Synthesis and Anti-H5N1 Activity of Substituted Pyridine Glycosides and (Oxadiazolyl)oxymethylpyridine Acyclic C-Nucleoside Analogues
- 作者: Soliman H.1, Kotb E.1, El-Bayaa M.1, Kutkat O.2, Abdel-Magied F.1
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隶属关系:
- Photochemistry Department
- Environmental Research Division
- 期: 卷 88, 编号 4 (2018)
- 页面: 815-824
- 栏目: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222157
- DOI: https://doi.org/10.1134/S1070363218040291
- ID: 222157
如何引用文章
详细
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.
作者简介
H. Soliman
Photochemistry Department
Email: emankotb60@hotmail.com
埃及, Dokki, Giza, 12622
E. Kotb
Photochemistry Department
编辑信件的主要联系方式.
Email: emankotb60@hotmail.com
埃及, Dokki, Giza, 12622
M. El-Bayaa
Photochemistry Department
Email: emankotb60@hotmail.com
埃及, Dokki, Giza, 12622
O. Kutkat
Environmental Research Division
Email: emankotb60@hotmail.com
埃及, Dokki, Cairo, 12622
F. Abdel-Magied
Photochemistry Department
Email: emankotb60@hotmail.com
埃及, Dokki, Giza, 12622