261909-90-4Relevant academic research and scientific papers
Synthesis and Anti-HCV Activity of a Novel 2′,3′-Dideoxy-2′-α-fluoro-2′-β-C-methyl Guanosine Phosphoramidate Prodrug
Yu, Wenquan,Li, Ertong,Lv, Zhigang,Liu, Ke,Guo, Xiaohe,Liu, Yuan,Chang, Junbiao
, p. 682 - 684 (2017)
A novel 2′,3′-dideoxy-2′-α-fluoro-2′-β-C-methyl-6-methoxy guanosine (8) and its phosphoramidate prodrug (1) have been designed and synthesized. Their biological activity was evaluated in both cytotoxicity and cell-based HCV replicon assays. Neither compounds exhibited cytotoxicity up to the highest concentration tested (100 μM) in the Huh-7 cell line. The prodrug (1) displayed nanomolar level antiviral activity (EC50 = 0.39-1.1 μM) against the HCV genotype (GT) 1a, 1b, 2a, and 1b S282T replicons.
HCV POLYMERASE INHIBITORS
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Page/Page column 28; 29, (2013/06/27)
The invention provides compounds of the formula:(I) which are of use in the treatment or prophylaxis of hepatitis C virus infection, and related aspects.
HCV Polymerase Inhibitors
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Paragraph 0147; 0148, (2013/06/26)
The invention provides compounds of the formula: which are of use in the treatment or prophylaxis of hepatitis C virus infection, and related aspects.
