5-Substituted Arabinofuranosyluracil Nucleosides as Antiherpesvirus Agents: From araT to BV-araU
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Springer US
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http://link.springer.com/content/pdf/10.1007/978-1-4615-2824-1_13.pdf
Reference77 articles.
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4. H. Machida, S. Sakata, A. Kuninaka, H. Yoshino, C. Nakayama, and M. Saneyoshi. In vitro antiherpes-viral activity of 5-alkyl derivatives of l-ß-D-arabinofuranosyluracil. Antimicrob. Agents Chemother. 16:158 (1979).
5. H. Machida, A. Kuninaka, H. Yoshino, K. Ikeda, and Y. Mizuno. Antiherpersviral activity and inhibitory action on cell growth of 5-alkenyl derivatives of l-ß-D-arabinofuranosyluracil. Antimicrob. Agents Chemother. 17:1030 (1980).
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1. Synthesis of 4′-Thionucleosides as Antitumor and Antiviral Agents;Chemical and Pharmaceutical Bulletin;2018
2. Anti-herpesvirus activity profile of 4′-thioarabinofuranosyl purine and uracil nucleosides and activity of 1-β-d-2′-fluoro-4′-thioarabinofuranosyl guanine and 2,6-diaminopurine against clinical isolates of human cytomegalovirus;Antiviral Research;1998-08
3. Nucleosides and Nucleotides, Part 144 Synthesis and Antiviral Activity of 5-Substituted (2′S)-2′-Deoxy-2′-C-Methylcytidines and -uridines[1];Archiv der Pharmazie;1996
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