Synthesis and biological evaluation of N-acetylneuraminic acid-based rotavirus inhibitors

被引:62
作者
Kiefel, MJ
Beisner, B
Bennett, S
Holmes, ID
vonItzstein, M
机构
[1] MONASH UNIV,VICTORIAN COLL PHARM,DEPT MED CHEM,PARKVILLE,VIC 3052,AUSTRALIA
[2] UNIV MELBOURNE,DEPT MICROBIOL,PARKVILLE,VIC 3052,AUSTRALIA
关键词
D O I
10.1021/jm950611f
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Rotavirus can cause several gastrointestinal disease, especially in infants and young children, and is particularly prevalent in Third-World countries. Therefore, the development of potential inhibitors of this virus is of great interest. The present study describes the synthesis and in vitro biological evaluation of a number of N-acethyneuraminic acid-based compounds as potential rotavirus inhibitors. Our data suggests that it is indeed possible to inhibit adhesion of the virus, and hence in vitro replication, with carbohydrate-based molecules, although this inhibition, dues appear to be strain dependent.
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页码:1314 / 1320
页数:7
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