Literature DB >> 12459010

A thymidine phosphorylase-stable analogue of BVDU with significant antiviral activity.

Sven Guenther1, Jan Balzarini, Erik De Clercq, Vasu Nair.   

Abstract

(E)-5-(2-Bromovinyl)isodideoxyuridine (BVisoDDU), synthesized on the basis of molecular modeling, is selectively active against HSV-1 (three different strains) but inactive against HSV-2. Unlike BVDU, BVisoDDU is completely resistant to cleavage by thymidine phosphorylase. BVisoDDU is also the first nucleoside analogue lacking OH groups at both the 2'- and 3'-position that shows pronounced activity against HSV-1 replication.

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Year:  2002        PMID: 12459010     DOI: 10.1021/jm025569k

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  2 in total

1.  Base-functionalized carbocyclic nucleosides: design, synthesis, and mechanism of antiviral activity.

Authors:  Vasu Nair; Fan Zhang; Xiaohui Ma; Eric Bonsu
Journal:  Nucleosides Nucleotides Nucleic Acids       Date:  2009-05       Impact factor: 1.381

2.  Synthesis and anti-HIV activity of D- and L-thietanose nucleosides.

Authors:  Hyunah Choo; Xin Chen; Vikas Yadav; Jianing Wang; Raymond F Schinazi; Chung K Chu
Journal:  J Med Chem       Date:  2006-03-09       Impact factor: 7.446

  2 in total

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