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: Kozlov M.V.1, Malikova A.Z.1, Kamarova K.A.1, Konduktorov K.A.1, Kochetkov S.N.1
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Affiliations:
- Engelhardt Institute of Molecular Biology
- Issue: Vol 44, No 4 (2018)
- Pages: 453-460
- Section: Article
- URL: https://journals.rcsi.science/1068-1620/article/view/228984
- DOI: https://doi.org/10.1134/S1068162018040118
- ID: 228984
Cite item
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.
About the authors
M. V. Kozlov
Engelhardt Institute of Molecular Biology
Author for correspondence.
Email: kozlovmavi@gmail.com
Russian Federation, Moscow, 119991
A. Z. Malikova
Engelhardt Institute of Molecular Biology
Email: kozlovmavi@gmail.com
Russian Federation, Moscow, 119991
K. A. Kamarova
Engelhardt Institute of Molecular Biology
Email: kozlovmavi@gmail.com
Russian Federation, Moscow, 119991
K. A. Konduktorov
Engelhardt Institute of Molecular Biology
Email: kozlovmavi@gmail.com
Russian Federation, Moscow, 119991
S. N. Kochetkov
Engelhardt Institute of Molecular Biology
Email: kozlovmavi@gmail.com
Russian Federation, Moscow, 119991