Synthesis and Anti-H5N1 Activity of Substituted Pyridine Glycosides and (Oxadiazolyl)oxymethylpyridine Acyclic C-Nucleoside Analogues
- Авторлар: Soliman H.1, Kotb E.1, El-Bayaa M.1, Kutkat O.2, Abdel-Magied F.1
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Мекемелер:
- Photochemistry Department
- Environmental Research Division
- Шығарылым: Том 88, № 4 (2018)
- Беттер: 815-824
- Бөлім: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222157
- DOI: https://doi.org/10.1134/S1070363218040291
- ID: 222157
Дәйексөз келтіру
Аннотация
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.
Негізгі сөздер
Авторлар туралы
H. Soliman
Photochemistry Department
Email: emankotb60@hotmail.com
Египет, Dokki, Giza, 12622
E. Kotb
Photochemistry Department
Хат алмасуға жауапты Автор.
Email: emankotb60@hotmail.com
Египет, Dokki, Giza, 12622
M. El-Bayaa
Photochemistry Department
Email: emankotb60@hotmail.com
Египет, Dokki, Giza, 12622
O. Kutkat
Environmental Research Division
Email: emankotb60@hotmail.com
Египет, Dokki, Cairo, 12622
F. Abdel-Magied
Photochemistry Department
Email: emankotb60@hotmail.com
Египет, Dokki, Giza, 12622