Amantadine analogues - synthesis and biological activity

被引:0
|
作者
Chayrov, R. [1 ]
Mukova, L. [2 ]
Galabov, A. [2 ]
Mitrev, Y. [3 ]
Stankova, I. [1 ]
机构
[1] South West Univ Neofit Rilsky, Dept Chem, Blagoevgrad, Bulgaria
[2] Bulgarian Acad Sci, Stefan Angeloff Inst Microbiol, BU-1113 Sofia, Bulgaria
[3] Ctr Phytochem, Inst Organ Chem, Lab Bulgarian NMR Ctr, Sofia 1113, Bulgaria
来源
关键词
adamantanes; amino asids; amino acid amides; antiviral activity; VIRUSES;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The biological activity of adamantane derivatives is due to the symmetry and steric bulkiness of the structure and the significant lipophilicity of the rigid hydrocarbon framework. This enables them to penetrate easily through biological membranes. Therefore, modification of organic compounds by an adamantyl radical changes significantly their biological activity, often enhancing it. A large number of strains that are completely resistant to amantadine are currently known. The number of resistant influenza strains increases every year because of spontaneous mutations in the virus genome. This necessitates expanded research on the reasons for the development of resistance and ways of overcoming it by creating new antiviral drugs [1].
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页码:61 / 63
页数:3
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