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Bioorg Med Chem ; 24(12): 2716-24, 2016 06 15.
Article in English | MEDLINE | ID: mdl-27157005

ABSTRACT

Seventeen silyl- and trityl-modified (5'-O- and 3',5'-di-O-) nucleosides were synthesized with the aim of investigating the in vitro antiproliferative activities of these nucleoside derivatives. A subset of the compounds was evaluated at a fixed concentration of 100µM against a small panel of tumor cell lines (HL-60, K-562, Jurkat, Caco-2 and HT-29). The entire set was also tested at varying concentrations against two human glioma lines (U373 and Hs683) to obtain GI50 values, with the best results being values of ∼25µM.


Subject(s)
Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacology , Cell Proliferation/drug effects , Nucleosides/chemistry , Nucleosides/pharmacology , Antineoplastic Agents/chemical synthesis , Cell Line, Tumor , Humans , Neoplasms/drug therapy , Nucleosides/chemical synthesis , Structure-Activity Relationship
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