DESIGN, SYNTHESIS AND ANTIVIRAL ACTIVITY OF ALPHA-L-ARABINOFURANOSYL DERIVATIVES OF 2-SUBSTITUTED-5,6-DICHLOROBENZIMIDAZOLES

Citation
Jl. Girardet et al., DESIGN, SYNTHESIS AND ANTIVIRAL ACTIVITY OF ALPHA-L-ARABINOFURANOSYL DERIVATIVES OF 2-SUBSTITUTED-5,6-DICHLOROBENZIMIDAZOLES, Nucleosides & nucleotides, 17(12), 1998, pp. 2389-2401
Citations number
28
Categorie Soggetti
Biology
Journal title
ISSN journal
07328311
Volume
17
Issue
12
Year of publication
1998
Pages
2389 - 2401
Database
ISI
SICI code
0732-8311(1998)17:12<2389:DSAAAO>2.0.ZU;2-X
Abstract
A number of ichloro-1-(alpha-L-arabinofuranosyl)benzimidazoles have be en prepared by condensation of 2-bromo-5,6-dichlorobenzimidazole or 2, 5,6-trichlorobenzimidazole with tetra-O-acetyl-L-arabinofuranose. 2-Al kylamino derivatives were prepared by a substitution of the 2-chloro g roup with the appropriate amines. All target compounds were evaluated for activity against HCMV and HSV-1. The 2-chloro and 2-bromo derivati ves showed moderate activity against HCMV at non-cytotoxic concentrati ons.