In Vitro Activity of 2,4-Diamino-6-[2-(Phosphonomethoxy)Ethoxy]-Pyrimidine against Multidrug-Resistant Hepatitis B Virus Mutants

  • M. N. Brunelle
    INSERM, U871, 151 Cours Albert Thomas, 69003 Lyon, France
  • J. Lucifora
    INSERM, U871, 151 Cours Albert Thomas, 69003 Lyon, France
  • J. Neyts
    Rega Institute for Medical Research, Katholieke Universiteit Leuven, Leuven, Belgium
  • S. Villet
    INSERM, U871, 151 Cours Albert Thomas, 69003 Lyon, France
  • A. Holy
    Institute of Organic Chemistry and Biochemistry, Academy of Sciences of the Czech Republic, Prague, Czech Republic
  • C. Trepo
    INSERM, U871, 151 Cours Albert Thomas, 69003 Lyon, France
  • F. Zoulim
    INSERM, U871, 151 Cours Albert Thomas, 69003 Lyon, France

書誌事項

公開日
2007-06
権利情報
  • https://journals.asm.org/non-commercial-tdm-license
DOI
  • 10.1128/aac.01440-06
公開者
American Society for Microbiology

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説明

<jats:title>ABSTRACT</jats:title><jats:p>The susceptibilities of drug-resistant hepatitis B virus (HBV) mutants to lamivudine, adefovir, tenofovir, entecavir, and 2,4-diamino-6-[2-(phosphonomethoxy)ethoxy]-pyrimidine (PMEO-DAPym), a novel acyclic pyrimidine analogue, were assessed in vitro. Most drug-resistant mutants, including multidrug-resistant strains, remained sensitive to tenofovir and PMEO-DAPym. Therefore, the latter molecule deserves further evaluation for the treatment of HBV infection.</jats:p>

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