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Nucleoside dimers analogues with a 1,2,3-triazole linkage: conjugation of floxuridine and thymidine provides novel tools for cancer treatment. Part II
Authors:Dagmara Baraniak  Daniel Baranowski  Piotr Ruszkowski  Jerzy Boryski
Affiliation:1. Institute of Bioorganic Chemistry, Polish Academy of Sciences, Poznań, Poland;2. baraniak@ibch.poznan.pl;4. Department of Pharmacology, Faculty of Pharmacy, Poznań University of Medical Sciences, Poznań, Poland
Abstract:Abstract

The fluorinated nucleoside dimers with a 1,2,3-triazole linkage are novel compounds within the field of bioorganic chemistry. We report on the synthesis and properties of two groups of nucleoside dimers analogs possessing a different arrangement of the 1,4-disubstituted 1,2,3-triazole linkage. Based on analysis of the 3JHH, 3JH1′C2, and 3JH1′C6 we estimated conformational preferences of sugar part and orientation around glycosidic bond. These compounds show moderate anticancer activity, with cytostatic studies in three different cancer cell lines.
Keywords:Floxuridine  nucleoside dimers derivatives  1,3-dipolar cycloaddition  cancer therapy
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