Synthesis and Anti-H5N1 Activity of Substituted Pyridine Glycosides and (Oxadiazolyl)oxymethylpyridine Acyclic C-Nucleoside Analogues
- Authors: Soliman H.A.1, Kotb E.R.1, El-Bayaa M.N.1, Kutkat O.M.2, Abdel-Magied F.M.1
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Affiliations:
- Photochemistry Department
- Environmental Research Division
- Issue: Vol 88, No 4 (2018)
- Pages: 815-824
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222157
- DOI: https://doi.org/10.1134/S1070363218040291
- ID: 222157
Cite item
Abstract
New aryl- and heteroaryl-substituted pyridinyl sugar hydrazones and their derivatives, 1,3,4-oxadiazole acyclic C-nucleosides, were synthesized. Novel O-glycoside derivatives of the substituted pyridines were prepared. The antiviral activity against avian influenza H5N1 virus was studied and compounds 5a, 9a, and 14 demonstrated high inhibition activity.
Keywords
About the authors
H. A. Soliman
Photochemistry Department
Email: emankotb60@hotmail.com
Egypt, Dokki, Giza, 12622
E. R. Kotb
Photochemistry Department
Author for correspondence.
Email: emankotb60@hotmail.com
Egypt, Dokki, Giza, 12622
M. N. El-Bayaa
Photochemistry Department
Email: emankotb60@hotmail.com
Egypt, Dokki, Giza, 12622
O. M. Kutkat
Environmental Research Division
Email: emankotb60@hotmail.com
Egypt, Dokki, Cairo, 12622
F. M. E. Abdel-Magied
Photochemistry Department
Email: emankotb60@hotmail.com
Egypt, Dokki, Giza, 12622