1. Academic Validation
  2. Inhibition of adenovirus replication by a trisubstituted piperazin-2-one derivative

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

  • Antiviral Res. 2014 Aug:108:65-73. doi: 10.1016/j.antiviral.2014.05.010.
Javier Sanchez-Cespedes 1 Crystal L Moyer 1 Landon R Whitby 2 Dale L Boger 2 Glen R Nemerow 3
Affiliations

Affiliations

  • 1 Department of Immunology and Microbial Science, The Scripps Research Institute, 10550 N. Torrey Pines Road, Mailcode IMM4, La Jolla, CA 92037, USA.
  • 2 Department of Chemistry, The Scripps Research Institute, 10550 N. Torrey Pines Road, Mailcode BCC483, La Jolla, CA 92037, USA.
  • 3 Department of Immunology and Microbial Science, The Scripps Research Institute, 10550 N. Torrey Pines Road, Mailcode IMM4, La Jolla, CA 92037, USA. Electronic address: gnemerow@scripps.edu.
Abstract

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.

Keywords

Adenovirus; Antiviral compound; DNA replication inhibitor.

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