Literature DB >> 16290162

Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 5'-alpha-hydroxyphosphonates.

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.

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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


  2 in total

Review 1.  H-Phosphonate Chemistry in the Synthesis of Electrically Neutral and Charged Antiviral and Anticancer Pronucleotides.

Authors:  Adam Kraszewski; Michal Sobkowski; Jacek Stawinski
Journal:  Front Chem       Date:  2020-11-13       Impact factor: 5.221

2.  Lewis acid-catalyzed Pudovik reaction-phospha-Brook rearrangement sequence to access phosphoric esters.

Authors:  Jin Yang; Dang-Wei Qian; Shang-Dong Yang
Journal:  Beilstein J Org Chem       Date:  2022-09-09       Impact factor: 2.544

  2 in total

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