Inhibition of adenovirus replication by a trisubstituted piperazin-2-one derivative

被引:28
作者
Sanchez-Cespedes, Javier [1 ]
Moyer, Crystal L. [1 ]
Whitby, Landon R. [2 ]
Boger, Dale L. [2 ]
Nemerow, Glen R. [1 ]
机构
[1] Scripps Res Inst, Dept Immunol & Microbial Sci, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
关键词
Adenovirus; Antiviral compound; DNA replication inhibitor; TARGETING PROTEIN-PROTEIN; ORGAN TRANSPLANT RECIPIENTS; HUMAN ALPHA-DEFENSINS; ENTRY INHIBITORS; COMBINATORIAL LIBRARIES; CHROMATIN-STRUCTURE; VIRAL-INFECTIONS; ANTIVIRAL DRUGS; GENE-TRANSFER; IN-VITRO;
D O I
10.1016/j.antiviral.2014.05.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The number of disseminated adenovirus (Ad) infections continues to increase mostly due to the growing use of immunosuppressive treatments. Recipients of solid organ or hematopoietic stem cell transplants, mainly in pediatric units, exhibit a high morbidity and mortality due to these infections. Unfortunately, there are no Ad-specific antiviral drugs currently approved for medical use. To address this situation, we used high-throughput screening (HTS) of synthetic small molecule libraries to identify compounds that restrict Ad infection. Among the more than 25,000 compounds screened, we identified a hit compound that significantly inhibited Ad infection. The compound (15D8) is a trisubstituted piperazin-2-one derivative that showed substantial antiviral activity with little or no cytotoxicity at low micromolar concentrations. Compound 15D8 selectively inhibits Ad DNA replication in the nucleus, providing a potential candidate for the development of a new class of antiviral compounds to treat Ad infections. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:65 / 73
页数:9
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