Aurintricarboxylic acid inhibits influenza virus neuraminidase

Hui Chen Hung, Ching Ping Tseng, Jinn Moon Yang, Yi Wei Ju, Sung Nain Tseng, Yen Fu Chen, Yu Sheng Chao, Hsing Pang Hsieh, Shin Ru Shih, John T.A. Hsu

研究成果: Article同行評審

90 引文 斯高帕斯(Scopus)

摘要

There is a continuing threat that the highly pathogenic avian influenza virus will cause future influenza pandemics. In this study, we screened a library of compounds that are biologically active and structurally diverse for inhibitory activity against influenza neuraminidase (NA). We found that aurintricarboxylic acid (ATA) is a potent inhibitor of NA activity of both group-1 and group-2 influenza viruses with IC50s (effective concentration to inhibit NA activity by 50%) values at low micromolar concentrations. ATA was equally potent in inhibiting the NA activity derived from wild-type NA and its H274Y mutant which renders NA resistance to inhibition by oseltamivir. Although ATA is structurally distinct from sialic acid, molecular modeling experiments suggested that ATA binds to NA at the enzyme's substrate binding site. These results indicate that ATA may be a good starting material for the design of a novel class of NA inhibitors for the treatment influenza viruses.

原文English
頁(從 - 到)123-131
頁數9
期刊Antiviral Research
81
發行號2
DOIs
出版狀態Published - 2009 二月

All Science Journal Classification (ASJC) codes

  • Pharmacology
  • Virology

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