Literature DB >> 10788594

Design and evaluation of hepatitis B virus inhibitors.

O Hantz1, J L Kraus, F Zoulim.   

Abstract

Antiviral therapy of chronic hepatitis B remains a major clinical problem worldwide. The design of new nucleoside analogs that inhibit hepatitis B virus (HBV) replication allowed their evaluation in in vitro and in vivo experimental models of HBV infection. This research has led to the discovery of the anti-HBV activity of lamivudine and its approval for the therapy of chronic hepatitis B. However, due to the development of viral resistance, strategies based on the combination of new inhibitors of HBV replication with immune modulatory approaches are urgently required.

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Year:  2000        PMID: 10788594     DOI: 10.2174/1381612003400740

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  2 in total

1.  Effects of two novel nucleoside analogues on different hepatitis B virus promoters.

Authors:  Xing-Xing He; Ju-Sheng Lin; Ying Chang; Ying-Hui Zhang; Yan Li; Xiao-Yan Wang; Dong Xu; Xiao-Ming Cheng
Journal:  World J Gastroenterol       Date:  2008-03-28       Impact factor: 5.742

2.  The optimal threshold: Baseline serum hepatitis B virus DNA and alanine transaminase levels can predict the 2-Year on-treatment virological response to lamivudine.

Authors:  Jie Yan; Wen Xie; Qi Wang; Yue Li; Xing Feng; Jun Cheng
Journal:  Hepat Mon       Date:  2011-05       Impact factor: 0.660

  2 in total

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