| Literature DB >> 16290162 |
Agnieszka Szymańska1, Marzena Szymczak, Jerzy Boryski, Jacek Stawiński, Adam Kraszewski, Gabriella Collu, Giseppina Sanna, Gabriele Giliberti, Roberta Loddo, Paolo La Colla.
Abstract
Aryl nucleoside 5'-H-phosphonates 4 bearing AZT or 2',3'-dideoxyuridine moieties were subjected to reaction with various aromatic aldehydes to produce nucleoside 5'-alpha-hydroxyphosphonate derivatives 2 as potential anti-HIV agents. Stability of the title compounds in cell culture media was investigated and three distinct decomposition pathways were identified. The anti-HIV activity of hydroxyphosphonates 2 correlates well with the type and extent of their chemical or enzymatic degradation in culture medium (RPMI 1640 containing 10% FBS), suggesting that aryl nucleoside 5'-hydroxyphosphonates 2 act as depot forms of the parent antiviral nucleosides.Entities:
Mesh:
Substances:
Year: 2005 PMID: 16290162 DOI: 10.1016/j.bmc.2005.10.048
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641