Analogues of Uridinediphosphatehexoses. A New Type of Protein Glycosylation Inhibitors That Show Antiviral Activity
A series of analogues of UDP-Glc and UDP-GlcNAc prepared by reaction of protected hexoses with ClSO 2 NCO and 2′3′-O-isopropylideneuridine, inhibited glycosylation of proteins in HSV-1 infected HeLa cells and were active against several enveloped viruses.
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Veröffentlicht in: | Nucleosides & nucleotides 1985-02, Vol.4 (1-2), p.149-151 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A series of analogues of UDP-Glc and UDP-GlcNAc prepared by reaction of protected hexoses with ClSO
2
NCO and 2′3′-O-isopropylideneuridine, inhibited glycosylation of proteins in HSV-1 infected HeLa cells and were active against several enveloped viruses. |
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ISSN: | 0732-8311 |
DOI: | 10.1080/07328318508077841 |