## Abstract The compounds (I)β(III) are screened for their antiviral activity against hepatitis B virus.
Synthesis and antiviral activity of new substituted pyrimidine glycosides
β Scribed by Mahmoud M. M. Ramiz; Wael A. El-Sayed; Ezzat Hagag; Adel A.-H. Abdel-Rahman
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2011
- Tongue
- English
- Weight
- 192 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.686
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β¦ Synopsis
Abstract
A number of Nβsubstituted pyrimidine glycosides were synthesized by coupling reaction of the pyrimidine base with acetobromosugars followed by deprotection. The synthesized compounds were tested for their antiviral activity against Hepatitis B Virus (HBV). Plaque reduction infectivity assay was used to determine virus count reduction as a result of treatment with tested compounds which showed moderate to high anti viral activities. J. Heterocyclic Chem., (2011).
π SIMILAR VOLUMES
5'-O-[N-(Anhacyl w imtxy~yJ)sulfi~noyl]uridines 4a+ 5a-e and 5'4-[N~isopoprl)sulh~yI]~ytibs 7-9 have been 8 -d and testcd againat herpes simplex Virus rype 2. condensation of 2',3'-0-isoproWlide-nv5'4-sulfamoyluridim with the N-hydmxysuccinimide esters of Boc-GIy, Boc-LA4 Boc-D-Ah and Boc-LPhe, gave
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
## Abstract magnified image Some molecular modifications were attempted to find antiviral active compounds in the class of triarylmethanes against herpes simplex virus type 1 (HSVβ1). All the synthesized compounds were evaluated for antiviral activity with HSVβ1 by a plaque reduction assay. Some of
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