Synthesis and Cytotoxicity Evaluation of Phosphorylated Derivatives of Ribavirin

Novel phosphorylated derivatives of ribavirin 5-16 were synthesized by the reaction of 4-nitrophenyl phosphorodichloridate with various amino acid esters in the presence of triethylamine in dry tetrahydrofuran through the intermediates 3. On further reaction of 3 with ribavirin in THF and pyridine i...

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Veröffentlicht in:Journal of the Korean Chemical Society 2011, 55(6), , pp.952-959
Hauptverfasser: Rao, Valasani Koteswara, Reddy, Sanapalli Subba, Babu, Kilaru Raveendra, Kumar, Kuntrapakam Hema, Ghosh, Sunil Kumar, Raju, Chamarthi Naga
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Sprache:eng
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Zusammenfassung:Novel phosphorylated derivatives of ribavirin 5-16 were synthesized by the reaction of 4-nitrophenyl phosphorodichloridate with various amino acid esters in the presence of triethylamine in dry tetrahydrofuran through the intermediates 3. On further reaction of 3 with ribavirin in THF and pyridine in the presence of TEA afforded the title compounds 5-16. Their structures were characterized by IR, ^1H, ^13C, ^31P NMR and mass spectral analyses. All the title compounds were found to exhibit potent in vitro anticancer activity against MCF-7 breast cancer cell lines. KCI Citation Count: 0
ISSN:1017-2548
2234-8530
DOI:10.5012/jkcs.2011.55.6.952