| Literature DB >> 21822360 |
Abstract
Several N-6 substituted derivatives (4-11) of (+)-4'-deoxy-5'-noraristeromycin (2) and its unsaturated counterpart (3) have been prepared. The derivatives are designed to systematically vary the hydrophobic/hydrophilic balance of the lead compounds. These compounds were evaluated against a large number of viruses but, no significant antiviral activity was observed. Also, no cytotoxicity to host cells was found.Entities:
Year: 2010 PMID: 21822360 PMCID: PMC3149869 DOI: 10.4314/bcse.v24i3.60692
Source DB: PubMed Journal: Bull Chem Soc Ethiop ISSN: 1011-3924 Impact factor: 1.330