| Literature DB >> 11886808 |
A Cipollone1, M Berettoni, M Bigioni, M Binaschi, C Cermele, E Monteagudo, L Olivieri, D Palomba, F Animati, C Goso, C A Maggi.
Abstract
Several observations highlight the importance of the carbohydrate moiety for the biological activity of antitumoural anthracyclines. Here is reported the synthesis, cytotoxicity and topoisomerase II-mediated DNA cleavage intensity of the new oligosaccharide anthracyclines 1--4 modified in the sugar residue. Evaluation of cytotoxic potency on different cell lines, resulted in quite similar values among the different analogues. On the other hand, topoisomerase II-mediated DNA breaks level was different for the various compounds, and was not related to cytotoxicity, thus supporting previous observations reported for some monosaccharide anthracyclines modified in the carbohydrate portion.Entities:
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Year: 2002 PMID: 11886808 DOI: 10.1016/s0968-0896(01)00411-4
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641