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Synthesis and DNA topoisomerase-II inhibitory activity of unnatural nucleosides
The synthesis and biological activities of a number of unnatural nucleosides (23-43) is described. Nucleosides have been synthesized by SnCl4-catalyzed condensation of amino sugar acetates and silylated modified pyrimidines. Few of the 2'-O-acetyl derivatives of the nucleosides were hydrolyzed...
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Published in: | Nucleosides, nucleotides & nucleic acids nucleotides & nucleic acids, 2005, Vol.24 (1), p.15-35 |
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container_title | Nucleosides, nucleotides & nucleic acids |
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creator | Mishra, Ram Chandra Dwivedi, Namrata Rama, Pati Tripathi Bansal, Iti Saxena, Jitendra Kumar |
description | The synthesis and biological activities of a number of unnatural nucleosides (23-43) is described. Nucleosides have been synthesized by SnCl4-catalyzed condensation of amino sugar acetates and silylated modified pyrimidines. Few of the 2'-O-acetyl derivatives of the nucleosides were hydrolyzed to the respective hydroxy derivatives by treatment with methanol saturated with ammonia. The compounds were screened against Filarial DNA-topoisomerase-II but only one of the compounds (29) inhibited this enzyme at 40 microg/mL of reaction mixture. |
doi_str_mv | 10.1081/NCN-200046776 |
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subjects | Acetates - chemistry Ammonia - chemistry Catalysis Hydrolysis Methanol - chemistry Nucleosides - chemical synthesis Nucleosides - chemistry Nucleosides - metabolism Pyrimidines - chemistry Tin Compounds - chemistry Topoisomerase II Inhibitors |
title | Synthesis and DNA topoisomerase-II inhibitory activity of unnatural nucleosides |
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