Literature DB >> 20183611

Synthesis and antiviral evaluation of 2'-C-methyl analogues of 5-alkynyl- and 6-alkylfurano- and pyrrolo[2,3-d]pyrimidine ribonucleosides.

Piotr Januszczyk1, Joanna Fogt, Jerzy Boryski, Kunisuke Izawa, Tomoyuki Onishi, Johan Neyts, Erik De Clercq.   

Abstract

A series of novel 2'-C-methylribonucleosides, involving 5-iodo and 5-alkynyl uridine analogues as well as related bicyclic furano- and pyrrolo[2,3-d]pyrimidinone compounds, has been synthesized and evaluated for their inhibitory effect on replication of the hepatitis C virus (HCV). The new nucleoside analogues did not show meaningful anti-HCV activity.

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Year:  2009        PMID: 20183611     DOI: 10.1080/15257770903128870

Source DB:  PubMed          Journal:  Nucleosides Nucleotides Nucleic Acids        ISSN: 1525-7770            Impact factor:   1.381


  1 in total

1.  Continuous-flow retro-Diels-Alder reaction: an efficient method for the preparation of pyrimidinone derivatives.

Authors:  Imane Nekkaa; Márta Palkó; István M Mándity; Ferenc Fülöp
Journal:  Beilstein J Org Chem       Date:  2018-02-01       Impact factor: 2.883

  1 in total

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