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Synthesis of Pyridyl-4-Oxy-Substituted N-Hydroxy Amides of Cinnamic Acid as New Inhibitors of Histone Deacetylase Activity and Hepatitis C Virus Replication
Authors:M. V. Kozlov  A. Z. Malikova  K. A. Kamarova  K. A. Konduktorov  S. N. Kochetkov
Affiliation:1.Engelhardt Institute of Molecular Biology,Russian Academy of Sciences,Moscow,Russia
Abstract:Three structural isomers of pyridyl-4-oxy-substituted N-hydroxy amides of cinnamic acid (PyOCHA) have been synthesized for the first time. The relationship between their antiviral activity against hepatitis C virus (HCV) and inhibition of histone deacetylases of different cellular localization has been studied.
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