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Synthesis of New Nucleoside Analogues from Theobromine

Authors: Thanaa M. Al-Mouamin --- Sumaya J. Abid
Journal: Al-Nahrain Journal of Science مجلة النهرين للعلوم ISSN: (print)26635453,(online)26635461 Year: 2019 Volume: 00 Issue: 2 Pages: 17-29
Publisher: Al-Nahrain University جامعة النهرين


Nucleoside Analogues play important role in different medical drugs,therefor we synthesized new nucleoside analogues using theobromine as a nucleobase, for the first time, by convertion to it's mercury salt, [1]. Then coupled with three kinds of sugar, including (glucose, galactose and mannose), after protection [2-4] and activation as bromo sugar [5-7] afforded blocked nucleoside analogues [8-10] which subsequently hydrolyzed to give our synthetic goal the free nucleoside analogues [11-13]. All prepared compounds were identify by FT-IR and some of them with 1H-NMR spectroscopy. The synthesized compounds (11-13) were screened for their in-vitro antibacterial and antifungal activity.

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