Synthesis of Pyridyl-4-Oxy-Substituted N-Hydroxy Amides of Cinnamic Acid as New Inhibitors of Histone Deacetylase Activity and Hepatitis C Virus Replication
- 作者: Kozlov M.1, Malikova A.1, Kamarova K.1, Konduktorov K.1, Kochetkov S.1
-
隶属关系:
- Engelhardt Institute of Molecular Biology
- 期: 卷 44, 编号 4 (2018)
- 页面: 453-460
- 栏目: Article
- URL: https://journals.rcsi.science/1068-1620/article/view/228984
- DOI: https://doi.org/10.1134/S1068162018040118
- ID: 228984
如何引用文章
详细
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.
作者简介
M. Kozlov
Engelhardt Institute of Molecular Biology
编辑信件的主要联系方式.
Email: kozlovmavi@gmail.com
俄罗斯联邦, Moscow, 119991
A. Malikova
Engelhardt Institute of Molecular Biology
Email: kozlovmavi@gmail.com
俄罗斯联邦, Moscow, 119991
K. Kamarova
Engelhardt Institute of Molecular Biology
Email: kozlovmavi@gmail.com
俄罗斯联邦, Moscow, 119991
K. Konduktorov
Engelhardt Institute of Molecular Biology
Email: kozlovmavi@gmail.com
俄罗斯联邦, Moscow, 119991
S. Kochetkov
Engelhardt Institute of Molecular Biology
Email: kozlovmavi@gmail.com
俄罗斯联邦, Moscow, 119991