV-2 RNA cap <i>N</i>7-guanine-methyltransferase nsp14 | Litcius