| Literature DB >> 25614455 |
Jin-Ching Lee1, Chin-Kai Tseng2, Yu-Hsuan Wu3, Neerja Kaushik-Basu4, Chun-Kuang Lin5, Wei-Chun Chen6, Huey-Nan Wu7.
Abstract
Dengue virus (DENV) is a severe mosquito-borne viral pathogen. Neither vaccines nor antiviral therapy is currently available to treat DENV infection. Nucleoside inhibitors targeting viral polymerase have proved promising for the development of drugs against viruses. In this study, we report a nucleoside analog, 2'-C-methylcytidine (2CMC), which exerts potent anti-DENV activity in DENV subgenomic RNA replicon and infectious systems, with an IC50 value of 11.2±0.3μM. This study utilized both cell-based and cell-free reporter assay systems to reveal the specific anti-DENV RNA polymerase activity of 2CMC. In addition, both xenograft bioluminescence-based DENV replicon and DENV-infected Institute of Cancer Research (ICR) suckling mice models evaluated the anti-DENV replication activity of 2CMC in vivo. Collectively, these findings provide a promising compound for the development of direct-acting antivirals against DENV infection.Entities:
Keywords: 2′-C-methylcytidine; Dengue virus; RNA polymerase
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Year: 2015 PMID: 25614455 DOI: 10.1016/j.antiviral.2015.01.002
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970